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Page 1
The genetics of migraine.
Ducros A, Tournier-Lasserve E, Bousser MG. Ducros A, et al. Among authors: bousser mg. Lancet Neurol. 2002 Sep;1(5):285-93. doi: 10.1016/s1474-4422(02)00134-5. Lancet Neurol. 2002. PMID: 12849426 Review.
[Hemiplegic migraine].
Joutel A, Tournier-Lasserve E, Bousser MG. Joutel A, et al. Among authors: bousser mg. Presse Med. 1995 Feb 25;24(8):411-4. Presse Med. 1995. PMID: 7899422 Review. French.
Notch3 mutations in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), a mendelian condition causing stroke and vascular dementia.
Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Maréchal E, Maciazek J, Vayssière C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: bousser mg. Ann N Y Acad Sci. 1997 Sep 26;826:213-7. doi: 10.1111/j.1749-6632.1997.tb48472.x. Ann N Y Acad Sci. 1997. PMID: 9329692 Review.
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. Among authors: bousser mg. Am J Hum Genet. 1999 Jan;64(1):89-98. doi: 10.1086/302192. Am J Hum Genet. 1999. PMID: 9915947 Free PMC article.
De novo mutation in the Notch3 gene causing CADASIL.
Joutel A, Dodick DD, Parisi JE, Cecillon M, Tournier-Lasserve E, Bousser MG. Joutel A, et al. Among authors: bousser mg. Ann Neurol. 2000 Mar;47(3):388-91. Ann Neurol. 2000. PMID: 10716263
549 results