Diagnosing nocturnal paroxysmal hemoglobinuria: a single-center 4-year experience-Reference-Cited by-同舟云学术

Diagnosing nocturnal paroxysmal hemoglobinuria: a single-center 4-year experience

Published:2017-04-13 Issue:3 Volume:39 Page:329-336
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Mercier T.¹,Devos T.²³,Mukovnikova M.⁴,Boeckx N.⁴⁵

Affiliation:

1. Department of Internal Medicine; University Hospitals Leuven; Leuven Belgium

2. Department of Hematology; University Hospitals Leuven; Leuven Belgium

3. Department of Microbiology and Immunology; KU Leuven; Leuven Belgium

4. Department of Laboratory Medicine; University Hospitals Leuven; Leuven Belgium

5. Department of Oncology; KU Leuven; Leuven Belgium

Publisher

Wiley

Subject

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

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12631/fullpdf

Reference23 articles.

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3. Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria;Takeda;Cell,1993

4. Paroxysmal nocturnal hemoglobinuria;Brodsky;Blood,2014

5. Guidelines for the diagnosis and monitoring of paroxysmal nocturnal hemoglobinuria and related disorders by flow cytometry;Borowitz;Cytometry B Clin Cytom,2010

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