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Neutral lipid storage disease with myopathy: A 10-year follow-up case report
1847Downloads: 806HTML: 54 -
Prevalence of muscular dystrophy in patients with muscular disorders in Tehran, Iran
1393Downloads: 778HTML: 174 -
Salivary and serum irisin in healthy adults before and after exercise
2251Downloads: 1261HTML: 89 -
Innervation of the thoracolumbar fascia
4433Downloads: 2222HTML: 253 -
Muscle pathology in upper motor neuron paraplegia
2305Downloads: 7065 -
11 | Human immortalized myoblasts/induced pluripotent stem cell derived skeletal muscle model to investigate cystinosis myopathy Jianhao Zhang1, R. Mora De La Serna2, M. Smits2, V. Marini1, A. Wang1, M. Biglietto1, M. Campaner Socias1, L. Rinvenuto1, Z. Ge1, R. Gijsbers2|3, M. Sampaolesi1|4 | 1Translational Cardiomyology Laboratory, Stem Cell and Developmental Biology, Department of Development and Regeneration, KU Leuven, Leuven, Belgium; 2Laboratory for Molecular Virology and Gene Therapy, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium; 3Leuven Viral Vector Core, KU Leuven, Leuven, Belgium; 4Histology and Medical Embryology Unit, Department of Anatomy, Histology, Forensic Medicine and Orthopedics, Sapienza University of Rome, Rome, Italy.
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Abstract 025 | Proteomic profiling of the biofluid marker signature of dystrophinopathies Kay Ohlendieck 1|2, Dieter Swandulla 3, Paul Dowling 1|2 | 1Department of Biology, Maynooth University, Maynooth, Co. Kildare, Ireland; 2Kathleen Lonsdale Institute for Human Health Research, Maynooth University, Maynooth, Co. Kildare, Ireland; 3Institute of Physiology, Faculty of Medicine, University of Bonn, Bonn, Germany.
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