Tournier-Lasserve E - Search Results

1

Truncating mutations in CCM1, encoding KRIT1, cause hereditary cavernous angiomas.

Laberge-le Couteulx S, Jung HH, Labauge P, Houtteville JP, Lescoat C, Cecillon M, Marechal E, Joutel A, Bach JF, Tournier-Lasserve E. Laberge-le Couteulx S, et al. Nat Genet. 1999 Oct;23(2):189-93. doi: 10.1038/13815. Nat Genet. 1999. PMID: 10508515

2

Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia.

Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Nature. 1996 Oct 24;383(6602):707-10. doi: 10.1038/383707a0. Nature. 1996. PMID: 8878478

3

Genetic heterogeneity and absence of founder effect in a series of 36 French cerebral cavernous angiomas families.

Laberge S, Labauge P, Maréchal E, Maciazek J, Tournier-Lasserve E. Laberge S, et al. Eur J Hum Genet. 1999 May-Jun;7(4):499-504. doi: 10.1038/sj.ejhg.5200324. Eur J Hum Genet. 1999. PMID: 10352941

4

Krit1/cerebral cavernous malformation 1 mRNA is preferentially expressed in neurons and epithelial cells in embryo and adult.

Denier C, Gasc JM, Chapon F, Domenga V, Lescoat C, Joutel A, Tournier-Lasserve E. Denier C, et al. Mech Dev. 2002 Sep;117(1-2):363-7. doi: 10.1016/s0925-4773(02)00209-5. Mech Dev. 2002. PMID: 12204286 Free article.

5

Mutations within the MGC4607 gene cause cerebral cavernous malformations.

Denier C, Goutagny S, Labauge P, Krivosic V, Arnoult M, Cousin A, Benabid AL, Comoy J, Frerebeau P, Gilbert B, Houtteville JP, Jan M, Lapierre F, Loiseau H, Menei P, Mercier P, Moreau JJ, Nivelon-Chevallier A, Parker F, Redondo AM, Scarabin JM, Tremoulet M, Zerah M, Maciazek J, Tournier-Lasserve E; Société Française de Neurochirurgie. Denier C, et al. Am J Hum Genet. 2004 Feb;74(2):326-37. doi: 10.1086/381718. Epub 2004 Jan 22. Am J Hum Genet. 2004. PMID: 14740320 Free PMC article.

6

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. Ann Neurol. 1995 Mar;37(3):289-93. doi: 10.1002/ana.410370304. Ann Neurol. 1995. PMID: 7695228

7

[Hemiplegic migraine].

Joutel A, Tournier-Lasserve E, Bousser MG. Joutel A, et al. Presse Med. 1995 Feb 25;24(8):411-4. Presse Med. 1995. PMID: 7899422 Review. French.

8

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12.

Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, et al. Tournier-Lasserve E, et al. Nat Genet. 1993 Mar;3(3):256-9. doi: 10.1038/ng0393-256. Nat Genet. 1993. PMID: 8485581

9

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. 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.

10

Hereditary cerebral cavernous angiomas: clinical and genetic features in 57 French families. Société Française de Neurochirurgie.

Labauge P, Laberge S, Brunereau L, Levy C, Tournier-Lasserve E. Labauge P, et al. Lancet. 1998 Dec 12;352(9144):1892-7. doi: 10.1016/s0140-6736(98)03011-6. Lancet. 1998. PMID: 9863787

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