Found: 4
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A second MNGIE patient without typical mitochondrial skeletal muscle involvement.
- Published in:
- Neurological Sciences, 2010, v. 31, n. 4, p. 491, doi. 10.1007/s10072-010-0225-5
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- Article
A novel mutation in the mitochondrial tRNA<sup>Pro</sup> gene associated with late-onset ataxia, retinitis pigmentosa, deafness, leukoencephalopathy and complex I deficiency.
- Published in:
- European Journal of Human Genetics, 2009, v. 17, n. 8, p. 1092, doi. 10.1038/ejhg.2009.12
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- Article
Structural and metabolic damage in brains of patients with SPG11-related spastic paraplegia as detected by quantitative MRI.
- Published in:
- Journal of Neurology, 2011, v. 258, n. 12, p. 2240, doi. 10.1007/s00415-011-6106-x
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- Publication type:
- Article
Association of the careggi collateral score with radiological outcomes after thrombectomy for stroke with an occlusion of the middle cerebral artery.
- Published in:
- Journal of Thrombosis & Thrombolysis, 2022, v. 54, n. 2, p. 309, doi. 10.1007/s11239-022-02647-z
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- Article