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B Schoser

Showing results (21-30 of 37) with videos related to

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Neuromuscular Disorders : NMD|January 29, 2025
Management of presymptomatic juvenile patients with late-onset Pompe disease (LOPD)M Porcino, O Musumeci, C Usbergo, et al.
Neuromuscular Disorders : NMD|May 9, 2018
A zebrafish model for FHL1-opathy reveals loss-of-function effects of human FHL1 mutationsM Keßler, A Kieltsch, E Kayvanpour, et al.
Neurology|August 19, 2009
Consequences of mutations within the C terminus of the FHL1 geneB Schoser, H H Goebel, I Janisch, et al.
Journal of Neurology|September 23, 2008
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and GermanyT Suominen, B Schoser, O Raheem, et al.
Journal of Neurology|December 22, 2010
Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degenerationJ Schessl, M Schuberth, P Reilich, et al.
Neuromuscular Disorders : NMD|January 24, 2018
Falls and resulting fractures in Myotonic Dystrophy: Results from a multinational retrospective surveyA C Jiménez-Moreno, J Raaphorst, H Babačić, et al.
Neuromuscular Disorders : NMD|May 11, 2006
140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on managementB Udd, G Meola, R Krahe, et al.
International Journal of Cardiology|December 26, 2012
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomesV A Sansone, E Brigonzi, B Schoser, et al.
Der Nervenarzt|November 23, 2013
[Diagnosis and therapy of late onset Pompe disease]A Schüller, C Kornblum, M Deschauer, et al.
Molecular Genetics and Metabolism|July 16, 2013
Pain in adult patients with Pompe disease: a cross-sectional surveyD Güngör, A K Schober, M E Kruijshaar, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
Neuromuscular Disorders : NMD|January 29, 2025
Management of presymptomatic juvenile patients with late-onset Pompe disease (LOPD)M Porcino, O Musumeci, C Usbergo, et al.
Neuromuscular Disorders : NMD|May 9, 2018
A zebrafish model for FHL1-opathy reveals loss-of-function effects of human FHL1 mutationsM Keßler, A Kieltsch, E Kayvanpour, et al.
Neurology|August 19, 2009
Consequences of mutations within the C terminus of the FHL1 geneB Schoser, H H Goebel, I Janisch, et al.
Journal of Neurology|September 23, 2008
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and GermanyT Suominen, B Schoser, O Raheem, et al.
Journal of Neurology|December 22, 2010
Long-term efficiency of intravenously administered immunoglobulin in anti-Yo syndrome with paraneoplastic cerebellar degenerationJ Schessl, M Schuberth, P Reilich, et al.
Neuromuscular Disorders : NMD|January 24, 2018
Falls and resulting fractures in Myotonic Dystrophy: Results from a multinational retrospective surveyA C Jiménez-Moreno, J Raaphorst, H Babačić, et al.
Neuromuscular Disorders : NMD|May 11, 2006
140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on managementB Udd, G Meola, R Krahe, et al.
International Journal of Cardiology|December 26, 2012
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomesV A Sansone, E Brigonzi, B Schoser, et al.
Der Nervenarzt|November 23, 2013
[Diagnosis and therapy of late onset Pompe disease]A Schüller, C Kornblum, M Deschauer, et al.
Molecular Genetics and Metabolism|July 16, 2013
Pain in adult patients with Pompe disease: a cross-sectional surveyD Güngör, A K Schober, M E Kruijshaar, et al.
Pageof 4