1. S. Lesage, E. Patin, C. Condroyer, A. L. Leutenegger, E. Lohmann, N. Giladi, A. Bar-Shira, S. Belarbi, N. Hecham, P. Pollak, A. M. Ouvrard-Hernandez, S. Bardien, J. Carr, T. Benhassine, H. Tomiyama, C. Pirkevi, T. Hamadouche, C. Cazeneuve, A. N. Basak, N. Hattori, A. Durr, M. Tazir, A. Orr-Urtreger, L. Quintana-Murci, and A. Brice. Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans. Hum Mol Genet, 2010. Note: For the French Parkinson's Disease Genetics Study GroupJournal article. [WWW]



2. S. Hanein, A. Durr, P. Ribai, S. Forlani, A. L. Leutenegger, I. Nelson, M. C. Babron, N. Elleuch, C. Depienne, C. Charon, A. Brice, and G. Stevanin. A novel locus for autosomal dominant ``uncomplicated'' hereditary spastic paraplegia maps to chromosome 8p21.1-q13.3. Hum Genet, 122(3-4):261-73, 2007. Note: Journal article. [WWW]



3. 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.



4. S. Lesage, A. Durr, M. Tazir, E. Lohmann, A. L. Leutenegger, S. Janin, P. Pollak, and A. Brice. LRRK2 G2019S as a cause of Parkinson's disease in North African Arabs. N Engl J Med, 354(4):422-3, 2006. Note: French Parkinson's Disease Genetics Study GroupLetterUnited States. [WWW] Keyword(s): Africa, Northern/ethnology, Arabs/*genetics, Heterozygote, Homozygote, Humans, Middle Aged, Mutation, Parkinson Disease/*genetics, Protein-Serine-Threonine Kinases/*genetics.



5. A. L. Leutenegger, M. A. Salih, P. Ibanez, M. M. Mukhtar, S. Lesage, A. Arabi, E. Lohmann, A. Durr, A. E. Ahmed, and A. Brice. Juvenile-onset Parkinsonism as a result of the first mutation in the adenosine triphosphate orientation domain of PINK1. Arch Neurol, 63(9):1257-61, 2006. Note: Ns 41723-01a1/ns/nindsComparative StudyJournal ArticleResearch Support, N.I.H., ExtramuralUnited States. [WWW] Keyword(s): Adenosine Triphosphate/*metabolism, Adolescent, Adult, Age of Onset, Alanine/genetics, Amino Acid Sequence, Aspartic Acid/genetics, DNA Mutational Analysis, *Family Health, Female, Genetic Predisposition to Disease, Humans, Male, Middle Aged, *Mutation, Parkinsonian Disorders/*genetics, Protein Kinases/*genetics, Sudan.



6. S. Lesage, P. Ibanez, E. Lohmann, P. Pollak, F. Tison, M. Tazir, A. L. Leutenegger, J. Guimaraes, A. M. Bonnet, Y. Agid, A. Durr, and A. Brice. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol, 58(5):784-7, 2005. Note: French Parkinson's Disease Genetics Study GroupComparative StudyJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adult, Africa, Northern/epidemiology/ethnology, Aged, Aged, 80 and over, DNA Mutational Analysis/methods, *Family Health, Female, France/epidemiology/ethnology, Gene Frequency, Genetic Predisposition to Disease, Genotype, Glycine/*genetics, Humans, Male, Mental Status Schedule/statistics & numerical data, Middle Aged, *Mutation, Parkinson Disease/*genetics, Protein-Serine-Threonine Kinases/*genetics, Serine/*genetics.



7. S. Lesage, A. L. Leutenegger, and A. Brice. [LRRK2: a gene belonging to the ROCO family is implicated in the Parkinson's disease]. Med Sci (Paris), 21(12):1015-7, 2005. Note: NewsFranceM/s. [WWW] Keyword(s): Humans, Parkinson Disease/*genetics, Protein-Serine-Threonine Kinases/*genetics.



8. S. Lesage, A. L. Leutenegger, P. Ibanez, S. Janin, E. Lohmann, A. Durr, and A. Brice. 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, 77(2):330-2, 2005. Note: French Parkinson's Disease Genetics Study GroupLetterResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Africa, Northern, African Continental Ancestry Group, European Continental Ancestry Group, Family Health, *Founder Effect, Genetic Markers, Genotype, *Haplotypes, Humans, Microsatellite Repeats, Middle Aged, *Mutation, Parkinson Disease/*genetics, Protein-Serine-Threonine Kinases/*genetics.



9. C. Verny, N. Ravise, A. L. Leutenegger, F. Pouplard, O. Dubourg, S. Tardieu, F. Dubas, A. Brice, E. Genin, and E. LeGuern. Coincidence of two genetic forms of Charcot-Marie-Tooth disease in a single family. Neurology, 63(8):1527-9, 2004. Note: Case ReportsJournal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Charcot-Marie-Tooth Disease/*genetics, *Chromosome Aberrations, Chromosomes, Human, Pair 17/*genetics, DNA Mutational Analysis, Disease Progression, Family Health, Female, Genes, Recessive/genetics, Genetic Predisposition to Disease/*genetics, Genetic Screening, Humans, Inheritance Patterns/*genetics, Male, Muscle Weakness/genetics/pathology/physiopathology, Mutation/*genetics, Nerve Fibers, Myelinated/pathology, Pedigree, Peripheral Nerves/pathology/physiopathology, Protein-Tyrosine-Phosphatase/genetics.

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