Denier C - Search Results

1

Frequency of retinal cavernomas in 60 patients with familial cerebral cavernomas: a clinical and genetic study.

Labauge P, Krivosic V, Denier C, Tournier-Lasserve E, Gaudric A. Labauge P, et al. Among authors: denier c. Arch Ophthalmol. 2006 Jun;124(6):885-6. doi: 10.1001/archopht.124.6.885. Arch Ophthalmol. 2006. PMID: 16769843

2

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.

Denier C, Ducros A, Vahedi K, Joutel A, Thierry P, Ritz A, Castelnovo G, Deonna T, Gérard P, Devoize JL, Gayou A, Perrouty B, Soisson T, Autret A, Warter JM, Vighetto A, Van Bogaert P, Alamowitch S, Roullet E, Tournier-Lasserve E. Denier C, et al. Neurology. 1999 Jun 10;52(9):1816-21. doi: 10.1212/wnl.52.9.1816. Neurology. 1999. PMID: 10371528

3

CACNA1A gene de novo mutation causing hemiplegic migraine, coma, and cerebellar atrophy.

Vahedi K, Denier C, Ducros A, Bousson V, Levy C, Chabriat H, Haguenau M, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Among authors: denier c. Neurology. 2000 Oct 10;55(7):1040-2. doi: 10.1212/wnl.55.7.1040. Neurology. 2000. PMID: 11061267

4

Missense CACNA1A mutation causing episodic ataxia type 2.

Denier C, Ducros A, Durr A, Eymard B, Chassande B, Tournier-Lasserve E. Denier C, et al. Arch Neurol. 2001 Feb;58(2):292-5. doi: 10.1001/archneur.58.2.292. Arch Neurol. 2001. PMID: 11176968

5

Sporadic late onset paroxysmal cerebellar ataxia in four unrelated patients: a new disease?

Julien J, Denier C, Ferrer X, Ducros A, Saintarailles J, Lagueny A, Tournier-Lasserve E, Vital C. Julien J, et al. Among authors: denier c. J Neurol. 2001 Mar;248(3):209-14. doi: 10.1007/s004150170228. J Neurol. 2001. PMID: 11355155

6

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: denier c. N Engl J Med. 2001 Jul 5;345(1):17-24. doi: 10.1056/NEJM200107053450103. N Engl J Med. 2001. PMID: 11439943 Free article.

7

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.

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

9

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.

10

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

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