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Brain Communications
|
November 21, 2025
Novel, complex configurations of the <i>MARCHF6</i> repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy
Mark F Bennett, Mark A Corbett, Thessa Kroes, et al.
Human Molecular Genetics
|
May 9, 2015
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia
John A Damiano, Zaid Afawi, Melanie Bahlo, et al.
British Journal of Sports Medicine
|
September 24, 2013
Position statement on youth resistance training: the 2014 International Consensus
Rhodri S Lloyd, Avery D Faigenbaum, Michael H Stone, et al.
Neurology. Genetics
|
November 17, 2021
Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases
Laura Canafoglia, Silvana Franceschetti, Antonio Gambardella, et al.
Cell
|
August 2, 2015
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis
Michael J Parsons, Marco Brancaccio, Siddharth Sethi, et al.
Epilepsia
|
February 13, 2023
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
Karen L Oliver, Marina Trivisano, Simone A Mandelstam, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2022
Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability
David I Francis, Zornitza Stark, Ingrid E Scheffer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 2, 2020
Transgenic Mice Expressing Human α-Synuclein in Noradrenergic Neurons Develop Locus Ceruleus Pathology and Nonmotor Features of Parkinson's Disease
Laura M Butkovich, Madelyn C Houser, Termpanit Chalermpalanupap, et al.
Research Involvement and Engagement
|
July 19, 2022
Standardised data on initiatives-STARDIT: Beta version
Jack S Nunn, Thomas Shafee, Steven Chang, et al.
Brain : a Journal of Neurology
|
December 19, 2018
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features
Samuel F Berkovic, Karen L Oliver, Laura Canafoglia, et al.
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of 88
Search research articles
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Showing results (781-790 of 874) with videos related to
Sort By:
Page
of 88
Brain Communications
|
November 21, 2025
Novel, complex configurations of the <i>MARCHF6</i> repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy
Mark F Bennett, Mark A Corbett, Thessa Kroes, et al.
Human Molecular Genetics
|
May 9, 2015
Mutation of the nuclear lamin gene LMNB2 in progressive myoclonus epilepsy with early ataxia
John A Damiano, Zaid Afawi, Melanie Bahlo, et al.
British Journal of Sports Medicine
|
September 24, 2013
Position statement on youth resistance training: the 2014 International Consensus
Rhodri S Lloyd, Avery D Faigenbaum, Michael H Stone, et al.
Neurology. Genetics
|
November 17, 2021
Progressive Myoclonus Epilepsies: Diagnostic Yield With Next-Generation Sequencing in Previously Unsolved Cases
Laura Canafoglia, Silvana Franceschetti, Antonio Gambardella, et al.
Cell
|
August 2, 2015
The Regulatory Factor ZFHX3 Modifies Circadian Function in SCN via an AT Motif-Driven Axis
Michael J Parsons, Marco Brancaccio, Siddharth Sethi, et al.
Epilepsia
|
February 13, 2023
WWOX developmental and epileptic encephalopathy: Understanding the epileptology and the mortality risk
Karen L Oliver, Marina Trivisano, Simone A Mandelstam, et al.
European Journal of Human Genetics : EJHG
|
November 29, 2022
Comparing saliva and blood for the detection of mosaic genomic abnormalities that cause syndromic intellectual disability
David I Francis, Zornitza Stark, Ingrid E Scheffer, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 2, 2020
Transgenic Mice Expressing Human α-Synuclein in Noradrenergic Neurons Develop Locus Ceruleus Pathology and Nonmotor Features of Parkinson's Disease
Laura M Butkovich, Madelyn C Houser, Termpanit Chalermpalanupap, et al.
Research Involvement and Engagement
|
July 19, 2022
Standardised data on initiatives-STARDIT: Beta version
Jack S Nunn, Thomas Shafee, Steven Chang, et al.
Brain : a Journal of Neurology
|
December 19, 2018
Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features
Samuel F Berkovic, Karen L Oliver, Laura Canafoglia, et al.
Page
of 88