Brice A - Search Results

1

Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines.

Mitsui J, Takahashi Y, Goto J, Tomiyama H, Ishikawa S, Yoshino H, Minami N, Smith DI, Lesage S, Aburatani H, Nishino I, Brice A, Hattori N, Tsuji S. Mitsui J, et al. Among authors: brice a. Am J Hum Genet. 2010 Jul 9;87(1):75-89. doi: 10.1016/j.ajhg.2010.06.006. Am J Hum Genet. 2010. PMID: 20598272 Free PMC article.

2

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century.

Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Lesage S, et al. Among authors: brice a. Am J Hum Genet. 2005 Aug;77(2):330-2. doi: 10.1086/432422. Am J Hum Genet. 2005. PMID: 16145815 Free PMC article. No abstract available.

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. Among authors: brice a. 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: brice a. Brain. 2006 Mar;129(Pt 3):686-94. doi: 10.1093/brain/awl005. Epub 2006 Jan 9. Brain. 2006. PMID: 16401616

5

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

Lesage S, Dürr A, Brice A. Lesage S, et al. Among authors: brice a. 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.

6

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: brice a. Arch Neurol. 2006 Sep;63(9):1257-61. doi: 10.1001/archneur.63.9.1257. Arch Neurol. 2006. PMID: 16966503

7

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. Among authors: brice a. Hum Mutat. 2007 Jan;28(1):27-32. doi: 10.1002/humu.20436. Hum Mutat. 2007. PMID: 17068781

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. Among authors: brice a. 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. Among authors: brice a. Hum Genet. 2008 Feb;123(1):114. Hum Genet. 2008. PMID: 18386383 No abstract available.

10

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms.

Ibáñez P, Lesage S, Janin S, Lohmann E, Durif F, Destée A, Bonnet AM, Brefel-Courbon C, Heath S, Zelenika D, Agid Y, Dürr A, Brice A; French Parkinson's Disease Genetics Study Group. Ibáñez P, et al. Among authors: brice a. Arch Neurol. 2009 Jan;66(1):102-8. doi: 10.1001/archneurol.2008.555. Arch Neurol. 2009. PMID: 19139307

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