Biomedical subjects
J P Colombo
Publications and source records attributed to J P Colombo.
[Indications of renal and intestinal amino acid malabsorption in Lowe's syndrome].
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Plasma glutamine in a phenylketonuric family with normal and mentally defective members.
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[Hereditary enzyme defects of the urea cycle].
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Congenital disorders of the urea cycle and ammonia detoxication.
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[Detection of congenital metabolic diseases with mental retardation].
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[Hyperargininemia wityh arginase deficiency. A new familial metabolic disease. I. Clinical studies].
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[Hyperargininemia with arginase deficiency. A new familial metabolic disease. II. Biochemical studies].
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[Sulfobromophthalein test in infancy].
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Periodic attacks of lethargy in a baby with ammonia intoxication due to a congenital defect in ureogenesis.
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[Enzymatic disturbances in the urea cycle].
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[Presymptomatic and hepatic forms of Wilson's disease in childhood. Long-term therapy with D-penicillamine].
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[The diagnostic value of alkaline phosphatase, leucine aminopeptidase and gamma-glutamytranspeptidase in diseases of the biliary tract].
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Urea cycle enzymes in the developing human fetus.
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Sweat composition in relation to rate of sweating in patients with cystic fibrosis of the pancreas.
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[Studies on the L-tryptophan metabolism in children with Down's syndrome].
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[L-tryptophan metabolism in phenylketonuria].
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