Relevant bibliographies by topics / Foetal Hemoglobin

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Foetal Hemoglobin'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "Foetal Hemoglobin"

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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2

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>&nbsp;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>&nbsp;Maternal haemoglobin levels affect pregnancy outcomes and the mother&rsquo;s and neonate&rsquo;s health. This cohort study examined the relationship between the mother&rsquo;s blood haemoglobin levels over the three trimesters and the neonates at birth.&nbsp;<strong>Methods:</strong>&nbsp;About 200 pregnant Territory Care Centre patients participated in the study. Researchers measured the mother&rsquo;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 &amp; sickle cell disease are the important challenges for tribal populations in India. Many study demonstrated the prevalence of haemoglobinopathies in India &amp; 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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7

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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8

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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9

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 &amp; 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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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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Dissertations / Theses on the topic "Foetal Hemoglobin"

1

Baudin-Chich, Véronique. "Interactions entre les sous-unites d'hemoglobines humaines adultes et foetales : les variantes pathologiques de l'interface alpha 1 beta 1 et l'hemoglobine s." Paris 6, 1988. http://www.theses.fr/1988PA066045.

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Exploration de l'interface entre les sousunites de l'hemoglobine d'un meme dimere et de la surface externe en utilisant cinq variants de l'interface alpha 1 beta 1 et l'hemoglobine s. Il a ete trouve une instabilite moleculaire pour ces variants. Le comportement electrophoretique de ces variants est proche de celui de l'hemoglobine a suggerant un masquage dans cette region. Etude des interactions entre l'hemoglobine foetale et l'hemoglobine s modulant l'expression phenotypique de la drepanocytose
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Antoniani, Chiara. "A genome editing approach to induce fetal hemoglobin expression for the treatment of β-hemoglobinopathies". Thesis, Sorbonne Paris Cité, 2017. http://www.theses.fr/2017USPCB077.

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Les β-hémoglobinopathies (β-thalassémies et drépanocytose) sont des anémies génétiques qui touchent des milliers de nouveaux nés chaque année dans le monde. Ces maladies sont causées par des mutations affectant l'expression de l'hémoglobine chez l'adulte. Le seul traitement disponible est la transfusion sanguine à vie, associée à une chélation du fer. Pour les patients les plus touchés, la greffe de cellule souche hématopoïétique (CSH) demeure le seul traitement curatif. Néanmoins, la transplantation autologue de cellules souches génétiquement corrigées représente une alternative thérapeutique
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3

El, Hoss Sara. "Novel insights into the role of fetal hemoglobin in spleen function, red cell survival and ineffective erythropoiesis in sickle cell disease." Thesis, Université de Paris (2019-....), 2019. https://theses.md.univ-paris-diderot.fr/ELHOSS_Sara_va2_20190924.pdf.

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La drépanocytose est une maladie génétique héréditaire récessive causée par la substitution d'un acide aminé dans la chaîne β-globine aboutissant à la production d'hémoglobine anormale (HbS). Dans des conditions hypoxiques, l’HbS polymérise entraînant une falciformation et une perte de déformabilité des globules rouges (GR). Au cours de la drépanocytose, le dysfonctionnement splénique entraîne des complications potentiellement mortelles, en particulier chez les jeunes enfants. Généralement, une asplénie fonctionnelle précède la survenue d’une asplénie anatomique avec cependant une grande varia
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4

Weber, Leslie. "New therapeutic strategies for the treatment of β-hemoglobinopathies". Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC272.

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Le développement de stratégies thérapeutiques curatives pour les patients affectés de β-hémoglobinopathies, c’est à dire drépanocytose et β-thalassémies, fait face à une grande demande. En effet, un accès restreint à des donneurs compatibles limite l’unique thérapie définitive autorisée, la transplantation allogénique de cellules souches hématopoïétiques (CSH). Au cours de la première partie de cette thèse,nous avons optimisé une alternative thérapeutique,la transplantation autoloque de CSH corrigées par le biais de lentivirus (LV). Le développement de lentivirus exprimant la β-globine et l’am
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