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Neurology. Genetics

Showing results (271-280 of 1,012) with videos related to

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Neurology. Genetics|May 12, 2021
Expanding the Spectrum of Movement Disorders Associated With <i>C9orf72</i> Hexanucleotide ExpansionsCarlos Estevez-Fraga, Francesca Magrinelli, Davina Hensman Moss, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
Neurology. Genetics|August 4, 2021
Mutation in <i>ZDHHC15</i> Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual DisabilitySara A Lewis, Somayeh Bakhtiari, Jennifer Heim, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.
Neurology. Genetics|March 31, 2017
<i>GNAO1</i> encephalopathy: Broadening the phenotype and evaluating treatment and outcomeFederica Rachele Danti, Serena Galosi, Marta Romani, et al.
Neurology. Genetics|April 7, 2017
Familial childhood-onset progressive cerebellar syndrome associated with the <i>ATP1A3</i> mutationFatima Jaffer, Katherine Fawcett, David Sims, et al.
Neurology. Genetics|April 12, 2017
Camptocormia and shuffling gait due to a novel <i>MT-TV</i> mutation: Diagnostic pitfallsJens Reimann, Diana Lehmann, Steven A Hardy, et al.
Neurology. Genetics|October 30, 2016
Helix: October 2016 issueStefan M Pulst
Neurology. Genetics|February 10, 2017
Precision therapy for a new disorder of AMPA receptor recycling due to mutations in <i>ATAD1</i>Rebecca C Ahrens-Nicklas, George K E Umanah, Neal Sondheimer, et al.
Pageof 102

Showing results (271-280 of 1,012) with videos related to

Sort By:
Pageof 102
Neurology. Genetics|May 12, 2021
Expanding the Spectrum of Movement Disorders Associated With <i>C9orf72</i> Hexanucleotide ExpansionsCarlos Estevez-Fraga, Francesca Magrinelli, Davina Hensman Moss, et al.
Neurology. Genetics|May 14, 2021
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor SubtypesIsabel Alfradique-Dunham, Rami Al-Ouran, Rainer von Coelln, et al.
Neurology. Genetics|August 4, 2021
Mutation in <i>ZDHHC15</i> Leads to Hypotonic Cerebral Palsy, Autism, Epilepsy, and Intellectual DisabilitySara A Lewis, Somayeh Bakhtiari, Jennifer Heim, et al.
Neurology. Genetics|November 23, 2016
De novo <i>FGF12</i> mutation in 2 patients with neonatal-onset epilepsyIlaria Guella, Linda Huh, Marna B McKenzie, et al.
Neurology. Genetics|December 14, 2016
Clinical and genetic study of hereditary spastic paraplegia in CanadaNicolas Chrestian, Nicolas Dupré, Ziv Gan-Or, et al.
Neurology. Genetics|March 31, 2017
<i>GNAO1</i> encephalopathy: Broadening the phenotype and evaluating treatment and outcomeFederica Rachele Danti, Serena Galosi, Marta Romani, et al.
Neurology. Genetics|April 7, 2017
Familial childhood-onset progressive cerebellar syndrome associated with the <i>ATP1A3</i> mutationFatima Jaffer, Katherine Fawcett, David Sims, et al.
Neurology. Genetics|April 12, 2017
Camptocormia and shuffling gait due to a novel <i>MT-TV</i> mutation: Diagnostic pitfallsJens Reimann, Diana Lehmann, Steven A Hardy, et al.
Neurology. Genetics|October 30, 2016
Helix: October 2016 issueStefan M Pulst
Neurology. Genetics|February 10, 2017
Precision therapy for a new disorder of AMPA receptor recycling due to mutations in <i>ATAD1</i>Rebecca C Ahrens-Nicklas, George K E Umanah, Neal Sondheimer, et al.
Pageof 102