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Janbernd Kirschner

Showing results (61-70 of 173) with videos related to

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Journal of Neurology|June 22, 2017
A multi-source approach to determine SMA incidence and research ready populationIngrid E C Verhaart, Agata Robertson, Rebecca Leary, et al.
Journal of Neurology|December 25, 2014
Adult care for Duchenne muscular dystrophy in the UKSunil Rodger, Katherine L Woods, Catherine L Bladen, et al.
Neuromuscular Disorders : NMD|May 18, 2004
A case of childhood Pompe disease demonstrating phenotypic variability of p.Asp645AsnMarian A Kroos, Janbernd Kirschner, Frank N Gellerich, et al.
Annals of Neurology|December 29, 2004
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeriaJanbernd Kirschner, Thomas Brune, Manfred Wehnert, et al.
Journal of Neuromuscular Diseases|October 10, 2019
Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 - A Prospective Observational StudyMaggie C Walter, Stephan Wenninger, Simone Thiele, et al.
Journal of the Neurological Sciences|February 2, 2010
Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locusMichael Kottlors, Olaf Moske-Eick, Angela Huebner, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|March 12, 2022
Development and Pilot Test of the Registry Evaluation and Quality Standards Tool: An Information Technology-Based Tool to Support and Review RegistriesAlexander Allen, Hannah Patrick, Jorg Ruof, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|November 17, 2016
Long-Term Follow-Up on Health-Related Quality of Life After Mechanical Circulatory Support in ChildrenThilo P K Fleck, Georg Dangel, Felix Bächle, et al.
Journal of Neuromuscular Diseases|May 17, 2024
Increased Diagnostic Yield by Reanalysis of Whole Exome Sequencing Data in Mitochondrial DiseaseCatarina Olimpio, Ida Paramonov, Leslie Matalonga, et al.
CNS Drugs|January 26, 2022
Restoration of Nusinersen Levels Following Treatment Interruption in People With Spinal Muscular Atrophy: Simulations Based on a Population Pharmacokinetic ModelDrew MacCannell, Zdenek Berger, Janbernd Kirschner, et al.
Pageof 18

Showing results (61-70 of 173) with videos related to

Sort By:
Pageof 18
Journal of Neurology|June 22, 2017
A multi-source approach to determine SMA incidence and research ready populationIngrid E C Verhaart, Agata Robertson, Rebecca Leary, et al.
Journal of Neurology|December 25, 2014
Adult care for Duchenne muscular dystrophy in the UKSunil Rodger, Katherine L Woods, Catherine L Bladen, et al.
Neuromuscular Disorders : NMD|May 18, 2004
A case of childhood Pompe disease demonstrating phenotypic variability of p.Asp645AsnMarian A Kroos, Janbernd Kirschner, Frank N Gellerich, et al.
Annals of Neurology|December 29, 2004
p.S143F mutation in lamin A/C: a new phenotype combining myopathy and progeriaJanbernd Kirschner, Thomas Brune, Manfred Wehnert, et al.
Journal of Neuromuscular Diseases|October 10, 2019
Safety and Treatment Effects of Nusinersen in Longstanding Adult 5q-SMA Type 3 - A Prospective Observational StudyMaggie C Walter, Stephan Wenninger, Simone Thiele, et al.
Journal of the Neurological Sciences|February 2, 2010
Late-onset autosomal dominant limb girdle muscular dystrophy and Paget's disease of bone unlinked to the VCP gene locusMichael Kottlors, Olaf Moske-Eick, Angela Huebner, et al.
Value in Health : the Journal of the International Society for Pharmacoeconomics and Outcomes Research|March 12, 2022
Development and Pilot Test of the Registry Evaluation and Quality Standards Tool: An Information Technology-Based Tool to Support and Review RegistriesAlexander Allen, Hannah Patrick, Jorg Ruof, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|November 17, 2016
Long-Term Follow-Up on Health-Related Quality of Life After Mechanical Circulatory Support in ChildrenThilo P K Fleck, Georg Dangel, Felix Bächle, et al.
Journal of Neuromuscular Diseases|May 17, 2024
Increased Diagnostic Yield by Reanalysis of Whole Exome Sequencing Data in Mitochondrial DiseaseCatarina Olimpio, Ida Paramonov, Leslie Matalonga, et al.
CNS Drugs|January 26, 2022
Restoration of Nusinersen Levels Following Treatment Interruption in People With Spinal Muscular Atrophy: Simulations Based on a Population Pharmacokinetic ModelDrew MacCannell, Zdenek Berger, Janbernd Kirschner, et al.
Pageof 18