Movement Disorders (revue) - Merge (PascalFrancis)

Index « FA11s1.i » - entrée « OZELIUS (Laurie J.) »
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List of bibliographic references

Number of relevant bibliographic references: 14.
Ident.Authors (with country if any)Title
000C13 (2004) Christoph Kamm ; Joanne Leung ; Soni Joseph ; William B. Dobyns ; Alison Brashear ; Xandra O. Breakefield ; Laurie J. OzeliusRefined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene
000C71 (2004) Katja Hedrich ; Cordula Eskelson ; Beth Wilmot ; Karen Marder ; Juliette Harris ; Jennifer Garrels ; Helen Meija-Santana ; Peter Vieregge ; Helfried Jacobs ; Susan B. Bressman ; Anthony E. Lang ; Martin Kann ; Giovanni Abbruzzese ; Paolo Martinelli ; Eberhard Schwinger ; Laurie J. Ozelius ; Peter P. Pramstaller ; Christine Klein ; Patricia KramerDistribution, type, and origin of Parkin mutations: Review and case studies
000C84 (2004) Patricia De Carvalho Aguiar ; Melissa Fazzari ; Joseph Jankovic ; Laurie J. OzeliusExamination of the SGCE gene in Tourette's syndrome patients with obsessive-compulsive disorder
000D38 (2004) Sean O'Riordan ; Laurie J. Ozelius ; Patricia De Carvalho Aguiar ; Michael Hutchinson ; Mary King ; Tim LynchInherited myoclonus-dystonia and epilepsy: Further evidence of an association?
000D39 (2004) Jacek Zaremba ; Hanna Mierzewska ; Zofia Lysiak ; Patricia Kramer ; Laurie J. Ozelius ; Allison BrashearRapid-onset Dystonia-Parkinsonism: A fourth family consistent with linkage to chromosome 19q13
001575 (2007) Laurie J. Ozelius ; Tatiana Foroud ; Susanne May ; Geetha Senthil ; Paola Sandroni ; Phillip A. Low ; Stephen Reich ; Amy Colcher ; Matthew B. Stern ; William G. Ondo ; Joseph Jankovic ; NENG HUANG ; Caroline M. Tanner ; Peter Novak ; Sid Gilman ; Frederick J. Marshall ; G. Frederick Wooten ; Thomas C. Chelimsky ; Clifford W. ShultsG2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy
001710 (2007) Andrew Mckeon ; Laurie J. Ozelius ; Oria Hardiman ; Matthew J. Greenway ; Sean J. PittockHeterogeneity of presentation and outcome in the irish rapid-onset dystonia-parkinsonism kindred
001792 (2007) Jee-Young Lee ; Seema Gollamudi ; Laurie J. Ozelius ; Ji-Young Kim ; Beom S. JeonATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism
002451 (2010) Nutan Sharma ; Ramon A. Jr Franco ; John K. Kuster ; Adele A. Mitchell ; Tania Fuchs ; Rachel Saunders-Pullman ; Deborah Raymond ; Mitchell F. Brin ; Andrew Blitzer ; Susan B. Bressman ; Laurie J. OzeliusGenetic Evidence for an Association of the TOR1A Locus with Segmental/Focal Dystonia
002506 (2010) Rachel Saunders-Pullman ; Matthew J. Barrett ; Kaili M. Stanley ; Marta San Luciano ; Vicki Shanker ; Lawrence Severt ; Ann Hunt ; Deborah Raymond ; Laurie J. Ozelius ; Susan B. BressmanLRRK2 G2019S Mutations are Associated with an Increased Cancer Risk in Parkinson Disease
002512 (2010) Marta San Luciano ; Richard B. Lipton ; CUILING WANG ; Mindy Katz ; Molly E. Zimmerman ; Amy E. Sanders ; Laurie J. Ozelius ; Susan B. Bressman ; Rachel Saunders-PullmanClinical Expression of LRRK2 G2019S Mutations in the Elderly
002753 (2011) Laurie J. Ozelius ; Naomi Lubarr ; Susan B. BressmanMilestones in Dystonia
002852 (2011) Rachel Saunders-Pullman ; Jose Cabassa ; Marta San Luciano ; Kaili Stanley ; Deborah Raymond ; Laurie J. Ozelius ; Susan B. BressmanLRRK2 G2019S Mutations May Be Increased in Puerto Ricans
002913 (2011) Nutan Sharma ; Ioanna A. Armata ; Trisha J. Multhaupt-Buell ; Laurie J. Ozelius ; WINNIE XIN ; Katherine B. SimsMutation in 5' Upstream Region of GCHI Gene Causes Familial Dopa-Responsive Dystonia

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