Familial erythrocytosis

Known as: ERYTHROCYTOSIS, PRIMARY FAMILIAL, Erythrocytosis autosomal dominant benign, PFCP 
Polycythemia that occurs in groups of related individuals.
National Institutes of Health

Topic mentions per year

Topic mentions per year

1967-2018
02419672018

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2014
2014
Congenital erythrocytosis (CE), or congenital polycythemia, represents a rare and heterogeneous clinical entity. It is caused by… (More)
  • table 1
  • figure 1
  • table 2
  • table 3
  • table 4
Is this relevant?
2009
2009
Epo-induced endocytosis of EpoR plays important roles in the down-regulation of EpoR signaling and is the primary means that… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2008
2008
PURPOSE To investigate the effect of concomitant administration of pilocarpine during radiotherapy for head-and-neck squamous… (More)
Is this relevant?
1999
1999
Inherited mutations in the erythropoietin receptor (EPOR) causing premature termination of the receptor cytoplasmic region are… (More)
  • figure 1
  • table 1
Is this relevant?
1998
1998
Familial erythrocytosis, associated with high haemoglobin levels and low serum erythropoietin (Epo), has been shown to co… (More)
Is this relevant?
1997
1997
Familial erythrocytosis (familial polycythemia) inherited as an autosomal dominant trait has recently been reported to be… (More)
  • table 1
  • figure 1
  • figure 2
  • figure 3
  • figure 5
Is this relevant?
1997
1997
Primary polycythemias are caused by an acquired or inborn mutation affecting hematopoietic/erythroid progenitors that results in… (More)
  • figure 1
  • figure 2
  • table 1
Is this relevant?
1997
1997
Primary familial and congenital polycythaemia (PFCP) is a rare disease characterized by congenital erythrocytosis inherited in an… (More)
Is this relevant?
1995
1995
Primary familial and congenital polycythemia (PFCP) is characterized by erythrocytosis with normal arterial PO2, blood P50, and… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
1993
1993
Familial erythrocytosis is heterogeneous with diverse causes. Using a highly informative, simple sequence repeat polymorphism in… (More)
Is this relevant?