Genton P - Search Results

1

[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.

2

[Limitations of the concept of idiopathic generalized epilepsy].

Genton P. Genton P. Rev Neurol (Paris). 1999 Feb;155(2):121-8. Rev Neurol (Paris). 1999. PMID: 10226315 Review. French.

3

[Ring chromosome 20: an identifiable epileptic syndrome].

Roubertie A, Petit J, Genton P. Roubertie A, et al. Among authors: genton p. Rev Neurol (Paris). 2000 Feb;156(2):149-53. Rev Neurol (Paris). 2000. PMID: 10743013 French.

4

Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.

Caraballo R, Pavek S, Lemainque A, Gastaldi M, Echenne B, Motte J, Genton P, Cersósimo R, Humbertclaude V, Fejerman N, Monaco AP, Lathrop MG, Rochette J, Szepetowski P. Caraballo R, et al. Among authors: genton p. Am J Hum Genet. 2001 Mar;68(3):788-94. doi: 10.1086/318805. Epub 2001 Feb 13. Am J Hum Genet. 2001. PMID: 11179027 Free PMC article.

5

[Psychiatric disorders in juvenile myoclonic epilepsy].

Gélisse P, Genton P, Samuelian JC, Thomas P, Bureau M. Gélisse P, et al. Among authors: genton p. Rev Neurol (Paris). 2001 Mar;157(3):297-302. Rev Neurol (Paris). 2001. PMID: 11319492 French.

6

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.

7

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.

8

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.

9

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.

10

Familial generalized epilepsy in Bulgarian Roma.

Tournev I, Royer B, Szepetowski P, Guergueltcheva V, Radionova M, Velizarova R, Yonova M, Lathrop M, Jamali S, Petkov R, Raycheva M, Genton P. Tournev I, et al. Among authors: genton p. Epileptic Disord. 2007 Sep;9(3):300-6. doi: 10.1684/epd.2007.0125. Epub 2007 Sep 20. Epileptic Disord. 2007. PMID: 17884754 Free article.

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