Hélène Ogier

Neurologic Crises in Hereditary Tyrosinemia

Grant A. Mitchell, Jean Larochelle, Marie Lambert et al. · New England Journal of Medicine · 1990 · 235 citations

Medicine, Neurology, Pediatrics +16

Risk of developing a mitochondrial DNA deletion disorder

Patrick F. Chinnery, Salvatore DiMauro, Sara Shanske et al. · The Lancet · 2004 · 230 citations

Life Sciences, Genetics, Molecular Genetics +11

Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece

Bénédicte Héron, Yann Mikaeloff, Roseline Froissart et al. · American Journal of Medical Genetics Part A · 2010 · 165 citations

Medicine, Neurology, Pediatrics +13

LPIN1 gene mutations: a major cause of severe rhabdomyolysis in early childhood

Caroline Michot, Laurence Hubert, Michèle Brivet et al. · Human Mutation · 2010 · 132 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Hepatic peroxisomes are deficient in infantile refsum disease: A cytochemical study of 4 cases

Frank Roels, Alfons Cornelis, Bwee Tien Poll‐The et al. · American Journal of Medical Genetics · 1986 · 101 citations

Medicine, Pathology, Pediatrics +17