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Peter Hedera

Showing results (61-70 of 134) with videos related to

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Pediatric Neurology|June 15, 2007
Infantile onset of hereditary spastic paraplegia poorly predicts the genotypeMarcia A Blair, Megan E Riddle, Jennifer F Wells, et al.
Neurotoxicology|September 8, 2009
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zincPeter Hedera, Amanda Peltier, John K Fink, et al.
BMC Neurology|September 19, 2012
Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesiaPeter Hedera, Jianfeng Xiao, Andreas Puschmann, et al.
Parkinsonism & Related Disorders|May 11, 2013
FUS in familial essential tremor - the search for common causes is still onPeter Hedera, Thomas L Davis, Fenna T Phibbs, et al.
Advances in Therapy|February 20, 2026
Patient Burden in the Treatment of Wilson Disease in the United States: An Analysis of Real-World Health Insurance Claims Data from the Komodo databasePeter Hedera, Megan Teynor, Carey Strader, et al.
Epilepsy Research|July 15, 2006
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsyShaochun Ma, Marcia A Blair, Bassel Abou-Khalil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 19, 2008
Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanismJiali Zhao, Dawn S Matthies, Emmanuel J Botzolakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 2, 2009
Positive family history of essential tremor influences the motor phenotype of Parkinson's diseasePeter Hedera, John Y Fang, Fenna Phibbs, et al.
SAGE Open Medical Case Reports|November 21, 2022
Treatment of segmental continuous hypertrophic myokymia of the limb with botulinum A toxinMuhammad Ismail Khalid Yousaf, Mohammad Ravi Ghani, Talita D'Aguiar Rosa, et al.
Neuroscience Letters|November 1, 2005
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizuresShaochun Ma, Bassel Abou-Khalil, Marcia A Blair, et al.
Pageof 14

Showing results (61-70 of 134) with videos related to

Sort By:
Pageof 14
Pediatric Neurology|June 15, 2007
Infantile onset of hereditary spastic paraplegia poorly predicts the genotypeMarcia A Blair, Megan E Riddle, Jennifer F Wells, et al.
Neurotoxicology|September 8, 2009
Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. The denture cream is a primary source of excessive zincPeter Hedera, Amanda Peltier, John K Fink, et al.
BMC Neurology|September 19, 2012
Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesiaPeter Hedera, Jianfeng Xiao, Andreas Puschmann, et al.
Parkinsonism & Related Disorders|May 11, 2013
FUS in familial essential tremor - the search for common causes is still onPeter Hedera, Thomas L Davis, Fenna T Phibbs, et al.
Advances in Therapy|February 20, 2026
Patient Burden in the Treatment of Wilson Disease in the United States: An Analysis of Real-World Health Insurance Claims Data from the Komodo databasePeter Hedera, Megan Teynor, Carey Strader, et al.
Epilepsy Research|July 15, 2006
Mutations in the GABRA1 and EFHC1 genes are rare in familial juvenile myoclonic epilepsyShaochun Ma, Marcia A Blair, Bassel Abou-Khalil, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|December 19, 2008
Hereditary spastic paraplegia-associated mutations in the NIPA1 gene and its Caenorhabditis elegans homolog trigger neural degeneration in vitro and in vivo through a gain-of-function mechanismJiali Zhao, Dawn S Matthies, Emmanuel J Botzolakis, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 2, 2009
Positive family history of essential tremor influences the motor phenotype of Parkinson's diseasePeter Hedera, John Y Fang, Fenna Phibbs, et al.
SAGE Open Medical Case Reports|November 21, 2022
Treatment of segmental continuous hypertrophic myokymia of the limb with botulinum A toxinMuhammad Ismail Khalid Yousaf, Mohammad Ravi Ghani, Talita D'Aguiar Rosa, et al.
Neuroscience Letters|November 1, 2005
Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizuresShaochun Ma, Bassel Abou-Khalil, Marcia A Blair, et al.
Pageof 14