Secondary Hypertension, Erythrocytosis, and Unilateral Renal Cystic Disease in a Submariner: A Case Report.
Forbes, Angela S; Yeo, Fred E.
J Spec Oper Med
; 16(4): 1-5, Winter 2016.
Artigo em Inglês | MEDLINE | ID: mdl-28088811
Genetic basis of congenital erythrocytosis: mutation update and online databases.
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range.
Thrombocytopenia and erythrocytosis in mice with a mutation in the gene encoding the hemoglobin ß minor chain.
A knock-in mouse model of human PHD2 gene-associated erythrocytosis establishes a haploinsufficiency mechanism.
The complete evaluation of erythrocytosis: congenital and acquired.
RUNX1 and NF-E2 upregulation is not specific for MPNs, but is seen in polycythemic disorders with augmented HIF signaling.
Poliglobulia e hidronefrosis de riñón en herradura
Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis: Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms.
Idiopathic erythrocytosis and other non-clonal polycythemias.
Idiopathic erythrocytosis in dialysis patients: a case report and literature review.