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Page 1
Partial epilepsy and 47,XXX karyotype: report of four cases.
Roubertie A, Humbertclaude V, Leydet J, Lefort G, Echenne B. Roubertie A, et al. Among authors: humbertclaude v. Pediatr Neurol. 2006 Jul;35(1):69-74. doi: 10.1016/j.pediatrneurol.2006.01.003. Pediatr Neurol. 2006. PMID: 16814091
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene.
Delcourt M, Riant F, Mancini J, Milh M, Navarro V, Roze E, Humbertclaude V, Korff C, Des Portes V, Szepetowski P, Doummar D, Echenne B, Quintin S, Leboucq N, Singh Amrathlal R, Rochette J, Roubertie A. Delcourt M, et al. Among authors: humbertclaude v. J Neurol Neurosurg Psychiatry. 2015 Jul;86(7):782-5. doi: 10.1136/jnnp-2014-309025. Epub 2015 Jan 16. J Neurol Neurosurg Psychiatry. 2015. PMID: 25595153
[Benign familial infantile convulsions].
Echenne B, Rivier F, Humbertclaude V, Roubertie A, Cheminal R, Malafosse A. Echenne B, et al. Among authors: humbertclaude v. Arch Pediatr. 1999 Jan;6(1):54-8. doi: 10.1016/S0929-693X(99)80075-X. Arch Pediatr. 1999. PMID: 9974098 French.
[The varied etiologies of childhood-onset dystonia].
Roubertie A, Rivier F, Humbertclaude V, Tuffery S, Cavalier L, Cheminal R, Coubes P, Echenne B. Roubertie A, et al. Among authors: humbertclaude v. Rev Neurol (Paris). 2002 Apr;158(4):413-24. Rev Neurol (Paris). 2002. PMID: 11984483 Review. French.
53 results