Campion D - Search Results

1

Evidence of chromosomal inversion using fluorescence in situ hybridization to stretched DNA.

Salomon-Nguyen F, Le Coniat-Busson M, Heilig R, Campion D, Weissenbach J, Berger R. Salomon-Nguyen F, et al. Among authors: campion d. C R Acad Sci III. 1998 Jun;321(6):447-52. doi: 10.1016/s0764-4469(98)80775-0. C R Acad Sci III. 1998. PMID: 9769858

2

A rare allele of a microsatellite located in the tyrosine hydroxylase gene found in schizophrenic patients.

Meloni R, Laurent C, Campion D, Ben Hadjali B, Thibaut F, Dollfus S, Petit M, Samolyk D, Martinez M, Poirier MF, et al. Meloni R, et al. Among authors: campion d. C R Acad Sci III. 1995 Jul;318(7):803-9. C R Acad Sci III. 1995. PMID: 7583768

3

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

4

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

5

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. Hum Mol Genet. 1995 Dec;4(12):2373-7. doi: 10.1093/hmg/4.12.2373. Hum Mol Genet. 1995. PMID: 8634712

6

Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives.

Pérez-Tur J, Campion D, Martinez M, Brice A, Tardieu S, Hannequin D, Agid Y, Delacourte A, Clerget-Darpoux F, Chartier-Harlin MC. Pérez-Tur J, et al. Among authors: campion d. Am J Med Genet. 1995 Dec 18;60(6):550-3. doi: 10.1002/ajmg.1320600613. Am J Med Genet. 1995. PMID: 8825894

7

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. Neuroreport. 1996 Jul 8;7(10):1582-4. doi: 10.1097/00001756-199607080-00009. Neuroreport. 1996. PMID: 8904759

8

De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group.

Dumanchin C, Brice A, Campion D, Hannequin D, Martin C, Moreau V, Agid Y, Martinez M, Clerget-Darpoux F, Frebourg T. Dumanchin C, et al. Among authors: campion d. J Med Genet. 1998 Aug;35(8):672-3. doi: 10.1136/jmg.35.8.672. J Med Genet. 1998. PMID: 9719376 Free PMC article.

9

Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families.

Campion D, d'Amato T, Laklou H, Sabate O, Jay M, Leboyer M, Malafosse A, Gorwood P, Babron MC, Hillaire D, et al. Campion D, et al. Among authors: d amato t. Psychiatry Res. 1992 Dec;44(3):171-9. doi: 10.1016/0165-1781(92)90021-t. Psychiatry Res. 1992. PMID: 1363250

10

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

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