C. Marsac - Concepedia

Author

C. Marsac

Also Known As

C MARSAC, C Marsac, C. MARSAC, C. Marsac, C. Marsac, Cecile Marsac, Cécile Marsac, CÉCILE MARSAC, Cécile MARSAC, Cécile Marsac

126

Publications

4.5K

Citations

H-Index

119

Concepts

All Affiliations

Inserm Institut Necker Enfants Malades Hôpital Necker-Enfants Malades Hôpital Saint-Vincent-de-Paul Université Paris Cité

About

C. Marsac is an author at Inserm specializing in medicine, physiology, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	30	44	2.6K
2	Health Sciences	10	10	607
3	Natural Sciences	10	10	390
4	Social Sciences	1	1	38
5	Allergy	1	1	27

C. Marsac

Publications

4.2K

Citations

H-Index

Page 1

	Year	Citations
Mitochondria are selective targets for the protective effects of heat shock against oxidative injury. Barbara S. Polla, S Kantengwa, D. François, Proceedings of the National Academy of Sciences Cell DeathMitochondrial BiologyRedox BiologyOxidative StressInflammation	1996	402
Zidovudine myopathy: A distinctive disorder associated with mitochondrial dysfunction Chokri Mhiri, Magalie Baudrimont, Gisèle Bonne, Annals of Neurology	1991	185
Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency P.F. Bougneres, Jean-M. Saudubray, C. Marsac, The Journal of Pediatrics Metabolic SyndromeHepatologyMetabolic DisorderLiver PhysiologyDiabetes	1981	179
Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome Béatrice Parfait, Delphine Chrétien, Agnès Rötig, Human Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic Disease	2000	175
Pyruvate dehydrogenase complex deficiency: four neurological phenotypes with differing pathogenesis Christine Barnérias, Jean‐Marie Saudubray, Guy Touati, Developmental Medicine & Child Neurology	2009	171
Homozygous Deletion in the Coding Sequence of the c-mer Gene in RCS Rats Unravels General Mechanisms of Physiological Cell Adhesion and Apoptosis Emeline F. Nandrot, Éric Dufour, Alexandra Provost, Neurobiology of Disease Knockout MouseHomozygous DeletionSignal TransductionMolecular PhysiologyCell Regulation	2000	134
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiency Eric Boitier, Françoise Degoul, Isabelle Desguerre, Journal of the Neurological Sciences Mitochondrial MyopathyMitochondrial FunctionPhysiologyPathologyDegenerative Disease	1998	126
Mutations in the<i>SURF1</i>gene associated with Leigh syndrome and cytochrome<i>c</i>oxidase deficiency Marie O. Péquignot, Runu Dey, Massimo Zeviani, Human Mutation	2001	104
Pyruvate carboxylase deficiency: Metabolic characteristics and new neurological aspects Àngels García‐Cazorla, Daniel Rabier, Guy Touati, Annals of Neurology	2005	97
Phosphorus NMR spectroscopy study of muscular enzyme deficiencies involving glycogenolysis and glycolysis Denis Duboc, P Jehenson, S. Tran Dinh, Neurology Muscle FunctionNmr SpectroscopyKinesiologySkeletal MuscleBioenergetics	1987	94

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