Hereditary methemoglobinemia with and without mental retardation
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference45 articles.
1. Methemoglobinemia in man;Jaffé,1964
2. The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia;Gibson;Biochem. J.,1948
3. The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia;Scott;J. Clin. Invest.,1960
4. Metabolic processes involved in the formation and reduction of methempglobin in human erythrocytes;Jaffé,1964
5. The reduction of methemoglobin in erythrocytes of a patient with congenital methemoglobinemia, subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency, and normal individuals;Jaffé;Blood,1963
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1. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: Determination of the molecular basis;HUM MUTAT;2000
2. A case of methemoglobinemia type II due to NADH-cytochrome b5 reductase deficiency: Determination of the molecular basis;Human Mutation;2000
3. Treatment of high-risk, refractory acquired methemoglobinemia with automated red blood cell exchange;Journal of Clinical Apheresis;1998
4. Evidence that NADPH-dependent methemoglobin reductase and administered riboflavin protect tissues from oxidative injury;American Journal of Hematology;1993-01
5. Landmark perspective: The legacy of well-water methemoglobinemia;JAMA: The Journal of the American Medical Association;1987-05-22
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