[Mucopolysaccharidosis without mucopolysacchariduria].
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Dwarfism↗
Biomedical subjects
R Humbel
Publications and source records attributed to R Humbel.
[Determination of arylsulfatase activity in urine. Clinical significance].
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Adult↗
[Systematic detection of hereditary metabolic encephalopathies].
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Alkaptonuria↗
[Atypical forms of metachromatic leukodystrophy].
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Child↗
[Retarded rejection of renal transplants pretreated with nucleic acid].
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Animals↗
[Clinical, biological and genetic study of a family of phenylketonuric subjects].
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Adolescent↗
[L-tryptophan metabolism in phenylketonuria].
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Adolescent↗
[Simple method for study of tyrosyluria].
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Colorimetry↗
[Determination of blood urea nitrogen by a new rapid test].
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Blood Urea Nitrogen↗
[Systematic studies of phenylketonuria with phenistix].
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Cyclohexanes↗
Lysine intolerance with periodic ammonia intoxication.
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Amino Acid Metabolism, Inborn Errors↗
[Systematic screening for phenylketonuria with Phenistix].
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Humans↗
Phenylketonuria, a family study. Borderline intelligence in two siblings with mentally retarded children.
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Adolescent↗
[Biochemical study of fructosuria. Considerations apropos an case of essential fructosuria].
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Carbohydrate Metabolism, Inborn Errors↗
[Detection and diagnosis of homocystinuria].
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Chromatography, Paper↗
[Disorders of amino acid metabolism associated with mental retardation].
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Amino Acid Metabolism, Inborn Errors↗
[Determination of o-hydroxyphenylacetic acid in the urine].
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Chromatography, Paper↗
[Proceedings: Diagnosis of mannosidase deficiency].
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Disaccharidases↗