Zaloguj się

Gotowe bibliografie tematyczne / Spherocytosis / Artykuły w czasopismach

Kliknij ten link, aby zobaczyć inne rodzaje publikacji na ten temat: Spherocytosis.

Artykuły w czasopismach na temat „Spherocytosis”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

Utwórz poprawne odniesienie w stylach APA, MLA, Chicago, Harvard i wielu innych

Wybierz rodzaj źródła:

Sprawdź 50 najlepszych artykułów w czasopismach naukowych na temat „Spherocytosis”.

Przycisk „Dodaj do bibliografii” jest dostępny obok każdej pracy w bibliografii. Użyj go – a my automatycznie utworzymy odniesienie bibliograficzne do wybranej pracy w stylu cytowania, którego potrzebujesz: APA, MLA, Harvard, Chicago, Vancouver itp.

Możesz również pobrać pełny tekst publikacji naukowej w formacie „.pdf” i przeczytać adnotację do pracy online, jeśli odpowiednie parametry są dostępne w metadanych.

Przeglądaj artykuły w czasopismach z różnych dziedzin i twórz odpowiednie bibliografie.

1

LI, Ying, Liyuan Lu, and Juan LI. "Topological Structures and Membrane Nanostructures of Erythrocytes after Splenectomy in Hereditary Spherocytosis Patients via Atomic Force Microscopy." Cell Biochemistry and Biophysics 74, no. 3 (2016): 365–71. http://dx.doi.org/10.1007/s12013-016-0755-4.

Pełny tekst źródła

Streszczenie:

Abstract Hereditary spherocytosis is an inherited red blood cell membrane disorder resulting from mutations of genes encoding erythrocyte membrane and cytoskeletal proteins. Few equipments can observe the structural characteristics of hereditary spherocytosis directly expect for atomic force microscopy In our study, we proved atomic force microscopy is a powerful and sensitive instrument to describe the characteristics of hereditary spherocytosis. Erythrocytes from hereditary spherocytosis patients were small spheroidal, lacking a well-organized lattice on the cell membrane, with smaller cell

Style APA, Harvard, Vancouver, ISO itp.

2

Shah, S., and R. Vega. "Hereditary Spherocytosis." Pediatrics in Review 25, no. 5 (2004): 168–72. http://dx.doi.org/10.1542/pir.25-5-168.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

3

Mahajan, Vasudha, and Sunil K. Jain. "Hereditary Spherocytosis." NeoReviews 17, no. 12 (2016): e697-e704. http://dx.doi.org/10.1542/neo.17-12-e697.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

4

Kalyan, Meenakshi, ShubhangiA Kanitkar, AnuN Gaikwad, and Harsh Kumar. "Hereditary spherocytosis." Medical Journal of Dr. D.Y. Patil University 7, no. 2 (2014): 229. http://dx.doi.org/10.4103/0975-2870.126357.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

5

Koju, Surendra, and Ramesh Makaju. "Hereditary Spherocytosis." Journal of Lumbini Medical College 6, no. 1 (2018): 41–43. http://dx.doi.org/10.22502/jlmc.v6i1.202.

Pełny tekst źródła

Streszczenie:

Introduction: Hereditary spherocytosis is a red cell membrane disorder that causes hemolytic anemia. Due to defective cell membrane, red cells are spherical shaped and result in their early lysis. Osmotic fragility of spherocytic red cell is increased. Case report: A 22 year old female presented with chief complain of abdominal pain. Initially she was diagnosed as cholelithiasis. Under laboratory evaluation she was found to be anemic with reticulocytosis. In peripheral blood smear, spherocytes were moderately distributed. Antihuman globulin test was negative but osmotic fragility was hig

Style APA, Harvard, Vancouver, ISO itp.

6

CROOM, ROBERT D., CAMPBELL W. MCMILLAN, GEORGE F. SHELDON, and EUGENE P. ORRINGER. "Hereditary Spherocytosis." Annals of Surgery 203, no. 1 (1986): 34–39. http://dx.doi.org/10.1097/00000658-198601000-00007.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

7

Perrotta, Silverio, Patrick G. Gallagher, and Narla Mohandas. "Hereditary spherocytosis." Lancet 372, no. 9647 (2008): 1411–26. http://dx.doi.org/10.1016/s0140-6736(08)61588-3.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

8

Iolascon, A., R. A. Avvisati, and C. Piscopo. "Hereditary spherocytosis." Transfusion Clinique et Biologique 17, no. 3 (2010): 138–42. http://dx.doi.org/10.1016/j.tracli.2010.05.006.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

9

Trompeter, Sara, and May-Jean King. "Hereditary spherocytosis." Paediatrics and Child Health 25, no. 8 (2015): 381–86. http://dx.doi.org/10.1016/j.paed.2015.04.003.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

10

Trompeter, Sara, and May-Jean King. "Hereditary spherocytosis." Paediatrics and Child Health 29, no. 8 (2019): 359–64. http://dx.doi.org/10.1016/j.paed.2019.05.006.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

11

Agre, Peter. "Hereditary Spherocytosis." JAMA: The Journal of the American Medical Association 262, no. 20 (1989): 2887. http://dx.doi.org/10.1001/jama.1989.03430200131039.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

12

Agre, P. "Hereditary spherocytosis." JAMA: The Journal of the American Medical Association 262, no. 20 (1989): 2887–90. http://dx.doi.org/10.1001/jama.262.20.2887.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

13

Asatryan, T. T., M. N. Zenina, and L. B. Gaikovaya. "Modern approaches to laboratory diagnostic of microspherocytic anemia." Medical alphabet 3, no. 22 (2019): 22–25. http://dx.doi.org/10.33667/2078-5631-2019-3-22(397)-22-25.

Pełny tekst źródła

Streszczenie:

Diagnosis of hereditary spherocytosis, as the most common form of membranopathy, is improved, thanks to advances in biotechnology and the presence of a large number of modern automatic analyzers. All this leads to a reduction in the number of patients with undiagnosed hereditary spherocytosis and a decrease in the incidence of complications. However, despite the improvement of various methods of evaluation of red blood cells, some difficulties in the diagnosis of hereditary spherocytosis remain. In this study, the authors developed an algorithm for the laboratory diagnosis of anemias microperi

Style APA, Harvard, Vancouver, ISO itp.

14

M. D., Balaji, Vadlamudy Vinay, and Shankar Vangalpudi V. "Aplastic crisis in a child with hereditary spherocytosis with a strong family history resolving with supportive care." International Journal of Contemporary Pediatrics 5, no. 3 (2018): 1150. http://dx.doi.org/10.18203/2349-3291.ijcp20181562.

Pełny tekst źródła

Streszczenie:

Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity. Clinical features range from asymptomatic to fulminant hemolytic anaemia. The Human Parvovirus Virus B19 induced aplastic crisis can unmask several hereditary hematological disorders that have been normally compensated. Among these conditions, hereditary spherocytosis has been extensively reported. The clinical importance of this report is that in the case of an abrupt onset of unexplained severe anemia and jaundice, one should consider underlying hemolytic anemias mostly hereditary spherocytosis complica

Style APA, Harvard, Vancouver, ISO itp.

15

Santoso, F. X., Sukardi Sukardi, Bambang Permono, Netty R. H. T., and S. Untario. "Hereditary Spherocytosis : A Clinical Experience." Paediatrica Indonesiana 28, no. 1-2 (2019): 27–35. http://dx.doi.org/10.14238/pi28.1-2.1988.27-35.

Pełny tekst źródła

Streszczenie:

Although hereditary spherocytosis is a common cause of hemolytic anemia among whites of Northern European descent, it is uncommon in Asia. In the past 8.5 years (from December 1978 to June 1987), we found only six cases of hereditary spherocytosis. They were 3 males and 3 females, and their ages ranged from 3 months to 8 years, with a mean age of 3.3 years. The most common presenting complaint was anemia (6 cases) followed by jaundice (4 cases) and splenomegaly (4 cases). Other symptoms were fever, abdominal pain and hepatomegaly. The mean hemoglobin concentration of these patients was 7.5 g/d

Style APA, Harvard, Vancouver, ISO itp.

16

Kasula, Lingareddy, Swapna Lingaldinna, Rakesh Kotha, and Alimelu Madireddi. "Hereditary Spherocytosis in a Neonate with a New Frameshift Deletion- A Case Report." Asian Journal of Pediatric Research 13, no. 2 (2023): 21–25. http://dx.doi.org/10.9734/ajpr/2023/v13i2258.

Pełny tekst źródła

Streszczenie:

Introduction: Hemolytic anaemias often occur in neonates, often presenting with jaundice or encephalopathy. Hereditary spherocytosis is the most common cause, followed by glucose-6-phosphate-dehydrogenase deficiency and ABO isoimmunization. Early diagnosis and laboratory evaluation are crucial for effective interventions and preventing complications. This case report helps to recognise the clinical signs of hereditary spherocytosis early. And to emphasise the importance of the HS ratio in the diagnostic approach to hereditary spherocytosis. Case Report: A 20-day-old first-born female bab

Style APA, Harvard, Vancouver, ISO itp.

17

Park, Tae Yeong, Jae Hyuck Jun, Huapyong Kang, et al. "Cholangitis Caused by Hereditary Spherocytosis in Adulthood Treated by Endoscopic Retrograde Cholangiopancreatography." Korean Journal of Pancreas and Biliary Tract 25, no. 2 (2020): 123–27. http://dx.doi.org/10.15279/kpba.2020.25.2.123.

Pełny tekst źródła

Streszczenie:

Hereditary spherocytosis is a disease caused by deficiency of erythrocyte lipid membrane protein. Hereditary spherocytosis shows hemolysis of erythrocyte, and it leads to anemia, jaundice by elevation of indirect bilirubin. Almost of patients are diagnosed in their infancy, and can be cured by splenectomy about their age 6–7. Herein, we report a rare case of 33-year-old male was suffered from gallbladder stone and cholangitis those are thought to be the late complications of hereditary spherocytosis. We performed endoscopic retrograde cholangiopancreaticography to remove common bile duct stone

Style APA, Harvard, Vancouver, ISO itp.

18

Schrier, S. "Hereditary Spherocytosis (HS)." ASH Image Bank 2001, no. 1205 (2001): 100214. http://dx.doi.org/10.1182/ashimagebank-2001-100214.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

19

Reznikoff-Etievant, M. F., C. Bonaiti, P. Maigret, et al. "HEREDITARY SPHEROCYTOSIS LINKAGE." British Journal of Haematology 46, no. 1 (2008): 153–55. http://dx.doi.org/10.1111/j.1365-2141.1980.tb05949.x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

20

Schuettge, Anna Gould. "Management of Spherocytosis." Journal of Pediatric Surgical Nursing 3, no. 1 (2014): 13–15. http://dx.doi.org/10.1097/jps.0000000000000010.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

21

Chuyko, Ya M., E. A. Seregina, T. A. Vuimo, A. V. Poletaev, and N. S. Smetanina. "Endothelial dysfunction in patients with hereditary spherocytosis and b-thalassemia." Pediatric Hematology/Oncology and Immunopathology 20, no. 3 (2021): 52–59. http://dx.doi.org/10.24287/1726-1708-2021-20-3-52-59.

Pełny tekst źródła

Streszczenie:

Patients with hereditary spherocytosis and b-Thalassemia are characterized by the increased risk of thrombosis. The early manifestation of thrombotic complications can occur even in childhood especially after surgery. Hypercoagulability can be associated with endothelial dysfunction. The aim of this study was to investigate the hemostatic state and endothelial function in children with hereditary spherocytosis and b-thalassemia. The study was approved by the Independent Ethics Committee of the Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology. Th

Style APA, Harvard, Vancouver, ISO itp.

22

Dr., Ramesh Chandra, Mayank Gupta Dr., Gaurav Chauhan Dr., Sunil Mahavar Dr., Swati Srivastava Dr., and Raman Sharma Dr. "Hereditary Spherocytosis in a 17 year girl: A case report." International Multispeciality Journal of Health 3, no. 7 (2017): 226–29. https://doi.org/10.5281/zenodo.837959.

Pełny tekst źródła

Streszczenie:

<strong><em>Abstract—</em></strong> <em>Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from an asymptomatic condition to a fulminate haemolytic anaemia. Although a positive family history of spherocytosis increases the risk for this disorder, it may be sporadic in some cases. Seventeen years old girl presented with mild anaemia, jaundice and moderate splenomegaly. Her haematological parameters supported diagnosis of hereditary spherocytosis. Appropriate treatment was started with an advice to patient to undergo splenectomy

Style APA, Harvard, Vancouver, ISO itp.

23

Mitsura, E. F. "HEREDITARY SPHEROCYTOSIS IN CHILDREN: MODERN CONCEPTION (literature review)." Health and Ecology Issues, no. 2 (June 28, 2011): 39–44. http://dx.doi.org/10.51523/2708-6011.2011-8-2-7.

Pełny tekst źródła

Streszczenie:

The modern conception of hereditary spherocytosis has been considered in the article. Hereditary spherocytosis is a common inherited disease declaring itself in haemolytic anaemia, jaundice and splenomegaly. The contemporary classification, approaches to the diagnosis and treatment depending on severity of the disease course and presence of the most frequent complications have been given.

Style APA, Harvard, Vancouver, ISO itp.

24

Bordyugova, O. V., E. N. Marchenko, S. A. Yuldasheva, and E. I. Shevtsova. "Cholelithiasis in children with hereditary spherocytosis." Experimental and Clinical Gastroenterology, no. 11 (November 20, 2019): 31–35. http://dx.doi.org/10.31146/1682-8658-ecg-171-11-31-35.

Pełny tekst źródła

Streszczenie:

Hereditary spherocytosis (Minkowski-Shoffar disease) - protein-dependent mebranopathy, leading to the destruction of red blood cells, is one of the causes of gallstone disease. The purpose of this work: to acquaint doctors of various specialties with a possible complication of hereditary spherocytosis in the form of cholelithiasis. The article briefly presents etiopathogenesis, clinical features, diagnosis and treatment of this disease. Two clinical cases of cholelithiasis with hereditary hemolytic microspherocytic anemia of Minkowski-Shoffar are described. Results. In the cases presented, the

Style APA, Harvard, Vancouver, ISO itp.

25

J., Brandenberg, F. Demarmels Biasiutti, Lutz H., and Wuillemin W. "Hereditary spherocytosis and hemochromatosis." Annals of Hematology 81, no. 4 (2002): 202–9. http://dx.doi.org/10.1007/s00277-002-0432-0.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

26

Bolton-Maggs, P. H. B. "Hereditary spherocytosis; new guidelines." Archives of Disease in Childhood 89, no. 9 (2004): 809–12. http://dx.doi.org/10.1136/adc.2003.034587.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

27

Pajor, A., D. Lehoczky, and Z. Szakács. "Pregnancy and hereditary spherocytosis." Archives of Gynecology and Obstetrics 253, no. 1 (1993): 37–42. http://dx.doi.org/10.1007/bf02770632.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

28

Mechery, Joseph, Claudia Hardy, and Christos Spyroulis. "Hereditary spherocytosis complicating pregnancy." European Journal of Obstetrics & Gynecology and Reproductive Biology 206 (November 2016): e109. http://dx.doi.org/10.1016/j.ejogrb.2016.07.284.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

29

Warkentin, TE, RD Barr, MA Ali, and N. Mohandas. "Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis." Blood 75, no. 1 (1990): 266–70. http://dx.doi.org/10.1182/blood.v75.1.266.266.

Pełny tekst źródła

Streszczenie:

Abstract A 14-year-old boy with hemoglobin SC disease and alpha-thalassemia-2 experienced five episodes of acute splenic sequestration crisis (ASSC), while two of his siblings with identical globin genotypes (SC and - alpha/alpha alpha) had no such experience. To determine if an additional red blood cell (RBC) defect was responsible for the unusual occurrence of frequent ASSCs, we performed detailed rheologic characterization and membrane protein analysis on RBCs from the proband and other members of his family. Reduced surface area, increased mechanical instability, and decreased spectrin con

Style APA, Harvard, Vancouver, ISO itp.

30

Warkentin, TE, RD Barr, MA Ali, and N. Mohandas. "Recurrent acute splenic sequestration crisis due to interacting genetic defects: hemoglobin SC disease and hereditary spherocytosis." Blood 75, no. 1 (1990): 266–70. http://dx.doi.org/10.1182/blood.v75.1.266.bloodjournal751266.

Pełny tekst źródła

Streszczenie:

A 14-year-old boy with hemoglobin SC disease and alpha-thalassemia-2 experienced five episodes of acute splenic sequestration crisis (ASSC), while two of his siblings with identical globin genotypes (SC and - alpha/alpha alpha) had no such experience. To determine if an additional red blood cell (RBC) defect was responsible for the unusual occurrence of frequent ASSCs, we performed detailed rheologic characterization and membrane protein analysis on RBCs from the proband and other members of his family. Reduced surface area, increased mechanical instability, and decreased spectrin content of t

Style APA, Harvard, Vancouver, ISO itp.

31

Barella, Susanna, Ramon Simon-Lopez, Nicola Di Gaetano, and Renzo Galanello. "Hereditary Spherocytosis: How the New Information Provided by the Routine Hematology Analysers May Help in Its Differential Diagnosis or Flagging." Blood 120, no. 21 (2012): 5163. http://dx.doi.org/10.1182/blood.v120.21.5163.5163.

Pełny tekst źródła

Streszczenie:

Abstract Abstract 5163 Introduction: Hereditary Spherocytosis (HS) is one of the most common inherited hemolytic anemias. Many of them are autosomal dominant, being about 25% of the cases transmitted recessively. Diagnostic of HS: Classic testing for HS includes: Hematologic testing of red blood cell indices (RDW, MCHC, Reticulocyte count), peripheral blood smear (presence of spherocytes), osmotic fragility and Eosin-5-maleimide binding to band 3 and Rh-related proteins forms that may be used as screening tests for hereditary spherocytosis. Objective: Recently have been developed new parameter

Style APA, Harvard, Vancouver, ISO itp.

32

Prudinnik, D. S., L. D. Koleva, E. A. Bovt, et al. "Red blood cell filterability measurement in the diagnosis of hereditary spherocytosis." Pediatric Hematology/Oncology and Immunopathology 23, no. 2 (2024): 145–51. http://dx.doi.org/10.24287/1726-1708-2024-23-2-145-151.

Pełny tekst źródła

Streszczenie:

The differential diagnosis of hereditary spherocytosis is a great challenge because of the similar clinical and laboratory signs it shares with other hereditary hemolytic anemias as well as due to the limited availability of molecular genetic testing. The development of easy-to-perform laboratory tests for the differential diagnosis of hereditary hemolytic anemias remains as relevant as ever. Here, a method of measuring red blood cell filterability for the diagnosis of hereditary spherocytosis is proposed for the first time. The aim of our study was to compare red blood cell filterability meas

Style APA, Harvard, Vancouver, ISO itp.

33

Sultana, Mst Musarrat, Md Shafiqul Islam, and Md Sanaul Haque Mia. "Hereditary Spherocytosis in a 22 Month Old Child." TAJ: Journal of Teachers Association 30, no. 2 (2018): 79–82. http://dx.doi.org/10.3329/taj.v30i2.39143.

Pełny tekst źródła

Streszczenie:

Hereditary spherocytosis (HS) is a familial hemolytic disorder with marked heterogeneity of clinical features, ranging from asymptomatic condition to a fulminant hemolytic anemia. Although a positive family history of spherocytosis increases the risk for this disorder, it may be sporadic in some case. A 22-month old girl was admitted in Rajshahi Medical College Hospital with pallor and jaundice. Her parents gave history of repeated episodes of pallor and jaundice since 8 month of age with negative family history. Blood film showed plenty of spherocytes, reticulocytosis of 15.0%, negative direc

Style APA, Harvard, Vancouver, ISO itp.

34

Waheed, Waqar, Anjali L. Varigonda, Chris E. Holmes, Christopher Trevino, Neil M. Borden, and W. Pendlebury. "Spinal Cord Infarction in a Patient with Hereditary Spherocytosis: A Case Report and Discussion." Case Reports in Neurological Medicine 2016 (2016): 1–7. http://dx.doi.org/10.1155/2016/7024120.

Pełny tekst źródła

Streszczenie:

The etiology of spinal cord infarcts (SCIs), besides being related to aortic perioperative events, in large subset of SCIs, remains cryptogenic. We present a first case of SCI in a patient with hereditary spherocytosis and discuss the potential pathophysiologic considerations for vascular compromise. A 43-year-old woman with a history of hereditary spherocytosis, post splenectomy status, presented with chest, back, and shoulder pain with subsequent myelopathic picture; SCI extending from C4-T2 was confirmed by MRI. Despite aggressive treatment her stroke progressed leading to her demise. Her a

Style APA, Harvard, Vancouver, ISO itp.

35

Asatryan, Tatevik T., Marina N. Zenina, Nataliya Yu Chernysh, and Larisa B. Gaikovaya. "Clinical and laboratory profile of hereditary spherocytosis." HERALD of North-Western State Medical University named after I.I. Mechnikov 11, no. 1 (2019): 65–72. http://dx.doi.org/10.17816/mechnikov201911165-72.

Pełny tekst źródła

Streszczenie:

Diagnostics of hereditary spherocytosis is usually based on clinical picture, family history and laboratory tests. The list of laboratory tests includes osmotic fragility test, a glycerol lysis test, an eosin-5-maleimide binding test and others. None of the following methods identify all cases of hereditary spherocytosis. The article discusses the problems of diagnosing congenital microspherocytic anemia and provides the detailed analysis of informational value of various research methods and their significance.

Style APA, Harvard, Vancouver, ISO itp.

36

Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.1124.

Pełny tekst źródła

Streszczenie:

Abstract Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect

Style APA, Harvard, Vancouver, ISO itp.

37

Pootrakul, P., K. Kitcharoen, P. Yansukon, et al. "The effect of erythroid hyperplasia on iron balance." Blood 71, no. 4 (1988): 1124–29. http://dx.doi.org/10.1182/blood.v71.4.1124.bloodjournal7141124.

Pełny tekst źródła

Streszczenie:

Measurements of erythropoiesis and iron balance were made in eight normal and 32 anemic subjects. The latter consisted of 12 individuals with ineffective erythropoiesis (beta-thalassemia/hemoglobin E), 13 subjects with ineffective erythropoiesis and hemolytic anemia (hemoglobin H), and seven subjects with hemolytic anemia (hereditary spherocytosis). A consistent relationship within each group existed between the degree of erythropoiesis and radioiron absorption. Although the effect of erythropoiesis on iron absorption was of similar magnitude in the two thalassemia groups, the effect in heredi

Style APA, Harvard, Vancouver, ISO itp.

38

Novikova, I. A., K. S. Makeyeva, and E. F. Mitsura. "Parameters of neutrophil functional activity in children with hereditary spherocytosis." Medical and Biological Problems of Life Activity, no. 2 (September 20, 2024): 121–26. https://doi.org/10.58708/2074-2088.2024-2(32)-121-126.

Pełny tekst źródła

Streszczenie:

This study investigates the functional activity of peripheral blood neutrophils in children with hereditary spherocytosis − one of the most common forms of congenital hemolytic anemias. For the first time, a comprehensive examination of various aspects of neutrophil reactivity in this pathology was conducted, including their ability to form reactive oxygen species and neutrophil extracellular traps (NETosis). The results revealed significant changes in neutrophil functional activity in patients with hereditary spherocytosis outside of hemolytic crisis, particularly an increased capacity for re

Style APA, Harvard, Vancouver, ISO itp.

39

Cheli, Estelle, Jocelyn Roze, Nadia Daouairi, et al. "Value of combined spherocytose osmotic and EMA tests in the diagnosis of hereditary spherocytosis." International Journal of Laboratory Hematology 41, no. 4 (2019): e84-e85. http://dx.doi.org/10.1111/ijlh.12976.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

40

Kibangou, Angela, Mounia Hanafi, Salima Hajjaji, Noufissa Benajiba, Khadija Maani, and Abdelhak Abkari. "Genetically Confirmed Hereditary Spherocytosis About 3 Cases." American Journal of Pediatrics 11, no. 2 (2025): 55–57. https://doi.org/10.11648/j.ajp.20251102.14.

Pełny tekst źródła

Streszczenie:

Hereditary spherocytosis, also known as Minkowski chauffard disease, is a constitutional red blood cell disease most common in North Africa with a prevalence of 1/2000. Autosomal dominant transmission. The disease is revealed by a chronic hemolysis chart made of a pallor, an icterus and a huge splenomegaly. The diagnosis is usually confirmed by a globular resistance test or better flow cytometry. It is easier when there is a family history associated with regenerative hemolytic anemia with the presence of spherocytosis. This assessment must be made before any transfusion of globular pellet. Th

Style APA, Harvard, Vancouver, ISO itp.

41

Papp, Zsuzsanna Erzsébet, Mihaela Chincesan, Adrienne Mária Horváth, and Izabella Kelemen. "Herediter spherocytosis a marosvásárhelyi gyermekhematológia osztály tapasztalatában." Orvosi Hetilap 160, no. 45 (2019): 1798–803. http://dx.doi.org/10.1556/650.2019.31345.

Pełny tekst źródła

Streszczenie:

Abstract: Introduction: Hereditary spherocytosis is a genetically determined familial hemolytic anemia. Clinically it is ranged from an asymptomatic condition to severe hemolytic anemia. The major complications are aplastic or megaloblastic crisis, hemolytic crisis, cholecystitis and cholelithiasis. Aim: To shortly summarize the most characteristic symptoms of hereditary spherocytosis from the prism of our centers in order to help primary care-physicians or pediatricians in this affection recognition. Method: In our retrospective study, we processed a period of 6 years between 2012–2017, we st

Style APA, Harvard, Vancouver, ISO itp.

42

Gallagher, Patrick G. "Red Cell Membrane Disorders." Hematology 2005, no. 1 (2005): 13–18. http://dx.doi.org/10.1182/asheducation-2005.1.13.

Pełny tekst źródła

Streszczenie:

Abstract Disorders of the erythrocyte membrane, including hereditary spherocytosis, hereditary elliptocytosis, hereditary pyropoikilocytosis, and hereditary stomatocytosis, comprise an important group of inherited hemolytic anemias. These syndromes are characterized by marked clinical and laboratory heterogeneity. Recent molecular studies have revealed that there is also significant genetic heterogeneity in these disorders. This is particularly true for the spherocytosis syndromes where each kindred has a private mutation in one of the spherocytosis genes. Treatment with splenectomy is curativ

Style APA, Harvard, Vancouver, ISO itp.

43

Shoda, Tetsuo, Minoru Yoshimura, Daishi Hayata, Yoshio Miyazawa, and Kiyoyuki Ogata. "Marked Spherocytosis in Clostridal Sepsis." International Journal of Hematology 83, no. 2 (2006): 179–80. http://dx.doi.org/10.1532/ijh97.05165.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

44

Unni, VN, A. Mathew, J. Varghese, and G. Kurian. "Hereditary spherocytosis with nephrotic syndrome." Indian Journal of Nephrology 17, no. 4 (2007): 174. http://dx.doi.org/10.4103/0971-4065.39173.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

45

Ceylan, Cengiz, Selda Çakın, and Ülkü Ergene. "Hereditary Spherocytosis In An Adult." Journal of Tepecik Education and Research Hospital 22, no. 1 (2012): 63–65. http://dx.doi.org/10.5222/terh.2012.60804.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

46

Becker, Pamela S., and Samuel E. Lux. "Hereditary Spherocytosis and Related Disorders." Clinics in Haematology 14, no. 1 (1985): 15–43. http://dx.doi.org/10.1016/s0308-2261(21)00461-6.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

47

LAWRENCE, P., I. ARONSON, N. SAXE, and P. JACOBS. "Leg ulcers in hereditary spherocytosis." Clinical and Experimental Dermatology 16, no. 1 (1991): 28–30. http://dx.doi.org/10.1111/j.1365-2230.1991.tb00289.x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

48

Snyder, C. L. "Partial Splenectomy for Hereditary Spherocytosis." AAP Grand Rounds 25, no. 5 (2011): 49. http://dx.doi.org/10.1542/gr.25-5-49.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

49

Agarwal, Archana M. "Ankyrin Mutations in Hereditary Spherocytosis." Acta Haematologica 141, no. 2 (2019): 63–64. http://dx.doi.org/10.1159/000495339.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

50

Zipursky, Alvin, Elizabeth J. Brown, and Dolores Momotiuk Chachula. "ERYTHROCYTE VACUOLES IN HEREDITARY SPHEROCYTOSIS." British Journal of Haematology 62, no. 4 (1986): 775–76. http://dx.doi.org/10.1111/j.1365-2141.1986.tb04102.x.

Pełny tekst źródła

Style APA, Harvard, Vancouver, ISO itp.

Oferujemy zniżki na wszystkie plany premium dla autorów, których prace zostały uwzględnione w tematycznych zestawieniach literatury. Skontaktuj się z nami, aby uzyskać unikalny kod promocyjny!