Works matching AU Yasuda, Rei
Results: 9
Aberrant astrocyte Ca<sup>2+</sup> signals “AxCa signals” exacerbate pathological alterations in an Alexander disease model.
- Published in:
- Glia, 2018, v. 66, n. 5, p. 1053, doi. 10.1002/glia.23300
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- Publication type:
- Article
Characteristics of cerebral lesions in adult-onset Alexander disease.
- Published in:
- 2020
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- Publication type:
- Letter
Towards genomic database of Alexander disease to identify variations modifying disease phenotype.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-51390-8
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- Publication type:
- Article
Clinical and radiological characteristics of older‐adult‐onset Alexander disease.
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- European Journal of Neurology, 2021, v. 28, n. 11, p. 3760, doi. 10.1111/ene.15017
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- Publication type:
- Article
Quantitative Evaluation of Brain Stem Atrophy Using Magnetic Resonance Imaging in Adult Patients with Alexander Disease.
- Published in:
- European Neurology, 2017, v. 77, n. 5/6, p. 296, doi. 10.1159/000475661
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- Publication type:
- Article
Substitution of Glu to Lys at Codon 332 on the GFAP Gene Alone Is Causative for Adult-onset Alexander Disease.
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- Internal Medicine, 2024, v. 63, n. 2, p. 309, doi. 10.2169/internalmedicine.1726-23
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- Publication type:
- Article
Recurrent ischemic strokes and elevated CA125 levels in a patient with Meigs syndrome: A case report.
- Published in:
- 2025
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- Publication type:
- Case Study
An autopsy case of intravascular large B‐cell lymphoma showing a rapid transition to embolic strokes with occlusion of the major cerebral arteries.
- Published in:
- Neuropathology, 2024, v. 44, n. 2, p. 135, doi. 10.1111/neup.12940
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- Publication type:
- Article
A Japanese case of oculopharyngeal muscular dystrophy (OPMD) with PABPN1 c.35G > C; p.Gly12Ala point mutation.
- Published in:
- 2021
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- Publication type:
- journal article