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Glia
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October 24, 2012
Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men
Gwendolyn Behrendt, Kristin Baer, Annalisa Buffo, et al.
Seizure
|
October 15, 2013
Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010
W Owen Pickrell, Arron S Lacey, Rhys H Thomas, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 19, 2014
Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1
Fouzia Hmami, Sian-Elin Wood, Sana Chaouki, et al.
Epilepsy & Behavior : E&B
|
June 19, 2014
A comprehensive neuropsychological description of cognition in drug-refractory juvenile myoclonic epilepsy
Rhys H Thomas, Jordana Walsh, Carla Church, et al.
European Journal of Medical Genetics
|
July 18, 2018
Tubulin genes and malformations of cortical development
Romina Romaniello, Filippo Arrigoni, Andrew E Fry, et al.
Brain : a Journal of Neurology
|
May 31, 2018
Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticus
Shira 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 gene
Jennifer L Gill, Deborah Capper, Jean-François Vanbellinghen, et al.
Australian Health Review : a Publication of the Australian Hospital Association
|
September 10, 2023
Development of a novel and more holistic approach for assessing impact in health and medical research: the Research Impact Assessment Framework
Robyn L Ward, Don Nutbeam, Wilfred Mijnhardt, et al.
Epilepsy & Behavior : E&B
|
June 20, 2020
Long-term outcomes after epilepsy surgery, a retrospective cohort study linking patient-reported outcomes and routine healthcare data
Bengi Kansu, William O Pickrell, Arron S Lacey, 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.
Page
of 9
Search research articles
Search
Showing results (21-30 of 82) with videos related to
Sort By:
Page
of 9
Glia
|
October 24, 2012
Dynamic changes in myelin aberrations and oligodendrocyte generation in chronic amyloidosis in mice and men
Gwendolyn Behrendt, Kristin Baer, Annalisa Buffo, et al.
Seizure
|
October 15, 2013
Trends in the first antiepileptic drug prescribed for epilepsy between 2000 and 2010
W Owen Pickrell, Arron S Lacey, Rhys H Thomas, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 19, 2014
Neonatal hyperekplexia with homozygous p.R392H mutation in GLRA1
Fouzia Hmami, Sian-Elin Wood, Sana Chaouki, et al.
Epilepsy & Behavior : E&B
|
June 19, 2014
A comprehensive neuropsychological description of cognition in drug-refractory juvenile myoclonic epilepsy
Rhys H Thomas, Jordana Walsh, Carla Church, et al.
European Journal of Medical Genetics
|
July 18, 2018
Tubulin genes and malformations of cortical development
Romina Romaniello, Filippo Arrigoni, Andrew E Fry, et al.
Brain : a Journal of Neurology
|
May 31, 2018
Expanding the phenotype of TRAK1 mutations: hyperekplexia and refractory status epilepticus
Shira 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 gene
Jennifer L Gill, Deborah Capper, Jean-François Vanbellinghen, et al.
Australian Health Review : a Publication of the Australian Hospital Association
|
September 10, 2023
Development of a novel and more holistic approach for assessing impact in health and medical research: the Research Impact Assessment Framework
Robyn L Ward, Don Nutbeam, Wilfred Mijnhardt, et al.
Epilepsy & Behavior : E&B
|
June 20, 2020
Long-term outcomes after epilepsy surgery, a retrospective cohort study linking patient-reported outcomes and routine healthcare data
Bengi Kansu, William O Pickrell, Arron S Lacey, 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.
Page
of 9