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Lesage S, Patin E, Condroyer C, Leutenegger AL, Lohmann E, Giladi N, et al. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Human molecular genetics. 2010.
Evangelou E, Maraganore DM, Annesi G, Brighina L, Brice A, Elbaz A, et al. Non-replication of association for six polymorphisms from meta-analysis of genome-wide association studies of Parkinson's disease: Large-scale collaborative study. Am J Med Genet B Neuropsychiatr Genet. 2009.
Ibáñez P, Lesage S, Janin S, Lohmann E, Durif F, Destée A, et al. Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms. Arch Neurol. 2009;66(1):102-8.
Ribeiro MJ, Thobois S, Lohmann E, du Montcel S, Lesage S, Pelissolo A, et al. A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations. J Nucl Med. 2009;50(8):1244-50.
Leutenegger AL, Salih MA, Ibáñez P, Mukhtar MM, Lesage S, Arabi A, et al. Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1. Arch Neurol. 2006;63(9):1257-61.
Ibáñez P, Lesage S, Lohmann E, Thobois S, De Michele G, Borg M, et al. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain. 2006;129(Pt 3):686-94.
Lesage S, Dürr A, Tazir M, Lohmann E, Leutenegger AL, Janin S, et al. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med. 2006;354(4):422-3.
Lesage S, Ibanez P, Lohmann E, Pollak P, Tison F, Tazir M, et al. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol. 2005;58(5):784-7.
Lesage S, Leutenegger AL, Ibanez P, Janin S, Lohmann E, Dürr A, et al. LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century. Am J Hum Genet. 2005;77(2):330-2.