Found: 7
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Japanese case of Emery-Dreifuss muscular dystrophy with a novel LMNA missense mutation.
- Published in:
- Neurology & Clinical Neuroscience, 2016, v. 4, n. 3, p. 124, doi. 10.1111/ncn3.12047
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- Publication type:
- Article
Impaired insulin signal transduction in neurons may be involved in β-amyloid-induced hyperphosphorylation of tau
- Published in:
- 2011
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- Publication type:
- Abstract
Reduced bowel sounds in Parkinson's disease and multiple system atrophy patients.
- Published in:
- Clinical Autonomic Research, 2011, v. 21, n. 3, p. 181, doi. 10.1007/s10286-010-0102-6
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- Publication type:
- Article
A Fulminant Case of Granulomatosis with Polyangiitis with Meningeal and Parenchymal Involvement.
- Published in:
- Case Reports in Neurology, 2015, v. 7, n. 1, p. 101, doi. 10.1159/000381942
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- Publication type:
- Article
A Patient with Fragile X-Associated Tremor/Ataxia Syndrome Presenting with Executive Cognitive Deficits and Cerebral White Matter Lesions.
- Published in:
- Case Reports in Neurology, 2011, v. 3, n. 2, p. 118, doi. 10.1159/000328838
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- Publication type:
- Article
Evidence for a Common Founder and Clinical Characteristics of Japanese Families with the MAPT R406W Mutation.
- Published in:
- Dementia & Geriatric Cognitive Disorders Extra, 2011, v. 1, n. 1, p. 267, doi. 10.1159/000331243
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- Publication type:
- Article
Development of a Novel Nutrition-Related Multivariate Biomarker for Mild Cognitive Impairment Based on the Plasma Free Amino Acid Profile.
- Published in:
- Nutrients, 2022, v. 14, n. 3, p. 637, doi. 10.3390/nu14030637
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- Publication type:
- Article