Genton P - Search Results

1

Severe epilepsy, retardation, and dysmorphic features with a 2q deletion including SCN1A and SCN2A.

Pereira S, Vieira JP, Barroca F, Roll P, Carvalhas R, Cau P, Sequeira S, Genton P, Szepetowski P. Pereira S, et al. Among authors: genton p. Neurology. 2004 Jul 13;63(1):191-2. doi: 10.1212/01.wnl.0000132844.20654.c1. Neurology. 2004. PMID: 15249644 No abstract available.

2

Antimyoclonic effects of alcohol in progressive myoclonus epilepsy.

Genton P, Guerrini R. Genton P, et al. Neurology. 1990 Sep;40(9):1412-6. doi: 10.1212/wnl.40.9.1412. Neurology. 1990. PMID: 2118240

3

Do carbamazepine and phenytoin aggravate juvenile myoclonic epilepsy?

Genton P, Gelisse P, Thomas P, Dravet C. Genton P, et al. Neurology. 2000 Oct 24;55(8):1106-9. doi: 10.1212/wnl.55.8.1106. Neurology. 2000. PMID: 11071486

4

Clinical and genetic analysis of a new multigenerational pedigree with GEFS+ (Generalized Epilepsy with Febrile Seizures Plus).

Gérard F, Pereira S, Robaglia-Schlupp A, Genton P, Szepetowski P. Gérard F, et al. Among authors: genton p. Epilepsia. 2002 Jun;43(6):581-6. doi: 10.1046/j.1528-1157.2002.43001.x. Epilepsia. 2002. PMID: 12060016 Free article.

5

[GEFS + syndrome: phenotypic variations from the newborn to the adult in a large French pedigree].

Audic-Gerard F, Szepetowski P, Genton P. Audic-Gerard F, et al. Among authors: genton p. Rev Neurol (Paris). 2003 Feb;159(2):189-95. Rev Neurol (Paris). 2003. PMID: 12660571 French.

6

Complete loss of the cytoplasmic carboxyl terminus of the KCNQ2 potassium channel: a novel mutation in a large Czech pedigree with benign neonatal convulsions or other epileptic phenotypes.

Pereira S, Roll P, Krizova J, Genton P, Brazdil M, Kuba R, Cau P, Rektor I, Szepetowski P. Pereira S, et al. Among authors: genton p. Epilepsia. 2004 Apr;45(4):384-90. doi: 10.1111/j.0013-9580.2004.47703.x. Epilepsia. 2004. PMID: 15030501 Free article.

7

Epilepsy and deletions at chromosome 2q24.

Pereira S, Vieira JP, Cau P, Genton P, Szepetowski P. Pereira S, et al. Among authors: genton p. Am J Med Genet A. 2006 Jun 15;140(12):1354-5. doi: 10.1002/ajmg.a.31299. Am J Med Genet A. 2006. PMID: 16700054 Free article. No abstract available.

8

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine.

Cloarec R, Bruneau N, Rudolf G, Massacrier A, Salmi M, Bataillard M, Boulay C, Caraballo R, Fejerman N, Genton P, Hirsch E, Hunter A, Lesca G, Motte J, Roubertie A, Sanlaville D, Wong SW, Fu YH, Rochette J, Ptácek LJ, Szepetowski P. Cloarec R, et al. Among authors: genton p. Neurology. 2012 Nov 20;79(21):2097-103. doi: 10.1212/WNL.0b013e3182752c46. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077017 Free PMC article.

9

Semi-late onset and rapidly progressive case of Lafora's disease with predominant cognitive symptoms.

Genton P, Borg M, Vigliano P, Pellissier JF, Roger J. Genton P, et al. Eur Neurol. 1989;29(6):333-8. doi: 10.1159/000116441. Eur Neurol. 1989. PMID: 2514103

10

Prognostic factors for childhood and juvenile absence epilepsies.

Bartolomei F, Roger J, Bureau M, Genton P, Dravet C, Viallat D, Gastaut JL. Bartolomei F, et al. Among authors: genton p. Eur Neurol. 1997;37(3):169-75. doi: 10.1159/000117429. Eur Neurol. 1997. PMID: 9137927

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