H syndrome mimicking Erdheim Chester disease: new entity and therapeutic perspectives-Reference-Cited by-同舟云学术

H syndrome mimicking Erdheim Chester disease: new entity and therapeutic perspectives

Published:2023-02-02 Issue:8 Volume:108 Page:2255-2260
ISSN:1592-8721
Container-title:Haematologica
language:
Short-container-title:haematol

Author:

Lequain Hippolyte,Gerfaud-Valentin Mathieu,Emile Jean-François,Gangloff Yann-Gaël,Boursier Guilaine,Deligny Christophe,Le Guenno Guillaume,Tantot Juliet,Valantin Julie,Savey Lea,Bachmeyer Claude,Jamilloux Yvan,Schaeffer Laurent,Leblanc Pascal,Sève Pascal

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Reference15 articles.

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3. Morgan NV, Morris MR, Cangul H. Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease. PLoS Genet. 2010; 6(2):e1000833.

4. Emile J-F, Abla O, Fraitag S. Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages. Blood. 2016; 127(22):2672-2681.

5. Young JD, Yao SYM, Baldwin JM, Cass CE, Baldwin SA. The human concentrative and equilibrative nucleoside transporter families, SLC28 and SLC29. Mol Aspects Med. 2013; 34(2-3):529-547.

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