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Robert Surtees

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Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Psychogenic movement disorders in children: a report of 15 cases and a review of the literaturePetra Schwingenschuh, Claustre Pont-Sunyer, Robert Surtees, et al.
Pediatric Radiology|June 8, 2006
Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblingsZarazuela Zolkipli, Hisham Dahmoush, Dawn E Saunders, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher diseaseKaren Woodward, Maria Cundall, Rodger Palmer, et al.
Seizure|August 14, 2003
Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable statusPeter Baxter, Antonia Clarke, Helen Cross, et al.
Brain : a Journal of Neurology|September 25, 2003
Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1Matthew Pitt, Henry Houlden, Jean Jacobs, et al.
The Biochemical Journal|January 22, 2003
L-serine in disease and developmentTom J de Koning, Keith Snell, Marinus Duran, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
Clinical Chemistry|April 30, 2002
Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiencyChike B Item, Carmen Stromberger, Adolf Mühl, et al.
AJNR. American Journal of Neuroradiology|October 10, 2002
New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellumMarjo S van der Knaap, SakkuBai Naidu, Petra J W Pouwels, et al.
Brain : a Journal of Neurology|February 4, 2005
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher diseaseNicole I Wolf, Erik A Sistermans, Maria Cundall, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Movement Disorders : Official Journal of the Movement Disorder Society|September 2, 2008
Psychogenic movement disorders in children: a report of 15 cases and a review of the literaturePetra Schwingenschuh, Claustre Pont-Sunyer, Robert Surtees, et al.
Pediatric Radiology|June 8, 2006
Pantothenate kinase 2 mutation with classic pantothenate-kinase-associated neurodegeneration without 'eye-of-the-tiger' sign on MRI in a pair of siblingsZarazuela Zolkipli, Hisham Dahmoush, Dawn E Saunders, et al.
American Journal of Medical Genetics. Part A|February 28, 2003
Complex chromosomal rearrangement and associated counseling issues in a family with Pelizaeus-Merzbacher diseaseKaren Woodward, Maria Cundall, Rodger Palmer, et al.
Seizure|August 14, 2003
Idiopathic catastrophic epileptic encephalopathy presenting with acute onset intractable statusPeter Baxter, Antonia Clarke, Helen Cross, et al.
Brain : a Journal of Neurology|September 25, 2003
Severe infantile neuropathy with diaphragmatic weakness and its relationship to SMARD1Matthew Pitt, Henry Houlden, Jean Jacobs, et al.
The Biochemical Journal|January 22, 2003
L-serine in disease and developmentTom J de Koning, Keith Snell, Marinus Duran, et al.
Neurogenetics|September 14, 2006
Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelinationNicole I Wolf, Maria Cundall, Paul Rutland, et al.
Clinical Chemistry|April 30, 2002
Denaturing gradient gel electrophoresis for the molecular characterization of six patients with guanidinoacetate methyltransferase deficiencyChike B Item, Carmen Stromberger, Adolf Mühl, et al.
AJNR. American Journal of Neuroradiology|October 10, 2002
New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellumMarjo S van der Knaap, SakkuBai Naidu, Petra J W Pouwels, et al.
Brain : a Journal of Neurology|February 4, 2005
Three or more copies of the proteolipid protein gene PLP1 cause severe Pelizaeus-Merzbacher diseaseNicole I Wolf, Erik A Sistermans, Maria Cundall, et al.
Pageof 2