Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?-Reference-Cited by-同舟云学术

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Screening for hereditary spherocytosis in daily practice: what is the best algorithm using erythrocyte and reticulocyte parameters?

Published:2022-04-22 Issue:7 Volume:101 Page:1485-1491
ISSN:0939-5555
Container-title:Annals of Hematology
language:en
Short-container-title:Ann Hematol

Author:

Adam Anne-Sophie^ORCID,Cotton Frédéric,Cantinieaux Brigitte,Benyaich Sara,Gulbis Béatrice

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Link

https://link.springer.com/content/pdf/10.1007/s00277-022-04845-4.pdf

Reference29 articles.

1. King MJ, Zanella A (2013) Hereditary red cell membrane disorders and laboratory diagnostic testing. Int J Lab Hematol 35(3):237–243

2. Narla J, Mohandas N (2017) Red cell membrane disorders. Int J Lab Hematol 39(Suppl 1):47–52

3. Barcellini W et al (2011) Hereditary red cell membrane defects: diagnostic and clinical aspects. Blood Transfus 9(3):274–277

4. King MJ et al (2015) ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders. Int J Lab Hematol 37(3):304–325

5. Christensen RD, Yaish HM, Gallagher PG (2015) A pediatrician’s practical guide to diagnosing and treating hereditary spherocytosis in neonates. Pediatrics 135(6):1107–1114

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