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Steven Frucht

Showing results (41-50 of 61) with videos related to

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Archives of Neurology|April 12, 2006
Case-control study of the parkin gene in early-onset Parkinson diseaseLorraine N Clark, Shehla Afridi, Eric Karlins, et al.
Parkinsonism & Related Disorders|July 25, 2018
Mirabegron in patients with Parkinson disease and overactive bladder symptoms: A retrospective cohortBenoit Peyronnet, Gregory Vurture, Jose-Alberto Palma, et al.
Frontiers in Neurology|May 19, 2017
Research Priorities in Limb and Task-Specific DystoniasSarah Pirio Richardson, Eckart Altenmüller, Katharine Alter, et al.
Parkinsonism & Related Disorders|December 12, 2024
IAPRD new consensus classification of myoclonusAnna Latorre, S van der Veen, Ashley Pena, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2004
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicityLorraine N Clark, Angelique Nicolai, Shehla Afridi, et al.
BMC Medical Genetics|August 5, 2011
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish populationXinmin Liu, Rong Cheng, Miguel Verbitsky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutationsLorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 8, 2015
Erratum to: Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 16, 2015
Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneLorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
Pageof 7

Showing results (41-50 of 61) with videos related to

Sort By:
Pageof 7
Archives of Neurology|April 12, 2006
Case-control study of the parkin gene in early-onset Parkinson diseaseLorraine N Clark, Shehla Afridi, Eric Karlins, et al.
Parkinsonism & Related Disorders|July 25, 2018
Mirabegron in patients with Parkinson disease and overactive bladder symptoms: A retrospective cohortBenoit Peyronnet, Gregory Vurture, Jose-Alberto Palma, et al.
Frontiers in Neurology|May 19, 2017
Research Priorities in Limb and Task-Specific DystoniasSarah Pirio Richardson, Eckart Altenmüller, Katharine Alter, et al.
Parkinsonism & Related Disorders|December 12, 2024
IAPRD new consensus classification of myoclonusAnna Latorre, S van der Veen, Ashley Pena, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 2, 2004
Pilot association study of the beta-glucocerebrosidase N370S allele and Parkinson's disease in subjects of Jewish ethnicityLorraine N Clark, Angelique Nicolai, Shehla Afridi, et al.
BMC Medical Genetics|August 5, 2011
Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish populationXinmin Liu, Rong Cheng, Miguel Verbitsky, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 16, 2004
Analysis of an early-onset Parkinson's disease cohort for DJ-1 mutationsLorraine N Clark, Shehla Afridi, Helen Mejia-Santana, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|November 8, 2015
Erratum to: Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|September 16, 2015
Strategies for treatment of dystoniaDirk Dressler, Eckart Altenmueller, Roongroj Bhidayasiri, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 7, 2007
Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin geneLorraine N Clark, Eneli Haamer, Helen Mejia-Santana, et al.
Pageof 7