1. S. Lesage, C. Condroyer, A. Lannuzel, E. Lohmann, A. Troiano, F. Tison, P. Damier, S. Thobois, A. M. Ouvrard-Hernandez, S. Rivaud-Pechoux, C. Brefel-Courbon, A. Destee, C. Tranchant, M. Romana, L. Leclere, A. Durr, and A. Brice. Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease. J Med Genet, 46(7):458-64, 2009. Note: French Parkinson's Disease Genetics Study GroupLetterResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Adolescent, Adult, African Continental Ancestry Group/genetics, Aged, Aged, 80 and over, Analysis of Variance, Chi-Square Distribution, DNA Mutational Analysis/methods, European Continental Ancestry Group/genetics, Female, Gene Frequency, Humans, Male, Middle Aged, Mutation, Parkinsonian Disorders/diagnosis/*genetics, Pedigree, Protein-Serine-Threonine Kinases/*genetics.



2. E. Lohmann, L. Leclere, F. De Anna, S. Lesage, B. Dubois, Y. Agid, A. Durr, and A. Brice. A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism Relat Disord, 15(4):273-6, 2009. Note: French Parkinson's Disease Genetics Study GroupJournal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Aged, DNA Mutational Analysis/methods, *Family Health, Female, France, *Genetic Predisposition to Disease, Glycine/genetics, Humans, Male, Middle Aged, Mutation/*genetics, Neuropsychological Tests, *Olfaction Disorders/etiology/genetics/psychology, *Parkinson Disease/complications/genetics/psychology, Protein-Serine-Threonine Kinases/*genetics, Serine/genetics.



3. E. Lohmann, L. Leclere, F. De Anna, S. Lesage, B. Dubois, Y. Agid, A. Durr, and A. Brice. A clinical, neuropsychological and olfactory evaluation of a large family with LRRK2 mutations. Parkinsonism Relat Disord, 2008. Note: The French Parkinson's Disease Genetics Study GroupJournal article. [WWW]



4. S. Lesage, S. Janin, E. Lohmann, A. L. Leutenegger, L. Leclere, F. Viallet, P. Pollak, F. Durif, S. Thobois, V. Layet, M. Vidailhet, Y. Agid, A. Durr, A. Brice, A. M. Bonnet, M. Borg, E. Broussolle, P. Damier, A. Destee, M. Martinez, C. Penet, O. Rasco, F. Tison, C. Tranchan, and M. Verin. LRRK2 exon 41 mutations in sporadic Parkinson disease in Europeans. Arch Neurol, 64(3):425-30, 2007. Note: French Parkinson's Disease Genetics Study GroupNs41723-01a1/ns/nindsComparative StudyJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Aged, Aged, 80 and over, DNA Mutational Analysis/methods, Europe, Exons/*genetics, Female, Histidine/genetics, Humans, Male, Middle Aged, *Mutation, Parkinson Disease/*genetics, Protein-Serine-Threonine Kinases/*genetics, Serine/genetics, Threonine/genetics, Tyrosine/genetics.



5. S. Lesage, L. Leclere, E. Lohmann, M. Borg, M. Ruberg, A. Durr, and A. Brice. Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease. Neurodegener Dis, 4(2-3):195-8, 2007. Note: French Parkinson's Disease Genetics Study GroupNs41723-01a1/ns/nindsJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tSwitzerland. [WWW]

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