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Peter Hedera

Showing results (11-20 of 134) with videos related to

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Annals of the New York Academy of Sciences|February 20, 2014
Treatment of Wilson's disease motor complications with deep brain stimulationPeter Hedera
Clinical Neuropharmacology|February 4, 2010
Rotigotine adverse effects affecting patient's sexual partnerPeter Hedera
Journal of the Neurological Sciences|October 1, 2013
Recurrent de novo c.316G>A mutation in NIPA1 hotspotPeter Hedera
Continuum (Minneapolis, Minn.)|April 4, 2018
Hereditary MyelopathiesPeter Hedera
Journal of Experimental Neuroscience|May 20, 2015
Strumpellin and Spartin, Hereditary Spastic Paraplegia Proteins, are Binding PartnersJiali Zhao, Peter Hedera
Molecular and Cellular Neurosciences|October 20, 2012
Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII traffickingJiali Zhao, Peter Hedera
Neurology|December 4, 2016
Hyperkinetic psychogenic movement disorders remain a diagnosis at first sightPeter Hedera, Antonio Gambardella
Neurology|April 17, 2008
Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emergingPeter Hedera, Oliver Bandmann
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2016
Speech-activated Myoclonus Mimicking Stuttering in a Patient with Myoclonus-Dystonia SyndromeDavid A Isaacs, Peter Hedera
American Journal of Medical Genetics. Part A|September 25, 2004
Two patients with monomelic ulnar duplication with mirror hand polydactyly: segmental Laurin-Sandrow syndromeJeffrey W Innis, Peter Hedera
Pageof 14

Showing results (11-20 of 134) with videos related to

Sort By:
Pageof 14
Annals of the New York Academy of Sciences|February 20, 2014
Treatment of Wilson's disease motor complications with deep brain stimulationPeter Hedera
Clinical Neuropharmacology|February 4, 2010
Rotigotine adverse effects affecting patient's sexual partnerPeter Hedera
Journal of the Neurological Sciences|October 1, 2013
Recurrent de novo c.316G>A mutation in NIPA1 hotspotPeter Hedera
Continuum (Minneapolis, Minn.)|April 4, 2018
Hereditary MyelopathiesPeter Hedera
Journal of Experimental Neuroscience|May 20, 2015
Strumpellin and Spartin, Hereditary Spastic Paraplegia Proteins, are Binding PartnersJiali Zhao, Peter Hedera
Molecular and Cellular Neurosciences|October 20, 2012
Hereditary spastic paraplegia-causing mutations in atlastin-1 interfere with BMPRII traffickingJiali Zhao, Peter Hedera
Neurology|December 4, 2016
Hyperkinetic psychogenic movement disorders remain a diagnosis at first sightPeter Hedera, Antonio Gambardella
Neurology|April 17, 2008
Complicated autosomal recessive hereditary spastic paraplegia: a complex picture is emergingPeter Hedera, Oliver Bandmann
Tremor and Other Hyperkinetic Movements (New York, N.Y.)|July 22, 2016
Speech-activated Myoclonus Mimicking Stuttering in a Patient with Myoclonus-Dystonia SyndromeDavid A Isaacs, Peter Hedera
American Journal of Medical Genetics. Part A|September 25, 2004
Two patients with monomelic ulnar duplication with mirror hand polydactyly: segmental Laurin-Sandrow syndromeJeffrey W Innis, Peter Hedera
Pageof 14