H. Ogier

A new peroxisomal disorder with enlarged peroxisomes and a specific deficiency of acyl-CoA oxidase (pseudo-neonatal adrenoleukodystrophy).

Bwee Tien Poll‐The, Frank Roels, H. Ogier et al. · PubMed · 1988 · 262 citations

Life Sciences, Biochemistry, Endocrinology +17

The fasting test in paediatrics: Application to the diagnosis of pathological hypo- and hyperketotic states

Jean‐Paul Bonnefont, Norma Spécola, Anne Vassault et al. · European Journal of Pediatrics · 1990 · 169 citations

Medicine, Endocrinology, Pediatrics +6

Infantile Refsum disease: an inherited peroxisomal disorder

Bwee Tien Poll‐The, J. M. Saudubray, H. Ogier et al. · European Journal of Pediatrics · 1987 · 132 citations

Life Sciences, Genetics, Pediatrics +9

Clinical outcome of long-term management of patients with vitamin B12-unresponsive methylmalonic acidemia

S. B. van der Meer, F Poggi, Marco Spada et al. · The Journal of Pediatrics · 1994 · 131 citations

Public Health, Internal Medicine, Micronutrient Deficiency +10

Clinical, metabolic, and genetic aspects of cytochrome C oxidase deficiency in Saguenay-Lac-Saint-Jean.

C Morin, Grant A. Mitchell, Jonathan R. LaRochelle et al. · PubMed · 1993 · 101 citations

Life Sciences, Genetics, Molecular Genetics +10