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Saskia A J Lesnik Oberstein

Showing results (1-10 of 48) with videos related to

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Stroke|August 17, 2021
Hereditary Cerebral Small Vessel Diseases and Stroke: A Guide for Diagnosis and ManagementStéphanie Guey, Saskia A J Lesnik Oberstein, Elisabeth Tournier-Lasserve, et al.
Cephalalgia : an International Journal of Headache|November 2, 2010
CADASIL and migraine: A narrative reviewMichael K Liem, Saskia A J Lesnik Oberstein, Jeroen van der Grond, et al.
Radiology|November 1, 2003
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR imaging findings at different ages--3rd-6th decadesRivka van den Boom, Saskia A J Lesnik Oberstein, Michel D Ferrari, et al.
Journal of the American Society for Mass Spectrometry|September 16, 2015
In-Depth Characterization of Protein Disulfide Bonds by Online Liquid Chromatography-Electrochemistry-Mass SpectrometryLinda Switzar, Simone Nicolardi, Julie W Rutten, et al.
Expert Review of Molecular Diagnostics|May 22, 2014
Interpretation of NOTCH3 mutations in the diagnosis of CADASILJulie W Rutten, Joost Haan, Gisela M Terwindt, et al.
Stroke|March 18, 2022
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic <i>NOTCH3</i> Variant Can Have a Normal Brain Magnetic Resonance Imaging and Skin Biopsy Beyond Age 50 YearsRemco J Hack, Gido Gravesteijn, Minne N Cerfontaine, et al.
Radiology|August 31, 2002
Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyRivka van Den Boom, Saskia A J Lesnik Oberstein, Sjoerd G van Duinen, et al.
Stroke|November 9, 2020
Cysteine-Altering <i>NOTCH3</i> Variants Are a Risk Factor for Stroke in the Elderly PopulationRemco J Hack, Julie W Rutten, Thomas N Person, et al.
Stem Cell Reports|September 3, 2021
Engineered 3D vessel-on-chip using hiPSC-derived endothelial- and vascular smooth muscle cellsMarc Vila Cuenca, Amy Cochrane, Francijna E van den Hil, et al.
American Journal of Human Genetics|August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseSaskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Stroke|August 17, 2021
Hereditary Cerebral Small Vessel Diseases and Stroke: A Guide for Diagnosis and ManagementStéphanie Guey, Saskia A J Lesnik Oberstein, Elisabeth Tournier-Lasserve, et al.
Cephalalgia : an International Journal of Headache|November 2, 2010
CADASIL and migraine: A narrative reviewMichael K Liem, Saskia A J Lesnik Oberstein, Jeroen van der Grond, et al.
Radiology|November 1, 2003
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: MR imaging findings at different ages--3rd-6th decadesRivka van den Boom, Saskia A J Lesnik Oberstein, Michel D Ferrari, et al.
Journal of the American Society for Mass Spectrometry|September 16, 2015
In-Depth Characterization of Protein Disulfide Bonds by Online Liquid Chromatography-Electrochemistry-Mass SpectrometryLinda Switzar, Simone Nicolardi, Julie W Rutten, et al.
Expert Review of Molecular Diagnostics|May 22, 2014
Interpretation of NOTCH3 mutations in the diagnosis of CADASILJulie W Rutten, Joost Haan, Gisela M Terwindt, et al.
Stroke|March 18, 2022
Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts and Leukoencephalopathy Family Members With a Pathogenic <i>NOTCH3</i> Variant Can Have a Normal Brain Magnetic Resonance Imaging and Skin Biopsy Beyond Age 50 YearsRemco J Hack, Gido Gravesteijn, Minne N Cerfontaine, et al.
Radiology|August 31, 2002
Subcortical lacunar lesions: an MR imaging finding in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathyRivka van Den Boom, Saskia A J Lesnik Oberstein, Sjoerd G van Duinen, et al.
Stroke|November 9, 2020
Cysteine-Altering <i>NOTCH3</i> Variants Are a Risk Factor for Stroke in the Elderly PopulationRemco J Hack, Julie W Rutten, Thomas N Person, et al.
Stem Cell Reports|September 3, 2021
Engineered 3D vessel-on-chip using hiPSC-derived endothelial- and vascular smooth muscle cellsMarc Vila Cuenca, Amy Cochrane, Francijna E van den Hil, et al.
American Journal of Human Genetics|August 16, 2006
Peters Plus syndrome is caused by mutations in B3GALTL, a putative glycosyltransferaseSaskia A J Lesnik Oberstein, Marjolein Kriek, Stefan J White, et al.
Pageof 5