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Christopher Troedson

Showing results (11-20 of 36) with videos related to

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Movement Disorders Clinical Practice|September 16, 2022
Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in <i>AFG3L2</i>Wui-Kwan Wong, Christopher Troedson, Russell C Dale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2015
Mild encephalopathy with reversible splenial lesion: an important differential of encephalitisAmy Ka, Philip Britton, Christopher Troedson, et al.
Mitochondrion|August 17, 2010
Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers SyndromeAlison G Compton, Christopher Troedson, Meredith Wilson, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 4, 2022
BCAS3-Related Neurodevelopmental Disorder Shows Magnetic Resonance Imaging Features Resembling Brain Iron AccumulationWui-Kwan Wong, Christopher Troedson, Markus Damme, et al.
JAMA Neurology|March 28, 2022
Incidence and Natural History of Pediatric Large Vessel Occlusion Stroke: A Population StudyKartik D Bhatia, Romain Briest, Robert Goetti, et al.
Interactive Cardiovascular and Thoracic Surgery|December 12, 2017
Contemporary incidence of stroke (focal infarct and/or haemorrhage) determined by neuroimaging and neurodevelopmental disability at 12 months of age in neonates undergoing cardiac surgery utilizing cardiopulmonary bypassCharlotte E Verrall, Karen Walker, Alison Loughran-Fowlds, et al.
Brain & Development|October 27, 2021
Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsyHannah F Jones, Marion Stoll, Gladys Ho, et al.
Epilepsy & Behavior Reports|July 28, 2022
Predictors of longitudinal seizure outcomes after epilepsy surgery in childhoodAmy Ka, Amir Taher, Stephanie D'Souza, et al.
Neurology. Genetics|December 25, 2019
Yield of comparative genomic hybridization microarray in pediatric neurology practiceShibalik Misra, Greg Peters, Elizabeth Barnes, et al.
Pageof 4

Showing results (11-20 of 36) with videos related to

Sort By:
Pageof 4
Movement Disorders Clinical Practice|September 16, 2022
Levodopa Responsive Dystonia Parkinsonism, Intellectual Disability, and Optic Atrophy Due to a Heterozygous Missense Variant in <i>AFG3L2</i>Wui-Kwan Wong, Christopher Troedson, Russell C Dale, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|February 25, 2015
Mild encephalopathy with reversible splenial lesion: an important differential of encephalitisAmy Ka, Philip Britton, Christopher Troedson, et al.
Mitochondrion|August 17, 2010
Application of oligonucleotide array CGH in the detection of a large intragenic deletion in POLG associated with Alpers SyndromeAlison G Compton, Christopher Troedson, Meredith Wilson, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 4, 2022
BCAS3-Related Neurodevelopmental Disorder Shows Magnetic Resonance Imaging Features Resembling Brain Iron AccumulationWui-Kwan Wong, Christopher Troedson, Markus Damme, et al.
JAMA Neurology|March 28, 2022
Incidence and Natural History of Pediatric Large Vessel Occlusion Stroke: A Population StudyKartik D Bhatia, Romain Briest, Robert Goetti, et al.
Interactive Cardiovascular and Thoracic Surgery|December 12, 2017
Contemporary incidence of stroke (focal infarct and/or haemorrhage) determined by neuroimaging and neurodevelopmental disability at 12 months of age in neonates undergoing cardiac surgery utilizing cardiopulmonary bypassCharlotte E Verrall, Karen Walker, Alison Loughran-Fowlds, et al.
Brain & Development|October 27, 2021
Autosomal dominant ADAR c.3019G>A (p.(G1007R)) variant is an important mimic of hereditary spastic paraplegia and cerebral palsyHannah F Jones, Marion Stoll, Gladys Ho, et al.
Epilepsy & Behavior Reports|July 28, 2022
Predictors of longitudinal seizure outcomes after epilepsy surgery in childhoodAmy Ka, Amir Taher, Stephanie D'Souza, et al.
Neurology. Genetics|December 25, 2019
Yield of comparative genomic hybridization microarray in pediatric neurology practiceShibalik Misra, Greg Peters, Elizabeth Barnes, et al.
Pageof 4