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Life (Basel, Switzerland)|October 27, 2022
Isolation and Characterization of Primary DMD Pig Muscle Cells as an In Vitro Model for Preclinical Research on Duchenne Muscular DystrophyTina Donandt, Stefan Hintze, Sabine Krause, et al.
Life (Basel, Switzerland)|June 28, 2023
Nuclear Small Dystrophin Isoforms during Muscle DifferentiationTina Donandt, Vanessa Todorow, Stefan Hintze, et al.
Human Mutation|February 5, 2011
Alterations of excitation-contraction coupling and excitation coupled Ca(2+) entry in human myotubes carrying CAV3 mutations linked to rippling muscleNina D Ullrich, Dirk Fischer, Cornelia Kornblum, et al.
Brain : a Journal of Neurology|July 3, 2004
Homozygosity for CCTG mutation in myotonic dystrophy type 2Benedikt G H Schoser, Wolfram Kress, Maggie C Walter, et al.
Arthritis and Rheumatism|November 1, 2008
Human muscle cells express the costimulatory molecule B7-H3, which modulates muscle-immune interactionsAnne Waschbisch, Sabine Wintterle, Hanns Lochmüller, et al.
Ideggyogyaszati Szemle|May 12, 2005
[Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family]Rita Horváth, Maggie C Walter, Hanns Lochmüller, et al.
Neuromuscular Disorders : NMD|March 30, 2010
Novel missense mutation p.A310P in the GNE gene in autosomal-recessive hereditary inclusion-body myopathy/distal myopathy with rimmed vacuoles in an Italian familyAndrea Stober, Angelo Aleo, Valerio Kuhl, et al.
Der Nervenarzt|November 20, 2020
[Expert recommendation: treatment of nonambulatory patients with Duchenne muscular dystrophy]Guenther Bernert, Andreas Hahn, Cornelia Köhler, et al.
Neuromuscular Disorders : NMD|October 27, 2021
Congenital myopathy and epidermolysis bullosa due to PLEC variantMaggie C Walter, Peter Reilich, Sabine Krause, et al.
Fortschritte Der Neurologie-Psychiatrie|December 18, 2019
[Spinal Muscular Atrophy - expert recommendations for the use of nusinersen in adult patients]Tim Hagenacker, Andreas Hermann, Christoph Kamm, et al.
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