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Ronald Wanders

Showing results (1-10 of 19) with videos related to

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Handbook of Clinical Neurology|April 30, 2013
Peroxisomal disordersPatrick Aubourg, Ronald Wanders
Brain Pathology (Zurich, Switzerland)|July 15, 2010
Biochemical aspects of X-linked adrenoleukodystrophyStephan Kemp, Ronald Wanders
Journal of Inherited Metabolic Disease|November 13, 2014
Complex lipidsJean-Marie Saudubray, Matthias R Baumgartner, Ronald Wanders
Brain & Development|August 22, 2006
D-bifunctional protein deficiency associated with drug resistant infantile spasmsSabrina Buoni, Raffaella Zannolli, Hans Waterham, et al.
The Journal of Pediatrics|October 1, 2003
MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiencyUte Spiekerkoetter, Bin Sun, Thomas Zytkovicz, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 1, 2017
Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophyMalu-Clair van de Beek, Rob Ofman, Inge Dijkstra, et al.
Annales De Medecine Interne|September 10, 2002
[Sjogren-Larsson syndrome: two cases with delayed diagnosis]Laurent Misery, Jean-Christophe Antoine, Renaud Touraine, et al.
Brain : a Journal of Neurology|August 16, 2014
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolismHeidi Peters, Nicole Buck, Ronald Wanders, et al.
Pediatric Transplantation|February 18, 2018
Living-donor liver transplantation for mild Zellweger spectrum disorder: Up to 17 years follow-upTanguy Demaret, Sharat Varma, Xavier Stephenne, et al.
JIMD Reports|February 23, 2013
Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene MutationsAndrea Mignarri, Claudia Vinciguerra, Antonio Giorgio, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Handbook of Clinical Neurology|April 30, 2013
Peroxisomal disordersPatrick Aubourg, Ronald Wanders
Brain Pathology (Zurich, Switzerland)|July 15, 2010
Biochemical aspects of X-linked adrenoleukodystrophyStephan Kemp, Ronald Wanders
Journal of Inherited Metabolic Disease|November 13, 2014
Complex lipidsJean-Marie Saudubray, Matthias R Baumgartner, Ronald Wanders
Brain & Development|August 22, 2006
D-bifunctional protein deficiency associated with drug resistant infantile spasmsSabrina Buoni, Raffaella Zannolli, Hans Waterham, et al.
The Journal of Pediatrics|October 1, 2003
MS/MS-based newborn and family screening detects asymptomatic patients with very-long-chain acyl-CoA dehydrogenase deficiencyUte Spiekerkoetter, Bin Sun, Thomas Zytkovicz, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|July 1, 2017
Lipid-induced endoplasmic reticulum stress in X-linked adrenoleukodystrophyMalu-Clair van de Beek, Rob Ofman, Inge Dijkstra, et al.
Annales De Medecine Interne|September 10, 2002
[Sjogren-Larsson syndrome: two cases with delayed diagnosis]Laurent Misery, Jean-Christophe Antoine, Renaud Touraine, et al.
Brain : a Journal of Neurology|August 16, 2014
ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolismHeidi Peters, Nicole Buck, Ronald Wanders, et al.
Pediatric Transplantation|February 18, 2018
Living-donor liver transplantation for mild Zellweger spectrum disorder: Up to 17 years follow-upTanguy Demaret, Sharat Varma, Xavier Stephenne, et al.
JIMD Reports|February 23, 2013
Zellweger Spectrum Disorder with Mild Phenotype Caused by PEX2 Gene MutationsAndrea Mignarri, Claudia Vinciguerra, Antonio Giorgio, et al.
Pageof 2