Allogeneic bone marrow transplantation for treatment of severe hemolytic anemia attributable to hexokinase deficiency
Author:
Affiliation:
1. Pediatric Marrow and Blood Cell Transplantation Program, Children’s Hospital at Montefiore, Albert Einstein College of Medicine, Bronx, NY; and
2. Departments of Pediatrics, Pathology, and Genetics, Yale University, New Haven, CT
Publisher
American Society of Hematology
Subject
Cell Biology,Hematology,Immunology,Biochemistry
Link
http://ashpublications.org/blood/article-pdf/128/5/735/1397569/735.pdf
Reference12 articles.
1. Hexokinase mutations that produce nonspherocytic hemolytic anemia.;Bianchi;Blood Cells Mol Dis,1995
2. Congenital nonspherocytic hemolytic anemia with an unstable hexokinase variant.;Board;Blood,1978
3. Hereditary hemolytic anemia with hexokinase deficiency. Role of hexokinase in erythrocyte aging.;Valentine;N Engl J Med,1967
4. The energy-less red blood cell is lost: erythrocyte enzyme abnormalities of glycolysis.;van Wijk;Blood,2005
5. Generalized hexokinase deficiency in the blood cells of a patient with nonspherocytic hemolytic anemia.;Rijksen;Blood,1983
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Novel pathogenic variant c.2714C>A (p. Thr905Lys) in the HK1 gene causing severe haemolytic anaemia with developmental delay in an Indian family;Journal of Clinical Pathology;2020-12-25
2. A nonsense variant in the Hexokinase 1 gene ( HK 1 ) causing severe non‐spherocytic haemolytic anaemia: genetic analysis exemplifies ambiguity due to multiple Isoforms;British Journal of Haematology;2019-05-23
3. How I do in front of an hemolytic anemia of unknown etiology?;HEMATOLOGIE;2019
4. How I do in front of an hemolytic anemia of unknown etiology?;ANN BIOL CLIN-PARIS;2018
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