Hannequin D - Search Results

1

Segregation of a missense mutation in the microtubule-associated protein tau gene with familial frontotemporal dementia and parkinsonism.

Dumanchin C, Camuzat A, Campion D, Verpillat P, Hannequin D, Dubois B, Saugier-Veber P, Martin C, Penet C, Charbonnier F, Agid Y, Frebourg T, Brice A. Dumanchin C, et al. Among authors: hannequin d. Hum Mol Genet. 1998 Oct;7(11):1825-9. doi: 10.1093/hmg/7.11.1825. Hum Mol Genet. 1998. PMID: 9736786

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. Among authors: hannequin d. 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. Among authors: hannequin d. 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. Among authors: hannequin d. Neurology. 1995 Jan;45(1):80-5. doi: 10.1212/wnl.45.1.80. Neurology. 1995. PMID: 7824141 Clinical Trial.

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

6

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: hannequin d. Am J Med Genet. 1996 Feb 16;67(1):9-12. doi: 10.1002/ajmg.1320670102. Am J Med Genet. 1996. PMID: 8678122

7

[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. Rev Neurol (Paris). 1995 Dec;151(12):682-90. Rev Neurol (Paris). 1995. PMID: 8787098 Review. French.

8

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: hannequin d. Am J Med Genet. 1995 Dec 18;60(6):550-3. doi: 10.1002/ajmg.1320600613. Am J Med Genet. 1995. PMID: 8825894

9

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: hannequin d. 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.

10

[Genetics of Alzheimer's disease].

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

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