Genetic heterogeneity of hereditary stomatocytosis syndromes showing pseudohyperkalemia.

No abstract is available for this paper.

• Publication year

  1999

• Venue

  Haematologica

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  PMID 10477465
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• A variant of hereditary stomatocytosis with marked pseudohyperkalaemia

  1999cited by this paper
• Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).

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• Familial pseudohyperkalaemia. A new syndrome.

  1979cited by this paper
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  1965cited by this paper
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  1961cited by this paper

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  2004cites this paper
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  2004cites this paper
• The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.

  2004cites this paper
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  2004cites this paper
• Hemolytic disease due to membrane ion channel disorders

  2004cites this paper
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  2003cites this paper
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  2003cites this paper
• Molecular Basis of Red Cell Membrane Disorders

  2002cites this paper
• A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis

  2001cites this paper
• Pleiotropic syndrome of dehydrated hereditary stomatocytosis, pseudohyperkalemia, and perinatal edema maps to 16q23-q24.

  2000cites this paper