Malafosse A - Search Results

1

Validity of diagnosis using the French translation of the semi-structured interview for seizure classification.

Picot MC, Crespel A, Tricot M, Daurès JP, Valton L, Malafosse A, Baldy-Moulinier M. Picot MC, et al. Among authors: malafosse a. Epilepsia. 1999 Nov;40(11):1649-56. doi: 10.1111/j.1528-1157.1999.tb02052.x. Epilepsia. 1999. PMID: 10565595 Free article.

2

GABA receptor 1 polymorphism (G1465A) and temporal lobe epilepsy.

Salzmann A, Moulard B, Crespel A, Baldy-Moulinier M, Buresi C, Malafosse A. Salzmann A, et al. Among authors: malafosse a. Epilepsia. 2005 Jun;46(6):931-3. doi: 10.1111/j.1528-1167.2005.40304.x. Epilepsia. 2005. PMID: 15946333 Free article.

3

Suicidal behaviors and the tryptophan hydroxylase gene.

Abbar M, Courtet P, Amadéo S, Caer Y, Mallet J, Baldy-Moulinier M, Castelnau D, Malafosse A. Abbar M, et al. Among authors: malafosse a. Arch Gen Psychiatry. 1995 Oct;52(10):846-9. doi: 10.1001/archpsyc.1995.03950220056011. Arch Gen Psychiatry. 1995. PMID: 7575104

4

A fok1 polymorphism in the human neuronal nicotinic acetylcholine receptor alpha 4 subunit gene.

Guipponi M, Baldy-Moulinier M, Malafosse A. Guipponi M, et al. Among authors: malafosse a. Clin Genet. 1997 Jan;51(1):78-9. Clin Genet. 1997. PMID: 9084944 No abstract available.

5

Linkage mapping of benign familial infantile convulsions (BFIC) to chromosome 19q.

Guipponi M, Rivier F, Vigevano F, Beck C, Crespel A, Echenne B, Lucchini P, Sebastianelli R, Baldy-Moulinier M, Malafosse A. Guipponi M, et al. Among authors: malafosse a. Hum Mol Genet. 1997 Mar;6(3):473-7. doi: 10.1093/hmg/6.3.473. Hum Mol Genet. 1997. PMID: 9147652

6

Replication of association between a SCN1A splice variant and febrile seizures.

Le Gal F, Salzmann A, Crespel A, Malafosse A. Le Gal F, et al. Among authors: malafosse a. Epilepsia. 2011 Oct;52(10):e135-8. doi: 10.1111/j.1528-1167.2011.03164.x. Epub 2011 Jul 18. Epilepsia. 2011. PMID: 21762453 Free article.

7

Lack of association between juvenile myoclonic epilepsy and GABRA5 and GABRB3 genes.

Guipponi M, Thomas P, Girard-Reydet C, Feingold J, Baldy-Moulinier M, Malafosse A. Guipponi M, et al. Among authors: malafosse a. Am J Med Genet. 1997 Apr 18;74(2):150-3. Am J Med Genet. 1997. PMID: 9129713

8

[Recent insights about genetics of human idiopathic epilepsies and febrile seizures].

Moulard B, Crespel A, Malafosse A, Baldy-Moulinier M. Moulard B, et al. Among authors: malafosse a. Rev Neurol (Paris). 2000 Oct;156(10):819-28. Rev Neurol (Paris). 2000. PMID: 11033510 Review. French.

9

Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations.

Moulard B, Genton P, Grid D, Jeanpierre M, Ouazzani R, Mrabet A, Morris M, LeGuern E, Dravet C, Mauguière F, Utermann B, Baldy-Moulinier M, Belaidi H, Bertran F, Biraben A, Ali Chérif A, Chkili T, Crespel A, Darcel F, Dulac O, Geny C, Humbert-Claude V, Kassiotis P, Buresi C, Malafosse A. Moulard B, et al. Among authors: malafosse a. Hum Genet. 2002 Sep;111(3):255-62. doi: 10.1007/s00439-002-0755-x. Epub 2002 Jul 23. Hum Genet. 2002. PMID: 12215838

10

Serotonin transporter gene may be involved in short-term risk of subsequent suicide attempts.

Courtet P, Picot MC, Bellivier F, Torres S, Jollant F, Michelon C, Castelnau D, Astruc B, Buresi C, Malafosse A. Courtet P, et al. Among authors: malafosse a. Biol Psychiatry. 2004 Jan 1;55(1):46-51. doi: 10.1016/j.biopsych.2003.07.004. Biol Psychiatry. 2004. PMID: 14706424

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