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Joseph Jankovic

Showing results (531-540 of 574) with videos related to

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Frontiers in Neurology|October 4, 2021
Oromandibular Dystonia: A Clinical Examination of 2,020 CasesLaura M Scorr, Stewart A Factor, Sahyli Perez Parra, et al.
Annals of Neurology|June 11, 2015
Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trialC Warren Olanow, Raymond T Bartus, Tiffany L Baumann, et al.
Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2008
Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing resultsChristopher G Goetz, Barbara C Tilley, Stephanie R Shaftman, et al.
The Lancet. Neurology|October 26, 2010
Gene delivery of AAV2-neurturin for Parkinson's disease: a double-blind, randomised, controlled trialWilliam J Marks, Raymond T Bartus, Joao Siffert, et al.
Molecular Genetics & Genomic Medicine|May 16, 2019
Autosomal dominant mitochondrial membrane protein-associated neurodegeneration (MPAN)Allison Gregory, Mitesh Lotia, Suh Young Jeong, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
The Lancet. Neurology|January 14, 2012
Subthalamic deep brain stimulation with a constant-current device in Parkinson's disease: an open-label randomised controlled trialMichael S Okun, Bruno V Gallo, George Mandybur, et al.
Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Brain : a Journal of Neurology|February 2, 2026
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's diseaseRuth B De-Paula, Jonggeol Kim, Herve Rhinn, et al.
Pageof 58

Showing results (531-540 of 574) with videos related to

Sort By:
Pageof 58
Frontiers in Neurology|October 4, 2021
Oromandibular Dystonia: A Clinical Examination of 2,020 CasesLaura M Scorr, Stewart A Factor, Sahyli Perez Parra, et al.
Annals of Neurology|June 11, 2015
Gene delivery of neurturin to putamen and substantia nigra in Parkinson disease: A double-blind, randomized, controlled trialC Warren Olanow, Raymond T Bartus, Tiffany L Baumann, et al.
Neurology. Genetics|August 18, 2020
Integrated sequencing and array comparative genomic hybridization in familial Parkinson diseaseLaurie A Robak, Renqian Du, Bo Yuan, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 26, 2008
Movement Disorder Society-sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS): scale presentation and clinimetric testing resultsChristopher G Goetz, Barbara C Tilley, Stephanie R Shaftman, et al.
The Lancet. Neurology|October 26, 2010
Gene delivery of AAV2-neurturin for Parkinson's disease: a double-blind, randomised, controlled trialWilliam J Marks, Raymond T Bartus, Joao Siffert, et al.
Molecular Genetics & Genomic Medicine|May 16, 2019
Autosomal dominant mitochondrial membrane protein-associated neurodegeneration (MPAN)Allison Gregory, Mitesh Lotia, Suh Young Jeong, et al.
JAMA Neurology|November 24, 2015
Whole-Exome Sequencing in Familial Parkinson DiseaseJanice L Farlow, Laurie A Robak, Kurt Hetrick, et al.
The Lancet. Neurology|January 14, 2012
Subthalamic deep brain stimulation with a constant-current device in Parkinson's disease: an open-label randomised controlled trialMichael S Okun, Bruno V Gallo, George Mandybur, et al.
Movement Disorders Clinical Practice|February 11, 2022
Current Guidelines for Classifying and Diagnosing Cervical Dystonia: Empirical Evidence and RecommendationsGamze Kilic-Berkmen, Sarah Pirio Richardson, Joel S Perlmutter, et al.
Brain : a Journal of Neurology|February 2, 2026
Mapping the causal chain from genetic risk variants to lipid dysmetabolism in Parkinson's diseaseRuth B De-Paula, Jonggeol Kim, Herve Rhinn, et al.
Pageof 58