C Largillière

Very long chain acyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid oxidation in fibroblasts

C. Bertrand, C Largillière, Marie Thérèse Zabot et al. · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · 1993 · 121 citations

Aldehyde Dehydrogenase, Mitochondrial Function, Biochemistry +8

Free malondialdehyde determination in human plasma by high-performance liquid chromatography

C Largillière, Serge B. Melançon · Analytical Biochemistry · 1988 · 116 citations

Biochemistry, Gas Chromatography, Medicine +10

Point mutation of the mitochondrial tRNA(Leu) gene (A 3243 G) in maternally inherited hypertrophic cardiomyopathy, diabetes mellitus, renal failure, and sensorineural deafness.

Sylvie Manouvrier, Agnès Rötig, G Hannebique et al. · Journal of Medical Genetics · 1995 · 77 citations · Full text

Metabolic Disorder, Genetics, Genetic Epidemiology +19

Liver transplantation for ornithine transcarbamylase deficiency in a girl

C Largillière, D Houssin, Frédèric Gottrand et al. · The Journal of Pediatrics · 1989 · 70 citations

Hepatology, Liver Physiology, Pathology +4

Diagnosis of variants of hyperphenylalaninemia by determination of pterins in urine

Jean‐Louis Dhondt, C Largillière, Patrick Ardouin et al. · Clinica Chimica Acta · 1981 · 42 citations

Urology, Medicine, Renal Pathology +2