Search Results - "Miyashita, Akinori"

Correction: Polygenic effects on the risk of Alzheimer's disease in the Japanese population.

Authors: Kikuchi, Masataka Miyashita, Akinori Hara, Norikazu et al.

Source: Alzheimer's Research & Therapy. 7/10/2024, Vol. 16 Issue 1, p1-2. 2p.

Polygenic effects on the risk of Alzheimer's disease in the Japanese population.

Authors: Kikuchi, Masataka Miyashita, Akinori Hara, Norikazu et al.

Source: Alzheimer's Research & Therapy. 2/27/2024, Vol. 16 Issue 1, p1-20. 20p.

Neurofibrillary tangle-predominant dementia followed by amyloid β pathology: a clinico-radio-pathological case providing insights into current disease-modifying therapeutic strategy.

Authors: Matsubara, Tomoyasu Ishii, Kenji Saito, Yoko et al.

Source: Acta Neuropathologica Communications. 6/17/2024, Vol. 12 Issue 1, p1-4. 4p.

Novel Aspects of Hereditary Spastic Paraplegia: A Clinicopathologic and Biochemical Study of a Patient With a Heterozygous GCH1 Variant.

Authors: Hongo, Shoko Ikeda, Tetsuhiko Tada, Mari et al.

Source: Neuropathology & Applied Neurobiology. Feb2025, Vol. 51 Issue 1, p1-5. 5p.

Association of Plasma Placental Growth Factor with White Matter Hyperintensities in Alzheimer's Disease.

Authors: Igarashi, Kazuya Tsukie, Tamao Washiyama, Kazuo et al.

Source: Biomolecules (2218-273X). Oct2025, Vol. 15 Issue 10, p1367. 17p.

Clinicopathologic features of two unrelated autopsied patients with Charcot-Marie-Tooth disease carrying MFN2 gene mutation.

Authors: Hayashi, Hideki Saito, Rie Tanaka, Hidetomo et al.

Source: Acta Neuropathologica Communications. 12/20/2023, Vol. 11 Issue 1, p1-6. 6p.

Missense mutation of NRAS is associated with malignant progression in neurocutaneous melanosis.

Authors: Takahashi, Haruhiko Natsumeda, Manabu Hara, Norikazu et al.

Source: Acta Neuropathologica Communications. 1/22/2024, Vol. 12 Issue 1, p1-11. 11p.

Amygdala granular fuzzy astrocytes are independently associated with both LATE neuropathologic change and argyrophilic grains: a study of Japanese series with a low to moderate Braak stage.

Authors: Yokota, Osamu Miki, Tomoko Nakashima-Yasuda, Hanae et al.

Source: Acta Neuropathologica Communications. 9/11/2023, Vol. 11 Issue 1, p1-7. 7p.

Oculopharyngodistal myopathy with coexisting histology of systemic neuronal intranuclear inclusion disease: Clinicopathologic features of an autopsied patient harboring CGG repeat expansions in LRP12.

Authors: Saito, Rie Shimizu, Hiroshi Miura, Takeshi et al.

Source: Acta Neuropathologica Communications. 6/3/2020, Vol. 8 Issue 1, p1-5. 5p.

Brain TDP‐43 pathology in corticobasal degeneration: Topographical correlation with neuronal loss.

Authors: Sainouchi, Makoto Tada, Mari Fitrah, Yusran Ady et al.

Source: Neuropathology & Applied Neurobiology. Apr2022, Vol. 48 Issue 3, p1-12. 12p.

Four‐repeat tauopathies and late‐onset psychiatric disorders: Etiological relevance or incidental findings?

Authors: Yokota, Osamu Miki, Tomoko Ishizu, Hideki et al.

Source: Neuropathology. Feb2023, Vol. 43 Issue 1, p51-71. 21p.

Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases.

Authors: Yamasaki, Maria Makino, Takashi Khor, Seik-Soon et al.

Source: BMC Medical Genomics. 3/29/2020, Vol. 13 Issue 1, p1-13. 13p.

Pure argyrophilic grain disease revisited: independent effects on limbic, neocortical, and striato-pallido-nigral degeneration and the development of dementia in a series with a low to moderate Braak stage.

Authors: Yokota, Osamu Miki, Tomoko Nakashima-Yasuda, Hanae et al.

Source: Acta Neuropathologica Communications. 7/31/2024, Vol. 12 Issue 1, p1-24. 24p.

SORL1 Is Genetically Associated with Late-Onset Alzheimer’s Disease in Japanese, Koreans and Caucasians.

Authors: Miyashita, Akinori Koike, Asako Jun, Gyungah et al.

Source: PLoS ONE. Apr2013, Vol. 8 Issue 4, p1-11. 11p.

Genetic Deficiency of Plasma Lipoprotein-Associated Phospholipase A2 (PLA2G7 V297F Null Mutation) and Risk of Alzheimer's Disease in Japan.

Authors: Koshy, Beena Miyashita, Akinori St. Jean, Pamela et al.

Source: Journal of Alzheimer's Disease. 2010, Vol. 21 Issue 3, p775-780. 6p. 1 Chart, 1 Graph.

Novel CHP1 mutation in autosomal-recessive cerebellar ataxia: autopsy features of two siblings.

Authors: Saito, Rie Hara, Norikazu Tada, Mari et al.

Source: Acta Neuropathologica Communications. 8/12/2020, Vol. 8 Issue 1, p1-6. 6p.

Effective simulations of interacting active droplets.

Authors: Kulkarni, Ajinkya Vidal-Henriquez, Estefania Zwicker, David

Source: Scientific Reports. 1/13/2023, Vol. 13 Issue 1, p1-10. 10p.

Multi‐omics insights into Alzheimer's disease stratification using a microglial polygenic risk score.

Authors: Kikuchi, Masataka Miyashita, Akinori Hirota, Yu et al.

Source: Alzheimer's & dementia: the journal of the Alzheimer's Association Dec2025 Supplement; Vol. 21 (S1).

Journal Info: Publisher: Wiley-Blackwell ISSN: 1552-5260

Association of rare APOE missense variants with Alzheimer's disease in the Japanese population.

Authors: Miyashita, Akinori Obinata, Ai Hara, Norikazu et al.

Source: Alzheimer's & dementia: the journal of the Alzheimer's Association Dec2025 Supplement; Vol. 21 (S1).

Journal Info: Publisher: Wiley-Blackwell ISSN: 1552-5260

Alteration of POLDIP3 Splicing Associated with Loss of Function of TDP-43 in Tissues Affected with ALS.

Authors: Shiga, Atsushi Ishihara, Tomohiko Miyashita, Akinori et al.

Source: PLoS ONE. Aug2012, Vol. 7 Issue 8, Special section p1-11. 11p.