Cecillon M - Search Results

1

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. Among authors: cecillon m. Ann Neurol. 1997 Dec;42(6):885-90. doi: 10.1002/ana.410420610. Ann Neurol. 1997. PMID: 9403481

2

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: cecillon m. Ann Neurol. 2000 Mar;47(3):388-91. Ann Neurol. 2000. PMID: 10716263

3

The clinical spectrum of familial hemiplegic migraine associated with mutations in a neuronal calcium channel.

Ducros A, Denier C, Joutel A, Cecillon M, Lescoat C, Vahedi K, Darcel F, Vicaut E, Bousser MG, Tournier-Lasserve E. Ducros A, et al. Among authors: cecillon m. N Engl J Med. 2001 Jul 5;345(1):17-24. doi: 10.1056/NEJM200107053450103. N Engl J Med. 2001. PMID: 11439943 Free article.

4

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. Among authors: cecillon m. Ann Neurol. 2004 Feb;55(2):213-20. doi: 10.1002/ana.10804. Ann Neurol. 2004. PMID: 14755725

5

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. Among authors: cecillon m. Nat Genet. 1999 Oct;23(2):189-93. doi: 10.1038/13815. Nat Genet. 1999. PMID: 10508515

6

[CADASIL: genetics and physiopathology].

Joutel A, François A, Chabriat H, Vahedi K, Andreux F, Domenga V, Cecillon M, Maciazek J, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: cecillon m. Bull Acad Natl Med. 2000;184(7):1535-42; discussion 1542-4. Bull Acad Natl Med. 2000. PMID: 11261257 Review. French.

7

Skin biopsy immunostaining with a Notch3 monoclonal antibody for CADASIL diagnosis.

Joutel A, Favrole P, Labauge P, Chabriat H, Lescoat C, Andreux F, Domenga V, Cécillon M, Vahedi K, Ducros A, Cave-Riant F, Bousser MG, Tournier-Lasserve E. Joutel A, et al. Among authors: cecillon m. Lancet. 2001 Dec 15;358(9298):2049-51. doi: 10.1016/S0140-6736(01)07142-2. Lancet. 2001. PMID: 11755616

8

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. Among authors: cecillon m. Eur J Hum Genet. 2002 Nov;10(11):733-40. doi: 10.1038/sj.ejhg.5200870. Eur J Hum Genet. 2002. PMID: 12404106

9

The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients.

Joutel A, Andreux F, Gaulis S, Domenga V, Cecillon M, Battail N, Piga N, Chapon F, Godfrain C, Tournier-Lasserve E. Joutel A, et al. Among authors: cecillon m. J Clin Invest. 2000 Mar;105(5):597-605. doi: 10.1172/JCI8047. J Clin Invest. 2000. PMID: 10712431 Free PMC article.

10

Evaluation of DHPLC analysis in mutational scanning of Notch3, a gene with a high G-C content.

Escary JL, Cécillon M, Maciazek J, Lathrop M, Tournier-Lasserve E, Joutel A. Escary JL, et al. Among authors: cecillon m. Hum Mutat. 2000 Dec;16(6):518-26. doi: 10.1002/1098-1004(200012)16:6<518::AID-HUMU9>3.0.CO;2-Q. Hum Mutat. 2000. PMID: 11102981

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