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Deep Brain Stimulation in Isolated Dystonia With a GNAL Mutation.
- Published in:
- 2019
- By:
- Publication type:
- letter
In memoriam: Robert E. Burke, MD, 1949-2018.
- Published in:
- 2019
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- Publication type:
- journal article
Increased substantia nigra echogenicity in LRRK2 family members without mutations.
- Published in:
- 2018
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- Publication type:
- letter
Application of the Movement Disorder Society prodromal criteria in healthy G2019S-LRRK2 carriers.
- Published in:
- 2018
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- Publication type:
- journal article
Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.
- Published in:
- 2017
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- Publication type:
- journal article
Arm swing as a potential new prodromal marker of Parkinson's disease.
- Published in:
- 2016
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- Publication type:
- journal article
Clinical and scientific perspectives on movement disorders: Stanley Fahn's contributions.
- Published in:
- 2015
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- Publication type:
- journal article
REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.
- Published in:
- 2015
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- Publication type:
- journal article
Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.
- Published in:
- Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213
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- Publication type:
- Article
Disclosure of research results in genetic studies of Parkinson's disease caused by LRRK2 mutations.
- Published in:
- Movement Disorders, 2015, v. 30, n. 7, p. 904, doi. 10.1002/mds.26250
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- Publication type:
- Article
Low-variance RNAs identify Parkinson's disease molecular signature in blood.
- Published in:
- Movement Disorders, 2015, v. 30, n. 6, p. 813, doi. 10.1002/mds.26205
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- Publication type:
- Article
The relationship between obsessive-compulsive symptoms and PARKIN genotype: The CORE-PD study.
- Published in:
- Movement Disorders, 2015, v. 30, n. 2, p. 278, doi. 10.1002/mds.26065
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- Publication type:
- Article
Peptidoglycan recognition protein genes and risk of Parkinson's disease.
- Published in:
- Movement Disorders, 2014, v. 29, n. 9, p. 1171, doi. 10.1002/mds.25895
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- Publication type:
- Article
A voxel-based morphometry and diffusion tensor imaging analysis of asymptomatic Parkinson's disease-related G2019S LRRK2 mutation carriers.
- Published in:
- Movement Disorders, 2014, v. 29, n. 6, p. 823, doi. 10.1002/mds.25827
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- Publication type:
- Article
Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.
- Published in:
- Movement Disorders, 2014, v. 29, n. 6, p. 812, doi. 10.1002/mds.25818
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- Publication type:
- Article
Reply: Dystonia after severe head injuries.
- Published in:
- Movement Disorders, 2014, v. 29, n. 4, p. 578, doi. 10.1002/mds.25861
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- Publication type:
- Article
Fall risk and gait in Parkinson's disease: The role of the LRRK2 G2019S mutation.
- Published in:
- Movement Disorders, 2013, v. 28, n. 12, p. 1683, doi. 10.1002/mds.25587
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- Publication type:
- Article
Phenomenology and classification of dystonia: A consensus update.
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- Movement Disorders, 2013, v. 28, n. 7, p. 863, doi. 10.1002/mds.25475
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- Publication type:
- Article
Primary dystonia: Moribund or viable.
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- Movement Disorders, 2013, v. 28, n. 7, p. 906, doi. 10.1002/mds.25528
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- Publication type:
- Article
Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.
- Published in:
- Movement Disorders, 2011, v. 26, n. 10, p. 1875, doi. 10.1002/mds.23746
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- Publication type:
- Article
LRRK2 G2019S mutations may be increased in Puerto Ricans.
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- Movement Disorders, 2011, v. 26, n. 9, p. 1771, doi. 10.1002/mds.23632
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- Publication type:
- Article
Inclusion and exclusion criteria for DBS in dystonia.
- Published in:
- 2011
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- Publication type:
- journal article
Inclusion and exclusion criteria for DBS in dystonia.
- Published in:
- Movement Disorders, 2011, v. 26, p. S5, doi. 10.1002/mds.23482
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- Publication type:
- Article
Pre-operative evaluations for DBS in dystonia.
- Published in:
- Movement Disorders, 2011, v. 26, p. S17, doi. 10.1002/mds.23481
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- Publication type:
- Article
Milestones in dystonia.
- Published in:
- Movement Disorders, 2011, v. 26, n. 6, p. 1106, doi. 10.1002/mds.23775
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- Publication type:
- Article
Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.
- Published in:
- Movement Disorders, 2011, v. 26, n. 5, p. 885, doi. 10.1002/mds.23644
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- Publication type:
- Article
Phenotypic spectrum of musician's dystonia: A task-specific disorder?
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- Movement Disorders, 2011, v. 26, n. 3, p. 546, doi. 10.1002/mds.23526
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- Publication type:
- Article
LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease.
- Published in:
- Movement Disorders, 2010, v. 25, n. 15, p. 2536, doi. 10.1002/mds.23314
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- Publication type:
- Article
Clinical expression of LRRK2 G2019S mutations in the elderly.
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- Movement Disorders, 2010, v. 25, n. 15, p. 2571, doi. 10.1002/mds.23330
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- Publication type:
- Article
Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.
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- Movement Disorders, 2010, v. 25, n. 13, p. 2183, doi. 10.1002/mds.23225
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- Publication type:
- Article
Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization.
- Published in:
- Movement Disorders, 2010, v. 25, n. 10, p. 1364, doi. 10.1002/mds.23046
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- Publication type:
- Article
Evidence for pre and postsynaptic nigrostriatal dysfunction in the fragile X tremor-Ataxia syndrome.
- Published in:
- Movement Disorders, 2009, v. 24, n. 8, p. 1245, doi. 10.1002/mds.22267
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- Publication type:
- Article
Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.
- Published in:
- Movement Disorders, 2008, v. 23, n. 4, p. 588, doi. 10.1002/mds.21785
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- Publication type:
- Article
Validity of spiral analysis in early Parkinson's disease.
- Published in:
- Movement Disorders, 2008, v. 23, n. 4, p. 531, doi. 10.1002/mds.21874
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- Publication type:
- Article
Microstructural white matter changes in primary torsion dystonia.
- Published in:
- Movement Disorders, 2008, v. 23, n. 2, p. 234, doi. 10.1002/mds.21806
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- Publication type:
- Article
Distribution, type, and origin of Parkin mutations: Review and case studies.
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- Movement Disorders, 2004, v. 19, n. 10, p. 1146, doi. 10.1002/mds.20234
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- Publication type:
- Article
State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.
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- Movement Disorders, 2003, v. 18, n. 1, p. 3, doi. 10.1002/mds.10338
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- Publication type:
- Article
Parkinsonism, dystonia, and hemiatrophy.
- Published in:
- 2000
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- Publication type:
- journal article
Multiple sclerosis in LRRK2 G2019S Parkinson's disease and isolated nigral degeneration in a homozygous variant carrier.
- Published in:
- Frontiers in Neurology, 2024, p. 01, doi. 10.3389/fneur.2024.1450654
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- Publication type:
- Article
Interest in Genetic Testing in Ashkenazi Jewish Parkinson's Disease Patients and Their Unaffected Relatives.
- Published in:
- Journal of Genetic Counseling, 2015, v. 24, n. 2, p. 238, doi. 10.1007/s10897-014-9756-x
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- Publication type:
- Article
Cerebellothalamocortical Connectivity Regulates Penetrance in Dystonia.
- Published in:
- Journal of Neuroscience, 2009, v. 29, n. 31, p. 9740, doi. 10.1523/JNEUROSCI.2300-09.2009
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- Publication type:
- Article
What’s new in dystonia?
- Published in:
- Current Neurology & Neuroscience Reports, 2009, v. 9, n. 4, p. 278, doi. 10.1007/s11910-009-0042-5
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- Publication type:
- Article
Parkinson's disease variant detection and disclosure: PD GENEration, a North American study.
- Published in:
- Brain: A Journal of Neurology, 2024, v. 147, n. 8, p. 2668, doi. 10.1093/brain/awae142
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- Publication type:
- Article
Estimation of genetic risk function with covariates in the presence of missing genotypes.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Reply to: Cognitive Effects of Deep Brain Stimulation in GBA‐Related Parkinson's Disease.
- Published in:
- Annals of Neurology, 2022, v. 92, n. 2, p. 345, doi. 10.1002/ana.26433
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- Publication type:
- Article
Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation Carriers.
- Published in:
- Annals of Neurology, 2022, v. 91, n. 3, p. 424, doi. 10.1002/ana.26302
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- Publication type:
- Article
Genomewide Association Studies of LRRK2 Modifiers of Parkinson's Disease.
- Published in:
- 2021
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- Publication type:
- journal article
Efficient estimation of nonparametric genetic risk function with censored data.
- Published in:
- Biometrika, 2015, v. 102, n. 3, p. 515, doi. 10.1093/biomet/asv030
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- Publication type:
- Article
Benign SLC39A14 Course of Dystonia‐Parkinsonism Secondary to Inherited Manganese Accumulation.
- Published in:
- Movement Disorders Clinical Practice, 2020, v. 7, n. 5, p. 569, doi. 10.1002/mdc3.12947
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- Publication type:
- Article
Sex differences in LRRK2 G2019S and idiopathic Parkinson's Disease.
- Published in:
- Annals of Clinical & Translational Neurology, 2017, v. 4, n. 11, p. 801, doi. 10.1002/acn3.489
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- Publication type:
- Article