Lesage S - Search Results

1

Detection of ATXN2 Expansions in an Exome Dataset: An Underdiagnosed Cause of Parkinsonism.

Casse F, Courtin T, Tesson C, Ferrien M, Noël S, Fauret-Amsellem AL, Gareau T, Guegan J, Anheim M, Mariani LL, Le Forestier N, Tranchant C, Corvol JC, Lesage S, Brice A; French Parkinson's disease genetics study group (PDG). Casse F, et al. Among authors: lesage s. Mov Disord Clin Pract. 2023 Mar 7;10(4):664-669. doi: 10.1002/mdc3.13699. eCollection 2023 Apr. Mov Disord Clin Pract. 2023. PMID: 37070044 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

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

4

[LRRK2 is a major gene in North African parkinsonism].

Lesage S, Dürr A, Brice A. Lesage S, et al. Med Sci (Paris). 2006 May;22(5):470-1. doi: 10.1051/medsci/2006225470. Med Sci (Paris). 2006. PMID: 16687108 Free article. French. No abstract available.

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

Deletion of the parkin and PACRG gene promoter in early-onset parkinsonism.

Lesage S, Magali P, Lohmann E, Lacomblez L, Teive H, Janin S, Cousin PY, Dürr A, Brice A; French Parkinson Disease Genetics Study Group. Lesage S, et al. Hum Mutat. 2007 Jan;28(1):27-32. doi: 10.1002/humu.20436. Hum Mutat. 2007. PMID: 17068781

7

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.

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

Are parkin patients particularly suited for deep-brain stimulation?

Lohmann E, Welter ML, Fraix V, Krack P, Lesage S, Laine S, Tanguy ML, Houeto JL, Mesnage V, Pollak P, Durr A, Agid Y, Brice A; French Parkinson's Disease Genetics study group. Lohmann E, et al. Among authors: lesage s. Mov Disord. 2008 Apr 15;23(5):740-3. doi: 10.1002/mds.21903. Mov Disord. 2008. PMID: 18228569

10

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.

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