Campion D - Search Results

1

Mutation of the PDGFRB gene as a cause of idiopathic basal ganglia calcification.

Nicolas G, Pottier C, Maltête D, Coutant S, Rovelet-Lecrux A, Legallic S, Rousseau S, Vaschalde Y, Guyant-Maréchal L, Augustin J, Martinaud O, Defebvre L, Krystkowiak P, Pariente J, Clanet M, Labauge P, Ayrignac X, Lefaucheur R, Le Ber I, Frébourg T, Hannequin D, Campion D. Nicolas G, et al. Among authors: campion d. Neurology. 2013 Jan 8;80(2):181-7. doi: 10.1212/WNL.0b013e31827ccf34. Epub 2012 Dec 19. Neurology. 2013. PMID: 23255827

2

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

3

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.

4

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

5

[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.

6

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.

7

[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.

8

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

9

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.

10

No association of apolipoprotein epsilon 4 allele with schizophrenia even in cognitively impaired patients.

Thibaut F, Coron B, Hannequin D, Segard L, Martin C, Dollfus S, Campion D, Frebourg T, Petit M. Thibaut F, et al. Among authors: campion d. Schizophr Res. 1998 Mar 10;30(2):149-53. doi: 10.1016/s0920-9964(97)00147-3. Schizophr Res. 1998. PMID: 9549778

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