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Harold G Marks

Showing results (1-10 of 8) with videos related to

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Journal of the Neurological Sciences|August 28, 2007
Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirableSurya N Gupta, Harold G Marks
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 7, 2012
Correction of a short cardiac PR interval in a 12-year-old girl with late-onset Pompe disease following enzyme replacement therapyCristina Fernández, Agustín Legido, Reena Jethva, et al.
Neurology|December 10, 2003
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problemRobert A Taylor, Erin M Simon, Harold G Marks, et al.
Pediatric Neurology|November 25, 2010
Microarray analysis in children with developmental disorder or epilepsyHerbert Ezugha, Carol E Anderson, Harold G Marks, et al.
Annals of Neurology|September 27, 2002
A PLP splicing abnormality is associated with an unusual presentation of PMDGrace M Hobson, Zhong Huang, Karen Sperle, et al.
Pediatric Neurology|September 26, 2006
Oxcarbazepine monotherapy in children and adolescents: a single-center clinical experienceSanjeev V Kothare, Divya S Khurana, Navid Mostofi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 1, 2008
Efficacy and safety of lamotrigine monotherapy in children and adolescents with epilepsyIgnacio Valencia, Gerard Piñol-Ripoll, Divya S Khurana, et al.
Pediatric Neurology|August 12, 2009
Efficacy and tolerability of topiramate in pediatric migraineMarcos J Cruz, Ignacio Valencia, Agustín Legido, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Journal of the Neurological Sciences|August 28, 2007
Spinocerebellar ataxia type 7 mimicking Kearns-Sayre syndrome: a clinical diagnosis is desirableSurya N Gupta, Harold G Marks
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 7, 2012
Correction of a short cardiac PR interval in a 12-year-old girl with late-onset Pompe disease following enzyme replacement therapyCristina Fernández, Agustín Legido, Reena Jethva, et al.
Neurology|December 10, 2003
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problemRobert A Taylor, Erin M Simon, Harold G Marks, et al.
Pediatric Neurology|November 25, 2010
Microarray analysis in children with developmental disorder or epilepsyHerbert Ezugha, Carol E Anderson, Harold G Marks, et al.
Annals of Neurology|September 27, 2002
A PLP splicing abnormality is associated with an unusual presentation of PMDGrace M Hobson, Zhong Huang, Karen Sperle, et al.
Pediatric Neurology|September 26, 2006
Oxcarbazepine monotherapy in children and adolescents: a single-center clinical experienceSanjeev V Kothare, Divya S Khurana, Navid Mostofi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|July 1, 2008
Efficacy and safety of lamotrigine monotherapy in children and adolescents with epilepsyIgnacio Valencia, Gerard Piñol-Ripoll, Divya S Khurana, et al.
Pediatric Neurology|August 12, 2009
Efficacy and tolerability of topiramate in pediatric migraineMarcos J Cruz, Ignacio Valencia, Agustín Legido, et al.
Pageof 1