Ducros A - Search Results

1

Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.

Riant F, Roos C, Roubertie A, Barbance C, Hadjadj J, Auvin S, Baille G, Beltramone M, Boulanger C, Cahn A, Cata F, Cheuret E, Cuvellier JC, Defo A, Demarquay G, Donnet A, Gaillard N, Massardier E, Guy N, Lamoureux S, Le Moigno L, Lucas C, Ratiu D, Redon S, Rey C, Thauvin C, Viallet F, Tournier-Lasserve E, Ducros A. Riant F, et al. Among authors: ducros a. Neurology. 2022 Jan 4;98(1):e51-e61. doi: 10.1212/WNL.0000000000012947. Epub 2021 Oct 14. Neurology. 2022. PMID: 34649875

2

A gene for hereditary paroxysmal cerebellar ataxia maps to chromosome 19p.

Vahedi K, Joutel A, Van Bogaert P, Ducros A, Maciazeck J, Bach JF, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Among authors: ducros a. Ann Neurol. 1995 Mar;37(3):289-93. doi: 10.1002/ana.410370304. Ann Neurol. 1995. PMID: 7695228

3

Monozygotic twins discordant for familial hemiplegic migraine.

Ducros A, Joutel A, Labauge P, Pagès M, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Neurology. 1995 Jun;45(6):1222. doi: 10.1212/wnl.45.6.1222. Neurology. 1995. PMID: 7783896 No abstract available.

4

Genetic heterogeneity of familial hemiplegic migraine.

Joutel A, Ducros A, Vahedi K, Labauge P, Delrieu O, Pinsard N, Mancini J, Ponsot G, Gouttière F, Gastaut JL, et al. Joutel A, et al. Among authors: ducros a. Am J Hum Genet. 1994 Dec;55(6):1166-72. Am J Hum Genet. 1994. PMID: 7977376 Free PMC article.

5

Mapping of a second locus for familial hemiplegic migraine to 1q21-q23 and evidence of further heterogeneity.

Ducros A, Joutel A, Vahedi K, Cecillon M, Ferreira A, Bernard E, Verier A, Echenne B, Lopez de Munain A, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Ann Neurol. 1997 Dec;42(6):885-90. doi: 10.1002/ana.410420610. Ann Neurol. 1997. PMID: 9403481

6

Recurrence of the T666M calcium channel CACNA1A gene mutation in familial hemiplegic migraine with progressive cerebellar ataxia.

Ducros A, Denier C, Joutel A, Vahedi K, Michel A, Darcel F, Madigand M, Guerouaou D, Tison F, Julien J, Hirsch E, Chedru F, Bisgård C, Lucotte G, Després P, Billard C, Barthez MA, Ponsot G, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192. Am J Hum Genet. 1999. PMID: 9915947 Free PMC article.

7

Recurrent episodes of coma: an unusual phenotype of familial hemiplegic migraine with linkage to chromosome 1.

Echenne B, Ducros A, Rivier F, Joutel A, Humbertclaude V, Roubertie A, Azaïs M, Bousser MG, Tournier-Lasserve E. Echenne B, et al. Among authors: ducros a. Neuropediatrics. 1999 Aug;30(4):214-7. doi: 10.1055/s-2007-973493. Neuropediatrics. 1999. PMID: 10569214

8

Decreased hemispheric water mobility in hemiplegic migraine related to mutation of CACNA1A gene.

Chabriat H, Vahedi K, Clark CA, Poupon C, Ducros A, Denier C, Le Bihan D, Bousser MG. Chabriat H, et al. Among authors: ducros a. Neurology. 2000 Jan 25;54(2):510-2. doi: 10.1212/wnl.54.2.510. Neurology. 2000. PMID: 10668728

9

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.

Vahedi K, Denier C, Ducros A, Bousson V, Levy C, Chabriat H, Haguenau M, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Among authors: ducros a. Neurology. 2000 Oct 10;55(7):1040-2. doi: 10.1212/wnl.55.7.1040. Neurology. 2000. PMID: 11061267

10

[Genetics of migraine].

Ducros A. Ducros A. Pathol Biol (Paris). 2000 Sep;48(7):658-62. Pathol Biol (Paris). 2000. PMID: 11072644 Review. French.

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