受强制性开放获取政策约束的文章 - Laurie Ozelius了解详情
无法在其他位置公开访问的文章：8 篇
Milestones in dystonia
LJ Ozelius, N Lubarr, SB Bressman
Movement disorders 26 (6), 1106-1126, 2011
强制性开放获取政策： US National Institutes of Health
Fall risk and gait in Parkinson's disease: the role of the LRRK2 G2019S mutation
A Mirelman, T Heman, K Yasinovsky, A Thaler, T Gurevich, K Marder, ...
Movement Disorders 28 (12), 1683-1690, 2013
强制性开放获取政策： US National Institutes of Health
Responsiveness to levodopa in epsilon‐sarcoglycan deletions
MS Luciano, L Ozelius, K Sims, D Raymond, L Liu, R Saunders‐Pullman
Movement disorders 24 (3), 425-428, 2009
强制性开放获取政策： US National Institutes of Health
Rapid-onset dystonia-parkinsonism: case report
M Svetel, LJ Ozelius, A Buckley, K Lohmann, L Brajković, C Klein, ...
Journal of neurology 257, 472-474, 2010
强制性开放获取政策： US National Institutes of Health
Clinical spectrum of disease associated with ATP1A3 mutations
LJ Ozelius
The Lancet Neurology 11 (9), 741-743, 2012
强制性开放获取政策： US National Institutes of Health
Genetics of dystonia
T Fuchs, LJ Ozelius
Seminars in neurology 31 (05), 441-448, 2011
强制性开放获取政策： US National Institutes of Health
Expression profiling in peripheral blood reveals signature for penetrance in DYT1 dystonia
M Walter, M Bonin, RS Pullman, EM Valente, M Loi, M Gambarin, ...
Neurobiology of Disease 38 (2), 192-200, 2010
强制性开放获取政策： US National Institutes of Health
Rapid-onset dystonia-parkinsonism: More than just dystonia
A Brashear, LJ Ozelius, KJ Sweadner
Handbook of Dystonia, 261-270, 2012
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：134 篇
Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia
T Fuchs, S Gavarini, R Saunders-Pullman, D Raymond, ME Ehrlich, ...
Nature genetics 41 (3), 286-288, 2009
强制性开放获取政策： US National Institutes of Health
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
KY Hui, H Fernandez-Hernandez, J Hu, A Schaffner, N Pankratz, NY Hsu, ...
Science translational medicine 10 (423), eaai7795, 2018
强制性开放获取政策： US National Science Foundation, US National Institutes of Health, UK Medical …
Mutations in GNAL cause primary torsion dystonia
T Fuchs, R Saunders-Pullman, I Masuho, MS Luciano, D Raymond, ...
Nature genetics 45 (1), 88-92, 2013
强制性开放获取政策： US National Institutes of Health
Distinct neurological disorders with ATP1A3 mutations
EL Heinzen, A Arzimanoglou, A Brashear, SJ Clapcote, F Gurrieri, ...
The Lancet Neurology 13 (5), 503-514, 2014
强制性开放获取政策： US National Institutes of Health, Canadian Institutes of Health Research
Dissecting the causal mechanism of X-linked dystonia-parkinsonism by integrating genome and transcriptome assembly
T Aneichyk, WT Hendriks, R Yadav, D Shin, D Gao, CA Vaine, RL Collins, ...
Cell 172 (5), 897-909. e21, 2018
强制性开放获取政策： US National Institutes of Health, Howard Hughes Medical Institute
Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study
SB Bressman, D Raymond, T Fuchs, GA Heiman, LJ Ozelius, ...
The Lancet Neurology 8 (5), 441-446, 2009
强制性开放获取政策： US National Institutes of Health
Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
S Carmi, KY Hui, E Kochav, X Liu, J Xue, F Grady, S Guha, K Upadhyay, ...
Nature communications 5 (1), 4835, 2014
强制性开放获取政策： US National Institutes of Health, Parkinson's Foundation, USA
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci
EE Kenny, I Pe'er, A Karban, L Ozelius, AA Mitchell, SM Ng, M Erazo, ...
PLoS genetics 8 (3), e1002559, 2012
强制性开放获取政策： US National Institutes of Health
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study
A Djarmati, SA Schneider, K Lohmann, S Winkler, H Pawlack, J Hagenah, ...
The Lancet Neurology 8 (5), 447-452, 2009
强制性开放获取政策： German Research Foundation
The p.L302P mutation in the lysosomal enzyme gene SMPD1 is a risk factor for Parkinson disease
Z Gan-Or, LJ Ozelius, A Bar-Shira, R Saunders-Pullman, A Mirelman, ...
Neurology 80 (17), 1606-1610, 2013
强制性开放获取政策： US National Institutes of Health
Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium
K Marder, Y Wang, RN Alcalay, H Mejia-Santana, MX Tang, A Lee, ...
Neurology 85 (1), 89-95, 2015
强制性开放获取政策： US National Institutes of Health
Monogenic variants in dystonia: an exome-wide sequencing study
M Zech, R Jech, S Boesch, M Škorvánek, S Weber, M Wagner, C Zhao, ...
The Lancet Neurology 19 (11), 908-918, 2020
强制性开放获取政策： US National Institutes of Health, German Research Foundation, Helmholtz …
出版信息和资助信息由计算机程序自动确定