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BMC Medical Genetics|September 18, 2013
Facioscapulohumeral muscular dystrophy and Charcot-Marie-Tooth neuropathy 1A - evidence for "double trouble" overlapping syndromesOlivia Schreiber, Peter Schneiderat, Wolfram Kress, et al.
Health and Quality of Life Outcomes|October 10, 2023
Inclusion body myositis-health-related quality of life and care situation during phases of the "patience journey" in Germany: results from a qualitative studyKatja C Senn, Simone Thiele, Laura Gumbert, et al.
Neuromuscular Disorders : NMD|January 27, 2009
Eosinophilic myositis as presenting symptom in gamma-sarcoglycanopathySarah K Baumeister, Slobodanka Todorovic, Vedrana Milić-Rasić, et al.
Orphanet Journal of Rare Diseases|June 16, 2022
The health-related quality of life, mental health and mental illnesses of patients with inclusion body myositis (IBM): results of a mixed methods systematic reviewKatja C Senn, Laura Gumbert, Simone Thiele, et al.
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.
Journal of Neurology|June 25, 2024
Analysis and occurrence of biallelic pathogenic repeat expansions in RFC1 in a German cohort of patients with a main clinical phenotype of motor neuron diseaseAnnalisa Schaub, Hannes Erdmann, Veronika Scholz, et al.
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