Campion D - Search Results

1

Brain calcification process and phenotypes according to age and sex: Lessons from SLC20A2, PDGFB, and PDGFRB mutation carriers.

Nicolas G, Charbonnier C, de Lemos RR, Richard AC, Guillin O, Wallon D, Legati A, Geschwind D, Coppola G, Frebourg T, Campion D, de Oliveira JR, Hannequin D; collaborators from the French IBGC study Group. Nicolas G, et al. Among authors: campion d. Am J Med Genet B Neuropsychiatr Genet. 2015 Oct;168(7):586-94. doi: 10.1002/ajmg.b.32336. Epub 2015 Jun 30. Am J Med Genet B Neuropsychiatr Genet. 2015. PMID: 26129893

2

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

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

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.

5

Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group.

Martinez M, Campion D, Babron MC, Hannequin D, Agid Y, Bellis M, Brice A, Mallet J, Michon A, Thomas-Anterion C, Clerget-Darpoux F. Martinez M, et al. Among authors: campion d. Am J Med Genet. 1996 Feb 16;67(1):9-12. doi: 10.1002/ajmg.1320670102. Am J Med Genet. 1996. PMID: 8678122

6

[Phenotype of familial forms of early-onset Alzheimer's disease linked to chromosome 14. Clinical and neuropsychological characteristics of a large group].

Hannequin D, Campion D, Tardieu S, Auzou P, Martinez M, Dubois B, Clerget-Darpoux F, Agid Y, Brice A. Hannequin D, et al. Among authors: campion d. Rev Neurol (Paris). 1995 Dec;151(12):682-90. Rev Neurol (Paris). 1995. PMID: 8787098 Review. French.

7

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

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. 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

[Genetics of Alzheimer's disease].

Hannequin D, Campion D, Brice A, Frebourg T, Martinez M, Clerget-Darpoux F, Agid Y. Hannequin D, et al. Among authors: campion d. Rev Med Interne. 1996;17(7):545-50. doi: 10.1016/0248-8663(96)83090-6. Rev Med Interne. 1996. PMID: 8881379 Review. French.

10

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

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