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Review
. 2001 Sep;175(3):193-6.
doi: 10.1136/ewjm.175.3.193.

Methemoglobinemia

Affiliations
Review

Methemoglobinemia

H U Rehman. West J Med. 2001 Sep.
No abstract available

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References

    1. Manabe J, Arya R, Sumimoto H, et al. Two novel mutations in the reduced nicotinamide adenine dinucleotide (NADH)-cytochrome b5 reductase gene of a patient with generalized type, hereditary methemoglobinemia. Blood 1996;88: 3208-3215. - PubMed
    1. Yawata Y, Ding L, Tanishima K, Tomoda A. New variant of cytochrome b5 reductase deficiency (b5Rkurashiki) in red cells, platelets, lymphocytes, and cultured fibroblasts with congenital methemoglobinemia, mental and neurological retardation, and skeletal anomalies. Am J Hematol 1992;40: 299-305. - PubMed
    1. Gibson QH. The reduction of methemoglobin in red blood cells and studies on the cause of idiopathic methemoglobinemia. Biochem J 1948;42: 13-23. - PMC - PubMed
    1. Worster-Drought C, White JC, Sargent F. Familial, idiopathic methaemoglobinaemia associated with mental deficiency and neurological abnormalities. Br Med J 1953;2: 114-118. - PMC - PubMed
    1. Askew GL, Finelli L, Genese CA, Sorhage FE, Sosin DM, Spitalny KC. Boilerbaisse: an outbreak of methemoglobinemia in New Jersey in 1992. Pediatrics 1994;94: 381-384. - PubMed

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