Polycythemia

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  Subject Areas on Research

  • A human erythropoietin receptor gene mutant causing familial erythrocytosis is associated with deregulation of the rates of Jak2 and Stat5 inactivation. 
  • A novel mutation in the erythropoietin receptor gene is associated with familial erythrocytosis. 
  • Anabolic steroids, acute myocardial infarction and polycythemia: a case report and review of the literature. 
  • Erythropoietin hypersensitivity in primary familial and congenital polycythemia: role of tyrosines Y285 and Y344 in erythropoietin receptor cytoplasmic domain. 
  • Evoked potentials in choreoacanthocytosis. 
  • Familial erythrocytosis associated with a short deletion in the erythropoietin receptor gene. 
  • Familial polycythemia due to truncations of the erythropoietin receptor. 
  • Global REACH 2018: High Blood Viscosity and Hemoglobin Concentration Contribute to Reduced Flow-Mediated Dilation in High-Altitude Excessive Erythrocytosis. 
  • Hypoxia Signaling Cascade for Erythropoietin Production in Hepatocytes. 
  • Losartan in post-transplant erythrocytosis. 
  • Ocular manifestations of hematologic disorders. 
  • Paraparesis, hypermanganesaemia, and polycythaemia: a novel presentation of cirrhosis. 
  • Post transplant erythrocytosis in hypercalcemic renal transplant recipients. 
  • Sequential activation of splenic nuclear RNA polymerases by erythropoietin. 
  • The clinical and laboratory evaluation of the patient with erythrocytosis. 
  • The distal cytoplasmic domain of the erythropoietin receptor induces granulocytic differentiation in 32D cells. 
  • The influence of hemoconcentration on hypoxic pulmonary vasoconstriction in acute, prolonged, and lifelong hypoxemia. 
  • Tubulovascular cross-talk by vascular endothelial growth factor a maintains peritubular microvasculature in kidney. 
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  Keywords of People

  • Sparks, Matthew A., Associate Professor of Medicine, Medicine, Nephrology