Erythrocytosis, methemoglobinemia, and the saturation gap

Author:

Koduri Prasad R.,Kedar Prabhakar S.,Warang Prashant

Publisher

Springer Science and Business Media LLC

Subject

Hematology,General Medicine

Reference8 articles.

1. Tefferi A (2004) Polycythemia vera evaluation algorithm revisited: in reply. Mayo Clin Proc 79:430–432

2. Jaffe ER (1966) Hereditary methemoglobinemias associated with abnormalities in the metabolism of erythrocytes. Am J Med 41:786–798

3. Fermo E, Bianchi P, Vercellati C et al (2008) Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene. Blood Cells Mol Dis 41:50–55

4. Warang PP, Kedar PS, Shanmukaiah C, Ghosh K, Colah RB (2013) Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India. Clin Genet. doi: 10.1111/cge.12326

5. Spivak JL (2012) Polycythemia vera and other myeloproliferative diseases. In: Longo DL, Kasper DL, Jameson JL, Fauci AS, Hauser SL, Loscalzo J (eds) Harrison’s principles of internal medicine, 18th edn. McGraw Hill, New York, p 899

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