Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Janbernd Kirschner

Showing results (51-60 of 173) with videos related to

Pageof 18
Sort By:
The Lancet. Neurology|May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy developmentRachel Thompson, Sally Spendiff, Andreas Roos, et al.
Muscle & Nerve|August 23, 2008
Predominant fiber atrophy and fiber type disproportion in early ullrich diseaseJoachim Schessl, Nathalie M Goemans, Alexandra I Magold, et al.
Orphanet Journal of Rare Diseases|June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in GermanyKirsten König, Astrid Pechmann, Simone Thiele, et al.
AIDS (London, England)|December 25, 2009
Oral uridine supplementation antagonizes the peripheral neuropathy and encephalopathy induced by antiretroviral nucleoside analoguesNils Venhoff, Dirk Lebrecht, Catherine Deveaud, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|September 10, 2010
Role of pyrimidine depletion in the mitochondrial cardiotoxicity of nucleoside analogue reverse transcriptase inhibitorsKerstin Balcarek, Nils Venhoff, Catherine Deveaud, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 2, 2020
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online surveyDavid C Schorling, Cornelia K Müller, Astrid Pechmann, et al.
Neuromuscular Disorders : NMD|March 6, 2015
Two novel nebulin variants in an adult patient with congenital nemaline myopathyAnne K Güttsches, Gabriele Dekomien, Kristl G Claeys, et al.
Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.
Orphanet Journal of Rare Diseases|August 13, 2025
Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysisJoanna Diesing, Janbernd Kirschner, Astrid Pechmann, et al.
Journal of Neuromuscular Diseases|September 24, 2023
A Mixed-method Approach to Develop an Ambulatory Module of the SMA Independence ScaleHannah Staunton, Sophie Cleanthous, Vanda Teodoro, et al.
Pageof 18

Showing results (51-60 of 173) with videos related to

Sort By:
Pageof 18
The Lancet. Neurology|May 30, 2020
Advances in the diagnosis of inherited neuromuscular diseases and implications for therapy developmentRachel Thompson, Sally Spendiff, Andreas Roos, et al.
Muscle & Nerve|August 23, 2008
Predominant fiber atrophy and fiber type disproportion in early ullrich diseaseJoachim Schessl, Nathalie M Goemans, Alexandra I Magold, et al.
Orphanet Journal of Rare Diseases|June 26, 2019
De-duplicating patient records from three independent data sources reveals the incidence of rare neuromuscular disorders in GermanyKirsten König, Astrid Pechmann, Simone Thiele, et al.
AIDS (London, England)|December 25, 2009
Oral uridine supplementation antagonizes the peripheral neuropathy and encephalopathy induced by antiretroviral nucleoside analoguesNils Venhoff, Dirk Lebrecht, Catherine Deveaud, et al.
Journal of Acquired Immune Deficiency Syndromes (1999)|September 10, 2010
Role of pyrimidine depletion in the mitochondrial cardiotoxicity of nucleoside analogue reverse transcriptase inhibitorsKerstin Balcarek, Nils Venhoff, Catherine Deveaud, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|July 2, 2020
Coagulation disorders in Duchenne muscular dystrophy? Results of a registry-based online surveyDavid C Schorling, Cornelia K Müller, Astrid Pechmann, et al.
Neuromuscular Disorders : NMD|March 6, 2015
Two novel nebulin variants in an adult patient with congenital nemaline myopathyAnne K Güttsches, Gabriele Dekomien, Kristl G Claeys, et al.
Neuromuscular Disorders : NMD|November 20, 2020
Tasks and interfaces in primary and specialized palliative care for Duchenne muscular dystrophy - A patients' perspectiveMaria Janisch, Kristin Boehme, Simone Thiele, et al.
Orphanet Journal of Rare Diseases|August 13, 2025
Epidemiology, disease burden and costs of Duchenne muscular dystrophy in Germany: an observational, retrospective health claims data analysisJoanna Diesing, Janbernd Kirschner, Astrid Pechmann, et al.
Journal of Neuromuscular Diseases|September 24, 2023
A Mixed-method Approach to Develop an Ambulatory Module of the SMA Independence ScaleHannah Staunton, Sophie Cleanthous, Vanda Teodoro, et al.
Pageof 18