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Janbernd Kirschner

Showing results (41-50 of 173) with videos related to

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Pharmacoeconomics|December 14, 2022
Caregiver Burden of Spinal Muscular Atrophy: A Systematic ReviewErik Landfeldt, Sophia Abner, Astrid Pechmann, et al.
Molecular and Cellular Probes|November 15, 2013
High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiencyMaria de los Angeles Beytía, Gabriele Dekomien, Sabine Hoffjan, et al.
Journal of Neuromuscular Diseases|January 11, 2021
Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec -A Single Centre ExperienceJohannes Friese, Stephanie Geitmann, Dorothea Holzwarth, et al.
The Patient|February 5, 2019
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic ReviewErik Landfeldt, Josefin Edström, Cecilia Jimenez-Moreno, et al.
Arthritis Research & Therapy|October 31, 2012
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathyNils Venhoff, Dirk Lebrecht, Dietmar Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 14, 2021
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiencyJan Schönberger, Matthias Eckenweiler, Kerstin Alexandra Klotz, et al.
Developmental Medicine and Child Neurology|March 18, 2006
'Why do children with cerebral palsy discontinue therapy with botulinum toxin A?'Michaela Linder-Lucht, Janbernd Kirschner, Jochen Herrmann, et al.
Antiviral Therapy|March 4, 2014
Zidovudine induces visceral mitochondrial toxicity and intra-abdominal fat gain in a rodent model of lipodystrophyUlrich A Walker, Dirk Lebrecht, Wilfried Reichard, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Neuropediatrics|June 20, 2017
Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of LiteratureDavid C Schorling, Tobias Dietel, Christina Evers, et al.
Pageof 18

Showing results (41-50 of 173) with videos related to

Sort By:
Pageof 18
Pharmacoeconomics|December 14, 2022
Caregiver Burden of Spinal Muscular Atrophy: A Systematic ReviewErik Landfeldt, Sophia Abner, Astrid Pechmann, et al.
Molecular and Cellular Probes|November 15, 2013
High creatine kinase levels and white matter changes: clinical and genetic spectrum of congenital muscular dystrophies with laminin alpha-2 deficiencyMaria de los Angeles Beytía, Gabriele Dekomien, Sabine Hoffjan, et al.
Journal of Neuromuscular Diseases|January 11, 2021
Safety Monitoring of Gene Therapy for Spinal Muscular Atrophy with Onasemnogene Abeparvovec -A Single Centre ExperienceJohannes Friese, Stephanie Geitmann, Dorothea Holzwarth, et al.
The Patient|February 5, 2019
Health-Related Quality of Life in Patients with Adult-Onset Myotonic Dystrophy Type 1: A Systematic ReviewErik Landfeldt, Josefin Edström, Cecilia Jimenez-Moreno, et al.
Arthritis Research & Therapy|October 31, 2012
Muscle-fiber transdifferentiation in an experimental model of respiratory chain myopathyNils Venhoff, Dirk Lebrecht, Dietmar Pfeifer, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|June 14, 2021
Facilitation of drug-resistant epilepsy and catastrophic status epilepticus in children with combined pituitary hormone deficiencyJan Schönberger, Matthias Eckenweiler, Kerstin Alexandra Klotz, et al.
Developmental Medicine and Child Neurology|March 18, 2006
'Why do children with cerebral palsy discontinue therapy with botulinum toxin A?'Michaela Linder-Lucht, Janbernd Kirschner, Jochen Herrmann, et al.
Antiviral Therapy|March 4, 2014
Zidovudine induces visceral mitochondrial toxicity and intra-abdominal fat gain in a rodent model of lipodystrophyUlrich A Walker, Dirk Lebrecht, Wilfried Reichard, et al.
Orphanet Journal of Rare Diseases|October 24, 2013
The TREAT-NMD care and trial site registry: an online registry to facilitate clinical research for neuromuscular diseasesSunil Rodger, Hanns Lochmüller, Adrian Tassoni, et al.
Neuropediatrics|June 20, 2017
Expanding Phenotype of De Novo Mutations in GNAO1: Four New Cases and Review of LiteratureDavid C Schorling, Tobias Dietel, Christina Evers, et al.
Pageof 18