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Martin Dichgans

Showing results (311-320 of 525) with videos related to

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Stroke|February 4, 2016
Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease SubtypeLoes C A Rutten-Jacobs, Matthew Traylor, Poneh Adib-Samii, et al.
Neuroimage. Clinical|July 31, 2022
Determining the OPTIMAL DTI analysis method for application in cerebral small vessel diseaseMarco Egle, Saima Hilal, Anil M Tuladhar, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 3, 2023
Blood-brain barrier leakage hotspots collocating with brain lesions due to sporadic and monogenic small vessel diseaseSalvatore Rudilosso, Michael S Stringer, Michael Thrippleton, et al.
Brain : a Journal of Neurology|June 12, 2015
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel diseaseEdgard Verdura, Dominique Hervé, Eva Scharrer, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Neurology|September 16, 2018
Serum neurofilament light: A biomarker of neuroaxonal injury after ischemic strokeSteffen Tiedt, Marco Duering, Christian Barro, et al.
Stroke|June 4, 2015
Family History in Young Patients With StrokeVincent Thijs, Ulrike Grittner, Martin Dichgans, et al.
Immunity|July 25, 2024
Innate immune training restores pro-reparative myeloid functions to promote remyelination in the aged central nervous systemVini Tiwari, Bharat Prajapati, Yaw Asare, et al.
Neurology|January 20, 2019
Genetic variation in <i>PLEKHG1</i> is associated with white matter hyperintensities (n = 11,226)Matthew Traylor, Daniel J Tozer, Iain D Croall, et al.
European Stroke Journal|July 11, 2023
Delivery of acute ischaemic stroke treatments in the European region in 2019 and 2020Diana Aguiar de Sousa, Arlene Wilkie, Bo Norrving, et al.
Pageof 53

Showing results (311-320 of 525) with videos related to

Sort By:
Pageof 53
Stroke|February 4, 2016
Association of MTHFR C677T Genotype With Ischemic Stroke Is Confined to Cerebral Small Vessel Disease SubtypeLoes C A Rutten-Jacobs, Matthew Traylor, Poneh Adib-Samii, et al.
Neuroimage. Clinical|July 31, 2022
Determining the OPTIMAL DTI analysis method for application in cerebral small vessel diseaseMarco Egle, Saima Hilal, Anil M Tuladhar, et al.
Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|May 3, 2023
Blood-brain barrier leakage hotspots collocating with brain lesions due to sporadic and monogenic small vessel diseaseSalvatore Rudilosso, Michael S Stringer, Michael Thrippleton, et al.
Brain : a Journal of Neurology|June 12, 2015
Heterozygous HTRA1 mutations are associated with autosomal dominant cerebral small vessel diseaseEdgard Verdura, Dominique Hervé, Eva Scharrer, et al.
Human Mutation|April 3, 2007
The novel p.L1649Q mutation in the SCN1A epilepsy gene is associated with familial hemiplegic migraine: genetic and functional studies. Mutation in brief #957. OnlineKaate R J Vanmolkot, Elena Babini, Boukje de Vries, et al.
Neurology|September 16, 2018
Serum neurofilament light: A biomarker of neuroaxonal injury after ischemic strokeSteffen Tiedt, Marco Duering, Christian Barro, et al.
Stroke|June 4, 2015
Family History in Young Patients With StrokeVincent Thijs, Ulrike Grittner, Martin Dichgans, et al.
Immunity|July 25, 2024
Innate immune training restores pro-reparative myeloid functions to promote remyelination in the aged central nervous systemVini Tiwari, Bharat Prajapati, Yaw Asare, et al.
Neurology|January 20, 2019
Genetic variation in <i>PLEKHG1</i> is associated with white matter hyperintensities (n = 11,226)Matthew Traylor, Daniel J Tozer, Iain D Croall, et al.
European Stroke Journal|July 11, 2023
Delivery of acute ischaemic stroke treatments in the European region in 2019 and 2020Diana Aguiar de Sousa, Arlene Wilkie, Bo Norrving, et al.
Pageof 53