Jean Marie Saudubray

Author

Also Known As

J M Saudubray, J SAUDUBRAY, J. -M. Saudubray, J. M. SAUDUBRAY, J. M. Saudubray, J.-M. Saudubray, J.M Saudubray, J.M. Saudubray, J.‐M. Saudubray, JEAN MARIE SAUDUBRAY

567

Publications

5.2K

Citations

H-Index

Concepts

All Affiliations

Hôpital Necker-Enfants Malades Hôpital des Enfants Inserm Bicêtre Hospital Institut Necker Enfants Malades

About

Jean Marie Saudubray is an author at Hôpital Necker-Enfants Malades specializing in medicine, pediatrics, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	38	1.9K
2	Health Sciences	14	14	626
3	Natural Sciences	3	3	244
4	Public Health	3	3	86
5	Arts	1	1	12

Jean Marie Saudubray

Publications

3.3K

Citations

H-Index

Page 1

	Year	Citations
The fasting test in paediatrics: Application to the diagnosis of pathological hypo- and hyperketotic states Jean‐Paul Bonnefont, Norma Spécola, Anne Vassault, European Journal of Pediatrics Fasting TestPathological Hypo-DiagnosisPediatricsHyperketotic States	1990	167
Clinical aspects of mitochondrial disorders Arnold Münnich, Pierre Rustin, Agnès Rötig, Journal of Inherited Metabolic Disease	1992	154
Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridation Ronald J. A. Wanders, Lodewijk IJlst, F Poggi, Biochemical and Biophysical Research Communications Metabolic SyndromeMetabolic DisorderMitochondrial FunctionBiochemistryMitochondrial Dynamic	1992	153
Diffuse and Focal Nesidioblastosis A. Goossens, W Gepts, Jean Marie Saudubray, The American Journal of Surgical Pathology	1989	147
Reference charts for respiratory chain activities in human tissues Dominique Chrétien, Pierre Rustin, Thomas Bourgeron, Clinica Chimica Acta AsthmaPhysiologyReference ChartsBiostatisticsRespiration (Physiology)	1994	137
Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation. Grant A. Mitchell, Damian Labuda, G Fontaine, Proceedings of the National Academy of Sciences Rna ProcessingMature MrnaExons 3Natural SciencesGenetics	1991	135
A deletion in the human QP-C gene causes a complex III deficiency resulting in hypoglycaemia and lactic acidosis Sandrine Haut, M. Brivet, Guy Touati, Human Genetics Lactic AcidosisMolecular PhysiologyComplex Iii DeficiencyMendelian DisorderGenetic Disorder	2003	132
The Molecular Basis of Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency in Compound Heterozygous Patients: Is There Correlation between Genotype and Phenotype? Brage Storstein Andresen, Peter Bross, Szabolcs Udvari, Human Molecular Genetics	1997	122
Methylmalonic and propionic acidurias: Management without or with a few supplements of specific amino acid mixture Guy Touati, Vassili Valayannopoulos, Karine Mention, Journal of Inherited Metabolic Disease	2006	113
Hyperinsulinism in children: Diagnostic value of pancreatic venous sampling correlated with clinical, pathological and surgical outcome in 25 cases Josée Dubois, Françis Brunelle, Guy Touati, Pediatric Radiology Surgical OutcomeDiabetesGastroenterologyDiagnostic ValuePediatrics	1995	113

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