[Therapeutic trials in amino acid disorders].
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Amino Acid Metabolism, Inborn Errors↗
Biomedical subjects
J Boisse
Publications and source records attributed to J Boisse.
[Amino acid transfer systems and their importance in pathology. II. Specific abnormalities in renal and intestinal amino acid transfer].
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Adolescent↗
[Hereditary ornithine-carbamyl-transferase deficiency with qualitative enzyme abnormality. Report of a form with neonatal revelation and fatal course in a boy].
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Amino Acid Metabolism, Inborn Errors↗
[New etiologic approach to periodic ketoacidosis in children].
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Alanine↗
[Evaluation of the activity of a phenylketonuria detection center. Analysis of the results of 500,000 tests].
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Adolescent↗
[Treatment of phenylketonuria. Principles, management and importance of a phenylalanine-free protein hydrolysate].
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Albumins↗
[Methylmalonic acidemia. A new cause of severe ketoacidosis. Study of a case].
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Acidosis↗
[The intermittent variant of leucinosis (study of a new case)].
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Acidosis↗
[How to detect avoidable mental retardation?].
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Diet Therapy↗
[Mass screening of phenylketonuria. Report on a screening center (October 1967-December 1968)].
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Adolescent↗
[Attempted clinical orientation in the diagnosis of amino-acidopathies. 3. Digestive symptoms, especially hepatic. IV. Evolutive mechanism].
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Amino Acid Metabolism, Inborn Errors↗
[Segmental hypoplasia of the kidney with arterial hypertension].
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Adolescent↗
[Acute glomerulonephritis with hypertensive encephalopathy and minor urinary manifestations].
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Adolescent↗
[Attempted clinical orientation in the diagnosis of amino-acidopathies. II. Dermatological, hematological, cardiovascular and renal symptoms].
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Amino Acid Metabolism, Inborn Errors↗
[Attempted clinical orientation in the diagnosis of amino acid metabolism disorders. I. Urinary symptoms, neuropsychic symptoms and ocular symtpoms].
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Amino Acid Metabolism, Inborn Errors↗
[Further problems and perspectives of phenylketonuria. Phenylketonuria and phenylalaninemia].
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Humans↗
[On a case of partial deletion of the short arm of chromosome 18, resulting in a familial 18c-17 translocation].
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Child, Preschool↗
[Tryptophan tolerance test in children].
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Adolescent↗