Found: 3
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Adult-onset nemaline myopathy due to a novel homozygous variant in the TNNT1 gene.
- Published in:
- 2022
- By:
- Publication type:
- letter
Distal hereditary motor neuronopathy as a new phenotype associated with variants in BAG3.
- Published in:
- Journal of Neurology, 2024, v. 271, n. 2, p. 986, doi. 10.1007/s00415-023-12039-9
- By:
- Publication type:
- Article
Serum GDF-15 Levels Accurately Differentiate Patients with Primary Mitochondrial Myopathy, Manifesting with Exercise Intolerance and Fatigue, from Patients with Chronic Fatigue Syndrome.
- Published in:
- Journal of Clinical Medicine, 2023, v. 12, n. 6, p. 2435, doi. 10.3390/jcm12062435
- By:
- Publication type:
- Article