Hannequin D - Search Results

1

Mutations in XPR1 cause primary familial brain calcification associated with altered phosphate export.

Legati A, Giovannini D, Nicolas G, López-Sánchez U, Quintáns B, Oliveira JR, Sears RL, Ramos EM, Spiteri E, Sobrido MJ, Carracedo Á, Castro-Fernández C, Cubizolle S, Fogel BL, Goizet C, Jen JC, Kirdlarp S, Lang AE, Miedzybrodzka Z, Mitarnun W, Paucar M, Paulson H, Pariente J, Richard AC, Salins NS, Simpson SA, Striano P, Svenningsson P, Tison F, Unni VK, Vanakker O, Wessels MW, Wetchaphanphesat S, Yang M, Boller F, Campion D, Hannequin D, Sitbon M, Geschwind DH, Battini JL, Coppola G. Legati A, et al. Among authors: hannequin d. Nat Genet. 2015 Jun;47(6):579-81. doi: 10.1038/ng.3289. Epub 2015 May 4. Nat Genet. 2015. PMID: 25938945 Free PMC article.

2

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

3

Severe myoclonus-dystonia syndrome associated with a novel epsilon-sarcoglycan gene truncating mutation.

Maréchal L, Raux G, Dumanchin C, Lefebvre G, Deslandre E, Girard C, Campion D, Parain D, Frebourg T, Hannequin D. Maréchal L, et al. Among authors: hannequin d. Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):114-7. doi: 10.1002/ajmg.b.10062. Am J Med Genet B Neuropsychiatr Genet. 2003. PMID: 12707948

4

[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.

5

Unusual cerebrotendinous xanthomatosis with fronto-temporal dementia phenotype.

Guyant-Maréchal L, Verrips A, Girard C, Wevers RA, Zijlstra F, Sistermans E, Vera P, Campion D, Hannequin D. Guyant-Maréchal L, et al. Among authors: hannequin d. Am J Med Genet A. 2005 Dec 1;139A(2):114-7. doi: 10.1002/ajmg.a.30797. Am J Med Genet A. 2005. PMID: 16278884

6

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

7

[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.

8

Progranulin null mutations in both sporadic and familial frontotemporal dementia.

Le Ber I, van der Zee J, Hannequin D, Gijselinck I, Campion D, Puel M, Laquerrière A, De Pooter T, Camuzat A, Van den Broeck M, Dubois B, Sellal F, Lacomblez L, Vercelletto M, Thomas-Antérion C, Michel BF, Golfier V, Didic M, Salachas F, Duyckaerts C, Cruts M, Verpillat P, Van Broeckhoven C, Brice A; French Research Network on FTD/FTD-MND. Le Ber I, et al. Among authors: hannequin d. Hum Mutat. 2007 Sep;28(9):846-55. doi: 10.1002/humu.20520. Hum Mutat. 2007. PMID: 17436289

9

Deletion of the progranulin gene in patients with frontotemporal lobar degeneration or Parkinson disease.

Rovelet-Lecrux A, Deramecourt V, Legallic S, Maurage CA, Le Ber I, Brice A, Lambert JC, Frébourg T, Hannequin D, Pasquier F, Campion D. Rovelet-Lecrux A, et al. Among authors: hannequin d. Neurobiol Dis. 2008 Jul;31(1):41-5. doi: 10.1016/j.nbd.2008.03.004. Epub 2008 Apr 7. Neurobiol Dis. 2008. PMID: 18479928

10

Association study of the NEDD9 gene with the risk of developing Alzheimer's and Parkinson's disease.

Chapuis J, Moisan F, Mellick G, Elbaz A, Silburn P, Pasquier F, Hannequin D, Lendon C, Campion D, Amouyel P, Lambert JC. Chapuis J, et al. Among authors: hannequin d. Hum Mol Genet. 2008 Sep 15;17(18):2863-7. doi: 10.1093/hmg/ddn183. Epub 2008 Jun 25. Hum Mol Genet. 2008. PMID: 18579580

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