Found: 10
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Primary mitochondrial myopathy: 12-month follow-up results of an Italian cohort.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 12, p. 6555, doi. 10.1007/s00415-022-11324-3
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- Publication type:
- Article
Adult-onset mitochondrial movement disorders: a national picture from the Italian Network.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 3, p. 1413, doi. 10.1007/s00415-021-10697-1
- By:
- Publication type:
- Article
Revisiting mitochondrial ocular myopathies: a study from the Italian Network.
- Published in:
- Journal of Neurology, 2017, v. 264, n. 8, p. 1777, doi. 10.1007/s00415-017-8567-z
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- Publication type:
- Article
Evaluation of muscle biopsy in late-onset GSDII patients before and after enzyme replacement therapy (ERT).
- Published in:
- 2013
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- Publication type:
- Abstract
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Multi-system neurological disease is common in patients with OPA1 mutations.
- Published in:
- Brain: A Journal of Neurology, 2010, v. 133, n. 3, p. 771, doi. 10.1093/brain/awq007
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- Publication type:
- Article
Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene.
- Published in:
- 2009
- By:
- Publication type:
- Report
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report.
- Published in:
- 2008
- By:
- Publication type:
- Correction notice
An apparently sporadic case of oculopharyngeal muscular dystrophy: the first Italian report.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Muscle glycogenoses.
- Published in:
- 2001
- By:
- Publication type:
- journal article