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P Bhatia

Showing results (751-760 of 797) with videos related to

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Nature Genetics|January 13, 2009
DCTN1 mutations in Perry syndromeMatthew J Farrer, Mary M Hulihan, Jennifer M Kachergus, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related ParkinsonismFrancesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
Minerva Urology and Nephrology|June 9, 2023
Influence of pre-stenting on RIRS outcomes. Inferences from patients of the Global Multicentre Flexible Ureteroscopy Outcome Registry (FLEXOR)Chu-Ann Chai, Yuen-Chun Teoh, Thomas Tailly, et al.
Neurology|October 19, 2012
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineAlice R Gardiner, Kailash P Bhatia, Maria Stamelou, et al.
Neurology|June 27, 2001
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotypeH Houlden, M Baker, H R Morris, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2024
Evaluation of Cerebrospinal Fluid α-Synuclein Seed Amplification Assay in Progressive Supranuclear Palsy and Corticobasal SyndromeDavid P Vaughan, Riona Fumi, Marte Theilmann Jensen, et al.
European Journal of Neurology|January 31, 2016
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromesA Valadas, M-F Contarino, A Albanese, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
NPJ Parkinson'S Disease|October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's diseaseClodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
Archives of Neurology|February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Pageof 80

Showing results (751-760 of 797) with videos related to

Sort By:
Pageof 80
Nature Genetics|January 13, 2009
DCTN1 mutations in Perry syndromeMatthew J Farrer, Mary M Hulihan, Jennifer M Kachergus, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2021
Dissecting the Phenotype and Genotype of PLA2G6-Related ParkinsonismFrancesca Magrinelli, Sahil Mehta, Giulia Di Lazzaro, et al.
Minerva Urology and Nephrology|June 9, 2023
Influence of pre-stenting on RIRS outcomes. Inferences from patients of the Global Multicentre Flexible Ureteroscopy Outcome Registry (FLEXOR)Chu-Ann Chai, Yuen-Chun Teoh, Thomas Tailly, et al.
Neurology|October 19, 2012
PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraineAlice R Gardiner, Kailash P Bhatia, Maria Stamelou, et al.
Neurology|June 27, 2001
Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotypeH Houlden, M Baker, H R Morris, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2024
Evaluation of Cerebrospinal Fluid α-Synuclein Seed Amplification Assay in Progressive Supranuclear Palsy and Corticobasal SyndromeDavid P Vaughan, Riona Fumi, Marte Theilmann Jensen, et al.
European Journal of Neurology|January 31, 2016
Management of dystonia in Europe: a survey of the European network for the study of the dystonia syndromesA Valadas, M-F Contarino, A Albanese, et al.
The Lancet. Neurology|June 10, 2008
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyDaniel G Healy, Mario Falchi, Sean S O'Sullivan, et al.
NPJ Parkinson'S Disease|October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's diseaseClodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
Archives of Neurology|February 16, 2011
Excessive daytime sleepiness in multiple system atrophy (SLEEMSA study)Claudia Moreno-López, Joan Santamaría, Manuel Salamero, et al.
Pageof 80