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U Schara

Showing results (11-20 of 25) with videos related to

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Klinische Padiatrie|December 22, 2007
[Muscular magnetic resonance imaging for evaluation of myopathies in children]S A Peters, C Köhler, U Schara, et al.
AJP Reports|July 18, 2014
Administration of Gemcitabine for Metastatic Adenocarcinoma during Pregnancy: A Case Report and Review of the LiteratureM Wiesweg, S Aydin, A Koeninger, et al.
Neuromuscular Disorders : NMD|December 14, 2020
Impaired secretion of platelet granules in patients with Duchenne muscular dystrophy - results of a prospective diagnostic studyD C Schorling, C K Müller, A Pechmann, et al.
Der Nervenarzt|November 5, 2017
[Spinal muscular atrophy : Time for newborn screening?]K Vill, A Blaschek, U Schara, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 15, 2009
Phenotypic variability in siblings with calpainopathy (LGMD2A)J Schessl, M C Walter, G Schreiber, et al.
Neuromuscular Disorders : NMD|October 20, 2009
Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutationsU Schara, N Barisic, M Deschauer, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Neuromuscular Disorders : NMD|December 5, 2013
Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot studyJ Kirschner, D Schorling, D Hauschke, et al.
Molecular and Cellular Pediatrics|June 1, 2026
Post-intensive care sequelae after severe bacterial infections in previously healthy childrenS C Goretzki, C Held, S Tschirner, et al.
Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Klinische Padiatrie|December 22, 2007
[Muscular magnetic resonance imaging for evaluation of myopathies in children]S A Peters, C Köhler, U Schara, et al.
AJP Reports|July 18, 2014
Administration of Gemcitabine for Metastatic Adenocarcinoma during Pregnancy: A Case Report and Review of the LiteratureM Wiesweg, S Aydin, A Koeninger, et al.
Neuromuscular Disorders : NMD|December 14, 2020
Impaired secretion of platelet granules in patients with Duchenne muscular dystrophy - results of a prospective diagnostic studyD C Schorling, C K Müller, A Pechmann, et al.
Der Nervenarzt|November 5, 2017
[Spinal muscular atrophy : Time for newborn screening?]K Vill, A Blaschek, U Schara, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 15, 2009
Phenotypic variability in siblings with calpainopathy (LGMD2A)J Schessl, M C Walter, G Schreiber, et al.
Neuromuscular Disorders : NMD|October 20, 2009
Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutationsU Schara, N Barisic, M Deschauer, et al.
Neurology|June 11, 2003
Rapsyn N88K is a frequent cause of congenital myasthenic syndromes in European patientsJ S Müller, G Mildner, W Müller-Felber, et al.
Neuromuscular Disorders : NMD|December 5, 2013
Somatropin treatment of spinal muscular atrophy: a placebo-controlled, double-blind crossover pilot studyJ Kirschner, D Schorling, D Hauschke, et al.
Molecular and Cellular Pediatrics|June 1, 2026
Post-intensive care sequelae after severe bacterial infections in previously healthy childrenS C Goretzki, C Held, S Tschirner, et al.
Clinical Genetics|April 9, 2015
Diagnostic algorithms in Charcot-Marie-Tooth neuropathies: experiences from a German genetic laboratory on the basis of 1206 index patientsS Rudnik-Schöneborn, D Tölle, J Senderek, et al.
Pageof 3