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M Synofzik

Showing results (11-20 of 32) with videos related to

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Der Nervenarzt|June 3, 2017
[Genetic architecture of amyotrophic lateral sclerosis and frontotemporal dementia : Overlap and differences]M Synofzik, M Otto, A Ludolph, et al.
Clinical Genetics|January 17, 2012
Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central EuropeJ Schicks, M Synofzik, C Beetz, et al.
Clinical Neuroradiology|November 29, 2015
Clinical Application of Fiber Visualization with LIC Maps Using Multidirectional Anisotropic Glyph Samples (A-Glyph LIC)M Höller, H-H Ehricke, M Synofzik, et al.
Deutsche Medizinische Wochenschrift (1946)|June 10, 2011
[Rare differential diagnosis of primary adrenal insufficiency: case 6/2011]F Blaschka, M Synofzik, L Schöls, et al.
BMC Neurology|September 15, 2016
A case of late-onset, thymoma-associated myasthenia gravis with ryanodine receptor and titin antibodies and concomitant granulomatous myositisM I Stefanou, L Komorowski, S Kade, et al.
Neurology|October 30, 2009
Intensive coordinative training improves motor performance in degenerative cerebellar diseaseW Ilg, M Synofzik, D Brötz, et al.
European Journal of Neurology|April 16, 2016
Slowly progressive LGI1 encephalitis with isolated late-onset cognitive dysfunction: a treatable mimic of Alzheimer's diseaseJ Marquetand, M van Lessen, B Bender, et al.
Disease Models & Mechanisms|October 24, 2020
CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neuronsS Schuster, E Heuten, A Velic, et al.
NPJ Digital Medicine|March 17, 2023
SARA<sup>speech</sup>-Feasibility of automated assessment of ataxic speech disturbanceM Grobe-Einsler, J Faber, A Taheri, et al.
Journal of Neurology|November 1, 2014
Boucher-Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literatureA A Tarnutzer, C Gerth-Kahlert, D Timmann, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Der Nervenarzt|June 3, 2017
[Genetic architecture of amyotrophic lateral sclerosis and frontotemporal dementia : Overlap and differences]M Synofzik, M Otto, A Ludolph, et al.
Clinical Genetics|January 17, 2012
Mutations in the PDYN gene (SCA23) are not a frequent cause of dominant ataxia in Central EuropeJ Schicks, M Synofzik, C Beetz, et al.
Clinical Neuroradiology|November 29, 2015
Clinical Application of Fiber Visualization with LIC Maps Using Multidirectional Anisotropic Glyph Samples (A-Glyph LIC)M Höller, H-H Ehricke, M Synofzik, et al.
Deutsche Medizinische Wochenschrift (1946)|June 10, 2011
[Rare differential diagnosis of primary adrenal insufficiency: case 6/2011]F Blaschka, M Synofzik, L Schöls, et al.
BMC Neurology|September 15, 2016
A case of late-onset, thymoma-associated myasthenia gravis with ryanodine receptor and titin antibodies and concomitant granulomatous myositisM I Stefanou, L Komorowski, S Kade, et al.
Neurology|October 30, 2009
Intensive coordinative training improves motor performance in degenerative cerebellar diseaseW Ilg, M Synofzik, D Brötz, et al.
European Journal of Neurology|April 16, 2016
Slowly progressive LGI1 encephalitis with isolated late-onset cognitive dysfunction: a treatable mimic of Alzheimer's diseaseJ Marquetand, M van Lessen, B Bender, et al.
Disease Models & Mechanisms|October 24, 2020
CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neuronsS Schuster, E Heuten, A Velic, et al.
NPJ Digital Medicine|March 17, 2023
SARA<sup>speech</sup>-Feasibility of automated assessment of ataxic speech disturbanceM Grobe-Einsler, J Faber, A Taheri, et al.
Journal of Neurology|November 1, 2014
Boucher-Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literatureA A Tarnutzer, C Gerth-Kahlert, D Timmann, et al.
Pageof 4