Search Results - "Hara, Norikazu"

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.

An early-onset case of adult-onset autosomal dominant leukodystrophy.

Authors: Mihashi, Izumi Ishii, Kazuhiro Hara, Norikazu et al.

Source: Neurological Sciences. Nov2024, Vol. 45 Issue 11, p5543-5545. 3p.

Subjects: Demyelination, Neuromyelitis optica, Symptoms, Nerve conduction studies, Neurological disorders, Leukodystrophy

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.

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.

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.

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.

Heterogenous Genetic, Clinical, and Imaging Features in Patients with Neuronal Intranuclear Inclusion Disease Carrying NOTCH2NLC Repeat Expansion.

Authors: Fitrah, Yusran Ady Higuchi, Yo Hara, Norikazu et al.

Source: Brain Sciences (2076-3425). Jun2023, Vol. 13 Issue 6, p955. 14p.

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.

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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.

Different CprABC amino acid sequences affect nisin A susceptibility in Clostridioides difficile isolates.

Authors: Ide, Noriaki Kawada-Matsuo, Miki Le, Mi Nguyen-Tra et al.

Source: PLoS ONE. 1/20/2023, Vol. 18 Issue 1, p1-18. 18p.

Age-related demethylation of the TDP-43 autoregulatory region in the human motor cortex.

Authors: Koike, Yuka Sugai, Akihiro Hara, Norikazu et al.

Source: Communications Biology. 9/21/2021, Vol. 4 Issue 1, p1-11. 11p.

Enhancer variants associated with Alzheimer's disease affect gene expression via chromatin looping.

Authors: Kikuchi, Masataka Hara, Norikazu Hasegawa, Mai et al.

Source: BMC Medical Genomics. 9/9/2019, Vol. 12 Issue 1, pN.PAG-N.PAG. 1p.

A novel missense variant of PSEN2 in a Japanese woman with hereditary Alzheimer's disease.

Authors: Nakamura, Katsuya Kasuga, Kazuki Yuzawa, Chinami et al.

Source: Alzheimer's & dementia: the journal of the Alzheimer's Association Dec2025 Supplement; Vol. 21 (S6).

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

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

Case of Barrett's adenocarcinoma with marked endoscopic morphological changes in Barrett's esophagus over a long follow-up period of 15 years.

Authors: Iwaya, Yugo Yamazaki, Tomoo Watanabe, Takayuki et al.

Source: Digestive Endoscopy. Jul2016, Vol. 28 Issue 5, p607-610. 4p.

Frequent Germline and Somatic Single Nucleotide Variants in the Promoter Region of the Ribosomal RNA Gene in Japanese Lung Adenocarcinoma Patients.

Authors: Ohashi, Riuko Umezu, Hajime Sato, Ayako et al.

Source: Cells (2073-4409). Nov2020, Vol. 9 Issue 11, p2409. 1p.