Paroxysmal nocturnal hemoglobinuria: Significant association with specific HLA-A, -B, -C, and -DR alleles in an Italian population-Reference-Cited by-同舟云学术

Paroxysmal nocturnal hemoglobinuria: Significant association with specific HLA-A, -B, -C, and -DR alleles in an Italian population

Published:2008-03 Issue:3 Volume:69 Page:202-206
ISSN:0198-8859
Container-title:Human Immunology
language:en
Short-container-title:Human Immunology

Author:

Lombardi Maria Luisa,Terrazzano Giuseppe,Cosentini Elena,Gargiulo Lucia,Risitano Antonio,Camerlingo Rosa,Sica Michela,Aufiero Daniela,Poggi Alessandro,Pirozzi Giuseppe,Luzzatto Lucio,Rotoli Bruno,Notaro Rosario,Alfinito Fiorella,Ruggiero Giuseppina

Publisher

Elsevier BV

Subject

General Medicine,Immunology,Immunology and Allergy

Reference31 articles.

1. Paroxysmal nocturnal hemoglobinuria: An acquired X-linked genetic disease with somatic-cell mosaicism;Luzzatto;Curr Opin Genet Dev,2006

2. Clonal population of hematopoietic cell with paroxysmal nocturnal hemoglobinuria phenotype are present in normal individuals;Araten;Proc Natl Acad Sci U S A,1999

3. Murine embrionic stem cells without pig-a gene activity are competent for hematopoiesis with the PNH phenotype but not for clonal expansion;Rosti;J Clin Invest,1997

4. Somatic mutations in paroxysmal nocturnal hemoglobinuria: A blessing in disguise?;Luzzatto;Cell,1997

5. The pathophysiology of acquired aplastic anemia;Young;N Engl J Med,1997

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