Profound spherocytosis in adulthood: Acquired, hereditary or both?-Reference-Cited by-同舟云学术

Profound spherocytosis in adulthood: Acquired, hereditary or both?

Published:2017-05-10 Issue:5 Volume:39 Page:e117-e120
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Langeveld T. J. C.¹^ORCID,van Rossum A. P.²,van der Zwaag B.³,van Wijk R.⁴,Vlasveld L. Th.⁵

Affiliation:

1. Department of Internal Medicine; Leiden University Medical Center; Leiden The Netherlands

2. Department of Clinical Chemistry; HMC (Haaglanden Medical Center); location Bronovo; The Hague The Netherlands

3. Department of Genetics; University Medical Center Utrecht; Utrecht The Netherlands

4. Department of Clinical Chemistry and Haematology; Laboratory for Red Blood Cell Research; University Medical Center Utrecht; Utrecht The Netherlands

5. Department of Internal Medicine; HMC (Haaglanden Medical Center), location Bronovo; The Hague The Netherlands

Publisher

Wiley

Subject

Biochemistry (medical),Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12685/fullpdf

Reference10 articles.

1. Guidelines for the diagnosis and management of hereditary spherocytosis - 2011 update;Bolton-Maggs;Br J Haematol,2012

2. ICSH guidelines for the laboratory diagnosis of nonimmune hereditary red cell membrane disorders;King;Int J Lab Hematol,2015

3. Advances in laboratory diagnosis of hereditary spherocytosis;Farias;Clin Chem Lab Med,2016

4. Autoimmune hemolytic anemia due to IgA class autoantibodies;Sokol;Immunohematology,1996

5. Direct antiglobulin (“Coombs”) test-negative autoimmune hemolytic anemia: a review;Segel;Blood Cell Mol Dis,2014