Erythrocytosis associated with <i>EPAS1</i>(<i>HIF2A</i>), <i>EGLN1</i>(<i>PHD2</i>), <i>VHL, EPOR</i> or <i>BPGM</i> mutations: The Mayo Clinic experience-Reference-Cited by-同舟云学术

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Erythrocytosis associated with <i>EPAS1</i>(<i>HIF2A</i>), <i>EGLN1</i>(<i>PHD2</i>), <i>VHL, EPOR</i> or <i>BPGM</i> mutations: The Mayo Clinic experience

Published:2022-02-10 Issue:5 Volume:107 Page:1201-1204
ISSN:1592-8721
Container-title:Haematologica
language:
Short-container-title:haematol

Author:

Gangat Naseema,Oliveira Jennifer L.,Porter Tavanna R,Hoyer James D.,Al-Kali Aref,Patnaik Mrinal M.,Pardanani Animesh,Tefferi Ayalew

Publisher

Ferrata Storti Foundation (Haematologica)

Subject

Hematology

Reference20 articles.

1. Gangat N, Szuber N, Pardanani A, Tefferi A. JAK2 unmutated erythrocytosis: current diagnostic approach and therapeutic views. Leukemia. 2021; 35(8):2166-2181.

2. Gangat N, Oliveira JL, Hoyer JD, Patnaik MM, Pardanani A, Tefferi A. High-oxygen-affinity hemoglobinopathy-associated erythrocytosis: Clinical outcomes and impact of therapy in 41 cases. Am J Hematol. 2021; 96(12):1647-1654.

3. Filser M, Aral B, Airaud F. Low incidence of EPOR mutations in idiopathic erythrocytosis. Haematologica. 2021; 106(1):299-301.

4. Oliveira JL, Coon LM, Frederick LA. Genotype-phenotype correlation of hereditary erythrocytosis mutations, a single center experience. Am J Hematol. 2018; 93(8):1029-1041.

5. Lorenzo FR, Yang C, Ng Tang Fui M. A novel EPAS1/HIF2A germline mutation in a congenital polycythemia with paraganglioma. J Mol Med (Berl). 2013; 91(4):507-512.

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