Campion D - Search Results

1

Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease.

Martinez M, Campion D, Brice A, Hannequin D, Dubois B, Didierjean O, Michon A, Thomas-Anterion C, Puel M, Frebourg T, Agid Y, Clerget-Darpoux F. Martinez M, et al. Among authors: campion d. Arch Neurol. 1998 Jun;55(6):810-6. doi: 10.1001/archneur.55.6.810. Arch Neurol. 1998. PMID: 9626772

2

More missense in amyloid gene.

Carter DA, Desmarais E, Bellis M, Campion D, Clerget-Darpoux F, Brice A, Agid Y, Jaillard-Serradt A, Mallet J. Carter DA, et al. Among authors: campion d. Nat Genet. 1992 Dec;2(4):255-6. doi: 10.1038/ng1292-255. Nat Genet. 1992. PMID: 1303275 No abstract available.

3

Allelic association at the D14S43 locus in early onset Alzheimer's disease. French Alzheimer's Disease Collaborative Study Group.

Brice A, Tardieu S, Campion D, Le Guern E, Martinez M, Carpentier A, Penet C, Dubois B, Bellis M, Mallet J, et al. Brice A, et al. Among authors: campion d. Am J Med Genet. 1995 Apr 24;60(2):91-3. doi: 10.1002/ajmg.1320600202. Am J Med Genet. 1995. PMID: 7485257

4

Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups.

Campion D, Martinez M, Hannequin D, Brice A, Thomas-Anterion C, Michon A, Babron MC, Dubois B, Goas Y, Jaillard-Serradt A, et al. Campion D, et al. Am J Med Genet. 1995 Jun 19;60(3):221-7. doi: 10.1002/ajmg.1320600310. Am J Med Genet. 1995. PMID: 7573175

5

The NACP/synuclein gene: chromosomal assignment and screening for alterations in Alzheimer disease.

Campion D, Martin C, Heilig R, Charbonnier F, Moreau V, Flaman JM, Petit JL, Hannequin D, Brice A, Frebourg T. Campion D, et al. Genomics. 1995 Mar 20;26(2):254-7. doi: 10.1016/0888-7543(95)80208-4. Genomics. 1995. PMID: 7601450

6

No major role for the dopamine D2 receptor Ser-->Cys311 mutation in schizophrenia.

Laurent C, Bodeau-Péan S, Campion D, d'Amato T, Jay M, Dollfus S, Thibault F, Petit M, Samolyk D, Martinez M, et al. Laurent C, et al. Among authors: campion d, d amato t. Psychiatr Genet. 1994 Winter;4(4):229-30. doi: 10.1097/00041444-199400440-00007. Psychiatr Genet. 1994. PMID: 7712120

7

A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization.

Campion D, Brice A, Hannequin D, Tardieu S, Dubois B, Calenda A, Brun E, Penet C, Tayot J, Martinez M, et al. Campion D, et al. Neurology. 1995 Jan;45(1):80-5. doi: 10.1212/wnl.45.1.80. Neurology. 1995. PMID: 7824141 Clinical Trial.

8

Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)?

Martinez M, Campion D, Babron MC, Clerget-Darpoux F. Martinez M, et al. Among authors: campion d. Genet Epidemiol. 1993;10(6):431-5. doi: 10.1002/gepi.1370100617. Genet Epidemiol. 1993. PMID: 8314039

9

Absence of the amyloid precursor protein gene mutation (APP717: Val->Ile) in 85 cases of early onset Alzheimer's disease.

Brice A, Boch AL, Stevanin G, Khati C, Dubois B, Agid Y, Campion D, Clerget F, Mallet J, Bellis M, et al. Brice A, et al. Among authors: campion d. J Neurol Neurosurg Psychiatry. 1993 Jan;56(1):112-3. doi: 10.1136/jnnp.56.1.112-a. J Neurol Neurosurg Psychiatry. 1993. PMID: 8429314 Free PMC article. No abstract available.

10

No mutation in codon 713 of the amyloid precursor gene in schizophrenic patients.

Carter D, Campion D, d'Amato T, Jay M, Brice A, Bellis M, Mallet J, Agid Y. Carter D, et al. Among authors: campion d, d amato t. Hum Mol Genet. 1993 Mar;2(3):321. doi: 10.1093/hmg/2.3.321. Hum Mol Genet. 1993. PMID: 8499923 No abstract available.

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