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Branched-chain organic aciduriasH. Ogier de Baulny; J.M. Saudubray · 2002
Macrocytoses d’origine métaboliqueSchiff, M.; Ogier de Baulny, H. · Archives de Pédiatrie · 2013
Remethylation defects: guidelines for clinical diagnosis and treatmentH. Ogier de Baulny, M. Gérard, J. M. Saudubray… · 1998
Mitochondria and diabetes mellitus: untangling a conflictive relationship?M. Schiff; S. Loublier; A. Coulibaly; P. Bénit; H. Ogier de Baulny; P. Rustin · 2009
Maternal and fetal tyrosinemia type IGarcia Segarra, N.; Roche, S.; Imbard, A.; Benoist, J. F.; Grenèche, M. O.; Davit-Spraul, A.; Ogier de Baulny, H. · Journal of Inherited Metabolic Disease · 2010
Early-onset hyperargininaemia: A severe disorder?Schiff, M.; Benoist, J.-F.; Cardoso, M. L.; Elmaleh-Bergès, M.; Forey, P.; Santiago, J.; Ogier de Baulny, H. · Journal of Inherited Metabolic Disease · 2009
Trastornos hereditarios del metabolismo de la galactosa y la fructosaTouati, G.; Brivet, M.; Ogier de Baulny, H. · EMC - Pediatría · 2012
Morphological studies of skeletal muscle in lactic acidosisN. B. Romero; A. Lombès; G. Touati; O. Rigal; P. Frachon; M. A. Cheval; M. Giraud; S. Possekel; M. Fardeau; H. Ogier de Baulny · 1996