Tournier-Lasserve E - Search Results

1

Distinct phenotypic and functional features of CADASIL mutations in the Notch3 ligand binding domain.

Monet-Leprêtre M, Bardot B, Lemaire B, Domenga V, Godin O, Dichgans M, Tournier-Lasserve E, Cohen-Tannoudji M, Chabriat H, Joutel A. Monet-Leprêtre M, et al. Brain. 2009 Jun;132(Pt 6):1601-12. doi: 10.1093/brain/awp049. Epub 2009 Mar 17. Brain. 2009. PMID: 19293235 Free PMC article.

2

Spectrum and expression analysis of KRIT1 mutations in 121 consecutive and unrelated patients with Cerebral Cavernous Malformations.

Cavé-Riant F, Denier C, Labauge P, Cécillon M, Maciazek J, Joutel A, Laberge-Le Couteulx S, Tournier-Lasserve E. Cavé-Riant F, et al. Eur J Hum Genet. 2002 Nov;10(11):733-40. doi: 10.1038/sj.ejhg.5200870. Eur J Hum Genet. 2002. PMID: 12404106

3

Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Ruchoux MM, Domenga V, Brulin P, Maciazek J, Limol S, Tournier-Lasserve E, Joutel A. Ruchoux MM, et al. Am J Pathol. 2003 Jan;162(1):329-42. doi: 10.1016/S0002-9440(10)63824-2. Am J Pathol. 2003. PMID: 12507916 Free PMC article.

4

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway.

Joutel A, Monet M, Domenga V, Riant F, Tournier-Lasserve E. Joutel A, et al. Am J Hum Genet. 2004 Feb;74(2):338-47. doi: 10.1086/381506. Epub 2004 Jan 8. Am J Hum Genet. 2004. PMID: 14714274 Free PMC article.

5

Clinical features of cerebral cavernous malformations patients with KRIT1 mutations.

Denier C, Labauge P, Brunereau L, Cavé-Riant F, Marchelli F, Arnoult M, Cecillon M, Maciazek J, Joutel A, Tournier-Lasserve E; Sociéte Française de Neurochirgurgie; Sociéte de Neurochirurgie de Langue Française. Denier C, et al. Ann Neurol. 2004 Feb;55(2):213-20. doi: 10.1002/ana.10804. Ann Neurol. 2004. PMID: 14755725

6

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

7

Notch3 is required for arterial identity and maturation of vascular smooth muscle cells.

Domenga V, Fardoux P, Lacombe P, Monet M, Maciazek J, Krebs LT, Klonjkowski B, Berrou E, Mericskay M, Li Z, Tournier-Lasserve E, Gridley T, Joutel A. Domenga V, et al. Genes Dev. 2004 Nov 15;18(22):2730-5. doi: 10.1101/gad.308904. Genes Dev. 2004. PMID: 15545631 Free PMC article.

8

Impaired vascular mechanotransduction in a transgenic mouse model of CADASIL arteriopathy.

Dubroca C, Lacombe P, Domenga V, Maciazek J, Levy B, Tournier-Lasserve E, Joutel A, Henrion D. Dubroca C, et al. Stroke. 2005 Jan;36(1):113-7. doi: 10.1161/01.STR.0000149949.92854.45. Epub 2004 Nov 29. Stroke. 2005. PMID: 15569862 Free PMC article.

9

Impaired cerebral vasoreactivity in a transgenic mouse model of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy arteriopathy.

Lacombe P, Oligo C, Domenga V, Tournier-Lasserve E, Joutel A. Lacombe P, et al. Stroke. 2005 May;36(5):1053-8. doi: 10.1161/01.STR.0000163080.82766.eb. Epub 2005 Apr 7. Stroke. 2005. PMID: 15817893

10

Genotype-phenotype correlations in cerebral cavernous malformations patients.

Denier C, Labauge P, Bergametti F, Marchelli F, Riant F, Arnoult M, Maciazek J, Vicaut E, Brunereau L, Tournier-Lasserve E. Denier C, et al. Ann Neurol. 2006 Nov;60(5):550-556. doi: 10.1002/ana.20947. Ann Neurol. 2006. PMID: 17041941

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