F. Coudé

发表

Inhibition of urea synthesis by pent-4-enoic acid: potentiation by ammonia.

G. Grimber, F. Coudé, 1984, Biochemical and biophysical research communications.

Discontinuity in the fall of left-handedness in a French population: A May '68 effect?

A. Munnich, S. Lyonnet, F. Coudé, 2006, Laterality.

Early Grade Repetition and Inattention Associated With Neurofibromatosis Type 1

A. Munnich, S. Lyonnet, F. Coudé, 2007, Journal of attention disorders.

Protective effects of SR 57746A in central and peripheral models of neurodegenerative disorders in rodents and primates

P. Soubrié, R. Steinberg, G. Fur, 1993, Neuroscience.

Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to age.

J. Saudubray, J. Limal, F. Coudé, 1981, The Journal of pediatrics.

Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency

A. Munnich, C. Griscelli, J. Frézal, 1981, Journal of Inherited Metabolic Disease.

Biotin dependent multiple carboxylase deficiency presenting as a congenital lactic acidosis

A. Munnich, J. Frézal, J. Saudubray, 1981, European Journal of Pediatrics.

Biotin-responsive immunoregulatory dysfunction in multiple carboxylase deficiency

A. Munnich, C. Griscelli, J. Frézal, 2004, Journal of Clinical Immunology.

Characterization of enzymatic deficiencies of branched chain amino-acid catabolism in human fibroblasts by genetic complementation.

G. Grimber, P. Parvy, J. Saudubray, 1983, Biochemical and biophysical research communications.

Hyperammonemia secondary to hereditary organic acidurias: a study of 29 cases.

P. Briand, J. Saudubray, F. Coudé, 1982, Advances in experimental medicine and biology.

FATTY-ACID-RESPONSIVE ALOPECIA IN MULTIPLE CARBOXYLASE DEFICIENCY

A. Munnich, J. Saurat, J. Frézal, 1980, The Lancet.

Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia.

W. Nyhan, F. Coudé, L. Sweetman, 1979, The Journal of clinical investigation.

Effect of overnight constant infusion of human growth hormone (GH)-releasing hormone-(1-44) on 24-hour GH secretion in children with partial GH deficiency.

F. Coudé, M. Morre, M. Tauber, 1986, The Journal of clinical endocrinology and metabolism.

Short Communication: Defective Insulin Response to Intravenous Glucose in Congenital Lactic Acidosis

A. Munnich, J. Saudubray, F. Coudé, 1982, Pediatric Research.

Acute glucagon treatment in rats fed various protein diets effect on n-acetyl glutamate concentration.

D. Rabier, F. Coudé, L. Cathelineau, 1982, Advances in experimental medicine and biology.

Dichloroacetate as treatment for congenital lactic acidosis.

J. Saudubray, F. Coudé, C. Marsac, 1978, The New England journal of medicine.

Growth hormone-releasing factor modifies dopaminergic but not serotonergic activity in the arcuate nucleus of hypothalamus in the rat, as recorded in vivo by differential pulse voltammetry

R. Roncucci, F. Coudé, F. Crespi, 1985, Brain Research.

A mechanism for valproate-induced hyperammonemia.

G. Grimber, D. Rabier, P. Parvy, 1982, Advances in experimental medicine and biology.

Effect of propionate and pyruvate on citrulline synthesis and ATP content in rat liver mitochondria.

P. Kamoun, F. Coudé, L. Cathelineau, 1979, Biochemical and biophysical research communications.

Role of N-acetylglutamate and acetyl-CoA in the inhibition of ureagenesis by isovaleric acid in isolated rat hepatocytes.

G. Grimber, D. Rabier, P. Parvy, 1983, Biochimica et biophysica acta.

Developmental changes of citrullinogenesis, mitochondrial N-acetylglutamate content and N-acetylglutamate synthetase in fetal and neonatal rats.

G. Grimber, P. Briand, D. Rabier, 1983, Biochimie.

CONGENITAL LACTIC ACIDOSIS, α‐KETOGLUTARIC ACIDURIA AND VARIANT FORM OF MAPLE SYRUP URINE DISEASE DUE TO A SINGLE ENZYME DEFECT: DIHYDROLIPOYL DEHYDROGENASE DEFICIENCY

A. Munnich, J. Frézal, F. Rocchiccioli, 1982, Acta paediatrica Scandinavica.

Results of 1-year growth hormone (GH)-releasing hormone-(1-44) treatment on growth, somatomedin-C, and 24-hour GH secretion in six children with partial GH deficiency.

C. Barbeau, F. Coudé, M. Arnone, 1987, The Journal of clinical endocrinology and metabolism.

Hudson memorial lecture. Neonatal management of organic acidurias. Clinical update.

A. Munnich, J. Frézal, J. Saudubray, 1984, Journal of inherited metabolic disease.

Inhibition of ureagenesis by valproate in rat hepatocytes. Role of N-acetylglutamate and acetyl-CoA.

G. Grimber, D. Rabier, P. Parvy, 1983, The Biochemical journal.

DEFECTIVE BIOTIN ABSORPTION IN MULTIPLE CARBOXYLASE DEFICIENCY

A. Munnich, J. Frézal, J. Saudubray, 1981, The Lancet.

Neonatal management of organic acidurias: clinical update

A. Munnich, J. Frézal, F. Coudé, 1984 .

Biotin dependent carboxylase activities in normal human and multicarboxylase deficient patient fibroblasts: relationship to the biotin content of the culture medium.

A. Munnich, J. Saudubray, F. Coudé, 1983, Clinica chimica acta; international journal of clinical chemistry.

Hudson memorial lecture

J. Frézal, J. Saudubray, F. Coudé, 1984, Journal of Inherited Metabolic Disease.

SECTION I: CLINICAL ASPECTS: MANAGEMENT AND OUTCOME

J., A. Munnich, J. Frézal, 2009 .

Oxidation of Fatty Acids in Cultured Fibroblasts: a Model System for the Detection and Study of Defects in Oxidation

K. Gibson, W. Nyhan, J. Saudubray, 1982, Pediatric Research.

[Multiple biotin-dependent carboxylase deficiencies (author's transl)].

A. Munnich, J. Frézal, J. Saudubray, 1981, Archives francaises de pediatrie.

Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder

J. Frézal, J. Saudubray, F. Coudé, 2004, Human Genetics.

Action of the antiepileptic drug, valproic acid, on fatty acid oxidation in isolated rat hepatocytes.

G. Grimber, F. Coudé, Y. Benoît, 1983, Biochemical and biophysical research communications.

Secondary citrullinemia with hyperammonemia in four neonatal cases of pyruvate carboxylase deficiency.

A. Munnich, J. Saudubray, F. Coudé, 1981, Pediatrics.

Letter to the Editor: A Mechanism for Valproate-Induced Hyperammonemia

G. Grimber, D. Rabier, P. Parvy, 1981, Pediatric Research.

Correlation between blood ammonia concentration and organic acid accumulation in isovaleric and propionic acidemia.

G. Grimber, P. Parvy, J. Saudubray, 1982, Pediatrics.

EEG findings as an aid to the diagnosis of neonatal non-ketotic hyperglycinaemia

J. Saudubray, F. Coudé, C. Charpentier, 1982, Journal of Inherited Metabolic Disease.

[Prognosis of congenital methylmalonic aciduria. Correlations between tolerance to proteins, response to vitamin B12 and enzymatic defect (author's transl)].

J. Saudubray, F. Coudé, D. Gompertz, 1980, Archives francaises de pediatrie.

Amino acid profile in pyruvate carboxylase deficiency: Comparison with some other metabolic disorders

J. Saudubray, F. Coudé, A. Lemonnier, 1982, Journal of Inherited Metabolic Disease.

Potentiation by piridoxilate of the synthesis of hippurate from benzoate in isolated rat hepatocytes. An approach to the determination of new pathways of nitrogen excretion in inborn errors of urea synthesis.

G. Grimber, F. Coudé, M. Coudé, 1984, Clinica chimica acta; international journal of clinical chemistry.

Growth hormone releasing factor — production and potential uses in humanand veterinary medicine

R. Roncucci, F. Coudé, M. Morre, 1984 .

Academic Impairment is the Most Frequent Complication of Neurofibromatosis Type-1 (NF1) in Children

Arnold Munnich, A. Munnich, S. Lyonnet, 2006, Behavior genetics.