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RIG-I expression in perifascicular myofibers is a reliable biomarker of dermatomyositis.
- Published in:
- Arthritis Research & Therapy, 2017, v. 19, p. 1, doi. 10.1186/s13075-017-1383-0
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- Article
Preclinical Research in Glycogen Storage Diseases: A Comprehensive Review of Current Animal Models.
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- International Journal of Molecular Sciences, 2020, v. 21, n. 24, p. 9621, doi. 10.3390/ijms21249621
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- Article
Proteasome inhibitors reduce thrombospondin-1 release in human dysferlin-deficient myotubes.
- Published in:
- 2020
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- Publication type:
- journal article
Pathophysiological Underpinnings of Extra-Motor Neurodegeneration in Amyotrophic Lateral Sclerosis: New Insights From Biomarker Studies.
- Published in:
- Frontiers in Neurology, 2022, p. 1, doi. 10.3389/fneur.2021.750543
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- Article
Comparison of Dysferlin Expression in Human Skeletal Muscle with That in Monocytes for the Diagnosis of Dysferlin Myopathy.
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- PLoS ONE, 2011, v. 6, n. 12, p. 1, doi. 10.1371/journal.pone.0029061
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- Article
Antibodies against disialosyl and terminal NeuNAc( α2-3)Gal ganglioside epitopes in acute relapsing sensory ataxic neuropathy.
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- Journal of Neurology, 2008, v. 255, n. 5, p. 764, doi. 10.1007/s00415-008-0803-0
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- Publication type:
- Article
1α,25(OH)<sub>2</sub>-Vitamin D3 Increases Dysferlin Expression in vitro and in a Human Clinical Trial.
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- Molecular Therapy, 2012, v. 20, n. 10, p. 1988, doi. 10.1038/mt.2012.156
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- Publication type:
- Article
Downregulation of miR-335-5P in Amyotrophic Lateral Sclerosis Can Contribute to Neuronal Mitochondrial Dysfunction and Apoptosis.
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- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-61246-1
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- Publication type:
- Article
Knock-in mice for the R50X mutation in the PYGM gene present with McArdle disease.
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- Brain: A Journal of Neurology, 2012, v. 135, n. 7, p. 2048, doi. 10.1093/brain/aws141
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- Article
Autoantibody screening in Guillain-Barré syndrome.
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- 2021
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- Publication type:
- journal article
Identification of serum microRNAs as potential biomarkers in Pompe disease.
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- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 7, p. 1214, doi. 10.1002/acn3.50800
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- Publication type:
- Article
A novel, blood-based diagnostic assay for limb girdle muscular dystrophy 2B and Miyoshi myopathy.
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- 2002
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- Publication type:
- journal article
Nintedanib decreases muscle fibrosis and improves muscle function in a murine model of dystrophinopathy.
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- Cell Death & Disease, 2018, v. 9, n. 7, p. 1, doi. 10.1038/s41419-018-0792-6
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- Article
Genetic and Epigenetic Determinants of Low Dysferlin Expression in Monocytes.
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- Human Mutation, 2014, v. 35, n. 8, p. 990, doi. 10.1002/humu.22591
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- Article
Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-41414-8
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- Publication type:
- Article
RhoA/ROCK2 signalling is enhanced by PDGF‐AA in fibro‐adipogenic progenitor cells: implications for Duchenne muscular dystrophy.
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- Journal of Cachexia, Sarcopenia & Muscle, 2022, v. 13, n. 2, p. 1373, doi. 10.1002/jcsm.12923
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- Article
Clinical and serological features of acute sensory ataxic neuropathy with antiganglioside antibodies.
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- Journal of the Peripheral Nervous System, 2012, v. 17, n. 2, p. 158, doi. 10.1111/j.1529-8027.2012.00407.x
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- Article
Proteomics identification of differentially expressed proteins in the muscle of dysferlin myopathy patients.
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- Proteomics - Clinical Applications, 2009, v. 3, n. 4, p. 486, doi. 10.1002/prca.200800087
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- Publication type:
- Article