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Cell and Tissue Research|May 15, 2010
Elevated satellite cell number in Duchenne muscular dystrophyMichael Kottlors, Janbernd KirschnerJoint Bone Spine|June 16, 2009
Muscle hypertrophy of the lower leg caused by L5 radiculopathyMichael Kottlors, Klaus Mueller, Janbernd Kirschner, et al.Journal of Perinatal Medicine|September 9, 2021
Postnatal gene therapy for neuromuscular diseases - opportunities and limitationsJanbernd KirschnerHandbook of Clinical Neurology|April 19, 2011
SarcoglycanopathiesJanbernd Kirschner, Hanns LochmüllerDeutsches Arzteblatt International|February 27, 2021
Gene Therapy for Monogenic Inherited DisordersJanbernd Kirschner, Toni CathomenArchives of Neurology|February 18, 2004
The congenital and limb-girdle muscular dystrophies: sharpening the focus, blurring the boundariesJanbernd Kirschner, Carsten G BönnemannJournal 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.Neuropediatrics|August 14, 2019
Decision-Making Regarding Ventilator Support in Children with SMA Type 1-A Cross-Sectional Survey among PhysiciansAstrid Pechmann, Thorsten Langer, Janbernd KirschnerNeuropediatrics|February 23, 2022
Parents' Perspectives on Diagnosis and Decision-Making regarding Ventilator Support in Children with SMA Type 1Astrid Pechmann, Thorsten Langer, Janbernd KirschnerPageof 16