Polyglobulie rare par mutation du gène EGLN1 : à propos d’un cas et revue de la littérature-Reference-Cited by-同舟云学术

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Polyglobulie rare par mutation du gène EGLN1 : à propos d’un cas et revue de la littérature

Published:2020-03 Issue:3 Volume:41 Page:196-199
ISSN:0248-8663
Container-title:La Revue de Médecine Interne
language:fr
Short-container-title:La Revue de Médecine Interne

Author:

Bonnin A.,Gardie B.,Girodon F.,Airaud F.,Garrec C.,Bézieau S.,Vignon G.,Mottaz P.,Labrousse J.,Lellouche F.

Publisher

Elsevier BV

Subject

Gastroenterology,Internal Medicine

Reference21 articles.

1. Interpretation of measured red cell mass and plasma volume in adults: expert panel on radionuclides of the international council for standadization in haematology;Pearson;Br J Haematol,1995

2. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia;Arber;Blood,2016

3. New mutations and pathogenesis of myeloproliferative neoplasms;Vainchenker;Blood,2011

4. How I treat polycythemia vera;Vannucchi;Blood,2014

5. The role of PHD2 mutations in the pathogenesis of erythrocytosis;Gardie;Hypoxia,2014

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Characterization of genetic variants in the <i>EGLN1/PHD2</i> gene identified in a European collection of patients with erythrocytosis;Haematologica;2023-06-15

2. Myoblast differentiation of C2C12 cell may related with oxidative stress;Intractable & Rare Diseases Research;2021-08-31

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