F. X. Coudé - Concepedia

Author

F. X. Coudé

Also Known As

F X Coude, F X Coudé, F. X. COUDE, F. X. Coude, F. X. Coudé, F.X Coude, F.X. Coude, F.X. Coudé, Francois X Coude, Francois X. Coudè

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Hôpital des Enfants Inserm Bicêtre Hospital

About

F. X. Coudé is an author at Hôpital Necker-Enfants Malades specializing in medicine, metabolism, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	752
2	Biochemistry	10	11	533
3	Health Sciences	8	8	442
4	Natural Sciences	1	1	15
5	Clinical Nutrition	1	1	23

F. X. Coudé

Publications

854

Citations

H-Index

Page 1

	Year	Citations
Inhibition by propionyl-coenzyme A of N-acetylglutamate synthetase in rat liver mitochondria. A possible explanation for hyperammonemia in propionic and methylmalonic acidemia. F. X. Coudé, Lawrence Sweetman, William L. Nyhan Journal of Clinical Investigation Lipid PeroxidationActivation ConstantOxidative StressMethylmalonic AcidemiaHepatotoxicity	1979	213
Action of the antiepileptic drug, valproic acid, on fatty acid oxidation in isolated rat hepatocytes F. X. Coudé, G Grimber, Anna Pelet, Biochemical and Biophysical Research Communications Valproic AcidBiochemistryAntiepileptic DrugMedicinePhysiology	1983	65
CONGENITAL LACTIC ACIDOSIS, α‐KETOGLUTARIC ACIDURIA AND VARIANT FORM OF MAPLE SYRUP URINE DISEASE DUE TO A SINGLE ENZYME DEFECT: DIHYDROLIPOYL DEHYDROGENASE DEFICIENCY Arnold Münnich, Jean‐Marie Saudubray, Jennifer Taylor, Acta Paediatrica Dihydrolipoyl Dehydrogenase DeficiencyUrologyAldehyde DehydrogenaseBiochemistryInherited Metabolic Disease	1982	61
Inhibition of ureagenesis by valproate in rat hepatocytes. Role of <i>N</i>-acetylglutamate and acetyl-CoA F. X. Coudé, G Grimber, P Parvy, Biochemical Journal 0.5-5 MmCellular PharmacologyExperimental PharmacologyOxidative StressRenal Function	1983	57
Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: Relationship to age Jean Marie Saudubray, C. Marsac, J.M. Limal, The Journal of Pediatrics Hypoglycemic ChildrenPhysiological ResearchBody CompositionMedicinePhysiology	1981	53
Academic Impairment is the Most Frequent Complication of Neurofibromatosis Type-1 (NF1) in Children F. X. Coudé, Stanislas Lyonnet, Arnold Munnich Behavior Genetics Frequent ComplicationPathologyDegenerative DiseaseAcademic ImpairmentNeurology	2006	46
Hudson memorial lecture Jean Marie Saudubray, H. Ogier, C. Charpentier, Journal of Inherited Metabolic Disease	1984	42
Neonatal glutaric aciduria type II: An X-linked recessive inherited disorder F. X. Coudé, H. Ogier, C. Charpentier, Human Genetics UrologyGenetic DisorderInherited Metabolic DiseasePediatricsX-linked Recessive	1981	38
Effect of propionate and pyruvate on citrulline synthesis and ATP content in rat liver mitochondria L Cathelineau, Françoise Petit, F. X. Coudé, Biochemical and Biophysical Research Communications BiosynthesisEnergy MetabolismBiochemistryMitochondrial FunctionCitrulline Synthesis	1979	34
Hudson Memorial Lecture Neonatal Management of Organic Acidurias. Clinical Update Jean‐Marie Saudubray, H. Ogier, C. Charpentier, UrologyNeonatologyOrganic AciduriasInherited Metabolic DiseasePediatrics	1984	33

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