Campion D - Search Results

1

Amyloid imaging with AV45 ((18)F-florbetapir) in a cognitively normal AβPP duplication carrier.

Saint-Aubert L, Planton M, Hannequin D, Albucher JF, Delisle MB, Payoux P, Hitzel A, Viallard G, Péran P, Campion D, Laquerrière A, Barbeau EJ, Puel M, Raposo N, Chollet F, Pariente J. Saint-Aubert L, et al. Among authors: campion d. J Alzheimers Dis. 2012;28(4):877-83. doi: 10.3233/JAD-2011-111598. J Alzheimers Dis. 2012. PMID: 22156048

2

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

3

No effect of the alpha1-antichymotrypsin A allele in Alzheimer's disease.

Didierjean O, Martinez M, Campion D, Hannequin D, Dubois B, Martin C, Puel M, Thomas Anterion C, Pasquier F, Moreau O, Babron MC, Penet C, Agid Y, Clerget-Darpoux F, Frebourg T, Brice A. Didierjean O, et al. Among authors: campion d. J Neurol Neurosurg Psychiatry. 1997 Jul;63(1):103-5. doi: 10.1136/jnnp.63.1.103. J Neurol Neurosurg Psychiatry. 1997. PMID: 9221977 Free PMC article.

4

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. Am J Hum Genet. 1999 Sep;65(3):664-70. doi: 10.1086/302553. Am J Hum Genet. 1999. PMID: 10441572 Free PMC article.

5

[Dominant forms of Alzheimer's disease: from genotype to phenotype].

Hannequin D, Campion D. Hannequin D, et al. Among authors: campion d. Rev Neurol (Paris). 2001 Apr;157(4):384-92. Rev Neurol (Paris). 2001. PMID: 11398010 Review. French.

6

Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population.

Verpillat P, Bouley S, Campion D, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Antérion C, Agid Y, Brice A, Clerget-Darpoux F. Verpillat P, et al. Among authors: campion d. Eur J Hum Genet. 2001 Jun;9(6):464-8. doi: 10.1038/sj.ejhg.5200644. Eur J Hum Genet. 2001. PMID: 11436129

7

Apolipoprotein E gene in frontotemporal dementia: an association study and meta-analysis.

Verpillat P, Camuzat A, Hannequin D, Thomas-Anterion C, Puel M, Belliard S, Dubois B, Didic M, Lacomblez L, Moreaud O, Golfier V, Campion D, Brice A, Clerget-Darpoux F. Verpillat P, et al. Among authors: campion d. Eur J Hum Genet. 2002 Jul;10(7):399-405. doi: 10.1038/sj.ejhg.5200820. Eur J Hum Genet. 2002. PMID: 12107813

8

Polymorphisms of insulin degrading enzyme gene are not associated with Alzheimer's disease.

Boussaha M, Hannequin D, Verpillat P, Brice A, Frebourg T, Campion D. Boussaha M, et al. Among authors: campion d. Neurosci Lett. 2002 Aug 23;329(1):121-3. doi: 10.1016/s0304-3940(02)00586-4. Neurosci Lett. 2002. PMID: 12161276

9

[Familial forms of Alzheimer's disease].

Maréchal L, Campion D, Hannequin D. Maréchal L, et al. Among authors: campion d. Presse Med. 2003 May 10;32(16):756-63. Presse Med. 2003. PMID: 12856536 Review. French.

10

A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24.

Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D. Le Ber I, et al. Among authors: campion d. Brain. 2004 Sep;127(Pt 9):1979-92. doi: 10.1093/brain/awh216. Epub 2004 Jun 23. Brain. 2004. PMID: 15215218

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