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M Synofzik

Showing results (21-30 of 32) with videos related to

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Clinical Genetics|June 1, 2011
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patientsN A Schlipf, R Schüle, S Klimpe, et al.
Brain, Behavior, and Immunity|May 10, 2024
Corrigendum to "Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients" [Brain Behav. Immun. 117 (2024) 510-520]H B Duindam, D Mengel, M Kox, et al.
Brain, Behavior, and Immunity|February 9, 2024
Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patientsH B Duindam, D Mengel, M Kox, et al.
Progress in Brain Research|September 4, 2016
A cognitive brain-computer interface for patients with amyotrophic lateral sclerosisM R Hohmann, T Fomina, V Jayaram, et al.
Clinical Genetics|September 24, 2017
Expanding the phenotype of DNAJC3 mutations: A case with hypothyroidism additionally to diabetes mellitus and multisystemic neurodegenerationS K Bublitz, B Alhaddad, M Synofzik, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegiaR Schüle, N Schlipf, M Synofzik, et al.
Cerebellum (London, England)|April 10, 2026
RFC1-related disorders: A case series of 4-aminopyridine and acetyl-DL-leucine treatmentF Heindl, A Traschütz, M Synofzik, et al.
European Journal of Neurology|November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?A Pilotto, C Schulte, A K Hauser, et al.
Cerebellum (London, England)|November 14, 2013
Consensus paper: management of degenerative cerebellar disordersW Ilg, A J Bastian, S Boesch, et al.
Clinical Genetics|March 16, 2017
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegiaB Ozes, N Karagoz, R Schüle, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Clinical Genetics|June 1, 2011
Amplicon-based high-throughput pooled sequencing identifies mutations in CYP7B1 and SPG7 in sporadic spastic paraplegia patientsN A Schlipf, R Schüle, S Klimpe, et al.
Brain, Behavior, and Immunity|May 10, 2024
Corrigendum to "Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients" [Brain Behav. Immun. 117 (2024) 510-520]H B Duindam, D Mengel, M Kox, et al.
Brain, Behavior, and Immunity|February 9, 2024
Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patientsH B Duindam, D Mengel, M Kox, et al.
Progress in Brain Research|September 4, 2016
A cognitive brain-computer interface for patients with amyotrophic lateral sclerosisM R Hohmann, T Fomina, V Jayaram, et al.
Clinical Genetics|September 24, 2017
Expanding the phenotype of DNAJC3 mutations: A case with hypothyroidism additionally to diabetes mellitus and multisystemic neurodegenerationS K Bublitz, B Alhaddad, M Synofzik, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegiaR Schüle, N Schlipf, M Synofzik, et al.
Cerebellum (London, England)|April 10, 2026
RFC1-related disorders: A case series of 4-aminopyridine and acetyl-DL-leucine treatmentF Heindl, A Traschütz, M Synofzik, et al.
European Journal of Neurology|November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?A Pilotto, C Schulte, A K Hauser, et al.
Cerebellum (London, England)|November 14, 2013
Consensus paper: management of degenerative cerebellar disordersW Ilg, A J Bastian, S Boesch, et al.
Clinical Genetics|March 16, 2017
PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegiaB Ozes, N Karagoz, R Schüle, et al.
Pageof 4