[Study of homogentisic acid by thin layer chromatography].
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Alkaptonuria↗
Biomedical subjects
J Cotte
Publications and source records attributed to J Cotte.
[A variant of glucose-6-phosphate dehydrogenase: the Constantine type].
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Algeria↗
[Determination of cyanide ion in the atmosphere, drinking water, industrial effluents and biologic media by means of a specific electrode].
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Air Pollution↗
[Standardization of antilymphocyte serum].
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Animals↗
[Transient hypertyrosinemia secondary to hepatic involvement. 2 cases of different etiologies (galactosemia, hepatitis)].
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Female↗
[Glucose-6-phosphate dehydrogenase and genetics].
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Genetics, Population↗
[Glucose-6-phosphate dehydrogenase Debrousse type: problem of enzymatic type specific to Algerians of the Arabic race].
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Africa, Northern↗
[Intestinal disaccharidases in celiac disease in children: correlation with clinical and histologic data].
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Celiac Disease↗
[Study of exocrine pancreatic function in mucoviscidosis].
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Adolescent↗
[Phototherapy in Crigler Najjar syndrome: value and limitations].
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Female↗
[Contribution to the study of the mechanism of hypoglycemia in fructose intolerance].
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Adenosine Triphosphate↗
[Observation of a case of partial deficiency of intraerythrocyte ATPase].
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Adenosine Triphosphatases↗
[Thin layer chromatoelectrophretic separation of blood and urinary amino acids].
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Amino Acids↗
[Syntocinon and cesarean section].
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Cesarean Section↗
[Contribution to a study of the mechanism of hemolysis in the Von Jaksch Luzet Syndrome. Exploration of intraerythrocytic glycolytic enzymes].
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Anemia, Hemolytic, Congenital↗
[Detection of metabolic anomalies leading to avoidable mental retardation].
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Adolescent↗
[Neonatal discovery of hypophosphatasia. Bone improvement. Fatal convulsant encephalopathy].
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Alkaline Phosphatase↗
[Intolerance to fructose. Observation and physiopathological mechanism of hypoglycemia].
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Carbohydrate Metabolism, Inborn Errors↗