Martin C - Search Results

1

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T. Campion D, et al. Among authors: martin c. Am J Hum Genet. 1999 Sep;65(3):664-70. doi: 10.1086/302553. Am J Hum Genet. 1999. PMID: 10441572 Free PMC article.

2

Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques.

Dumanchin C, Tournier I, Martin C, Didic M, Belliard S, Carlander B, Rouhart F, Duyckaerts C, Pellissier JF, Latouche JB, Hannequin D, Frebourg T, Tosi M, Campion D. Dumanchin C, et al. Among authors: martin c. Hum Mutat. 2006 Oct;27(10):1063. doi: 10.1002/humu.9458. Hum Mutat. 2006. PMID: 16941492

3

Presenilins interact with Rab11, a small GTPase involved in the regulation of vesicular transport.

Dumanchin C, Czech C, Campion D, Cuif MH, Poyot T, Martin C, Charbonnier F, Goud B, Pradier L, Frebourg T. Dumanchin C, et al. Among authors: martin c. Hum Mol Genet. 1999 Jul;8(7):1263-9. doi: 10.1093/hmg/8.7.1263. Hum Mol Genet. 1999. PMID: 10369872

4

A novel presenilin 1 missense mutation (L153V) segregating with early-onset autosomal dominant Alzheimer's disease.

Raux G, Gantier R, Martin C, Pothin Y, Brice A, Frebourg T, Campion D. Raux G, et al. Among authors: martin c. Hum Mutat. 2000 Jul;16(1):95. doi: 10.1002/1098-1004(200007)16:1<95::AID-HUMU28>3.0.CO;2-H. Hum Mutat. 2000. PMID: 10874324 No abstract available.

5

APOE promoter polymorphisms do not confer independent risk for Alzheimer's disease in a French population.

Zurutuza L, Verpillat P, Raux G, Hannequin D, Puel M, Belliard S, Michon A, Pothin Y, Camuzat A, Penet C, Martin C, Brice A, Campion D, Clerget-Darpoux F, Frebourg T. Zurutuza L, et al. Among authors: martin c. Eur J Hum Genet. 2000 Sep;8(9):713-6. doi: 10.1038/sj.ejhg.5200513. Eur J Hum Genet. 2000. PMID: 10980578

6

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.

Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D. Raux G, et al. Among authors: martin c. J Med Genet. 2005 Oct;42(10):793-5. doi: 10.1136/jmg.2005.033456. Epub 2005 Jul 20. J Med Genet. 2005. PMID: 16033913 Free PMC article.

7

Mutations of the presenilin I gene in families with early-onset Alzheimer's disease.

Campion D, Flaman JM, Brice A, Hannequin D, Dubois B, Martin C, Moreau V, Charbonnier F, Didierjean O, Tardieu S, et al. Campion D, et al. Among authors: martin c. Hum Mol Genet. 1995 Dec;4(12):2373-7. doi: 10.1093/hmg/4.12.2373. Hum Mol Genet. 1995. PMID: 8634712

8

No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group.

Campion D, Brice A, Hannequin D, Charbonnier F, Dubois B, Martin C, Michon A, Penet C, Bellis M, Calenda A, Martinez M, Agid Y, Clerget-Darpoux F, Frebourg T. Campion D, et al. Among authors: martin c. J Med Genet. 1996 Aug;33(8):661-4. doi: 10.1136/jmg.33.8.661. J Med Genet. 1996. PMID: 8863158 Free PMC article.

9

A novel presenilin 1 mutation resulting in familial Alzheimer's disease with an onset age of 29 years.

Campion D, Brice A, Dumanchin C, Puel M, Baulac M, De La Sayette V, Hannequin D, Duyckaerts C, Michon A, Martin C, Moreau V, Penet C, Martinez M, Clerget-Darpoux F, Agid Y, Frebourg T. Campion D, et al. Among authors: martin c. Neuroreport. 1996 Jul 8;7(10):1582-4. doi: 10.1097/00001756-199607080-00009. Neuroreport. 1996. PMID: 8904759

10

Apolipoprotein E and Alzheimer disease: genotype-specific risks by age and sex.

Bickeböller H, Campion D, Brice A, Amouyel P, Hannequin D, Didierjean O, Penet C, Martin C, Pérez-Tur J, Michon A, Dubois B, Ledoze F, Thomas-Anterion C, Pasquier F, Puel M, Demonet JF, Moreaud O, Babron MC, Meulien D, Guez D, Chartier-Harlin MC, Frebourg T, Agid Y, Martinez M, Clerget-Darpoux F. Bickeböller H, et al. Among authors: martin c. Am J Hum Genet. 1997 Feb;60(2):439-46. Am J Hum Genet. 1997. PMID: 9012418 Free PMC article.

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