Imerslund-Gräsbeck Syndrome presenting with microangiopathic hemolytic anemia in a child
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference18 articles.
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2. Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anemia;Aminoff;Nat. Genet.,1999
3. Current hematological findings of cobalamin deficiency;Andres;Clin. Lab. Hematol.,2006
4. Pseudo-thrombotic microangiopathy related to cobalamin deficiency;Andres;Am. J. Med.,2006
5. Neglect‐induced pseudo‐thrombotic thrombocytopenic purpura due to vitamin B12 deficiency;Asano;Pediatr. Int.,2015
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1. Imerslund-Gräsbeck Syndrome in a child with a novel compound heterozygous mutations in the AMN gene: a case report;2023-11-14
2. Imerslund-Gräsbeck syndrome: a comprehensive review of reported cases;Orphanet Journal of Rare Diseases;2023-09-14
3. Pseudo-thrombotic microangiopathy due to folate deficiency;BMJ Case Reports;2023-01
4. Síndrome de Imerslund-Gränsbeck: revisión sistemática de casos clínicos;CES Medicina;2022-11-16
5. Metabolism-mediated thrombotic microangiopathy and B12;Vitamins and Hormones;2022
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