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Epilepsy & Behavior : E&B
|
March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy
Amanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One
|
January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood
Kenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2022
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
Haloom Rafehi, Cherie Green, Kiymet Bozaoglu, et al.
Developmental Medicine and Child Neurology
|
February 23, 2026
Developmental stuttering with common and complex phenotypes
Sarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
Epilepsia
|
August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsy
Meng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology
|
October 1, 1979
C-type virus-like particles specifically localized in Langerhans cells and related cells of skin and lymph nodes of patients with mycosis fungoides and Sezary's syndrome. A morphological and biochemical study
E M van der Loo, G N van Muijen, W A van Vloten, et al.
Journal of Medical Genetics
|
March 8, 2013
Recent advances in the molecular genetics of epilepsy
Michael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.
Developmental Medicine and Child Neurology
|
June 15, 2013
Head stereotypies in STXBP1 encephalopathy
Young Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.
Developmental Medicine and Child Neurology
|
March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizures
Rima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Epilepsy Research
|
April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsy
Alexander Peeraer, John A Damiano, Susannah T Bellows, et al.
Page
of 74
Search research articles
Search
Showing results (261-270 of 740) with videos related to
Sort By:
Page
of 74
Epilepsy & Behavior : E&B
|
March 2, 2010
Neuropsychological function in patients with a single gene mutation associated with autosomal dominant nocturnal frontal lobe epilepsy
Amanda G Wood, Michael M Saling, Marco Fedi, et al.
Plos One
|
January 21, 2018
KANSL1 variation is not a major contributing factor in self-limited focal epilepsy syndromes of childhood
Kenneth A Myers, Amelia McGlade, Bernd A Neubauer, et al.
European Journal of Human Genetics : EJHG
|
August 9, 2022
Unexpected diagnosis of myotonic dystrophy type 2 repeat expansion by genome sequencing
Haloom Rafehi, Cherie Green, Kiymet Bozaoglu, et al.
Developmental Medicine and Child Neurology
|
February 23, 2026
Developmental stuttering with common and complex phenotypes
Sarah E Horton, Daisy A Shepherd, Stephanie Siemers, et al.
Epilepsia
|
August 27, 2016
Hippocampal malrotation is an anatomic variant and has no clinical significance in MRI-negative temporal lobe epilepsy
Meng-Han Tsai, David N Vaughan, Yuliya Perchyonok, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology
|
October 1, 1979
C-type virus-like particles specifically localized in Langerhans cells and related cells of skin and lymph nodes of patients with mycosis fungoides and Sezary's syndrome. A morphological and biochemical study
E M van der Loo, G N van Muijen, W A van Vloten, et al.
Journal of Medical Genetics
|
March 8, 2013
Recent advances in the molecular genetics of epilepsy
Michael S Hildebrand, Hans-Henrik M Dahl, John Anthony Damiano, et al.
Developmental Medicine and Child Neurology
|
June 15, 2013
Head stereotypies in STXBP1 encephalopathy
Young Ok Kim, Christian M Korff, Mel Michel G Villaluz, et al.
Developmental Medicine and Child Neurology
|
March 5, 2019
Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizures
Rima Nabbout, Stephane Auvin, Catherine Chiron, et al.
Epilepsy Research
|
April 19, 2017
Evaluation of GLUT1 variation in non-acquired focal epilepsy
Alexander Peeraer, John A Damiano, Susannah T Bellows, et al.
Page
of 74