Tournier-Lasserve E - Search Results

1

Ducros A, Tournier-Lasserve E, Bousser MG. Ducros A, et al. Lancet Neurol. 2002 Sep;1(5):285-93. doi: 10.1016/s1474-4422(02)00134-5. Lancet Neurol. 2002. PMID: 12849426 Review.

2

Familial cluster headache: a series of 186 index patients.

El Amrani M, Ducros A, Boulan P, Aidi S, Crassard I, Visy JM, Tournier-Lasserve E, Bousser MG. El Amrani M, et al. Headache. 2002 Nov-Dec;42(10):974-7. doi: 10.1046/j.1526-4610.2002.02226.x. Headache. 2002. PMID: 12453028

3

New CACNA1A gene mutation in a case of familial hemiplegic migraine with status epilepticus.

Beauvais K, Cavé-Riant F, De Barace C, Tardieu M, Tournier-Lasserve E, Furby A. Beauvais K, et al. Eur Neurol. 2004;52(1):58-61. doi: 10.1159/000079546. Epub 2004 Jul 5. Eur Neurol. 2004. PMID: 15240985 No abstract available.

4

Migraine with aura and brain magnetic resonance imaging abnormalities in patients with CADASIL.

Vahedi K, Chabriat H, Levy C, Joutel A, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Arch Neurol. 2004 Aug;61(8):1237-40. doi: 10.1001/archneur.61.8.1237. Arch Neurol. 2004. PMID: 15313840

5

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E. Riant F, et al. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Hum Mutat. 2005. PMID: 16088919

6

Genetics of cavernous angiomas.

Labauge P, Denier C, Bergametti F, Tournier-Lasserve E. Labauge P, et al. Lancet Neurol. 2007 Mar;6(3):237-44. doi: 10.1016/S1474-4422(07)70053-4. Lancet Neurol. 2007. PMID: 17303530 Review.

7

COL4A1 mutation in a patient with sporadic, recurrent intracerebral hemorrhage.

Vahedi K, Kubis N, Boukobza M, Arnoult M, Massin P, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Stroke. 2007 May;38(5):1461-4. doi: 10.1161/STROKEAHA.106.475194. Epub 2007 Mar 22. Stroke. 2007. PMID: 17379824

8

PRRT2 mutations cause hemiplegic migraine.

Riant F, Roze E, Barbance C, Méneret A, Guyant-Maréchal L, Lucas C, Sabouraud P, Trébuchon A, Depienne C, Tournier-Lasserve E. Riant F, et al. Neurology. 2012 Nov 20;79(21):2122-4. doi: 10.1212/WNL.0b013e3182752cb8. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077016

9

A novel hereditary extensive vascular leukoencephalopathy mapping to chromosome 20q13.

Hervé D, Chabriat H, Rigal M, Dalloz MA, Kawkabani Marchini A, De Lepeleire J, Fontaine B, Ceuterick-de Groote C, Alili N, Mine M, Delaforge A, Bousser MG, Guichard JP, Martin JJ, Gray F, Tournier-Lasserve E. Hervé D, et al. Neurology. 2012 Dec 4;79(23):2283-7. doi: 10.1212/WNL.0b013e3182768954. Epub 2012 Nov 21. Neurology. 2012. PMID: 23175731

10

[Reference center for rare vascular diseases of the eye and brain].

Chabriat H; L'équipe et membres du centre de référence CERVCO. Chabriat H, et al. Rev Neurol (Paris). 2013 Feb;169 Suppl 1:S28-32. doi: 10.1016/S0035-3787(13)70057-2. Rev Neurol (Paris). 2013. PMID: 23452768 Review. French.

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