Hannequin D - Search Results

1

A study of the association between the ADAM12 and SH3PXD2A (SH3MD1) genes and Alzheimer's disease.

Laumet G, Petitprez V, Sillaire A, Ayral AM, Hansmannel F, Chapuis J, Hannequin D, Pasquier F, Scarpini E, Galimberti D, Lendon C, Campion D, Amouyel P, Lambert JC. Laumet G, et al. Among authors: hannequin d. Neurosci Lett. 2010 Jan 1;468(1):1-2. doi: 10.1016/j.neulet.2009.10.040. Epub 2009 Oct 22. Neurosci Lett. 2010. PMID: 19837132

2

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: hannequin d. Eur J Hum Genet. 2002 Jul;10(7):399-405. doi: 10.1038/sj.ejhg.5200820. Eur J Hum Genet. 2002. PMID: 12107813

3

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: hannequin d. Neurosci Lett. 2002 Aug 23;329(1):121-3. doi: 10.1016/s0304-3940(02)00586-4. Neurosci Lett. 2002. PMID: 12161276

4

Is the saitohin gene involved in neurodegenerative diseases?

Verpillat P, Ricard S, Hannequin D, Dubois B, Bou J, Camuzat A, Pradier L, Frebourg T, Brice A, Clerget-Darpoux F, Deleuze JF, Campion D; French Study Group on Alzheimer's Disease and Frontotemporal Dementia. Verpillat P, et al. Among authors: hannequin d. Ann Neurol. 2002 Dec;52(6):829-32. doi: 10.1002/ana.10384. Ann Neurol. 2002. PMID: 12447938

5

A risk for early-onset Alzheimer's disease associated with the APBB1 gene (FE65) intron 13 polymorphism.

Cousin E, Hannequin D, Ricard S, Macé S, Génin E, Chansac C, Brice A, Dubois B, Frebourg T, Mercken L, Benavides J, Pradier L, Campion D, Deleuze JF. Cousin E, et al. Among authors: hannequin d. Neurosci Lett. 2003 May 15;342(1-2):5-8. doi: 10.1016/s0304-3940(03)00225-8. Neurosci Lett. 2003. PMID: 12727304

6

[Familial forms of Alzheimer's disease].

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

7

No replication of the association between the Nicastrin gene and familial early-onset Alzheimer's disease.

Cousin E, Hannequin D, Macé S, Dubois B, Ricard S, Génin E, Brun C, Chansac C, Pradier L, Frebourg T, Brice A, Campion D, Deleuze JF. Cousin E, et al. Among authors: hannequin d. Neurosci Lett. 2003 Dec 19;353(2):153-5. doi: 10.1016/s0304-3940(03)01105-4. Neurosci Lett. 2003. PMID: 14664923

8

APP locus duplication causes autosomal dominant early-onset Alzheimer disease with cerebral amyloid angiopathy.

Rovelet-Lecrux A, Hannequin D, Raux G, Le Meur N, Laquerrière A, Vital A, Dumanchin C, Feuillette S, Brice A, Vercelletto M, Dubas F, Frebourg T, Campion D. Rovelet-Lecrux A, et al. Among authors: hannequin d. Nat Genet. 2006 Jan;38(1):24-6. doi: 10.1038/ng1718. Epub 2005 Dec 20. Nat Genet. 2006. PMID: 16369530

9

[APP duplication causes autosomal dominant Alzheimer disease with cerebral amyloid angiopathy].

Campion D, Hannequin D. Campion D, et al. Among authors: hannequin d. Med Sci (Paris). 2006 May;22(5):468-9. doi: 10.1051/medsci/2006225468. Med Sci (Paris). 2006. PMID: 16687107 Free article. French. No abstract available.

10

Biological effects of four PSEN1 gene mutations causing Alzheimer disease with spastic paraparesis and cotton wool plaques.

Dumanchin C, Tournier I, Martin C, Didic M, Belliard S, Carlander B, Rouhart F, Duyckaerts C, Pellissier JF, Latouche JB, Hannequin D, Frebourg T, Tosi M, Campion D. Dumanchin C, et al. Among authors: hannequin d. Hum Mutat. 2006 Oct;27(10):1063. doi: 10.1002/humu.9458. Hum Mutat. 2006. PMID: 16941492

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