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Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan.
- Published in:
- Journal of Human Genetics, 2009, v. 54, n. 7, p. 377, doi. 10.1038/jhg.2009.44
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- Article
Clinical and pathological studies of familial amyotrophic lateral sclerosis (FALS) with SOD1 H46R mutation in large Japanese families.
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- Acta Neuropathologica, 2003, v. 106, n. 6, p. 561, doi. 10.1007/s00401-003-0763-5
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- Article
Microbleed clustering in thalamus sign in CADASIL patients with NOTCH3 R75P mutation.
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- Frontiers in Neurology, 2023, p. 01, doi. 10.3389/fneur.2023.1241678
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- Article
Fine mapping of 16q-linked autosomal dominant cerebellar ataxia type III in Japanese families.
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- Neurogenetics, 2004, v. 5, n. 4, p. 215, doi. 10.1007/s10048-004-0194-z
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- Article
Long-term follow-up of patients with Duchenne muscular dystrophy receiving ventilatory support.
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- Muscle & Nerve, 1993, v. 16, n. 5, p. 554, doi. 10.1002/mus.880160519
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- Article