• A case of familial erythrocytosis type 2 caused by VHL gene mutation
• A clinical study of fetal outcome following early and delayed cord clamping in births associated with anemia in pregnancy
• A cross-sectional survey of symptoms and daily living among patients with polycythemia vera and their treating physicians in Japan
• A Kindred with a β-Globin Base Substitution [β89(F5)Ser→Arg (AG<em>T</em>&gt;AG<em>G</em>); <em>HBB</em>: c.270T&gt;G] Resulting in Hemoglobin Vanderbilt
• Association between polycythemia and risk of ischemic stroke in males based on the national health insurance service-health screening cohort
• Association of the <em>EPAS1</em> rs7557402 Polymorphism with Hemodynamically Significant Patent Ductus Arteriosus Closure Failure in Premature Newborns under Pharmacological Treatment with Ibuprofen
• Congenital erythrocytosis
• Congenital erythrocytosis - A condition behind recurrent thromboses: A case report and literature review
• Diagnosis and genetic analysis of polycythemia in children and a novel EPAS1 gene mutation
• Effects of idiopathic erythrocytosis on the left ventricular diastolic functions and the spectrum of genetic mutations: A case control study
• Elevated erythroferrone distinguishes erythrocytosis with inherited defects in oxygen-sensing pathway from primary familial and congenital polycythaemia
• Expression and Variations in <em>EPAS1</em> Associated with Oxygen Metabolism in Sheep
• Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient
• Genetic variability of hypoxia-inducible factor alpha (HIFA) genes in familial erythrocytosis: Analysis of the literature and genome databases
• Heritable disorders of oxygen sensing
• Heterozygosity for bisphosphoglycerate mutase deficiency expressing clinically as congenital erythrocytosis: A case series and literature review
• Heterozygous, germline JAK2 E846D substitution as the cause of familial erythrocytosis
• Hypoxia-inducible factor underlies von Hippel-Lindau disease stigmata
• Identification of Two Novel <em>EPOR</em> Gene Variants in Primary Familial Polycythemia: Case Report and Literature Review
• Insights into the Prognostic Role of Serum Interleukin-6 and Hematobiochemical Alterations in Cattle during Recent Outbreaks of Lumpy Skin Disease in Lodhran District, Pakistan
• JAK2 unmutated erythrocytosis: 2023 Update on diagnosis and management
• Janus kinase (JAK) inhibitors in the treatment of neoplastic and inflammatory disorders
• Novel mutations in EPO-R and oxygen-dependent degradation (ODD) domain of EPAS1 genes-a causative reason for Congenital Erythrocytosis
• Novel mutations in the EPO-R, VHL and EPAS1 genes in the Congenital Erythrocytosis patients
• Ruxolitinib Versus Best Available Therapy for Polycythemia Vera Intolerant or Resistant to Hydroxycarbamide in a Randomized Trial
• Structural basis for binding of the renal carcinoma target hypoxia-inducible factor 2α to prolyl hydroxylase domain 2
• The Outcome of Fatherhood in Patients With Philadelphia-Negative Myeloproliferative Neoplasms: A Single-Institution Experience
• Variants in the new E1' cryptic exon of the <em>VHL</em> gene associated with congenital erythrocytosis-Description of three cases
• Von Hipple-Lindau disease complicated with central retinal vein occlusion: a case report