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Alasdair Parker

Showing results (1-10 of 17) with videos related to

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Developmental Medicine and Child Neurology|September 15, 2015
Genomics in early infantile epileptic encephalopathies - trials and tribulationsAlasdair Parker
Developmental Medicine and Child Neurology|December 13, 2021
Harnessing the power of neuroimaging and whole genome sequencing from fetus to adulthoodAlasdair Parker
Developmental Medicine and Child Neurology|December 3, 2022
Rapid developments in paediatric neurology: Keeping up with the patient's voiceAlasdair Parker
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2016
Intracranial stimulation for children with epilepsy-early daysAlasdair Parker
Archives of Disease in Childhood|July 2, 2013
Investigating microcephalyC Geoffrey Woods, Alasdair Parker
Developmental Medicine and Child Neurology|May 24, 2014
Idiopathic intracranial hypertension in childhood: pitfalls in diagnosisDeepa Krishnakumar, John D Pickard, Zofia Czosnyka, et al.
Archives of Disease in Childhood|May 9, 2024
Consensus recommendations for the assessment and management of idiopathic intracranial hypertension in children and young peopleSam Amin, Marie Monaghan, Katharine Forrest, et al.
Brain : a Journal of Neurology|February 27, 2016
CCDC88A mutations cause PEHO-like syndrome in humans and mouseMichael S Nahorski, Masato Asai, Emma Wakeling, et al.
Biochimica Et Biophysica Acta|October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiencyAbdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delayEmma S Reid, Hywel Williams, Glenn Anderson, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Developmental Medicine and Child Neurology|September 15, 2015
Genomics in early infantile epileptic encephalopathies - trials and tribulationsAlasdair Parker
Developmental Medicine and Child Neurology|December 13, 2021
Harnessing the power of neuroimaging and whole genome sequencing from fetus to adulthoodAlasdair Parker
Developmental Medicine and Child Neurology|December 3, 2022
Rapid developments in paediatric neurology: Keeping up with the patient's voiceAlasdair Parker
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 31, 2016
Intracranial stimulation for children with epilepsy-early daysAlasdair Parker
Archives of Disease in Childhood|July 2, 2013
Investigating microcephalyC Geoffrey Woods, Alasdair Parker
Developmental Medicine and Child Neurology|May 24, 2014
Idiopathic intracranial hypertension in childhood: pitfalls in diagnosisDeepa Krishnakumar, John D Pickard, Zofia Czosnyka, et al.
Archives of Disease in Childhood|May 9, 2024
Consensus recommendations for the assessment and management of idiopathic intracranial hypertension in children and young peopleSam Amin, Marie Monaghan, Katharine Forrest, et al.
Brain : a Journal of Neurology|February 27, 2016
CCDC88A mutations cause PEHO-like syndrome in humans and mouseMichael S Nahorski, Masato Asai, Emma Wakeling, et al.
Biochimica Et Biophysica Acta|October 29, 2013
Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiencyAbdulraheem Almalki, Charlotte L Alston, Alasdair Parker, et al.
Journal of Inherited Metabolic Disease|March 4, 2017
Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delayEmma S Reid, Hywel Williams, Glenn Anderson, et al.
Pageof 2