8 results on '"Shimohata T"'
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2. The phenotype spectrum of Japanese multiple system atrophy
3. Identification of independent APP locus duplication in Japanese patients with early-onset Alzheimer disease
4. A novel autosomal dominant cerebellar ataxia associated with tremor. - Clinical features and molecular genetic analysis
5. Expanded polyglutamine stretches associated with CAG repeat diseases interact with [TAF.sub.U]130, interfering with CREB-dependent transcription
6. Neuronal intranuclear accumulation of mutant DRPLA protein with expanded polyglutamine stretches and transcriptional dysregulation in DRPLA transgenic mice (Q129)
7. Five year follow up of a patient with spinal and bulbar muscular atrophy treated with leuprorelin
8. Five year follow up of a patient with spinal and bulbar muscular atrophy treated with leuprorelin
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