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Showing results (31-40 of 37) with videos related to

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European Journal of Neurology|January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemiaT Kyriakides, K Aleksovska, C Angelini, et al.
Journal of Neuromuscular Diseases|November 25, 2017
Early-Onset Myopathies: Clinical Findings, Prevalence of Subgroups and Diagnostic Approach in a Single Neuromuscular Referral Center in GermanyK Vill, A Blaschek, D Gläser, et al.
European Journal of Neurology|May 7, 2017
European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experienceA T van der Ploeg, M E Kruijshaar, A Toscano, et al.
Neuropathology and Applied Neurobiology|September 24, 2019
An integrative correlation of myopathology, phenotype and genotype in late onset Pompe diseaseM Kulessa, I Weyer-Menkhoff, L Viergutz, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Neurology|May 19, 2010
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEOC Fratter, G S Gorman, J D Stewart, et al.
Neuromuscular Disorders : NMD|August 18, 2021
1st FSHD European Trial Network workshop:Working towards trial readiness across EuropeN C Voermans, M Vriens-Munoz Bravo, G W Padberg, et al.
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Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
European Journal of Neurology|January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemiaT Kyriakides, K Aleksovska, C Angelini, et al.
Journal of Neuromuscular Diseases|November 25, 2017
Early-Onset Myopathies: Clinical Findings, Prevalence of Subgroups and Diagnostic Approach in a Single Neuromuscular Referral Center in GermanyK Vill, A Blaschek, D Gläser, et al.
European Journal of Neurology|May 7, 2017
European consensus for starting and stopping enzyme replacement therapy in adult patients with Pompe disease: a 10-year experienceA T van der Ploeg, M E Kruijshaar, A Toscano, et al.
Neuropathology and Applied Neurobiology|September 24, 2019
An integrative correlation of myopathology, phenotype and genotype in late onset Pompe diseaseM Kulessa, I Weyer-Menkhoff, L Viergutz, et al.
Acta Neuropathologica Communications|February 5, 2016
New insights into the protein aggregation pathology in myotilinopathy by combined proteomic and immunolocalization analysesA Maerkens, M Olivé, A Schreiner, et al.
Neurology|May 19, 2010
The clinical, histochemical, and molecular spectrum of PEO1 (Twinkle)-linked adPEOC Fratter, G S Gorman, J D Stewart, et al.
Neuromuscular Disorders : NMD|August 18, 2021
1st FSHD European Trial Network workshop:Working towards trial readiness across EuropeN C Voermans, M Vriens-Munoz Bravo, G W Padberg, et al.
Pageof 4