Lesage S - Search Results

1

Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia.

Real R, Martinez-Carrasco A, Reynolds RH, Lawton MA, Tan MMX, Shoai M, Corvol JC, Ryten M, Bresner C, Hubbard L, Brice A, Lesage S, Faouzi J, Elbaz A, Artaud F, Williams N, Hu MTM, Ben-Shlomo Y, Grosset DG, Hardy J, Morris HR. Real R, et al. Among authors: lesage s. Brain. 2023 May 2;146(5):1873-1887. doi: 10.1093/brain/awac414. Brain. 2023. PMID: 36348503 Free PMC article.

2

G2019S LRRK2 mutation in French and North African families with Parkinson's disease.

Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, Leutenegger AL, Guimaraes J, Bonnet AM, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Ann Neurol. 2005 Nov;58(5):784-7. doi: 10.1002/ana.20636. Ann Neurol. 2005. PMID: 16240353

3

[LRRK2: a gene belonging to the ROCO family is implicated in the Parkinson's disease].

Lesage S, Leutenegger AL, Brice A. Lesage S, et al. Med Sci (Paris). 2005 Dec;21(12):1015-7. doi: 10.1051/medsci/200521121015. Med Sci (Paris). 2005. PMID: 16324633 Free article. French. No abstract available.

4

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.

Ibáñez P, Lesage S, Lohmann E, Thobois S, De Michele G, Borg M, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Ibáñez P, et al. Among authors: lesage s. Brain. 2006 Mar;129(Pt 3):686-94. doi: 10.1093/brain/awl005. Epub 2006 Jan 9. Brain. 2006. PMID: 16401616

5

Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1.

Leutenegger AL, Salih MA, Ibáñez P, Mukhtar MM, Lesage S, Arabi A, Lohmann E, Dürr A, Ahmed AE, Brice A. Leutenegger AL, et al. Among authors: lesage s. Arch Neurol. 2006 Sep;63(9):1257-61. doi: 10.1001/archneur.63.9.1257. Arch Neurol. 2006. PMID: 16966503

6

Subthalamic nucleus stimulation is efficacious in patients with Parkinsonism and LRRK2 mutations.

Schüpbach M, Lohmann E, Anheim M, Lesage S, Czernecki V, Yaici S, Worbe Y, Charles P, Welter ML, Pollak P, Dürr A, Agid Y, Brice A. Schüpbach M, et al. Among authors: lesage s. Mov Disord. 2007 Jan;22(1):119-22. doi: 10.1002/mds.21178. Mov Disord. 2007. PMID: 17080443 Clinical Trial.

7

LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans.

Lesage S, Janin S, Lohmann E, Leutenegger AL, Leclere L, Viallet F, Pollak P, Durif F, Thobois S, Layet V, Vidailhet M, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group; Bonnet AM, Borg M, Broussolle E, Damier P, Destée A, Martinez M, Penet C, Rasco O, Tison F, Tranchan C, Vérin M. Lesage S, et al. Arch Neurol. 2007 Mar;64(3):425-30. doi: 10.1001/archneur.64.3.425. Arch Neurol. 2007. PMID: 17353388

8

Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease.

Lesage S, Leclere L, Lohmann E, Borg M, Ruberg M, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Neurodegener Dis. 2007;4(2-3):195-8. doi: 10.1159/000101844. Neurodegener Dis. 2007. PMID: 17596714

9

Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive.

Lesage S, Lohmann E, Tison F, Durif F, Dürr A, Brice A. Lesage S, et al. Hum Genet. 2008 Feb;123(1):114. Hum Genet. 2008. PMID: 18386383 No abstract available.

10

Parkinson's disease: from monogenic forms to genetic susceptibility factors.

Lesage S, Brice A. Lesage S, et al. Hum Mol Genet. 2009 Apr 15;18(R1):R48-59. doi: 10.1093/hmg/ddp012. Hum Mol Genet. 2009. PMID: 19297401 Review.

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