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The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasiaS Portrat, P Mulatero, K M Curnow, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1985
Effects of hypopituitarism and growth hormone replacement therapy on the production and utilization of glucose in childhoodP F Bougneres, E Artavia-Loria, P Ferre, et al.Fertility and Sterility|November 1, 1993
A new mutation within the deoxyribonucleic acid-binding domain of the androgen receptor gene in a family with complete androgen insensitivity syndromeS Lumbroso, J M Lobaccaro, C Belon, et al.The Journal of Pediatrics|July 1, 1991
Near normalization of adolescent height with growth hormone therapy in very short children without growth hormone deficiencyC Lesage, J Walker, F Landier, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 1, 1996
[Association of mixed gonadal dysgenesis and non-classic 21-hydroxylase deficiency]O Del Pino, J C Carel, J P Barbet, et al.Journal De Radiologie|September 20, 2007
[Subtle brain abnormalities in adrenomyeloneuropathy]C Teriitehau, C Adamsbaum, V Merzoug, et al.Pediatric Radiology|November 1, 1996
Accelerated myelination in early Sturge-Weber syndrome: MRI-SPECT correlationsC Adamsbaum, F Pinton, Y Rolland, et al.Pediatric Radiology|November 1, 1995
Opercular malformations: clinical and MRI features in 11 childrenY Rolland, C Adamsbaum, N Sellier, et al.AJNR. American Journal of Neuroradiology|April 28, 2012
Toward a better understanding of brain lesions during metachromatic leukodystrophy evolutionA Martin, C Sevin, C Lazarus, et al.Archives Francaises De Pediatrie|January 1, 1992
[Neonatal cervical cord compression by a staphylococcal abscess]V Desportes, C Huon, C Adamsbaum, et al.Pageof 29