Literature DB >> 14248326

[A NEW CASE OF RECESSIVE CONGENITAL METHEMOGLOBINEMIA LINKED WITH A DIAPHORASE I DEFICIENCY].

H HARTLEYB, D FISCHER, P HEIDT, G W LOHR, C LAUSECKER.   

Abstract

Entities:  

Keywords:  ASCORBIC ACID, THERAPEUTIC; DRUG THERAPY; GENETICS, HUMAN; INFANT, NEWBORN; INFANT, NEWBORN, DISEASES; LIPOAMIDE DEHYDROGENASE; METABOLIC DISEASES; METHEMOGLOBINEMIA; METHYLENE BLUE; NAD; NADP

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Year:  1964        PMID： 14248326

Source DB:  PubMed          Journal:  Arch Fr Pediatr        ISSN： 0003-9764


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  1 in total

1.  [Familial deficiency of NADH-dependent methemoglobin-reductase associated with glycerin-1-phosphate-dehydrogenase activity in the erythrocytes].

Authors:  W Kübler; H Kuhn; H M Mertens; L Seipel
Journal:  Klin Wochenschr       Date:  1971-12-01
  1 in total

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