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Whole-exome sequencing in patients with protein aggregate myopathies reveals causative mutations associated with novel atypical phenotypes.
- Published in:
- Neurological Sciences, 2021, v. 42, n. 7, p. 2819, doi. 10.1007/s10072-020-04876-7
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- Publication type:
- Article
Benign acute viral myositis in African migrants: A clinical, serological, and pathological study.
- Published in:
- 2019
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- Publication type:
- journal article
Non-Hematologic Toxicity of Bortezomib in Multiple Myeloma: The Neuromuscular and Cardiovascular Adverse Effects.
- Published in:
- Cancers, 2020, v. 12, n. 9, p. 2540, doi. 10.3390/cancers12092540
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- Article
A novel in‐frame deletion in MYOT causes an early adult onset distal myopathy.
- Published in:
- Clinical Genetics, 2023, v. 104, n. 6, p. 705, doi. 10.1111/cge.14413
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- Publication type:
- Article
Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy.
- Published in:
- European Journal of Neuroscience, 2022, v. 56, n. 3, p. 4214, doi. 10.1111/ejn.15728
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- Publication type:
- Article
Multiple acyl-COA dehydrogenase deficiency in elderly carriers.
- Published in:
- Journal of Neurology, 2020, v. 267, n. 5, p. 1414, doi. 10.1007/s00415-020-09729-z
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- Publication type:
- Article
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey.
- Published in:
- Neurogenetics, 2020, v. 21, n. 2, p. 87, doi. 10.1007/s10048-019-00601-5
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- Publication type:
- Article