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The Journal of Pediatrics|June 1, 1981
Variation in plasma ketone bodies during a 24-hour fast in normal and in hypoglycemic children: relationship to ageJ M Saudubray, C Marsac, J M Limal, et al.Biochemical and Biophysical Research Communications|March 7, 1996
Biochemical investigations and immunoblot analyses of two unrelated patients with an isolated deficiency in complex II of the mitochondrial respiratory chainM A Birch-Machin, C Marsac, G Ponsot, et al.Journal of Inherited Metabolic Disease|March 1, 1997
A near homoplasmic T8993G mtDNA mutation in a patient with atypic Leigh syndrome not present in the mother's tissuesF Degoul, D François, M Diry, et al.Nucleic Acids Research|February 11, 1991
Different mechanisms inferred from sequences of human mitochondrial DNA deletions in ocular myopathiesF Degoul, I Nelson, S Amselem, et al.Journal of the Neurological Sciences|April 29, 1998
A case of mitochondrial encephalomyopathy associated with a muscle coenzyme Q10 deficiencyE Boitier, F Degoul, I Desguerre, et al.Disability and Rehabilitation|August 25, 2025
"The most important thing is having patience, both of us." Successful conversations from the perspective of people with aphasia and their primary conversation partnersA Rotherham, K Shrubsole, C Croteau, et al.Cancer Research|July 15, 1995
Impairment of the mitochondrial respiratory chain activity in diethylnitrosamine-induced rat hepatomas: possible involvement of oxygen free radicalsE Boitier, M Merad-Boudia, C Guguen-Guillouzo, et al.Journal of the Neurological Sciences|November 1, 1989
Immunocytological and histochemical correlation in Kearns-Sayre syndrome with mtDNA deletion and partial cytochrome c oxidase deficiency in skeletal muscleN B Romero, P Lestienne, C Marsac, et al.British Journal of Hospital Medicine (London, England : 2005)|July 9, 2019
Hepatitis E: a largely underestimated, emerging threatS J Wallace, C Crossan, S H Hussaini, et al.Digestive Diseases and Sciences|March 1, 1992
Chronic intestinal pseudoobstruction with myopathy and ophthalmoplegia. A muscular biochemical study of a mitochondrial disorderV Li, J Hostein, N B Romero, et al.Pageof 15