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Your search keyword '"Myoglobinuria metabolism"' showing total 2 results
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2 results on '"Myoglobinuria metabolism"'

1. Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.

Author

Dionisi Vici C, Burlina AB, Bertini E, Bachmann C, Mazziotta MR, Zacchello F, Sabetta G, and Hale DE

Subjects
3-Hydroxyacyl CoA Dehydrogenases deficiency, Biopsy, Carnitine administration & dosage, Child, Combined Modality Therapy, Dietary Fats administration & dosage, Humans, Male, Mitochondria, Muscle metabolism, Mitochondria, Muscle ultrastructure, Myoglobinuria metabolism, Myoglobinuria therapy, Nervous System Diseases metabolism, Nervous System Diseases therapy, Neurologic Examination, Recurrence, Starch administration & dosage, Myoglobinuria diagnosis, Nervous System Diseases diagnosis
Published
1991
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2. The glycogen storage diseases.

Author

Drash A and Field J

Subjects
Adipose Tissue metabolism, Adult, Blood Glucose metabolism, Carbohydrate Metabolism, Child, Child, Preschool, Female, Gluconeogenesis, Glucose metabolism, Glucose-6-Phosphate Isomerase metabolism, Glucosidases metabolism, Glucosyltransferases metabolism, Glycogen metabolism, Glycogen Storage Disease metabolism, Glycogen Storage Disease Type I metabolism, Glycoside Hydrolases metabolism, Hepatomegaly metabolism, Humans, Infant, Infant, Newborn, Liver metabolism, Male, Muscles metabolism, Myoglobinuria metabolism, Phosphofructokinase-1 metabolism, Phosphoglucomutase metabolism, Phosphorylases metabolism, Glycogen Storage Disease classification
Published
1971

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