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Journal articles on the topic 'Foetal Hemoglobin'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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1

SONIA SEBASTIAN. "A study to assess the effect of maternal hemoglobin level on foetal outcome among antenatal mothers in selected maternity hospitals at Mangalore." World Journal of Biology Pharmacy and Health Sciences 14, no. 1 (2023): 199–209. http://dx.doi.org/10.30574/wjbphs.2023.14.1.0179.

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In developing countries maternal anemia during pregnancy has been reported to increase the risk of unfavorable foetal outcome. According to the standard laid down by WHO, anemia in pregnancy is present when the hemoglobin concentration in the peripheral blood is 11gm\100ml or less. In India its prevalence has been found to be in the range of 50-90% in 3rd trimester of pregnancy according to different studies conducted in rural areas. Maternal anemia in pregnancy is commonly considered as risk factor for poor pregnancy outcome and can threaten the life of mother and foetus. However, the extent

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SONIA, SEBASTIAN. "A study to assess the effect of maternal hemoglobin level on foetal outcome among antenatal mothers in selected maternity hospitals at Mangalore." World Journal of Biology Pharmacy and Health Sciences 14, no. 1 (2023): 199–209. https://doi.org/10.5281/zenodo.8037672.

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In developing countries maternal anemia during pregnancy has been reported to increase the risk of unfavorable foetal outcome. According to the standard laid down by WHO, anemia in pregnancy is present when the hemoglobin concentration in the peripheral blood is 11gm\100ml or less. In India its prevalence has been found to be in the range of 50-90% in 3<sup>rd</sup> trimester of pregnancy according to different studies conducted in rural areas. Maternal anemia in pregnancy is commonly considered as risk factor for poor pregnancy outcome and can threaten the life of mother and foetus. Howe

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3

Dogonzo, Yusuf Ishaya, and Christopher Chimaobi Onyeabor. "How effective are antioxidants without fetal hemoglobin in tackling oxidative stress in sickle cell disease?" Journal of Clinical and Experimental Hematology 3, no. 1 (2024): 40–43. http://dx.doi.org/10.46439/hematol.3.017.

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In our previous work titled “Antioxidative potential of foetal haemoglobin in sickle cell disease”, we reported that fetal hemoglobin correlated directly with antioxidative markers and inversely with markers of oxidative stress in sickle cell subjects. Based on our observations, we concluded that fetal hemoglobin contributes to the cellular antioxidant defense system by limiting the rate of production of reactive oxygen species. In this current report, we aim to highlight the synergy between fetal hemoglobin and the antioxidant defense system in modulating oxidative stress in sickle cell disea

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Kumari, Tanuja, Bharti Archana, and H.P.Dubey. "Study of Relationship between Foetus, Neonatal & Maternal Hemoglobin Level." International Journal of Pharmaceutical and Clinical Research 16, no. 5 (2024): 1841–45. https://doi.org/10.5281/zenodo.12765427.

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<strong>Background:</strong> Maternal haemoglobin levels affect pregnancy outcomes and the mother’s and neonate’s health. This cohort study examined the relationship between the mother’s blood haemoglobin levels over the three trimesters and the neonates at birth. <strong>Methods:</strong> About 200 pregnant Territory Care Centre patients participated in the study. Researchers measured the mother’s haemoglobin in the third trimester. After giving birth, they checked foetal and neonatal cord blood levels. To summarise haemoglobin levels, descriptive statis

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Dulhani, Naveen, Pratima Koshewara, Rupendra K. Bharti, and Sanat K. Sharma. "Prevalence of Hemoglobinopathies in Tribal Region of India: A Retrospective Observational Study." Advances in Bioscience and Clinical Medicine 8, no. 4 (2020): 3. http://dx.doi.org/10.7575/aiac.abcmed.v.8n.4p.3.

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Hemoglobinopathies are the common inherited diseases around the world. Thalassemia & sickle cell disease are the important challenges for tribal populations in India. Many study demonstrated the prevalence of haemoglobinopathies in India & among tribes of India but limited data available from Baster tribal region. This study will further lightens the haemoglobinopathies among Baster region of Chhattisgarh state of India. Methods: It was an retrospective observational study, carried out in Late. BRKM Government Medical College, Dimrapal, Jagdalpur which was located at baster region of C

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Waghela, Sneha, Sujata Sharma, Nikita Shah, Harshada Uchil, and Radha Ghildiyal. "Varied clinical presentation of compound heterozygous thalassemia with delta beta or hereditary persistence of foetal hemoglobin." Pediatric Hematology Oncology Journal 8, no. 1 (2023): 31–33. http://dx.doi.org/10.1016/j.phoj.2023.01.002.

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A., Bhagyashree, Julie Thomas, and Shobha N. Gudi. "A prospective, randomized, cross sectional study of manual versus vacuum extraction of mobile head in caesarean section." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 7, no. 11 (2018): 4556. http://dx.doi.org/10.18203/2320-1770.ijrcog20184507.

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Background: Considering the high rate of caesarean section, and the difficulty during delivery of the floating foetal head even by the most experienced obstetrician, the use of vacuum has been described. The present study was undertaken with the hypothesis that, vacuum assisted foetal head delivery during caesarean section is safe and effective without increasing maternal and neonatal complications. The outcomes enumerated by the limited literature available need to be evaluated before it is used routinely.Methods: A prospective, randomized, comparative, cross sectional Hospital based study wa

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Yadav, Meetu, Pooja T, Sumit Dagar, Arti Dhingra, and Divya Mangla. "Outcome of newborns born to anaemic mother in a rural tertiary care hospital, comparative study." Indian Journal of Public Health Research & Development 16, no. 2 (2025): 191–98. https://doi.org/10.37506/8rd7y767.

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Background: Anemia is one of the most common nutritional deficiency issues in pregnant women. Maternal anemia has been linked (IUGR), LBW, and (PPH). Prematurity, poor Apgar scores, and intrauterine foetal mortality are more likely in anemic pregnant women than in nonanemic pregnant women.5 Maternal anemia increases the odds of preterm delivery and low birth weight of the newborns, which increases foetal morbidity and death.Hence, this study was aimed to assess neonatal outcomes among babies born to anemic mothers in comparison to Non-anemic and to find the correlation between maternal and neo

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Kazi, Asma, Aisha Aziz, Shoaib Ahmed, Sabeena Umer, Shazia Roman, and Faiza Irshad. "Iron Supplementation in Anemic Pregnant Women: A Comparison of Different Prescription Options in Pakistan." Pakistan Journal of Medical and Health Sciences 16, no. 7 (2022): 342–43. http://dx.doi.org/10.53350/pjmhs22167342.

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Background & objectives: Many pregnant women in Pakistan have iron deficiency anemia (IDA), a dietary deficit. It affects both the mother's and the foetal' health. Oral iron supplementation usually relieves IDA symptoms. Oral iron supplements are hazardous to the GI mucosa, and sensitivity is common. Poor therapeutic compliance leads to treatment failure. Ferrous ascorbate (FeA) and iron hydroxide polymaltose complex (IPC) reportedly improve gastrointestinal discomfort and increase patient compliance compared to ferrous sulphate (FS). These preparations reportedly improve hemoglobin levels

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10

Losekoot, M., R. Fodde, EJ Gerritsen, et al. "Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant." Blood 77, no. 4 (1991): 861–67. http://dx.doi.org/10.1182/blood.v77.4.861.861.

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Abstract We report two different disorders of the beta-globin gene cluster segregating in a Belgian family: a novel deletion that results in (G) gamma + ((A) gamma delta beta)(0)-thalassemia (thal) and a heterocellular hereditary persistence of foetal hemoglobin of the Swiss type linked to a delta(0)-thal gene (delta (0)-HPFH). Heterozygosity for the heterocellular HPFH brings about a moderate (3.4% to 8.24%) increase of hemoglobin (Hb) F having a G gamma/A gamma ratio of 4:1, whereas carriers of the G gamma + ((A) gamma delta beta)(0)-thal deletion show in their peripheral blood a considerabl

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11

Losekoot, M., R. Fodde, EJ Gerritsen, et al. "Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant." Blood 77, no. 4 (1991): 861–67. http://dx.doi.org/10.1182/blood.v77.4.861.bloodjournal774861.

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We report two different disorders of the beta-globin gene cluster segregating in a Belgian family: a novel deletion that results in (G) gamma + ((A) gamma delta beta)(0)-thalassemia (thal) and a heterocellular hereditary persistence of foetal hemoglobin of the Swiss type linked to a delta(0)-thal gene (delta (0)-HPFH). Heterozygosity for the heterocellular HPFH brings about a moderate (3.4% to 8.24%) increase of hemoglobin (Hb) F having a G gamma/A gamma ratio of 4:1, whereas carriers of the G gamma + ((A) gamma delta beta)(0)-thal deletion show in their peripheral blood a considerably higher

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12

OSMANA, Yasser, and Mashael ALKHALDIA. "Study of Haemolytic Disease of the Foetus and Newborn with Positive Direct Coomb’s Test in Single Centre." Documenta Haematologica - Revista Romana de Hematologie 2, no. 4 (2024): 167–75. https://doi.org/10.59854/dhrrh.2024.2.4.167.

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Objectives: HDFN is caused by maternal alloantibodies against foetal erythrocytes that might cause morbidity and mortality in the foetus and newborn. Our study aims to investigate the incidence of Haemolytic disease of foetus and newborn (HDFN), Direct Coomb’s test (DCT), cord blood and to identify the eluted antibodies in those patients. Besides, to evaluate the adapted protocol regarding Rosette and Kleihauer Betke test. Methods/Materials: A retrospective study of all newborns with positive DCT using cord blood samples. Descriptive data were analyzed as frequency and percentage or mean and r

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13

Punjaji Tambse, Manjusha, Maya Suresh Vasaikar, and Sunil Santaram Chavan. "Hemoglobin Patterns in Sickle Cell Hemoglobinopathies- A Large Prospective Study in North Maharashtra." MVP Journal of Medical Sciences 4, no. 1 (2017): 84. http://dx.doi.org/10.18311/mvpjms/0/v0/i0/11831.

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Introduction: Sickle cell haemoglobinopathy is an inherited hemoglobinopathy resulting from a mutation occurring in betaglobin gene, on chromosome 11. The gene is prevalent in some tribes of North Maharashtra. The main aim of the study is to determine haemoglobin patterns in cases with sickle cell hemoglobinoathies in North Maharashtra using HPLC testing system. Material and Methods: This is a prospective study done over a period of 6 years. 10081 patients having positive solubility test or negative solubility test but having clinical suspicion of Sickle cell hemoglobinopathies were studied in

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14

Rai, Lata, and Uttara kumar Chaturvedi. "Effect of Punarnavadi Mandoora in the Management of Garbhini Pandu w.s.r to Iron Deficiency Anemia in Pregnancy –A Review." International Research Journal of Ayurveda & Yoga 05, no. 03 (2022): 94–98. http://dx.doi.org/10.47223/irjay.2022.5313.

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India is one of the countries where anaemia during pregnancy is common. Anemia in pregnancy is caused by a various factors. The most common disorder in a pregnant woman is iron deficiency anaemia. Rasa Pradoshaja vikara is a disorder that arises due to inappropriate Rasa Dhatu in the mother and constantly rising foetal demands. According to Ayurvedic classics, for decades, a variety of Lauha preparations have been used to treat anaemia. Punarnava Mandoora is an Ayurvedic preparation that has been described in various Ayurvedic texts. It's a traditional Ayurvedic treatment for a variety of ailm

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15

Asif, Mohammad, Nishant Dangi, Vijay Rajak, Suresh Goyal, and Manoj K. Garg. "Study of hemoglobin and red blood cell indices during first week of life in normal term neonates." International Journal of Contemporary Pediatrics 9, no. 1 (2021): 75. http://dx.doi.org/10.18203/2349-3291.ijcp20214942.

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Background: Transition from foetal to neonatal life is associated with major changes in hemogram due to homeostatic control. There are very wide ranges of hemogram levels that seem to be abnormally high or low in healthy term neonate at birth and during first week of life but these were actually normal for that neonatal period depending upon gestational and post-natal age.Method: Hemogram was studied in 100 normal term neonates born in RNT medical college during June 2009 to Dec 2009.Results: The ranges of various hemogram indices at birth, 24 hours, 48 hours and 7 days are as follows: Hemoglo

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Nurdiana, Astri, Jenny Anna Siauta, and Rina Listiana. "Successful Pregnancy and Vaginal Delivery after Oxytocin Massage for Nulliparous Women with Anemia and Undetected Foetal Congenital Anomaly: An Indonesian Case Report." EAS Journal of Nursing and Midwifery 6, no. 01 (2024): 11–21. http://dx.doi.org/10.36349/easjnm.2024.v06i01.002.

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Background: A factor that contributes to the poor health of both the mother and the fetus is Anemia. Pregnant women must therefore receive prenatal care that includes the identification and management of Anemia properly. Case Presentation: This case report provides an analysis of the pregnancy circumstances of Mrs. R, a 22-year-old housewife from a middle-class socioeconomic background, who is anticipating her first child. From the pregnancy data obtained, Mrs. R experienced anemia, supported by supporting examinations of hemoglobin levels. The management provided included iron supplementation

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Vuong, Vu Viet Ha, Thinh Huy Tran, Phuoc-Dung Nguyen, et al. "Feasibility of combining short tandem repeats (STRs) haplotyping with preimplantation genetic diagnosis (PGD) in screening for beta thalassemia." PLOS ONE 17, no. 12 (2022): e0278539. http://dx.doi.org/10.1371/journal.pone.0278539.

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β-thalassemia is an autosomal recessive disease with the reduction or absence in the production of β-globin chain in the hemoglobin, which is caused by mutations in the Hemoglobin subunit beta (HBB) gene. In Vietnam, the number of β-thalassemia carriers range from 1.5 to 25.0%, depending on ethnic and geographical areas, which is much higher than WHO’s data worldwide (1.5%). Hence, preimplantation genetic diagnosis (PGD) plays a crucial role in reducing the rate of β-thalassemia affected patients/carriers. In this research, we report the feasibility and reliability of conducting PGD in combina

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Chavan, Niranjan, Umme Ammara, Deepali Kapote, Prasad Deshmukh, and Ashwini Sakhalkar. "Study of maternal and foetal outcome in COVID-19 anaemic patients during COVID pandemic in a tertiary centre." International Journal of Reproduction, Contraception, Obstetrics and Gynecology 11, no. 5 (2022): 1565. http://dx.doi.org/10.18203/2320-1770.ijrcog20221295.

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Background: The haemoglobin concentration is one of the most critical indicators of the blood's oxygen-carrying ability. Due to the hypermetabolic condition produced by infection, anaemia in COVID-19 positive pregnant women might result in tissue hypoxia due to increased peripheral tissue oxygen demands. Complications such as multi-organ failure and acute respiratory distress syndrome can worsen the prognosis. Since hemoglobin is necessary for tissue oxygenation, anaemia may have a substantial impact on the prognosis of COVID-19 pneumonia, where tissue hypoxia develops as a result of disease p

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Mayuranathan, Thiyagaraj, Janakiram Rayabaram, Reena Das та ін. "Molecular Basis Of (δβ)0 Thalassaemia and HPFH In Indian Population and The Role Of Non-Coding Transcripts In Increased Foetal Hemoglobin In Adults". Blood 122, № 21 (2013): 3446. http://dx.doi.org/10.1182/blood.v122.21.3446.3446.

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Abstract Hereditary persistence of fetal haemoglobin (HPFH) and (δβ)0-thalassaemia are conditions caused by large deletions of δ- and β-globin genes and are characterized by high fetal haemoglobin (HbF) in heterozygotes of these mutations. Complete characterization of these deletions is important for understanding the transcriptional and epigenetic mechanisms involved in increase in HbF levels by these mutations. Previous studies demonstrated that these large deletions remove the regulatory sequences which suppress γ-globin gene expression and increase the interaction of enhancers with γ-globi

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Hidayah, Mudita Sri. "Hubungan antara Kebiasaan Sarapan dan Status Gizi dengan Kejadian Anemia pada Remaja di Kawasan Bantaran Kali Winongo Kota Yogyakarta." Surya Medika: Jurnal Ilmiah Ilmu Keperawatan dan Ilmu Kesehatan Masyarakat 17, no. 2 (2022): 69–74. http://dx.doi.org/10.32504/sm.v17i2.187.

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Background: Nutritional anemia is one of Indinesia’s major public health problems. Anemia in adolescent girls contributes to maternal and foetal mortality and morbidity in future. The purpose of this study is to determine the prevalence of anemia among adolescent in a slum area Kali Winongio and and to determine the influence of breakfast habbits and body mass index (BMI) associated with it.Methods: A community-based cross-sectional study was conducted among 62 adolescent in a slum area at Kali Winongo Yogyakarta from September to December 2019. Information regarding socio-demographic and brea

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Auliva, Mira Nur, Mahfuzhah Deswita Puteri, and Nelly Mariati. "Relationship between nutritional status and anemia incidence in pregnant women at Kelua Health Center 2024." International Journal of Health Science and Technology 6, no. 2 (2024): 81–88. https://doi.org/10.31101/ijhst.v6i3.3633.

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A low hemoglobin level, known as anemia, raises the risk of maternal and foetal sickness or death and is among the most prevalent nutritional status concerns. The purpose of this research was to identify the rate of anemia among pregnant women in the Kelua Health Center's service area in Tabalong Regency in 2023 and to draw any conclusions about the association between nutritional status and this condition. The study is cross-sectional in nature and employs quantitative methods. The population and sample used the Total Sampling technique, which consisted of 42 respondents, and observations wer

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Gautam, Praveen Kumar, Beenu Prajapati, and Manju Lata Arya. "Hemoglobin status in pregnant women for diagnosis of anemia, assessment of severity and its socio-demographic determinants in rural area of Kanpur district, Uttar Pradesh, India." International Journal of Research in Medical Sciences 7, no. 1 (2018): 178. http://dx.doi.org/10.18203/2320-6012.ijrms20185376.

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Background: Anaemia is one of the most common nutritional deficiency disorders affecting the pregnant women in the developing countries. In India anaemia in pregnancy is a major health issue with adverse maternal and foetal outcome. Nutritional anaemia in pregnant women continues to be a cause of concern despite the fact that this problem is largely preventable and easily treatable. Objectives was to determine the prevalence and severity of anaemia in the pregnant women.Methods: Around 350 pregnant women in different trimesters of pregnancy were enrolled coming for the 1st time in outpatient d

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23

Shah, Ishan P., Manish Pandya, Bhamini Kadikar, Pankaj Nimbalkar, and Tejas Patel. "A prospective interventional study to observe the effectiveness of parenteral iron infusion of iron isomaltoside 1000 (Fur – IV) in obstetrics and gynecology patients suffering from moderate to severe iron deficiency anaemia." Indian Journal of Obstetrics and Gynecology Research 10, no. 2 (2023): 110–14. http://dx.doi.org/10.18231/j.ijogr.2023.026.

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Anaemia during pregnancy is allied with maternal and foetal complications like increased risk of intrauterine growth retardation, prematurity, low birth weight, and maternal and infant mortality. The agent iron isomaltose 1000 (Fur-IV) combines iron and isomaltose 1000 for slow, controlled release to reduce the risk of free iron toxicity and provide flexibility and convenience for high dose administration. Iron isomaltoside has been shown to be effective in the treatment of IDA in many treatment groups compared to intravenous iron sucrose and FCM. : It is a prospective interventional study whi

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Dhale, Dr Shruti. "Study on the Effect of Maternal Haemoglobin on Birth Weight of Newborn Babies." Journal of Medical Science and clinical Research 12, no. 04 (2024): 22–26. http://dx.doi.org/10.18535/jmscr/v12i04.05.

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Background: Anemia is a very common condition found in pregnant women, which has a deleterious effect on foetal wellbeing including weight gain of fetus. Studies indicate that anemia in pregnancy is a risk factor low birth weight and possibly for inferior neonatal health. The present study is done to determine the effect of the maternal hemoglobin on birth weight. Methods: An observational cross-sectional study was carried out at a tertiary care hospital in Mumbai. All pregnant females with single live pregnancy were included in this study. After the selection criteria was satisfied, all term

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Sonawane, Sangeeta V., Sampatti S. Todkar, and Sanjay Mulaje. "Prevalence of anemia and factors affecting anemia among adolescent girls under field practice area of rural health training centre of western Maharashtra." International Journal Of Community Medicine And Public Health 12, no. 1 (2024): 226–30. https://doi.org/10.18203/2394-6040.ijcmph20244023.

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Background: India has the largest adolescents population in the world, 253 million, nearly 23 percent of India’s population. Adolescents anemia is severe public health problem in India, 59.1% by NFHS. As adolescent age is formative years for development, anemia at this stage of life has some long-term consequences, as maternal and foetal deaths. Methods: It was observational cross sectional study under field practice area of Rural Health Training Centre of Western Maharashtra. 350 adolescent girls were interviewed using predesigned, pretested questionnaire and their anemic status was assessed

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Nair, Abhilasha, and Mohan K. Doibale. "Prevalence of Anemia among Adolescent Girls in Rural Area of a District of Maharashtra." Indian Journal of Community Health 35, no. 1 (2023): 21–26. http://dx.doi.org/10.47203/ijch.2023.v35i01.005.

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Introduction: Nutritional anemia is one of India’s major public health problems. Adolescence is a vulnerable period in the human life cycle for the development of nutritional anemia. Anemia in adolescent girls contributes to maternal and foetal mortality and morbidity in future. Aim and Objectives: To estimate the prevalence of anemia among adolescent girls and to study the sociodemographic factors associated with anemia. Method: It was a community based cross sectional study in 10 villages of a district. 420 adolescent girls were interviewed using a predesigned, pretested questionnaire, and t

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van Tuijn, Charlotte F. J., Roosmarijn G. van der Stap, Joris A. M. van der Post, Marjolein Peters, and Bart J. Biemond. "Pregnancy Complications In Sickle Cell Disease Are More Prevalent In Women with Vaso-Occlusion Related Organ Damage Than Hemolysis Related Organ Damage." Blood 116, no. 21 (2010): 2661. http://dx.doi.org/10.1182/blood.v116.21.2661.2661.

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Abstract Abstract 2661 Background: Patients with sickle cell disease (SCD) develop accumulating organ damage throughout their lives as result of chronic hemolytic anemia and ongoing microvascular vaso-occlusion. Chronic organ damage has been related to significant morbidity and increased mortality. Previous studies have shown significant increased foetal and maternal complications in patients with SCD. It is unclear whether the presence of chronic organ damage is related to pregnancy complications in these patients. Therefore, we determined the relation between chronic organ damage and pregnan

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Beris, Photis, Tanguy Araud, Lorella Clerici та ін. "A Deletion Of About 11kb Starting From 0.5 Kb 5’ To The β-Globin Gene Reactivates Foetal Haemoglobin and Leads To β Thalassemia Intermedia When Associated To a β-Zero Thalassemic Mutation". Blood 122, № 21 (2013): 4702. http://dx.doi.org/10.1182/blood.v122.21.4702.4702.

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Background and Aims Thalassemia intermedia is characterized by severe but not transfusion dependent anemia secondary to seriously decreased production of hemoglobin (Hb). In the majority of cases, thalassemia intermedia concerns β-globin gene pathology. The molecular basis of thalassemia intermedia is heterogeneous. Here we describe a case of an adopted child native of Myanmar suffering from β-thalassemia intermedia which was proved to be secondary to a β-zero thalassemia associated with a not yet described deletional form of HPFH. Patient, Material and Methods Male child born in 1994 with Hb

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Bianchi, Maria, Patrizia Papacci, Serena Spartano, et al. "Transfusion Of Very Low Birth Weight Neonates Using Allogeneic Cord Blood Derived RBC Units." Blood 122, no. 21 (2013): 2398. http://dx.doi.org/10.1182/blood.v122.21.2398.2398.

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Abstract Infants with very low birth weight (VLBW) frequently need transfusions of red blood cells (RBCs) during the first weeks of life. However, adult blood transfusions are acknowledged risk factors for several complications, including Retinopathy of Prematurity (ROP), cytomegalovirus infection and necrotizing enterocolitis. For ROP, for example, it is thought that adult hemoglobin (HbA), with lower affinity for oxygen than foetal HbF, may induce an oxidative damage (Romagnoli C. Early Hum Dev 2009; 85, 10 Suppl:S79-S82). Previous studies showed that autologous cord blood (CB) could serve a

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Purnima, Saxena, and Saxena Somya. "Comparison of Effectiveness between Intravenous Ferric-Carboxy Maltose and Iron Sucrose in Treatment of Anemia Complicating Pregnancy." International Journal of Pharmaceutical and Clinical Research 15, no. 2 (2023): 129–34. https://doi.org/10.5281/zenodo.12798366.

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<strong>Introduction: </strong>Anemia during pregnancy is most frequently caused by iron deficiency. Both the mother and the growing foetus may suffer negative effects. The goal of the current study was to examine the effectiveness of iron sucrose and intravenous ferric carboxy maltose (FCM) in treating anemia in pregnant women. <strong>Material and Methods:</strong> In this prospective observational study, 100 pregnant women between the ages of 14 and 35 weeks who had been diagnosed with iron deficiency anemia received either FCM or iron sucrose treatment for the condition duri

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Primiastanti, Petriana, and Ninik Sukartini. "KEKURANGAN ZAT BESI DI PEREMPUAN HAMIL MENGGUNAKAN HEMOGLOBIN RETIKULOSIT (RET-HE)." INDONESIAN JOURNAL OF CLINICAL PATHOLOGY AND MEDICAL LABORATORY 19, no. 3 (2016): 156. http://dx.doi.org/10.24293/ijcpml.v19i3.414.

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Iron deficiency is the most common nutrional deficiency in the world, mostly in developing and industrial countries. Population with highest risk of iron deficiency generally are reproductive-age women. In Indonesia, the prevalence of iron deficiency anemia in pregnant women is about 50.5%. Anemia due to iron deficiency in pregnancy can affect both mother as well as the foetus. In order to prevent permanent systemic complication, it is important to do early detection before iron deficiency anaemia developes. In the early phase of iron deficiency prior to anaemia, additional tests of ferritin,

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Mbah, Tihnje Abena, Agatha K. N. Tanya, and Julius Oben. "Nutritional status and haemoglobin levels of pregnant adolescent girls in the city of Yaoundé, Cameroon." Journal of the Cameroon Academy of Sciences 16, no. 2 (2021): 97–110. http://dx.doi.org/10.4314/jcas.v16i2.3.

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Recently, there has been so much attention on adolescent health issues such as adolescent pregnancy, sexually transmitted infections, and Human Immune Virus infections but adolescent pregnancy and nutrition have aroused very little interest. This cross-sectional study was carried out to evaluate the nutritional status of adolescents aged 15 to 19 years in the city of Yaoundé, Cameroon. Three referral hospitals were selected at random for the recruitment of subjects in Yaoundé. Body Mass Index (BMI), hemoglobin level, a 24-hour recall, food frequency and socio–demographic data were collected us

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Monteiro, Gearaldine, Subbalakshmi N. K., and Sheila R. Pai. "RELEVANCE OF MEASUREMENT OF HEMATOLOGICAL PARAMETERS IN SUBJECTS WITH PREGNANCY INDUCED HYPERTENSION." Journal of Health and Allied Sciences NU 04, no. 01 (2014): 015–20. http://dx.doi.org/10.1055/s-0040-1703724.

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Abstract: Background: The pregnancy induced hypertensive (PIH) mothers are at greater risk for intrauterine growth restriction (IUGR) and intrauterine death of foetus (IUD). But currently there are no suitable early indicators of PIH mothers at risk of IUGR and IUD. Aims/objectives: To assess the various routinely measured hematological parameters in assessment of PIH mothers at risk of IUGR and IUD. Methods: This was a retrospective study done in singleton mothers. Study Group: 75 subjects with PIH. They were divided in to: Group A (n=35): PIH subjects with IUGR and IUD. Group B (n=40): PIH s

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Devaux, Celine, Xiaoduan Weng, Louise Robin, Harold J. Olney, Gilbert Cornut та Denis Soulières. "Prevalence of Frequent α-Globin Gene Deletions in Neonates with HbH in Cord Blood." Blood 106, № 11 (2005): 3817. http://dx.doi.org/10.1182/blood.v106.11.3817.3817.

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Abstract Introduction: Increasing multiethnicity is likely to make α-thalassemia minor more prevalent in Western metropolitan areas. It also increases the probability of finding newborns with Hemoglobin H disease or hydrops foetalis. Therefore, there is a need to implement screening methods to detect α-thalassemia at birth. Screening should also identify patients and families with specific requirements in genetic counselling. The goal of the present study is to evaluate the value of HbH measurement in cord blood to identify patients with α-globin deletions and patients with genotypes at risk t

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Mahajan, Aarti Sood, and Akanksha Mahajan. "Competency Based Medical Education: Integrating two subjects- Physiology of Infancy." Journal of Bangladesh Society of Physiologist 19, no. 1 (2025): 35–45. https://doi.org/10.3329/jbsp.v19i1.79570.

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Infancy reflects a multisystem physiological transition from a dependent foetus to a newborn to a one-year-old child. This is a one-of-a-kind review of literature that is helpful for both medical graduates in concordance with the curriculum outlined by the National Medical Commission’s Competency Based Medical Education in India and for physicians to keep updated about infantile physiology. An in-depth review of literature shows a gradual transition in the physiology of different organ systems with unidirectional anatomical maturation. The respiratory system is characterised by increasing numb

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Bergeron, Julie, Xiaoduan Weng, Louise Robin, Harold J. Olney, and Denis Soulières. "Prevalence of Alpha-Globin Gene Deletions amongst Patients with Unexplained Microcytosis in a North-American Population." Blood 104, no. 11 (2004): 3762. http://dx.doi.org/10.1182/blood.v104.11.3762.3762.

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Abstract Introduction: Increasing multi-ethnicity is likely to make α-thalassemia more prevalent in western metropolitan areas. The current prevalence of α-thalassemia in regions outside the traditional thalassemia areas with the associated risk for HbH disease and hydrops foetalis is unknown. Genetic counseling for reproductive risks due to α-globin gene mutations requires adequate and precise genotyping. Objectives: To determine by multiplex polymerase chain reaction (m-PCR) the prevalence and genotypes of α-thalassemia among non selected, consecutive cases of unexplained microcytosis identi

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Zinzuwadiya, Shreya Ghanshyambhai, Nimesh P. Modi, and Keshini S. Dhande. "Management of iron deficiency anemia in pregnancy in India: A review of current practices and challenges." Indian Journal of Obstetrics and Gynecology Research 11, no. 2 (2024): 147–51. http://dx.doi.org/10.18231/j.ijogr.2024.031.

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Iron deficiency anaemia (IDA) is a major global health concern that can lead to difficulties for both the mother and the foetus, especially in pregnant women. The physiological demand of iron during pregnancy increases threefold to support fetoplacental development and maternal adaptation to pregnancy. This study aimed to identify gaps in current IDA management, limitations of conventional oral iron therapy, and the need for effective and well-tolerated treatments.The objective of this study was to understand the gap of current treatment options in IDA management, its limitations, and possible

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Tamašauskas, Oldas, and Ieva Šiaudinytė. "Žmogaus chorioninio gonadotropino reikšmė klinikinėje praktikoje." Lietuvos chirurgija 12, no. 4 (2013): 238–42. http://dx.doi.org/10.15388/lietchirur.2013.4.2839.

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Žmogaus chorioninio gonadotropino (hCG) koncentracijos nustatymas dažniausiai naudojamas ankstyvo nėštumo diagnostikai, trukmei nustatyti bei nėštumui stebėti. Be to, HCG yra vertingas diagnozuojant savaiminį persileidimą, nesivystantį arektopinį nėštumą. Šis hormonas leidžia prenataliai įvertinti vaisiaus apsigimimų riziką. Taip pat hCG labai svarbus trofoblastinių ligų ir tam tikrų lokalizacijų vėžio diagnostikai, gydymo efektyvumo vertinimui. Retai, tačiau galimi ir klaidingai teigiamityrimų rezultatai dėl analitinių klaidų, tyrimams naudojamų įrenginių, prietaisų gedimų ar tam tikrų kraujy

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Andre, E., E. Yaniz-Galende, C. Hamilton, et al. "Poster session 1Cell growth, differentiation and stem cells - Heart72Understanding the metabolism of cardiac progenitor cells: a first step towards controlling their proliferation and differentiation?73Expression of pw1/peg3 identifies a new cardiac adult stem cell population involved in post-myocardial infarction remodeling74Long-term stimulation of iPS-derived cardiomyocytes using optogenetic techniques to promote phenotypic changes in E-C coupling75Benefits of electrical stimulation on differentiation and maturation of cardiomyocytes from human induced pluripotent stem cells76Constitutive beta-adrenoceptor-mediated cAMP production controls spontaneous automaticity of human induced pluripotent stem cell-derived cardiomyocytes77Formation and stability of T-tubules in cardiomyocytes78Identification of miRNAs promoting human cardiomyocyte proliferation by regulating Hippo pathway79A direct comparison of foetal to adult epicardial cell activation reveals distinct differences relevant for the post-injury response80Role of neuropilins in zebrafish heart regeneration81Highly efficient immunomagnetic purification of cardiomyocytes derived from human pluripotent stem cells82Cardiac progenitor cells posses a molecular circadian clock and display large 24-hour oscillations in proliferation and stress tolerance83Influence of sirolimus and everolimus on bone marrow-derived mesenchymal stem cell biology84Endoglin is important for epicardial behaviour following cardiac injuryCell death and apoptosis - Heart87Ultrastructural alterations reflecting Ca2+ handling and cell-to-cell coupling disorders precede occurrence of severe arrhythmias in intact animal heart88Urocortin-1 promotes cardioprotection through ERK1/2 and EPAC pathways: role in apoptosis and necrosis89Expression p38 MAPK and Cas-3 in myocardium LV of rats with experimental heart failure at melatonin and enalapril introductionTranscriptional control and RNA species - Heart92Accumulation of beta-amyloid 1-40 in HF patients: the role of lncRNA BACE1-AS93Role of miR-182 in zebrafish and mouse models of Holt-Oram syndrome94Mir-27 distinctly regulates muscle-enriched transcription factors and growth factors in cardiac and skeletal muscle cells95AF risk factors impair PITX2 expression leading to Wnt-microRNA-ion channel remodelingCytokines and cellular inflammation - Heart98Post-infarct survival depends on the interplay of monocytes, neutrophils and interferon gamma in a mouse model of myocardial Infarction99Inflammatory cd11b/c cells play a protective role in compensated cardiac hypertrophy by promoting an orai3-related pro-survival signal100Anti-inflammatory effects of endothelin receptor blockade in the atrial tissue of spontaneously hypertensive rats101Mesenchymal stromal cells reduce NLRP3 inflammasome activity in Coxsackievirus B3-induced myocarditis102Mesenchymal stromal cells modulate monocytes trafficking in Coxsackievirus B3-induced myocarditis103The impact of regulatory T lymphocytes on long-term mortality in patients with chronic heart failure104Temporal dynamics of dendritic cells after ST-elevation myocardial infarction relate with improvement of myocardial functionGrowth factors and neurohormones - Heart107Preconditioning of hypertrophied heart: miR-1 and IGF-1 crosstalk108Modulation of catecholamine secretion from human adrenal chromaffin cells by manipulation of G protein-coupled receptor kinase-2 activity109Evaluation of cyclic adenosin-3,5- monophosphate and neurohormones in patients with chronic heart failureNitric oxide and reactive oxygen species - Heart112Hydrogen sulfide donor inhibits oxidative and nitrosative stress, cardiohemodynamics disturbances and restores cNOS coupling in old rats113Role and mechanisms of action of aldehydes produced by monoamine oxidase A in cardiomyocyte death and heart failure114Exercise training has contrasting effects in myocardial infarction and pressure-overload due to different endothelial nitric oxide synthase regulation115S-Nitroso Human Serum Albumin dose-dependently leads to vasodilation and alters reactive hyperaemia in coronary arteries of an isolated mouse heart model116Modulating endothelial nitric oxide synthase with folic acid attenuates doxorubicin-induced cardiomyopathy119Effects of long-term very high intensity exercise on aortic structure and function in an animal model120Electron paramagnetic resonance spectroscopy quantification of nitrosylated hemoglobin (HbNO) as an index of vascular nitric oxide bioavailability in vivo121Deletion of repressor activator protein 1 impairs acetylcholine-induced relaxation due to production of reactive oxygen speciesExtracellular matrix and fibrosis - Heart124MicroRNA-19b is associated with myocardial collagen cross-linking in patients with severe aortic stenosis. Potential usefulness as a circulating biomarker125A new ex vivo model to study cardiac fibrosis126Heterogeneity of fibrosis and fibroblast differentiation in the left ventricle after myocardial infarction127Effect of carbohydrate metabolism degree compensation to the level of galectin-3 changes in hypertensive patients with chronic heart failure and type 2 diabetes mellitus128Statin paradox in association with calcification of bicuspid aortic valve interstitial cells129Cardiac function remains impaired despite reversible cardiac fibrosis after healed experimental viral myocarditisIon channels, ion exchangers and cellular electrophysiology - Heart132Identifying a novel role for PMCA1 (Atp2b1) in heart rhythm instability133Mutations of the caveolin-3 gene as a predisposing factor for cardiac arrhythmias134The human sinoatrial node action potential: time for a computational model135iPSC-derived cardiomyocytes as a model to dissect ion current alterations of genetic atrial fibrillation136Postextrasystolic potentiation in healthy and diseased hearts: effects of the site of origin and coupling interval of the preceding extrasystole137Absence of Nav1.8-based (late) sodium current in rabbit cardiomyocytes and human iPSC-CMs138hiPSC-derived cardiomyocytes from Brugada Syndrome patients without identified mutations do not exhibit cellular electrophysiological abnormalitiesMicrocirculation141Atherogenic indices, collagen type IV turnover and the development of microvascular complications- study in diabetics with arterial hypertension142Changes in the microvasculature and blood viscosity in women with rheumatoid arthritis, hypercholesterolemia and hypertensionAtherosclerosis145Shear stress regulates endothelial autophagy: consequences on endothelial senescence and atherogenesis146Obstructive sleep apnea causes aortic remodeling in a chronic murine model147Aortic perivascular adipose tissue displays an aged phenotype in early and late atherosclerosis in ApoE-/- mice148A systematic evaluation of the cellular innate immune response during the process of human atherosclerosis149Inhibition of Coagulation factor Xa increases plaque stability and attenuates the onset and progression of atherosclerotic plaque in apolipoprotein e-deficient mice150Regulatory CD4+ T cells from patients with atherosclerosis display pro-inflammatory skewing and enhanced suppression function151Hypoxia-inducible factor (HIF)-1alpha regulates macrophage energy metabolism by mediating miRNAs152Extracellular S100A4 is a key player of smooth muscle cell phenotypic transition: implications in atherosclerosis153Microparticles of healthy origins improve atherosclerosis-associated endothelial progenitor cell dysfunction via microRNA transfer154Arterial remodeling and metabolism impairment in early atherosclerosis155Role of pannexin1 in atherosclerotic plaque formationCalcium fluxes and excitation-contraction coupling158Amphiphysin II induces tubule formation in cardiac cells159Interleukin 1 beta regulation of connexin 43 in cardiac fibroblasts and the effects of adult cardiac myocyte:fibroblast co-culture on myocyte contraction160T-tubular electrical defects contribute to blunted beta-adrenergic response in heart failure161Beat-to-beat variability of intracellular Ca2+ dynamics of Purkinje cells in the infarct border zone of the mouse heart revealed by rapid-scanning confocal microscopy162The efficacy of late sodium current blockers in hypertrophic cardiomyopathy is dependent on genotype: a study on transgenic mouse models with different mutations163Synthesis of cADPR and NAADP by intracellular CD38 in heart: role in inotropic and arrhythmogenic effects of beta-adrenoceptor signalingContractile apparatus166Towards an engineered heart tissue model of HCM using hiPSC expressing the ACTC E99K mutation167Diastolic mechanical load delays structural and functional deterioration of ultrathin adult heart slices in culture168Structural investigation of the cardiac troponin complex by molecular dynamics169Exercise training restores myocardial and oxidative skeletal muscle function from myocardial infarction heart failure ratsOxygen sensing, ischaemia and reperfusion172A novel antibody specific to full-length stromal derived factor-1 alpha reveals that remote conditioning induces its cleavage by endothelial dipeptidyl peptidase 4173Attenuation of myocardial and vascular arginase activity by vagal nerve stimulation via a mechanism involving alpha-7 nicotinic receptor during cardiac ischemia and reperfusion174Novel nanoparticle-mediated medicine for myocardial ischemia-reperfusion injury simultaneously targeting mitochondrial injury and myocardial inflammation175Acetylcholine plays a key role in myocardial ischaemic preconditioning via recruitment of intrinsic cardiac ganglia176The role of nitric oxide and VEGFR-2 signaling in post ischemic revascularization and muscle recovery in aged hypercholesterolemic mice177Efficacy of ischemic preconditioning to protect the human myocardium: the role of clinical conditions and treatmentsCardiomyopathies and fibrosis180Plakophilin-2 haploinsufficiency leads to impaired canonical Wnt signaling in ARVC patient181Improved technique for customized, easier, safer and more reliable transverse aortic arch banding and debanding in mice as a model of pressure overload hypertrophy182Late sodium current inhibitors for the treatment of inducible obstruction and diastolic dysfunction in hypertrophic cardiomyopathy: a study on human myocardium183Angiotensin II receptor antagonist fimasartan has protective role of left ventricular fibrosis and remodeling in the rat ischemic heart184Role of High-Mobility Group Box 1 (HMGB1) redox state on cardiac fibroblasts activities and heart function after myocardial infarction185Atrial remodeling in hypertrophic cardiomyopathy: insights from mouse models carrying different mutations in cTnT186Electrophysiological abnormalities in ventricular cardiomyocytes from a Maine Coon cat with hypertrophic cardiomyopathy: effects of ranolazine187ZBTB17 is a novel cardiomyopathy candidate gene and regulates autophagy in the heart188Inhibition of SRSF4 in cardiomyocytes induces left ventricular hypertrophy189Molecular characterization of a novel cardiomyopathy related desmin frame shift mutation190Autonomic characterisation of electro-mechanical remodeling in an in-vitro leporine model of heart failure191Modulation of Ca2+-regulatory function by three novel mutations in TNNI3 associated with severe infant restrictive cardiomyopathyAging194The aging impact on cardiac mesenchymal like stromal cells (S+P+)195Reversal of premature aging markers after bariatric surgery196Sex-associated differences in vascular remodeling during aging: role of renin-angiotensin system197Role of the receptor for advanced glycation end-products (RAGE) in age dependent left ventricle dysfunctionsGenetics and epigenetics200hsa-miR-21-5p as a key factor in aortic remodeling during aneurysm formation201Co-inheritance of mutations associated with arrhythmogenic and hypertrophic cardiomyopathy in two Italian families202Lamin a/c hot spot codon 190: form various amino acid substitutions to clinical effects203Treatment with aspirin and atorvastatin attenuate cardiac injury induced by rat chest irradiation: Implication of myocardial miR-1, miR-21, connexin-43 and PKCGenomics, proteomics, metabolomics, lipidomics and glycomics206Differential phosphorylation of desmin at serines 27 and 31 drives the accumulation of preamyloid oligomers in heart failure207Potential role of kinase Akt2 in the reduced recovery of type 2 diabetic hearts subjected to ischemia / reperfusion injury208A proteomics comparison of extracellular matrix remodelling in porcine coronary arteries upon stent implantationMetabolism, diabetes mellitus and obesity211Targeting grk2 as therapeutic strategy for cancer associated to diabetes212Effects of salbutamol on large arterial stiffness in patients with metabolic syndrome213Circulating microRNA-1 and microRNA-133a: potential biomarkers of myocardial steatosis in type 2 diabetes mellitus214Anti-inflammatory nutrigenomic effects of hydroxytyrosol in human adipocytes - protective mechanisms of mediterranean diets in obesity-related inflammation215Alterations in the metal content of different cardiac regions within a rat model of diabetic cardiomyopathyTissue engineering218A novel conductive patch for application in cardiac tissue engineering219Establishment of a simplified and improved workflow from neonatal heart dissociation to cardiomyocyte purification and characterization220Effects of flexible substrate on cardiomyocytes cell culture221Mechanical stretching on cardiac adipose progenitors upregulates sarcomere-related genes." Cardiovascular Research 111, suppl 1 (2016): S16—S42. http://dx.doi.org/10.1093/cvr/cvw135.

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Segbefia, Catherine, Yvonne Dei-Adomakoh, Enoch Mensah, Priya Thota, and Isaac Odame. "Point-of-care Diagnostic for Foetal Haemoglobin in Kids for Sickle Cell Disease in Ghana." Journal of Sickle Cell Disease 1, Supplement_1 (2024). http://dx.doi.org/10.1093/jscdis/yoae002.019.

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Abstract Presentation Date: 6/9/2024 Presentation Start Time: 2:30:00 PM Background Sickle cell disease (SCD) is an inherited blood disorder which causes acute and chronic complications and can result in early death. About three-fourth of patients with SCD live in sub-Saharan Africa; in Ghana, 1 in 50 newborns are affected with SCD. Foetal hemoglobin (Hb F) level is a strong modifier of SCD severity. High levels of Hb F inhibit sickling and hemolysis and reduce disease morbidity and mortality. Hb F monitoring is also used to assess adherence and response to disease modifying therapy such as hy

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Punjaji Tambse, Manjusha, Maya Suresh Vasaikar, and Sunil Santaram Chavan. "Hemoglobin Patterns in Sickle Cell Hemoglobinopathies- A Large Prospective Study in North Maharashtra." MVP Journal of Medical Sciences, May 23, 2017, 84–88. https://doi.org/10.18311/mvpjms/2017/v4i1/11831.

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Introduction: Sickle cell haemoglobinopathy is an inherited hemoglobinopathy resulting from a mutation occurring in betaglobin gene, on chromosome 11. The gene is prevalent in some tribes of North Maharashtra. The main aim of the study is to determine haemoglobin patterns in cases with sickle cell hemoglobinoathies in North Maharashtra using HPLC testing system. Material and Methods: This is a prospective study done over a period of 6 years. 10081 patients having positive solubility test or negative solubility test but having clinical suspicion of Sickle cell hemoglobinopathies were studied in

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Okeke, O. Chinwe, O. Ernest Ukaejiofo, E. Nnodu Obiageli, D. Ezigbo Eyiuche, and C. Okeke Chinedu. "Evaluation of Acute Painful Episodes with Foetal Hemoglobin Level and Other Haematological Parameters in Sickle Cell Patients in Abuja Nigeria." Journal of Advances in Medicine and Medical Research, August 31, 2019, 1–5. http://dx.doi.org/10.9734/jammr/2019/v30i730213.

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Introduction: Heterogeneity in sickle cell anaemia manifestations ranges from near asymptomatic cases to severe illness.  Objective: This study determined the relationship between foetal haemoglobin F level, other haematological parameters and acute painful episode score of sickle cell disease patients in FCT Abuja Nigeria. Methods: 60 Sickle cell patients were selected for the study. 20 severe crises, 20 non-severe crisis SS were enrolled in the study. Control group comprised 20 apparently healthy haemoglobin AA individuals. Data were analysed descriptively. Results: Hb F le

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Sharma, Achala sahai, Udit Mishra, Rajkishori Dandotiya, and Paribhashita Mishra. "A STUDY OF ASSOCIATED RISK FACTORS OF URINARY TRACT INFECTION AMONG PREGNANT WOMEN AT KAMLA RAJA HOSPITAL, GWALIOR." INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH, December 1, 2020, 35–37. http://dx.doi.org/10.36106/ijsr/7621461.

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Background Urinary tract infection (UTI) is an infection caused by presence and growth of microorganism anywhere in the urinary tract. Urinary tract infection in pregnancy may also lead to unfavorable pregnancy outcomes and complication such as pyelonephritis, hypertensive disease of pregnancy, anaemia, chronic renal failure, premature delivery, low birth weight and foetal mortality. Aims and objectives: To determine the overall prevalence of UTI among pregnant women and to identify bacterial uropathogen associated with UTI in pregnant women and determine their antibiotic susceptibility to sel

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Imtiaz, Amna, Noshina Noreen, Rabiah Asghar, Rabia Nazir, Rabeea Irfan, and Bushra Anam Ali. "Clinical Application of Reticulocyte Maturity Indices in Early Diagnosis of Iron Deficiency Anemia in the First Trimester of Pregnancy." Journal of Islamabad Medical & Dental College 13, no. 1 (2024). http://dx.doi.org/10.35787/jimdc.v13i1.1147.

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Background: Iron deficiency anemia (IDA) is a prevalent global health issue, particularly affecting pregnant females due to increased iron demands during pregnancy. In Pakistan, IDA remains a significant concern, posing challenges to maternal and child health. Early detection and management of iron deficiency are crucial for improving pregnancy outcomes. Objective: This study aims to investigate the iron status and associated hematological parameters among pregnant females during the first trimester in Islamabad, Pakistan. Methodology : This cross-sectional study, conducted in coll

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Oswaldo Margarito Torres-Chablé, Nadia Florencia Ojeda-Robertos, Paulo Sergio Zamudio-Ortiz, et al. "Haematological Status of Cows in Different Physiological Stages under Humid Tropic Condition." Acta Scientiae Veterinariae 52 (April 18, 2024). https://doi.org/10.22456/1679-9216.138187.

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Background: Baseline haematological data serve as reference for the evaluation of the health status of animals. In cows, physiological stages such as pregnant, calving and lactation represent challenges, which can affect their blood parameters. The prepartum and postpartum periods are important for the productive and reproductive efficiency of cows. There is a transition period involving several physiological adaptations in a short period of time that can lead to health problems, especially metabolic and infectious diseases. The aims of the present study were report haematological reference in

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Angèle, Albert Thierry NDIMBA Georges MISUMBA LUFULUABO BUSHABU KONGO PALUKU THEYTHEY Bob SENKER MVUMBI LELO. "INCOMPATIBILITÉ FŒTO-MATERNELLE ABO DANS TROIS FORMATIONS SANITAIRES DE KINSHASA (RDC) : PROFIL BIOLOGIQUE ET FACTEURS DE MAUVAIS PRONOSTIC." July 16, 2022. https://doi.org/10.5281/zenodo.15566781.

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En vue d'apporter notre contribution à l'étude de l'incompatibilité sanguine fœto-maternelle en RDC et précisément à Kinshasa, nous avions choisi trois formations médicales dans lesquelles nous avons eu à prélever 120 échantillons des couples mères nouveau-nés sur lesquelles nous avons effectué les analyses biologiques précises dont : le groupage sanguin, le test de Coombs direct et le taux d'hémoglobine. A l'issue de notre étude, les résultats suivants ont été obtenus : Chez les nouveau-nés, 57% étaient de sexe masculin contre 43% de sexe féminin ; Les données cliniques ont identifiés un ictè

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Angèle, Albert Thierry NDIMBA Georges MISUMBA LUFULUABO BUSHABU KONGO PALUKU THEYTHEY Bob SENKER MVUMBI LELO. "INCOMPATIBILITÉ FŒTO-MATERNELLE ABO DANS TROIS FORMATIONS SANITAIRES DE KINSHASA (RDC) : PROFIL BIOLOGIQUE ET FACTEURS DE MAUVAIS PRONOSTIC." July 16, 2022. https://doi.org/10.5281/zenodo.15566785.

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En vue d'apporter notre contribution à l'étude de l'incompatibilité sanguine fœto-maternelle en RDC et précisément à Kinshasa, nous avions choisi trois formations médicales dans lesquelles nous avons eu à prélever 120 échantillons des couples mères nouveau-nés sur lesquelles nous avons effectué les analyses biologiques précises dont : le groupage sanguin, le test de Coombs direct et le taux d'hémoglobine. A l'issue de notre étude, les résultats suivants ont été obtenus : Chez les nouveau-nés, 57% étaient de sexe masculin contre 43% de sexe féminin ; Les données cliniques ont identifiés un ictè

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Yelamali, B. C., Anita Daddi, Pallavi Charantimath, Sheela M S, and Rashmi N K. "TO STUDY THE EFFECT OF IMMEDIATE VERSUS DELAYED CORD CLAMPING ON HEMATOCRIT, HEMOGLOBIN AND BODY TEMPERATURE IN TERM NEONATES BORN BY CESAREAN SECTION- A RANDOMIZED CONTROL TRIAL." GLOBAL JOURNAL FOR RESEARCH ANALYSIS, May 15, 2024, 75–76. http://dx.doi.org/10.36106/gjra/3405481.

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The umbilical cord is the lifeline that connects the placenta to the foetus. Following birth, blood continues to ow through umbilical arteries (from the infant to the placenta) for approximately 20-25 seconds and is negligible by 45 seconds1. In the umbilical vein, however, blood continues to ow from the placenta to the infant for up to 3 minutes after delivery2. This additional blood volume transferred from the placenta to the neonate at birth through the umbilical vein is dened as Placental transfusion3. Neonatal anaemia is an important problem that has multiple sequelae on long term neur

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Biswas, Soumika, and Lekha Biswas. "“EVALUATION OF CORD BLOOD TO SCREEN FOR NEONATAL ANEMIA AND ITS CORRELATION WITH MATERNAL ANEMIA IN A TERTIARY MEDICAL COLLEGE IN EASTERN INDIA”." GLOBAL JOURNAL FOR RESEARCH ANALYSIS, October 15, 2022, 65–68. http://dx.doi.org/10.36106/gjra/8102420.

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An estimated 87% of pregnant women in India suffers from iron deciency anemia in some point in their pregnancy. Maternal anemia has been found to be associated with low birth weight babies, asphyxia, preterm delivery and neurological decits & the neonatal iron stores are solely dependent on the transplacental iron transport, about 1gm in term newborns. The transfer of iron from the mother to the foetus is tightly regulated by factors such as transferrin, coelomic uid and hepcidin. This study aims to nd whether maternal anemia has a correlation with neonatal anemia. Also, it aims to scr

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