Relevant bibliographies by topics / Anemia syndrome

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers

Academic literature on the topic 'Anemia syndrome'

Author: Grafiati
Published: 28 May 2022
Last updated: 18 July 2025

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Journal articles on the topic "Anemia syndrome"

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T., Glebova,. "Anemic Syndrome in Children in the Children’s Regional Hospital." Bulletin of Science and Practice, no. 1 (January 15, 2023): 197–99. http://dx.doi.org/10.33619/2414-2948/86/26.

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The study of a general blood test determining the nature of anemic syndrome in young children (0-12 years old) and children (3-6 years old) with infectious processes in the infectious department of the Penza Regional Children's Hospital was carried out. In the study, 4 groups were identified according to blood parameters in the age group 0-12 years. The study of the indicators of the general blood test showed that the first group cannot be attributed to the manifestations of severe anemia syndrome. In the second – normochromic, normocytic anemia syndrome. The third group had a manifestation of
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Gopchuk, O. M. "Iron deficiency anemia." HEALTH OF WOMAN, no. 9(145) (November 30, 2019): 32–37. http://dx.doi.org/10.15574/hw.2019.145.32.

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Iron deficiency anemia is the most common group of blood diseases in the population (80–95% of all anemias), characterized by a decrease in the number of circulating red blood cells and / or hemoglobin per unit volume of blood below normal for a given age and sex. The article deals with the role of iron in the human body, the conditions associated with its deficiency, causes, clinical symptoms, diagnosis of this pathology. Recommendations are given for the treatment of iron deficiency anemia by modern iron preparations, the advantages of using in the complex correction of heme iron deficiency,
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Lazrak FZ, Jahdaoui Adil, Yahyaoui Hicham, Ait Ameur Mustapha, and Chakour Mohamed. "Macrocytic anemia: Myelogram results in military hospital Avicenna in Marrakech." GSC Advanced Research and Reviews 13, no. 3 (2022): 212–15. http://dx.doi.org/10.30574/gscarr.2022.13.3.0275.

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Anemia is one of the most common health problems in the primary care setting. Macrocytosis in adults is defined as a red blood cell mean corpuscular volum >95 fL. Macrocytic anemias are generally classified into megaloblastic or non-megaloblastic anemia. Retrospective descriptive study included 340 samples of myelogram received in the Hematology Labortory belonging to patients admitted to the Military hospital of Avicenna in Marrakech, over a period of 48 months (from January 2016 to January 2020), aimed to assess the etiological profile of macrocytic anemia in patients whose bone marrow sm
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Lazrak, FZ, Adil Jahdaoui, Hicham Yahyaoui, Ameur Mustapha Ait, and Mohamed Chakour. "Macrocytic anemia: Myelogram results in military hospital Avicenna in Marrakech." GSC Advanced Research and Reviews 13, no. 3 (2022): 212–15. https://doi.org/10.5281/zenodo.7678386.

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Anemia is one of the most common health problems in the primary care setting. Macrocytosis in adults is defined as a red blood cell mean corpuscular volum >95 fL. Macrocytic anemias are generally classified into megaloblastic or non-megaloblastic anemia. Retrospective descriptive study included 340 samples of myelogram received in the Hematology Labortory belonging to patients admitted to the Military hospital of Avicenna in Marrakech, over a period of 48 months (from January 2016 to January 2020), aimed to assess the etiological profile of macrocytic anemia in patients whose bone marrow sm
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Mamchenko, I. L., E. G. Malaeva, Z. V. Grekova, O. A. Yarmolenko, I. A. Vasyukhina, and N. V. Kholupko. "Anemia syndrome of complex genesis." Health and Ecology Issues 19, no. 2 (2022): 134–39. http://dx.doi.org/10.51523/2708-6011.2022-19-2-17.

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Anemia is a clinical and hematological syndrome which is one of the most common diseases in the world. The clinical manifestations of anemia syndrome can be caused by both anemia itself and various manifestations of hypoxia and hypercapnia. Due to the similarity of the clinical manifestations, doctors of various specialties face a difficult task of the differential diagnosis of anemias and the selection of therapeutic tactics.The article presents a clinical case of anemia syndrome in a patient with comorbid pathology and latent vascular malformation. The presence of comorbid diseases in the pa
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Klimov, L. Ya, R. A. Zhetishev, T. A. Ivenskaya, et al. "PATHOGENETIC ASPECTS OF THE FORMATION OF ANEMIA IN CHILDREN WITH CELIAC DISEASE." Pediatria. Journal named after G.N. Speransky 101, no. 6 (2022): 116–25. http://dx.doi.org/10.24110/0031-403x-2022-101-6-116-125.

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Celiac disease (CD) is characterized by the formation of an anemic syndrome whose etiopathogenesis if of a multifactorial origin. The main types of anemias in children with celiac disease are iron deficiency anemia (IDA) and anemia of inflammation, also called anemia of chronic disease (ACD). This bibliographical review presents current information on the iron metabolism, morphological changes in the epithelium of the intestinal mucosa in celiac disease leading to the development of iron deficiency, pathogenesis of ACD formation in celiac disease, as well as the diagnosis of IDA and ACD in cel
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Urbanovych, A. M., and M. V. Yuskiv. "Peculiarities of the anemic syndrome course with thyroid dysfunction." INTERNATIONAL JOURNAL OF ENDOCRINOLOGY (Ukraine) 19, no. 5 (2023): 391–97. http://dx.doi.org/10.22141/2224-0721.19.5.2023.1304.

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This article was created on the basis of a literature review in the Web of Science, PubMed and Scopus databases and analyzes information on the prevalence, classification, etiopathogenetic mechanisms of anemia, evaluation of data from clinical studies and meta-analyses on the course of anemic syndrome in thyroid diseases. Anemia and thyroid dysfunction are common phenomena that often occur simultaneously. According to modern recommendations, it is worth evaluating the function of the thyroid gland when investigating anemia. With thyroid dysfunction, normocytic anemia is the most common, and mi
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Pavliukovych, N. D., O. V. Pavliukovych, and V. O. Shuper. "Structure of Anemic Syndrome in Patients with Chronic Forms of Coronary Artery Disease." Ukraïnsʹkij žurnal medicini, bìologìï ta sportu 7, no. 6 (2022): 95–99. http://dx.doi.org/10.26693/jmbs07.06.095.

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The purpose of the study was to determine the incidence and characteristic features of anemia in elderly and senile patients with chronic forms of coronary artery disease. Materials and methods. 1,993 case reports of patients with chronic forms of coronary artery disease with comorbid anemia were analyzed retrospectively. All patients were diagnosed with chronic coronary artery disease (stable angina pectoris of II-III functional classes, diffuse or focal (post-infarction) cardiosclerosis). Average age of investigated patients was 79.5 ± 5.24. Comorbid anemia was diagnosed in case of hemoglobi
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Alter, Blanche P. "Diagnosis, Genetics, and Management of Inherited Bone Marrow Failure Syndromes." Hematology 2007, no. 1 (2007): 29–39. http://dx.doi.org/10.1182/asheducation-2007.1.29.

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Abstract The inherited bone marrow failure syndromes are traditionally considered to be pediatric disorders, but in fact, many of the patients now are diagnosed as adults, and many diagnosed as children now live to reach adulthood. The most common of these rare disorders include Fanconi anemia, dyskeratosis congenita, Shwachman-Diamond syndrome and amegakaryocytic thrombocytopenia, which often develop aplastic anemia and may evolve into myelodysplastic syndrome and acute myeloid leukemia; and Diamond-Blackfan anemia, severe congenital neutropenia, and thrombocytopenia absent radii, single cyto
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Goryainova, Nadiya, Stanislav Vydyborets, Yurii Derpak, Olena Kucher, and Halyna Moroz. "Anemic Syndrome and Molecular Mechanisms and Regulation of Iron Absorption in Gastroenterological Diseases." Family medicine. European practices, no. 1 (February 28, 2023): 11–19. http://dx.doi.org/10.30841/2786-720x.1.2023.277472.

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Anemic syndrome is the most often extraintestinal complication in patients with diseases of the digestive tract (DT), which can significantly impair the quality of life. In the literature review, we tried to combine and systematize the accumulated information on the problem of anemic syndrome in DT diseases. Iron-deficiency anemia, chronic disease anemia, B12-deficiency and folio-deficiency anemia are determined depending on the combination of pathogenetic mechanisms. Other variants of anemia are rare. It is necessary to carry out a complex laboratory examination to establish the leading facto
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Dissertations / Theses on the topic "Anemia syndrome"

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Cherry, Anne Blanche Cresswell. "Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia." Thesis, Harvard University, 2014. http://dissertations.umi.com/gsas.harvard:11410.

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The effect of a single genetic mutation can vary greatly between different types of cells. The mutated gene may not be expressed in one tissue but may cause a devastating loss of function in another. To learn about disease mechanisms and generate novel therapies, genetic disorders must be studied in the types of cells where the mutations are most deleterious. Recently, scientists have begun manipulating cellular identity to create the cell types most affected by various genetic diseases. This dissertation describes the experience of generating reprogramming models for three genetic disorde
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SAVARESE, ALICE. "¿CARDIORENAL SYNDROME-ANEMIA¿ COMPLEX IN SMALL ANIMAL MEDICINE: RESEARCH IN DIAGNOSTIC." Doctoral thesis, Università degli Studi di Milano, 2019. http://hdl.handle.net/2434/626513.

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La sindrome cardiorenale (CRS) può essere definita come un disordine fisiopatologico di cuore e reni in cui la disfunzione acuta o cronica di un organo può indurre una disfunzione acuta o cronica dell'altro. La cardiopatia acquisita più comune che colpisce i cani anziani e che porta a insufficienza cardiaca congestizia (CHF) è la degenerazione mixomatosa della valvola mitrale (MMVD). Il peggioramento della performance cardiaca e la riduzione della perfusione renale contribuiscono allo sviluppo della malattia renale cronica (CKD) (CRS tipo 2). Nei gatti la più frequente malattia cardiaca è la
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Arruda, Daisy Maria Meireles. "Aloimmunity against HLA class I antigens in patients with myelodysplastic syndrome and aplastic anemia." Universidade Federal do CearÃ, 2005. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=38.

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CoordenaÃÃo de AperfeiÃoamento de Pessoal de NÃvel Superior<br>Myelodysplastic syndrome (MDS) and aplastic anemia (AA) are two of the hematological disorders which present peripheral cytopenias, with extensive clinical manifestations that vary from slight anemia to severe pancytopenia; the latter requiring continuous transfusional reposition of red cell (RC) and platelet concentrates (PC), which can induce aloimunization in patients. Such patients can develop a post-transfusional refractory state, rendering further transfusions unviable. The objective of the present study was to investigate th
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Wu, Katie Jennifer. "The influence of UBE3A, NEDD4L, and ARFGEF2 on the progression of Angelman syndrome and sickle cell anemia." Thesis, Boston University, 2012. https://hdl.handle.net/2144/12683.

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Thesis (M.A.)--Boston University PLEASE NOTE: Boston University Libraries did not receive an Authorization To Manage form for this thesis or dissertation. It is therefore not openly accessible, though it may be available by request. If you are the author or principal advisor of this work and would like to request open access for it, please contact us at open-help@bu.edu. Thank you.<br>This project investigates the impact of UBE3A, NEDD4L, and ARFGEF2 on disorder and disease in humans. UBE3A is a member of the homologous to E6AP COOH-terminus (HECT) E3 ubiquitin ligase family and is parentally
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Frick, Thomas Patrick. "Klinischer follow-up und biochemische Untersuchungen bei einem Patienten mit einem thiamine-responsive megaloblastic anemia (TRMA) syndrome /." [S.l.] : [s.n.], 2008. http://opac.nebis.ch/cgi-bin/showAbstract.pl?sys=000277059.

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Araújo, Jerônimo Gonçalves de. "Oximetria transcutânea na síndrome torácica aguda em pacientes com anemia falciforme." Universidade Federal de Sergipe, 2007. https://ri.ufs.br/handle/riufs/3720.

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Coordenação de Aperfeiçoamento de Pessoal de Nível Superior<br>Searching to trace the clinical profile, epidemiologist, evolution and laboratorial of the internments of patients with Sickle Cell Disease (SCD); to identify factors that can be related with the sprouting and evolution of Acute Chest Syndrome (ACS), as well as; to evaluate if the average saturation of oxygen through the oximetry of pulse is diagnosis or prognostic of ACS; a study of coorte with 168 carrying patients was carried through of SCD. During all the year of 2006, 168 patients with SCD had been studied, had predominance of
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Reed, Caroline. "Increasing Hydroxyurea Adherence for Pediatric Patients With Sickle Cell Anemia." Thesis, Walden University, 2016. http://pqdtopen.proquest.com/#viewpdf?dispub=10141603.

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<p> Sickle cell disease is a disabling chronic autosomal recessive blood disease characterized by abnormal hemoglobin, pain crises, and frequent emergency department visits. Adherence to hydroxyurea therapy has been shown to improve these patient outcomes. Guided by the theory of comfort, the purpose of this project was to determine if an educational intervention would increase adherence to hydroxyurea therapy in pediatric patients between 2 and 17 years of age recruited from an urban university hospital hematology clinic. The RE-AIM model was used to support the translation of evidence and th
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Sébert, Marie. "Génétique et évolution clonale des syndromes d’insuffisance médullaire." Thesis, Sorbonne Paris Cité, 2018. http://www.theses.fr/2018USPCC271.

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Les syndromes d’insuffisance médullaire sont liés à des mutations constitutionnelles à l’origine d’une hématopoïèse déficiente chez les patients atteints. Ils représentent un groupe hétérogène de maladies syndromiques, et impliquent plusieurs familles de gènes avec des mécanismes biologiques différents conduisant à l’insuffisance médullaire. Ces maladies prédisposent à une évolution clonale somatique, avec un risque accru de développer un syndrome myélodysplasique (SMD) ou une leucémie aigüe myéloïde (LAM) au cours du temps. Nous avons séquencé et analysé l’exome d’ADN fibroblastique d’une coh
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Гужва, Н. Ю. "Актуальні питання анемічного синдрому у хворих на ревматоїдний артрит фертильного віку". Thesis, Сумський державний університет, 2014. http://essuir.sumdu.edu.ua/handle/123456789/35688.

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Анемічний синдром відноситься до тих позасуглобових проявів РА, які впливають на ефективність лікування, якість та тривалість життя пацієнтів. РА відноситься до захворювань, які негативно впливають на фертильність. Анемія, що спостерігається у хворих на РА, має дві причини. Перша - алізодефіцитна анемія (ЗДА), що розвиваеться переважно внаслідок прихованих кровотеч з травного тракту, що ушкоджується агресивними лікувальними засобами; друга – анемія хронічного захворювання, або ж цитокінмедійована анемія (ЦМА), яка розвивається внаслідок гіперпродукції проанемічних цитокінів (ФНП-α, інтерлейкін
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Meroño, Dueñas Oona. "Comorbilidades en los pacientes con síndrome coronario agudo: nuevas evidencias de la anemia nosocomial y del déficit de hierro." Doctoral thesis, Universitat Autònoma de Barcelona, 2017. http://hdl.handle.net/10803/457624.

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El síndrome coronario agudo (SCA) es la principal complicación de la cardiopatía isquémica y se produce como consecuencia de la inestabilización de las placas de aterosclerosis de las arterias coronarias. Se sabe que la inflamación juega un papel importante en todas las fases de la enfermedad aterosclerosa; en el inicio de la formación de la placa, en la progresión de la misma y es máxima en el momento de inestabilización y aparición del SCA. Los objetivos de esta tesis son analizar el papel e implicaciones clínicas de la anemia adquirida intrahospitalariamente y del déficit de hierro (DH)
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Books on the topic "Anemia syndrome"

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Uzoegwu, Peter Nzeemdu. Families' guide against sickle cell syndrome. Sickle Cell Laboratory, University of Nigeria, 1995.

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Shahidi, Nasrollah T., ed. Aplastic Anemia and Other Bone Marrow Failure Syndromes. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3254-4.

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T, Shahidi Nasrollah, ed. Aplastic anemia and other bone marrow failure syndromes. Springer-Verlag, 1990.

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Cherry, Anne Blanche Cresswell. Reprogramming Pediatric Genetic Disorders: Pearson Syndrome, Ring 14 Syndrome, and Fanconi Anemia. 2014.

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Sybert, Virginia P. Disorders of Pigmentation. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780195397666.003.0004.

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Hyperpigmentation – Carney Complex – Dowling-Degos Disease – Dyskeratosis Congenita – Fanconi Anemia – Hemochromatosis – Incontinentia Pigmenti – LEOPARD Syndrome – Linear and Whorled Nevoid Hypermelanosis – McCune-Albright Syndrome – Naegeli Syndrome – Neurofibromatosis – Nevus Phakomatosis Pigmentovascularis – Peutz-Jeghers Syndrome – Universal Melanosis – Hypopigmentation – Albinisms – Albinism with Deafness – Hermansky-Pudlak Syndrome – Oculocutaneous Albinism Tyrosinase Negative – Oculocutaneous Albinism Tyrosinase Positive – Yellow Mutant Albinism – Cross Syndrome – Hypomelanosis of Ito
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Sybert, Virginia P. Disorders of Pigmentation. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780190276478.003.0004.

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Chapter 4 covers Hyperpigmentation (including Carney Complex, Dowling-Degos Disease, Dyskeratosis Congenita, Fanconi Anemia, H Syndrome, Hemochromatosis, Incontinentia Pigmenti, LEOPARD Syndrome, Linear and Whorled Nevoid Hypermelanosis, McCune-Albright Syndrome, Naegeli Syndrome, Neurofibromatosis, Nevus Phakomatosis Pigmentovascularis, Peutz-Jeghers Syndrome, and Universal Melanosis) and Hypopigmentation ( Albinisms, Albinism with Deafness, Hermansky-Pudlak Syndrome, Oculocutaneous Albinism Tyrosinase Negative, Oculocutaneous Albinism Tyrosinase Positive, Yellow Mutant Albinism, Cross Syndro
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Fridbinstons, Pit Alex. Causes of Thrombocytopenia: Enlarged Spleen, Anemia, Leukemia, Pregnancy, Heavy Alcohol Consumption, Viral Infections, Chemotherapy Medications, Hemolytic Uremic Syndrome, Thrombotic Thrombocytopenic Purpura. Independently Published, 2021.

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Publications, ICON Health. HELLP Syndrome - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References. ICON Health Publications, 2004.

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Ng, Dominic S. Familial Lecithin Cholesterol Acyl Transferase Deficiency Syndromes. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199972135.003.0034.

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Lecithin cholesterol ester transferase (LCAT) is the sole enzyme in the circulation that mediates the esterification of free cholesterol (FC) to cholesterol ester (CE) in lipoproteins. Mutations in the LCAT gene result in one of two clinical syndromes: complete LCAT deficiency syndrome, and “fish eye disease.” The former is characterized by a broad spectrum of clinical features, including profound high-density lipoprotein (HDL) deficiency, hypertriglyceridemia, corneal opacities, anemia, neuropathies, and nephropathy. In contrast, fish eye disease patients develop severe HDL deficiency and sev
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Ng, Ann, and Erin S. Williams. Sickle Cell Disease. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0033.

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Sickle cell anemia (sickle cell disease) is a common hemoglobinopathy with anywhere from 90,000 to 100,000 Americans affected. This chronic condition has a predominance in populations of African descent, occurring in approximately 1 out of 365 African American births, compared to 1 out of 16,300 Hispanic births. The sickle cell trait can be detected in 1 of 13 African American births. One of the most common complications associated with sickle cell anemia, vaso-occlusive crises by sickled cells, results in severe pain. Other issues associated with this condition include acute chest syndrome, l
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Book chapters on the topic "Anemia syndrome"

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von Haehling, Stephan, and Stefan D. Anker. "Cardio-Renal Anemia Syndrome." In Hemodialysis. KARGER, 2011. http://dx.doi.org/10.1159/000327342.

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Xu, Xiaoyi, Hong Cheng, and Weijing Bian. "A Case of Cardiorenal Anemia Syndrome Complicated with Malignant Hypertension." In Treatment of Refractory Renal Anemia. Springer Nature Singapore, 2025. https://doi.org/10.1007/978-981-97-7636-8_22.

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Bagby, Grover C. "The Preleukemic Syndrome (Hematopoietic Dysplasia)." In Aplastic Anemia and Other Bone Marrow Failure Syndromes. Springer New York, 1990. http://dx.doi.org/10.1007/978-1-4612-3254-4_17.

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Gupta, Arun. "Inherited Bone Marrow Failure Syndrome–Fanconi Anemia." In Decision Making Through Problem Based Learning in Hematology. Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-8933-1_24.

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Al-Salem, Ahmed. "The Acute Chest Syndrome in Sickle Cell Anemia." In Medical and Surgical Complications of Sickle Cell Anemia. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-24762-5_7.

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Young, Neal S., Jaroslaw P. Maciejewski, Elaine Sloand, et al. "The Enigma of the Aplastic Anemia/PNH Syndrome." In Paroxysmal Nocturnal Hemoglobinuria and Related Disorders. Springer Japan, 2003. http://dx.doi.org/10.1007/978-4-431-67867-0_13.

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Stone, Marvin J., and Sigbjorn Berentsen. "Hyperviscosity Syndrome, Cold Agglutinin Hemolytic Anemia, and Cryoglobulinemia." In Waldenström’s Macroglobulinemia. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-22584-5_12.

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Al-Salem, Ahmed. "The Hand-Foot Syndrome in Patients with Sickle Cell Anemia." In Medical and Surgical Complications of Sickle Cell Anemia. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-24762-5_11.

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Parker, Michelle Mason, and Mark Wigger. "Cardiorenal Syndrome, Chronic Kidney Disease, Anemia, and Heart Failure." In Managing Heart Failure in Primary Care: A Case Study Approach. Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-20193-6_11.

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Hilt, Henry, and Oyebimpe Adesina. "Hyperhemolysis Syndrome in a Pregnant Woman with Sickle Cell Anemia." In Transfusion Management of the Obstetrical Patient. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-77140-3_17.

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Conference papers on the topic "Anemia syndrome"

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Lodonio, Larissa Lacerda, Livia Romana Lima Gonçalves Arrais, David Nilson Gondim Alves, et al. "Acute chest syndrome in sickle cell anemia: Diagnostic challenges and therapeutic strategies." In VI Seven International Multidisciplinary Congress. Seven Congress, 2024. http://dx.doi.org/10.56238/sevenvimulti2024-066.

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Sickle cell disease is a genetic blood disorder caused by a mutation in the amino acid glutamic acid, which is replaced by valine in the beta chain of the hemoglobin molecule. In this context, acute chest syndrome is a serious disease with a high rate of morbidity and mortality, accounting for approximately 25% of deaths in patients with sickle cell anemia. Thus, the objective of this study is to describe the main aspects of Acute Chest Syndrome (ACS) in patients with sickle cell anemia. This is a review study of a scoping review in which data collection was carried out on the research portal
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Mahmood, B., D. Rao, Z. Ghazala, and Y. M. Rivera-Sanchez. "Diffuse Alveolar Hemorrhage with Possible Heiner Syndrome Mistaken for Autoimmune Hemolytic Anemia." In American Thoracic Society 2019 International Conference, May 17-22, 2019 - Dallas, TX. American Thoracic Society, 2019. http://dx.doi.org/10.1164/ajrccm-conference.2019.199.1_meetingabstracts.a7500.

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Patel, S. V., V. M. Patel, S. M. Patel, K. Vance, and C. Alexander. "Zieve Syndrome: A Rare Cause of Hemolytic Anemia in Alcohol Use Disorder." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a2133.

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Floccari, Fulvio. "Cardiorenal-anemia syndrome and iron deficiency: new challenges in prevention and treatment." In 7th International Congress of Cardionephrology KARNEF 2025. Punta Niš, 2025. https://doi.org/10.46793/karnef25.170f.

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Sapira, Violeta, Mihaiela Lungu, Alexandru Paul Baciu, et al. "FROM DEPRESSION TO HUMAN IMMUNODEFICIENCY VIRUS – A CASE REPORT." In The European Conference of Psychiatry and Mental Health "Galatia". Archiv Euromedica, 2023. http://dx.doi.org/10.35630/2022/12/psy.ro.19.

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Introduction: Human immunodeficiency virus (HIV) infection is often preceded or accompanied by neuropsychiatric symptoms, including depression. This fact has been evaluated in most of the clinical studies to date as associated with HIV infection already diagnosed. Case report: We report a case of a 46-year-old woman patient with no prior diagnosed pathology, suffering from depressive disorder for roughly 6 months, with a progressive evolution under treatment. Blood tests showed a moderate normochromic normocytic anemic syndrome of unspecified origin. Given the fact that depressive syndrome has
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Rodriguez-Segade Alonso, Santiago, Irene Nieto Codesido, Carmen Diego Roza, and Elvira Clavero Fernández. "Anemia and proBNP levels as risk factors for airflow limitation in patients with acute coronary syndrome." In ERS International Congress 2023 abstracts. European Respiratory Society, 2023. http://dx.doi.org/10.1183/13993003.congress-2023.pa1024.

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Hernandez, T. E., N. Guevara, R. Marques-Jones, V. Chapiolkina, and S. Roudsari. "Case Report of Angioimmunoblastic T-Cell Lymphoma Presenting as Spontaneous Lysis Tumor Syndrome and Hemolytic Anemia." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a1709.

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Lee, D. J., K. A. Ramones, and T. Ambooken. "Idiopathic Pauci-Immune Pulmonary Capillaritis in a Patient With Autoimmune Hemolytic Anemia and Mowat Wilson Syndrome." In American Thoracic Society 2024 International Conference, May 17-22, 2024 - San Diego, CA. American Thoracic Society, 2024. http://dx.doi.org/10.1164/ajrccm-conference.2024.209.1_meetingabstracts.a2280.

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Ofori-Acquah, Solomon, Samit Ghosh, and Olufolake Adisa. "Acute Elevation Of Protein-Free Plasma Heme Triggers Acute Chest Syndrome In Mouse Models Of Sickle Cell Anemia." In American Thoracic Society 2011 International Conference, May 13-18, 2011 • Denver Colorado. American Thoracic Society, 2011. http://dx.doi.org/10.1164/ajrccm-conference.2011.183.1_meetingabstracts.a3757.

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Brasil, Salomão Bruno Dos Santos, Matteus Gomes De Oliveira, Luis Felipe Ferreira Carneiro, Osmar Júnior Da Silva Silva, and Josuelem Portela Castro. "REVISÃO DE LITERATURA – ASSOCIAÇÃO ENTRE HIV E O DESENVOLVIMENTO CONCOMITANTE DE ANEMIA." In II Congresso Brasileiro de Hematologia Clínico-laboratorial On-line. Revista Multidisciplinar em Saúde, 2022. http://dx.doi.org/10.51161/hematoclil/129.

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Introdução: O HIV (human immunodeficiency virus) é um lentivírus isolado na década de 1980 que gerou uma pandemia com consequências hodiernas após o surgimento em massa inexplicável de pneumonia por Pneumocystis jirovecii e sarcoma de Kaposi em homossexuais previamente hígidos. O ciclo de replicação do vírus depende principalmente da interação bioquímica da proteína de superfície gp120 com o receptor CD4, encontrado principalmente nas Células T CD4. A anemia encontrada em pacientes positivados para o HIV se desenvolve por razões multifatoriais, representando importante objeto de investigação,
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