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Seo-Kyung Chung

Showing results (1-10 of 39) with videos related to

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Brain & Development|November 16, 2016
Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patientsAmira Masri, Seo-Kyung Chung, Mark I Rees
Advances in Protein Chemistry and Structural Biology|October 11, 2012
Next generation sequencing methodologies--an overviewWilliam O Pickrell, Mark I Rees, Seo-Kyung Chung
Advances in Protein Chemistry and Structural Biology|November 27, 2010
Fine architecture and mutation mapping of human brain inhibitory system ligand gated ion channels by high-throughput homology modelingJonathan G L Mullins, Seo-Kyung Chung, Mark I Rees
Epilepsy & Behavior : E&B|October 23, 2012
Translation of genetic findings to clinical practice in juvenile myoclonic epilepsyRhys H Thomas, Seo-Kyung Chung, Khalid Hamandi, et al.
Heart Rhythm|November 6, 2007
Coinheritance of long QT syndrome and Kearns-Sayre syndromeJonathan R Skinner, Tao Yang, Dianne Purvis, et al.
Frontiers in Molecular Neuroscience|October 24, 2008
A critical role for glycine transporters in hyperexcitability disordersRobert J Harvey, Eloisa Carta, Brian R Pearce, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 19, 2014
Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1Fouzia Hmami, Sian-Elin Wood, Sana Chaouki, et al.
Brain : a Journal of Neurology|May 31, 2018
Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticusShira Sagie, Tally Lerman-Sagie, Snezana Maljevic, et al.
Neurobiology of Disease|March 23, 2011
Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 geneJennifer L Gill, Deborah Capper, Jean-François Vanbellinghen, et al.
Heart Rhythm|December 2, 2010
Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: a marker of severe KCNQ1 dysfunction?Kathryn S Rice, Graeme Dickson, Mark Lane, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Brain & Development|November 16, 2016
Hyperekplexia: Report on phenotype and genotype of 16 Jordanian patientsAmira Masri, Seo-Kyung Chung, Mark I Rees
Advances in Protein Chemistry and Structural Biology|October 11, 2012
Next generation sequencing methodologies--an overviewWilliam O Pickrell, Mark I Rees, Seo-Kyung Chung
Advances in Protein Chemistry and Structural Biology|November 27, 2010
Fine architecture and mutation mapping of human brain inhibitory system ligand gated ion channels by high-throughput homology modelingJonathan G L Mullins, Seo-Kyung Chung, Mark I Rees
Epilepsy & Behavior : E&B|October 23, 2012
Translation of genetic findings to clinical practice in juvenile myoclonic epilepsyRhys H Thomas, Seo-Kyung Chung, Khalid Hamandi, et al.
Heart Rhythm|November 6, 2007
Coinheritance of long QT syndrome and Kearns-Sayre syndromeJonathan R Skinner, Tao Yang, Dianne Purvis, et al.
Frontiers in Molecular Neuroscience|October 24, 2008
A critical role for glycine transporters in hyperexcitability disordersRobert J Harvey, Eloisa Carta, Brian R Pearce, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 19, 2014
Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1Fouzia Hmami, Sian-Elin Wood, Sana Chaouki, et al.
Brain : a Journal of Neurology|May 31, 2018
Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticusShira Sagie, Tally Lerman-Sagie, Snezana Maljevic, et al.
Neurobiology of Disease|March 23, 2011
Startle disease in Irish wolfhounds associated with a microdeletion in the glycine transporter GlyT2 geneJennifer L Gill, Deborah Capper, Jean-François Vanbellinghen, et al.
Heart Rhythm|December 2, 2010
Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: a marker of severe KCNQ1 dysfunction?Kathryn S Rice, Graeme Dickson, Mark Lane, et al.
Pageof 4