Baulac M - Search Results

1

A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

Baulac S, Gourfinkel-An I, Picard F, Rosenberg-Bourgin M, Prud'homme JF, Baulac M, Brice A, LeGuern E. Baulac S, et al. Among authors: baulac m. Am J Hum Genet. 1999 Oct;65(4):1078-85. doi: 10.1086/302593. Am J Hum Genet. 1999. PMID: 10486327 Free PMC article.

2

A novel locus for generalized epilepsy with febrile seizures plus in French families.

Baulac S, Gourfinkel-An I, Couarch P, Depienne C, Kaminska A, Dulac O, Baulac M, LeGuern E, Nabbout R. Baulac S, et al. Among authors: baulac m. Arch Neurol. 2008 Jul;65(7):943-51. doi: 10.1001/archneur.65.7.943. Arch Neurol. 2008. PMID: 18625863

3

Fever, genes, and epilepsy.

Baulac S, Gourfinkel-An I, Nabbout R, Huberfeld G, Serratosa J, Leguern E, Baulac M. Baulac S, et al. Among authors: baulac m. Lancet Neurol. 2004 Jul;3(7):421-30. doi: 10.1016/S1474-4422(04)00808-7. Lancet Neurol. 2004. PMID: 15207799 Review.

4

Myoclonic seizures in the context of generalized epilepsy with febrile seizures plus (GEFS+).

Baulac M, Gourfinkel-An I, Baulac S, Leguern E. Baulac M, et al. Among authors: baulac s. Adv Neurol. 2005;95:119-25. Adv Neurol. 2005. PMID: 15508917 Review. No abstract available.

5

Evidence for digenic inheritance in a family with both febrile convulsions and temporal lobe epilepsy implicating chromosomes 18qter and 1q25-q31.

Baulac S, Picard F, Herman A, Feingold J, Genin E, Hirsch E, Prud'homme JF, Baulac M, Brice A, LeGuern E. Baulac S, et al. Among authors: baulac m. Ann Neurol. 2001 Jun;49(6):786-92. doi: 10.1002/ana.1014. Ann Neurol. 2001. PMID: 11409431

6

[Recent insights into the implication of ion channels in familial forms of epilepsies associated or non associated to febrile convulsions].

Gourfinkel-An I, Baulac S, Nabbout R, Brice A, Baulac M, Leguern E. Gourfinkel-An I, et al. Among authors: baulac m, baulac s. Rev Neurol (Paris). 2004 May;160(5 Pt 2):S90-7. doi: 10.1016/s0035-3787(04)71011-5. Rev Neurol (Paris). 2004. PMID: 15269666 Review. French.

7

First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene.

Baulac S, Huberfeld G, Gourfinkel-An I, Mitropoulou G, Beranger A, Prud'homme JF, Baulac M, Brice A, Bruzzone R, LeGuern E. Baulac S, et al. Among authors: baulac m. Nat Genet. 2001 May;28(1):46-8. doi: 10.1038/ng0501-46. Nat Genet. 2001. PMID: 11326274

8

Advances on the genetics of mendelian idiopathic epilepsies.

Baulac S, Baulac M. Baulac S, et al. Among authors: baulac m. Neurol Clin. 2009 Nov;27(4):1041-1061. doi: 10.1016/j.ncl.2009.07.001. Neurol Clin. 2009. PMID: 19853223 Review.

9

Advances on the genetics of Mendelian idiopathic epilepsies.

Baulac S, Baulac M. Baulac S, et al. Among authors: baulac m. Clin Lab Med. 2010 Dec;30(4):911-29. doi: 10.1016/j.cll.2010.07.008. Clin Lab Med. 2010. PMID: 20832659 Review.

10

Novel GABRG2 mutations cause familial febrile seizures.

Boillot M, Morin-Brureau M, Picard F, Weckhuysen S, Lambrecq V, Minetti C, Striano P, Zara F, Iacomino M, Ishida S, An-Gourfinkel I, Daniau M, Hardies K, Baulac M, Dulac O, Leguern E, Nabbout R, Baulac S. Boillot M, et al. Among authors: baulac m, baulac s. Neurol Genet. 2015 Nov 4;1(4):e35. doi: 10.1212/NXG.0000000000000035. eCollection 2015 Dec. Neurol Genet. 2015. PMID: 27066572 Free PMC article.

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