Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis-Reference-Cited by-同舟云学术

Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis

Published:2018-08-31 Issue:4 Volume:101 Page:566-569
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Orvain Corentin¹²³^ORCID,Da Costa Lydie⁴,Van Wijk Richard⁵,Pissard Serge⁶,Picard Véronique⁷,Mansour-Hendili Lamisse¹⁶,Cunat Séverine¹,Giansily-Blaizot Muriel¹,Cartron Guillaume⁸,Schved Jean-François¹,Aguilar-Martinez Patricia¹

Affiliation:

1. Department of Haematology Biology; Saint Eloi Hospital; Montpellier University Hospital; Montpellier France

2. Department of Blood Diseases; Angers University Hospital; Angers France

3. CRCINA, INSERM; Université de Nantes; Université d'Angers; Angers France

4. Department of Biological Haematology; AP-HP; Robert Debré University Hospital; Paris France

5. Department of Clinical Chemistry and Haematology; Utrecht University Medical Center; Utrecht The Netherlands

6. Department of Molecular Genetics; AP-HP; Henri Mondor University Hospital; Créteil France

7. Laboratory of Haematology; AP-HP; Bicêtre University Hospital; Le Kremlin-Bicêtre France

8. Department of Clinical Haematology; Saint Eloi Hospital; Montpellier University Hospital; Montpellier France

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.13135/fullpdf

Reference5 articles.

1. Mild dehydrated hereditary stomatocytosis revealed by marked hepatosiderosis;Syfuss;Clin Lab Haematol,2006

2. Thrombo-embolic disease after splenectomy for hereditary stomatocytosis;Stewart;Br J Haematol,1996

3. Iron overload in HFE C282Y heterozygotes at first genetic testing: a strategy for identifying rare HFE variants;Aguilar-Martinez;Haematologica,2011

4. Gender-specific phenotypic expression and screening strategies in C282Y-linked haemochromatosis: a study of 9396 French people;Deugnier;Br J Haematol,2002

5. HAMP promoter mutation nc.-153C>T in non p. C282Y homozygous patients with iron overload;Aguilar-Martinez;Haematologica,2010

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