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American Journal of Medical Genetics. Part A
|
April 28, 2015
Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome
Heather E Olson, Dimira Tambunan, Christopher LaCoursiere, et al.
Journal of Child Neurology
|
January 7, 2017
A Model Program for Translational Medicine in Epilepsy Genetics
Lacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Tissue Engineering. Part A
|
February 5, 2009
Neural stem cell- and Schwann cell-loaded biodegradable polymer scaffolds support axonal regeneration in the transected spinal cord
Heather E Olson, Gemma E Rooney, LouAnn Gross, et al.
Developmental Medicine and Child Neurology
|
May 24, 2021
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure
Heather E Olson, Julia G Costantini, Lindsay C Swanson, et al.
Journal of Neurointerventional Surgery
|
October 2, 2017
Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part II: synthesis of the literature and patient management
Edward Yang, Armide Storey, Heather E Olson, et al.
Journal of Neurointerventional Surgery
|
October 2, 2017
Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part I: review of experience at Boston Children's Hospital
Edward Yang, Armide Storey, Heather E Olson, et al.
Journal of Neurodevelopmental Disorders
|
October 24, 2025
Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome
Elise Brimble, Pam Ventola, Elizabeth Blomenberg, et al.
Epilepsia
|
August 29, 2013
Clinical application and evaluation of the Bien diagnostic criteria for Rasmussen encephalitis
Heather E Olson, Mirna Lechpammer, Sanjay P Prabhu, et al.
Pediatric Neurology
|
April 1, 2019
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review
Heather E Olson, Scott T Demarest, Elia M Pestana-Knight, et al.
Molecular Genetics and Metabolism
|
December 28, 2017
Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency
Stephanie J Sacharow, Elizabeth E Dudenhausen, Carrie L Lomelino, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 50) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics. Part A
|
April 28, 2015
Mutations in epilepsy and intellectual disability genes in patients with features of Rett syndrome
Heather E Olson, Dimira Tambunan, Christopher LaCoursiere, et al.
Journal of Child Neurology
|
January 7, 2017
A Model Program for Translational Medicine in Epilepsy Genetics
Lacey A Smith, Jeremy F P Ullmann, Heather E Olson, et al.
Tissue Engineering. Part A
|
February 5, 2009
Neural stem cell- and Schwann cell-loaded biodegradable polymer scaffolds support axonal regeneration in the transected spinal cord
Heather E Olson, Gemma E Rooney, LouAnn Gross, et al.
Developmental Medicine and Child Neurology
|
May 24, 2021
Cerebral visual impairment in CDKL5 deficiency disorder: vision as an outcome measure
Heather E Olson, Julia G Costantini, Lindsay C Swanson, et al.
Journal of Neurointerventional Surgery
|
October 2, 2017
Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part II: synthesis of the literature and patient management
Edward Yang, Armide Storey, Heather E Olson, et al.
Journal of Neurointerventional Surgery
|
October 2, 2017
Imaging features and prognostic factors in fetal and postnatal torcular dural sinus malformations, part I: review of experience at Boston Children's Hospital
Edward Yang, Armide Storey, Heather E Olson, et al.
Journal of Neurodevelopmental Disorders
|
October 24, 2025
Longitudinal characterization of clinical, developmental, and behavioral phenotypes in 101 children and adults with FOXG1 syndrome
Elise Brimble, Pam Ventola, Elizabeth Blomenberg, et al.
Epilepsia
|
August 29, 2013
Clinical application and evaluation of the Bien diagnostic criteria for Rasmussen encephalitis
Heather E Olson, Mirna Lechpammer, Sanjay P Prabhu, et al.
Pediatric Neurology
|
April 1, 2019
Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review
Heather E Olson, Scott T Demarest, Elia M Pestana-Knight, et al.
Molecular Genetics and Metabolism
|
December 28, 2017
Characterization of a novel variant in siblings with Asparagine Synthetase Deficiency
Stephanie J Sacharow, Elizabeth E Dudenhausen, Carrie L Lomelino, et al.
Page
of 5