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American Journal of Human Genetics|September 9, 2000
A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31V Cormier-Daire, N Dagoneau, R Nabbout, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|September 13, 2021
Pediatric hospital care organization: Cross-sectional enquiry in four regions in FranceO Gasmi, K Hodel, E Launay, et al.Pediatric Radiology|November 7, 1999
In vivo brain proton MR spectroscopy in a case of molybdenum cofactor deficiencyA M Salvan, B Chabrol, S Lamoureux, et al.European Journal of Medical Genetics|October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiencyG Barcia, C Barnerias, M Rio, et al.Journal of Medical Genetics|February 1, 2008
Deletion of C2orf34, PREPL and SLC3A1 causes atypical hypotonia-cystinuria syndromeB Chabrol, K Martens, S Meulemans, et al.Archives Francaises De Pediatrie|June 1, 1993
[Generalized epilepsy disclosing medium-chain-acyl-CoA dehydrogenase deficiency]B Chabrol, J Mancini, C Bertrand, et al.Der Urologe. Ausg. A|September 1, 1984
[Microsurgery of the renal arteries]J M Dubernard, A Gelet, X Martin, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 10, 2002
[Central alveolar hypoventilation syndrome and cerebral venous thrombosis: fortuitous association?]F Boubred, V Lethel, C Hugonencq, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 16, 2007
[Kystic pleuropulmonary blastoma fortuitly discovered in an infant]M David, E Bosdure, P de Lagausie, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|April 23, 2010
[Language disorders in children with morphologic abnormalities of the hippocampus]G Agostini, J Mancini, B Chabrol, et al.Pageof 19