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Jan C Pronk

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

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The Lancet. Neurology|April 25, 2006
Vanishing white matter diseaseMarjo S van der Knaap, Jan C Pronk, Gert C Scheper
Journal of Child Neurology|October 24, 2003
Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genesPeter A J Leegwater, Jan C Pronk, Marjo S van der Knaap
Mental Retardation and Developmental Disabilities Research Reviews|June 30, 2006
Vanishing white matter disease: a review with focus on its geneticsJan C Pronk, Barbara van Kollenburg, Gert C Scheper, et al.
Human Mutation|May 3, 2006
Megalencephalic leukoencephalopathy with subcortical cysts: an update and extended mutation analysis of MLC1P K Ilja Boor, Koen de Groot, Vlatka Mejaski-Bosnjak, et al.
Annals of Neurology|February 9, 2002
Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matterMarjo S van der Knaap, Peter A J Leegwater, Andrea A M Könst, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
MLC1: a novel protein in distal astroglial processesP K Ilja Boor, Koen de Groot, Quinten Waisfisz, et al.
Neurobiology of Disease|September 28, 2005
Regulation of protein synthesis in lymphoblasts from vanishing white matter patientsBarbara van Kollenburg, Adri A M Thomas, Gerre Vermeulen, et al.
Acta Neuropathologica|July 14, 2007
MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeetIlja Boor, Machiel Nagtegaal, Wouter Kamphorst, et al.
American Journal of Human Genetics|October 21, 2003
eIF2B-related disorders: antenatal onset and involvement of multiple organsMarjo S van der Knaap, Carola G M van Berkel, Jochen Herms, et al.
Nature Genetics|March 27, 2007
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevationGert C Scheper, Thom van der Klok, Rob J van Andel, et al.
Pageof 1

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

Sort By:
Pageof 1
The Lancet. Neurology|April 25, 2006
Vanishing white matter diseaseMarjo S van der Knaap, Jan C Pronk, Gert C Scheper
Journal of Child Neurology|October 24, 2003
Leukoencephalopathy with vanishing white matter: from magnetic resonance imaging pattern to five genesPeter A J Leegwater, Jan C Pronk, Marjo S van der Knaap
Mental Retardation and Developmental Disabilities Research Reviews|June 30, 2006
Vanishing white matter disease: a review with focus on its geneticsJan C Pronk, Barbara van Kollenburg, Gert C Scheper, et al.
Human Mutation|May 3, 2006
Megalencephalic leukoencephalopathy with subcortical cysts: an update and extended mutation analysis of MLC1P K Ilja Boor, Koen de Groot, Vlatka Mejaski-Bosnjak, et al.
Annals of Neurology|February 9, 2002
Mutations in each of the five subunits of translation initiation factor eIF2B can cause leukoencephalopathy with vanishing white matterMarjo S van der Knaap, Peter A J Leegwater, Andrea A M Könst, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
MLC1: a novel protein in distal astroglial processesP K Ilja Boor, Koen de Groot, Quinten Waisfisz, et al.
Neurobiology of Disease|September 28, 2005
Regulation of protein synthesis in lymphoblasts from vanishing white matter patientsBarbara van Kollenburg, Adri A M Thomas, Gerre Vermeulen, et al.
Acta Neuropathologica|July 14, 2007
MLC1 is associated with the dystrophin-glycoprotein complex at astrocytic endfeetIlja Boor, Machiel Nagtegaal, Wouter Kamphorst, et al.
American Journal of Human Genetics|October 21, 2003
eIF2B-related disorders: antenatal onset and involvement of multiple organsMarjo S van der Knaap, Carola G M van Berkel, Jochen Herms, et al.
Nature Genetics|March 27, 2007
Mitochondrial aspartyl-tRNA synthetase deficiency causes leukoencephalopathy with brain stem and spinal cord involvement and lactate elevationGert C Scheper, Thom van der Klok, Rob J van Andel, et al.
Pageof 1