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Padraic Grattan-Smith

Showing results (1-10 of 22) with videos related to

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Journal of Paediatrics and Child Health|July 15, 2010
Investigation of suspected Guillain-Barre syndrome in childhood: what is the role for gadolinium enhanced magnetic resonance imaging of the spine?Nicholas Smith, John Pereira, Padraic Grattan-Smith
DNA Repair|May 10, 2008
Defective responses to DNA single- and double-strand breaks in spinocerebellar ataxiaMartin F Lavin, Nuri Gueven, Padraic Grattan-Smith
Journal of Paediatrics and Child Health|December 17, 2011
Response to Zhang et alNicholas Jc Smith, John Pereira, Padraic Grattan-Smith
Journal of Paediatrics and Child Health|February 18, 2010
Acquired facial palsy with hypertension secondary to Guillain-Barre syndromeNicholas Smith, Padraic Grattan-Smith, Ian P Andrews, et al.
Developmental Medicine and Child Neurology|April 21, 2012
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre studyRussell C Dale, Padraic Grattan-Smith, Michelle Nicholson, et al.
Journal of Paediatrics and Child Health|December 4, 2015
Intravenous immunoglobulin in acute Sydenham's chorea: A systematic reviewShekeeb S Mohammad, Margherita Nosadini, Padraic Grattan-Smith, et al.
Neurology|September 24, 2011
Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletionRussell C Dale, Padraic Grattan-Smith, Victor S C Fung, et al.
Journal of Child Neurology|May 4, 2004
Neuroepithelial cysts in a patient with Joubert syndrome plus renal cystsSarah E Marsh, Padraic Grattan-Smith, John Pereira, et al.
Developmental Medicine and Child Neurology|March 2, 2010
Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiencyRussell C Dale, Anna Melchers, Victor S C Fung, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 8, 2004
Movement disorder emergenciesChristopher M Kipps, Victor S C Fung, Padraic Grattan-Smith, et al.
Pageof 3

Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
Journal of Paediatrics and Child Health|July 15, 2010
Investigation of suspected Guillain-Barre syndrome in childhood: what is the role for gadolinium enhanced magnetic resonance imaging of the spine?Nicholas Smith, John Pereira, Padraic Grattan-Smith
DNA Repair|May 10, 2008
Defective responses to DNA single- and double-strand breaks in spinocerebellar ataxiaMartin F Lavin, Nuri Gueven, Padraic Grattan-Smith
Journal of Paediatrics and Child Health|December 17, 2011
Response to Zhang et alNicholas Jc Smith, John Pereira, Padraic Grattan-Smith
Journal of Paediatrics and Child Health|February 18, 2010
Acquired facial palsy with hypertension secondary to Guillain-Barre syndromeNicholas Smith, Padraic Grattan-Smith, Ian P Andrews, et al.
Developmental Medicine and Child Neurology|April 21, 2012
Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre studyRussell C Dale, Padraic Grattan-Smith, Michelle Nicholson, et al.
Journal of Paediatrics and Child Health|December 4, 2015
Intravenous immunoglobulin in acute Sydenham's chorea: A systematic reviewShekeeb S Mohammad, Margherita Nosadini, Padraic Grattan-Smith, et al.
Neurology|September 24, 2011
Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletionRussell C Dale, Padraic Grattan-Smith, Victor S C Fung, et al.
Journal of Child Neurology|May 4, 2004
Neuroepithelial cysts in a patient with Joubert syndrome plus renal cystsSarah E Marsh, Padraic Grattan-Smith, John Pereira, et al.
Developmental Medicine and Child Neurology|March 2, 2010
Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiencyRussell C Dale, Anna Melchers, Victor S C Fung, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 8, 2004
Movement disorder emergenciesChristopher M Kipps, Victor S C Fung, Padraic Grattan-Smith, et al.
Pageof 3