Works by Onodera, Osamu

Results: 157

Clinical utility of CSF Aβ38 in Japanese research and clinical cohorts.

Published in:

Alzheimer's & Dementia: Diagnosis, Assessment & Disease Monitoring, 2025, v. 17, n. 2, p. 1, doi. 10.1002/dad2.70125

By:

Tsukie, Tamao;
Kasuga, Kensaku;
Kikuchi, Masataka;
Ishiguro, Takanobu;
Miyashita, Akinori;
Onodera, Osamu;
Iwatsubo, Takeshi;
Ikeuchi, Takeshi

Publication type:

Article

A case of cerebral amyloid angiopathy with ipsilateral tau and contralateral amyloid PET uptake related to cadaveric dura mater implanted in childhood.

Published in:

European Journal of Nuclear Medicine & Molecular Imaging, 2025, v. 52, n. 8, p. 2737, doi. 10.1007/s00259-024-07030-z

By:

Hatakeyama, Yuki;
Kimura, Atsushi Michael;
Tsuboguchi, Shintaro;
Ratanov, Mikhail;
Nakamura, Kosei;
Hatakeyama, Masahiro;
Nakamura, Yukimi;
Watanabe, Masaki;
Murakami, Yoshihiro;
Saito, Yuko;
Murayama, Shigeo;
Kasuga, Kensaku;
Ikeuchi, Takeshi;
Igarashi, Hironaka;
Onodera, Osamu;
Shimada, Hitoshi

Publication type:

Article

Identification of novel SNPs of ABCD1, ABCD2, ABCD3, and ABCD4 genes in patients with X-linked adrenoleukodystrophy (ALD) based on comprehensive resequencing and association studies with ALD phenotypes.

Published in:

Neurogenetics, 2011, v. 12, n. 1, p. 41, doi. 10.1007/s10048-010-0253-6

By:

Matsukawa, Takashi;
Asheuer, Muriel;
Takahashi, Yuji;
Goto, Jun;
Suzuki, Yasuyuki;
Shimozawa, Nobuyuki;
Takano, Hiroki;
Onodera, Osamu;
Nishizawa, Masatoyo;
Aubourg, Patrick;
Tsuji, Shoji

Publication type:

Article

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

Published in:

Communications Biology, 2021, v. 4, n. 1, p. 1, doi. 10.1038/s42003-021-02621-0

By:

Koike, Yuka;
Sugai, Akihiro;
Hara, Norikazu;
Ito, Junko;
Yokoseki, Akio;
Ishihara, Tomohiko;
Yamagishi, Takuma;
Tsuboguchi, Shintaro;
Tada, Mari;
Ikeuchi, Takeshi;
Kakita, Akiyoshi;
Onodera, Osamu

Publication type:

Article

Inappropriate interpretation of non‐pathogenic HTRA1 variant as pathogenic.

Published in:

Annals of Clinical & Translational Neurology, 2023, v. 10, n. 7, p. 1261, doi. 10.1002/acn3.51817

By:

Uemura, Masahiro;
Kitahara, Sho;
Kato, Taisuke;
Nozaki, Hiroaki;
Ando, Shoichiro;
Ishihara, Tomohiko;
Onodera, Osamu

Publication type:

Article

Pyloric-gland metaplasia may be an origin of cancer and intestinal metaplasia with possible CDX2 expression.

Published in:

Gastroenterology Report, 2021, v. 9, n. 4, p. 370, doi. 10.1093/gastro/goaa061

By:

Yagi, Kazuyoshi;
Tsuchiya, Atsunori;
Hashimoto, Satoru;
Kato, Taisuke;
Onodera, Osamu;
Terai, Shuji

Publication type:

Article

Do patients with multiple system atrophy have decreased nocturnal urinary concentration?

Published in:

2021

By:

Sakata, Yusuke;
Kanazawa, Masato;
Hatakeyama, Masahiro;
Konno, Takuya;
Ozawa, Tetsutaro;
Onodera, Osamu

Publication type:

Letter

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

By:

Ozawa, Tetsutaro;
Saji, Etsuji;
Yajima, Ryuji;
Onodera, Osamu;
Nishizawa, Masatoyo

Publication type:

Article

C9ORF72 repeat-associated non- ATG-translated polypeptides are distributed independently of TDP-43 in a Japanese patient with c9 ALS.

Published in:

Neuropathology & Applied Neurobiology, 2014, v. 40, n. 6, p. 783, doi. 10.1111/nan.12157

By:

Konno, Takuya;
Tada, Mari;
Shiga, Atsushi;
Tsujino, Akira;
Eguchi, Hiroto;
Masuda‐Suzukake, Masami;
Hasegawa, Masato;
Nishizawa, Masatoyo;
Onodera, Osamu;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Progressive myoclonus epilepsy: extraneuronal brown pigment deposition and system neurodegeneration in the brains of Japanese patients with novel SCARB2 mutations.

Published in:

Neuropathology & Applied Neurobiology, 2014, v. 40, n. 5, p. 551, doi. 10.1111/nan.12057

By:

Fu, Yong‐Juan;
Aida, Izumi;
Tada, Masayoshi;
Tada, Mari;
Toyoshima, Yasuko;
Takeda, Shigeki;
Nakajima, Takashi;
Naito, Haruhiko;
Nishizawa, Masatoyo;
Onodera, Osamu;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Novel Mutation in EIF2B Gene in a Case of Adult-Onset Leukoencephalopathy with Vanishing White Matter.

Published in:

European Neurology, 2007, v. 57, n. 1, p. 57, doi. 10.1159/000097120

By:

Matsui, Masaru;
Mizutani, Kotaro;
Ohtake, Hiroaki;
Miki, Yukio;
Ishizu, Koichi;
Fukuyama, Hidenao;
Shimohata, Takayoshi;
Onodera, Osamu;
Nishizawa, Masatoyo;
Takayama, Yoshihiro;
Shibasaki, Hiroshi

Publication type:

Article

Pathological and Clinical Spectrum of Progressive Supranuclear Palsy: With Special Reference to Astrocytic Tau Pathology.

Published in:

Brain Pathology, 2016, v. 26, n. 2, p. 155, doi. 10.1111/bpa.12265

By:

Yokoyama, Yuichi;
Toyoshima, Yasuko;
Shiga, Atsushi;
Tada, Mari;
Kitamura, Hideaki;
Hasegawa, Kazuko;
Onodera, Osamu;
Ikeuchi, Takeshi;
Someya, Toshiyuki;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Early-onset ataxia with ocular motor apraxia and hypoalbuminemia is caused by mutations in a new HIT superfamily gene.

Published in:

Nature Genetics, 2001, v. 29, n. 2, p. 184, doi. 10.1038/ng1001-184

By:

Date, Hidetoshi;
Onodera, Osamu;
Tanaka, Hajime;
Iwabuchi, Kiyoshi;
Uekawa, Kazutoshi;
Igarashi, Shuichi;
Koike, Ryoko;
Hiroi, Tadashi;
Yuasa, Tatsuhiko;
Awaya, Yutaka;
Sakai, Tetsuo;
Takahashi, Tatsuya;
Nagatomo, Hideki;
Sekijima, Yoshiki;
Kawachi, Izumi;
Takiyama, Yoshihisa;
Nishizawa, Masatoyo;
Fukuhara, Nobuyoshi;
Saito, Kayoko

Publication type:

Article

Expanded polyglutamine stretches interact with TAF<sub>II</sub>130, interfering with CREB-dependent transcription.

Published in:

Nature Genetics, 2000, v. 26, n. 1, p. 29, doi. 10.1038/79139

By:

Shimohata, Takayoshi;
Nakajima, Toshihiro;
Yamada, Mitsunori;
Uchida, Chiharu;
Onodera, Osamu;
Naruse, Satoshi;
Kimura, Tetsuya;
Koide, Reiji;
Nozaki, Kenkichi;
Sano, Yasuteru;
Ishiguro, Hiroshi;
Sakoe, Kumi;
Ooshima, Takayuki;
Sato, Aki;
Ikeuchi, Takeshi;
Oyake, Mutsuo;
Sato, Toshiya;
Aoyagi, Yasuyuki;
Hozumi, Isao

Publication type:

Article

Multiple system atrophy: clinicopathological characteristics in Japanese patients.

Published in:

Proceedings of the Japan Academy, Series B Physical & biological sciences, 2017, v. 93, n. 5, p. 251, doi. 10.2183/pjab.93.016

By:

Tetsutaro OZAWA;
Osamu ONODERA

Publication type:

Article

A case of isolated dystextia due to subcortical infarction: a novel condition of digital device era.

Published in:

2024

By:

Hatakeyama, Masahiro;
Kanayama, Takeshi;
Tokunaga, Saori;
Kizaki, Toshiya;
Tsuboguchi, Shintaro;
Kanazawa, Masato;
Onodera, Osamu

Publication type:

Case Study

A case report of reversible cerebral vasoconstriction syndrome with thunderclap headache significantly exacerbated in the supine position and alleviated in the standing position.

Published in:

2023

By:

Toyama, Genri;
Tsuboguchi, Shintaro;
Igarashi, Kazuya;
Saji, Etsuji;
Konno, Takuya;
Onodera, Osamu

Publication type:

Case Study

Accuracy of a machine learning method based on structural and locational information from AlphaFold2 for predicting the pathogenicity of TARDBP and FUS gene variants in ALS.

Published in:

BMC Bioinformatics, 2023, v. 24, n. 1, p. 1, doi. 10.1186/s12859-023-05338-5

By:

Hatano, Yuya;
Ishihara, Tomohiko;
Onodera, Osamu

Publication type:

Article

Quantitative evaluation of brainstem involvement in multiple system atrophy by diffusion-weighted MR imaging.

Published in:

Journal of Neurology, 2004, v. 251, n. 9, p. 1121, doi. 10.1007/s00415-004-0494-0

By:

Kanazawa, Masato;
Shimohata, Takayoshi;
Terajima, Kenshi;
Onodera, Osamu;
Tanaka, Keiko;
Tsuji, Shoji;
Okamoto, Kouichirou;
Nishizawa, Masatoyo

Publication type:

Article

Long-term disability and prognosis in dentatorubral-pallidoluysian atrophy: A correlation with CAG repeat length.

Published in:

Movement Disorders, 2010, v. 25, n. 11, p. 1694, doi. 10.1002/mds.23167

By:

Hasegawa, Arika;
Ikeuchi, Takeshi;
Koike, Ryoko;
Matsubara, Nae;
Tsuchiya, Miyuki;
Nozaki, Hiroaki;
Homma, Atsushi;
Idezuka, Jiro;
Nishizawa, Masatoyo;
Onodera, Osamu

Publication type:

Article

Novel GFAP mutation in patient with adult-onset Alexander disease presenting with spastic ataxia.

Published in:

Movement Disorders, 2009, v. 24, n. 9, p. 1393, doi. 10.1002/mds.22556

By:

Kaneko, Hiroyuki;
Hirose, Masaki;
Katada, Shinichi;
Takahashi, Toshiaki;
Naruse, Satoshi;
Tsuchiya, Miyuki;
Yoshida, Tomokatsu;
Nakagawa, Masanori;
Onodera, Osamu;
Nishizawa, Masatoyo;
Ikeuchi, Takeshi

Publication type:

Article

Sacsin-related ataxia with neither retinal hypermyelination nor spasticity.

Published in:

Movement Disorders, 2007, v. 22, n. 9, p. 1362, doi. 10.1002/mds.21557

By:

Hara, Kenju;
Shimbo, Junsuke;
Nozaki, Hiroaki;
Kikugawa, Koki;
Onodera, Osamu;
Nishizawa, Masatoyo

Publication type:

Article

Clinical and genetic characterizations of 16q-linked autosomal dominant spinocerebellar ataxia (AD-SCA) and frequency analysis of AD-SCA in the Japanese population.

Published in:

Movement Disorders, 2007, v. 22, n. 6, p. 857, doi. 10.1002/mds.21443

By:

Nozaki, Hiroaki;
Ikeuchi, Takeshi;
Kawakami, Akio;
Kimura, Akio;
Koide, Reiji;
Tsuchiya, Miyuki;
Nakmura, Yuusaku;
Mutoh, Tatsuro;
Yamamoto, Hiroko;
Nakao, Naoki;
Sahashi, Ko;
Nishizawa, Masatoyo;
Onodera, Osamu

Publication type:

Article

New mutation in the non-gigantic exon of SACS in Japanese siblings.

Published in:

Movement Disorders, 2007, v. 22, n. 5, p. 748, doi. 10.1002/mds.21365

By:

Takado, Yuhei;
Hara, Kenju;
Shimohata, Takayoshi;
Tokiguchi, Susumu;
Onodera, Osamu;
Nishizawa, Masatoyo

Publication type:

Article

Botulinum toxin A injections improve apraxia of eyelid opening without overt blepharospasm associated with neurodegenerative diseases.

Published in:

Movement Disorders, 2007, v. 22, n. 4, p. 597, doi. 10.1002/mds.21367

By:

Kanazawa, Masato;
Shimohata, Takayoshi;
Sato, Masahisa;
Onodera, Osamu;
Tanaka, Keiko;
Nishizawa, Masatoyo

Publication type:

Article

Sacsin-related autosomal recessive ataxia without prominent retinal myelinated fibers in Japan.

Published in:

Movement Disorders, 2005, v. 20, n. 3, p. 380, doi. 10.1002/mds.20315

By:

Hara, Kenju;
Onodera, Osamu;
Endo, Minoru;
Kondo, Hiroshi;
Shiota, Hiroshi;
Miki, Kenji;
Tanimoto, Naoyuki;
Kimura, Tetsuya;
Nishizawa, Masatoyo

Publication type:

Article

Sporadic ALS with compound heterozygous mutations in the SQSTM1 gene.

Published in:

2013

By:

Shimizu, Hiroshi;
Toyoshima, Yasuko;
Shiga, Atsushi;
Yokoseki, Akio;
Arakawa, Keiko;
Sekine, Yumi;
Shimohata, Takayoshi;
Ikeuchi, Takeshi;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Onodera, Osamu;
Takahashi, Hitoshi

Publication type:

Report

Involvement of Onuf’s nucleus in Machado–Joseph disease: a morphometric and immunohistochemical study.

Published in:

Acta Neuropathologica, 2010, v. 120, n. 4, p. 439, doi. 10.1007/s00401-010-0699-5

By:

Shimizu, Hiroshi;
Yamada, Mitsunori;
Toyoshima, Yasuko;
Ikeuchi, Takeshi;
Onodera, Osamu;
Takahashi, Hitoshi

Publication type:

Article

Sporadic four-repeat tauopathy with frontotemporal lobar degeneration, Parkinsonism, and motor neuron disease: a distinct clinicopathological and biochemical disease entity.

Published in:

Acta Neuropathologica, 2010, v. 120, n. 1, p. 21, doi. 10.1007/s00401-010-0649-2

By:

Yong-Juan Fu;
Nishihira, Yasushi;
Kuroda, Shigetoshi;
Toyoshima, Yasuko;
Ishihara, Tomohiko;
Shinozaki, Makoto;
Miyashita, Akinori;
Yue-Shan Piao;
Chun-Feng Tan;
Tani, Takashi;
Koike, Ryoko;
Iwanaga, Keisuke;
Tsujihata, Mitsuhiro;
Onodera, Osamu;
Kuwano, Ryozo;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Ikeuchi, Takeshi;
Takahashi, Hitoshi

Publication type:

Article

Selective occurrence of TDP-43-immunoreactive inclusions in the lower motor neurons in Machado–Joseph disease.

Published in:

Acta Neuropathologica, 2009, v. 118, n. 4, p. 553, doi. 10.1007/s00401-009-0552-x

By:

Chun-Feng Tan;
Yamada, Mitsunori;
Toyoshima, Yasuko;
Yokoseki, Akio;
Miki, Yukari;
Hoshi, Yasuhiro;
Kaneko, Hiroyuki;
Ikeuchi, Takeshi;
Onodera, Osamu;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Sporadic amyotrophic lateral sclerosis of long duration is associated with relatively mild TDP-43 pathology.

Published in:

Acta Neuropathologica, 2009, v. 117, n. 1, p. 45, doi. 10.1007/s00401-008-0443-6

By:

Nishihira, Yasushi;
Chun-Feng Tan;
Hoshi, Yasuhiro;
Iwanaga, Keisuke;
Yamada, Megumi;
Kawachi, Izumi;
Tsujihata, Mitsuhiro;
Hozumi, Isao;
Morita, Takashi;
Onodera, Osamu;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Cardiac sympathetic denervation in Parkinson’s disease linked to SNCA duplication.

Published in:

2008

By:

Orimo, Satoshi;
Uchihara, Toshiki;
Nakamura, Ayako;
Mori, Fumiaki;
Ikeuchi, Takeshi;
Onodera, Osamu;
Nishizawa, Masatoyo;
Ishikawa, Atsushi;
Kakita, Akiyoshi;
Wakabayashi, Koichi;
Takahashi, Hitoshi

Publication type:

Letter

Sporadic amyotrophic lateral sclerosis: two pathological patterns shown by analysis of distribution of TDP-43-immunoreactive neuronal and glial cytoplasmic inclusions.

Published in:

Acta Neuropathologica, 2008, v. 116, n. 2, p. 169, doi. 10.1007/s00401-008-0385-z

By:

Nishihira, Yasushi;
Chun-Feng Tan;
Onodera, Osamu;
Toyoshima, Yasuko;
Yamada, Mitsunori;
Morita, Takashi;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation.

Published in:

Acta Neuropathologica, 2007, v. 113, n. 5, p. 535, doi. 10.1007/s00401-007-0206-9

By:

Chun-Feng Tan;
Eguchi, Hiroto;
Tagawa, Asako;
Onodera, Osamu;
Iwasaki, Takuya;
Tsujino, Akira;
Nishizawa, Masatoyo;
Kakita, Akiyoshi;
Takahashi, Hitoshi

Publication type:

Article

Familial amyotrophic lateral sclerosis: a SOD1-unrelated Japanese family of bulbar type with Bunina bodies and ubiquitin-positive skein-like inclusions in lower motor neurons.

Published in:

Acta Neuropathologica, 2007, v. 113, n. 2, p. 205, doi. 10.1007/s00401-006-0151-z

By:

Tagawa, Asako;
Tan, Chun-Feng;
Kikugawa, Koki;
Fukase, Masayuki;
Nakano, Ryoichi;
Onodera, Osamu;
Nishizawa, Masatoyo;
Takahashi, Hitoshi

Publication type:

Article

Apolipoprotein E ε4 allele and progression of cortical Lewy body pathology in Parkinson’s disease.

Published in:

Acta Neuropathologica, 1998, v. 95, n. 5, p. 450, doi. 10.1007/s004010050824

By:

Wakabayashi, K.;
Kakita, Akiyoshi;
Hayashi, Shintaro;
Okuizumi, Kaoru;
Onodera, Osamu;
Tanaka, Hajime;
Ishikawa, Atsushi;
Tsuji, Shoji;
Takahashi, Hitoshi

Publication type:

Article

Pick’s disease: selective occurrence of apolipoprotein E-immunoreactive Pick bodies in the limbic system.

Published in:

Acta Neuropathologica, 1997, v. 95, n. 1, p. 1, doi. 10.1007/s004010050759

By:

Hayashi, S.;
Wakabayashi, Koichi;
Iwanaga, Keisuke;
Kakita, Akiyoshi;
Seki, Koji;
Tanaka, Masaharu;
Okuizumi, Kaoru;
Onodera, Osamu;
Tanaka, Hajime;
Tsuji, Shoji;
Takahashi, Hitoshi

Publication type:

Article

Is the population of Sado Island genetically close to the population of western Japan?

Published in:

Human Genome Variation, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41439-019-0058-6

By:

Misawa, Kazuharu;
Watanabe, Hiroshi;
Yokoseki, Akio;
Wakasugi, Minako;
Onodera, Osamu;
Narita, Ichiei;
Momotsu, Takeshi;
Sato, Kenji;
Endo, Naoto

Publication type:

Article

Correction to: A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.

Published in:

2021

By:

Sainouchi, Makoto;
Hatano, Yuya;
Tada, Mari;
Ishihara, Tomohiko;
Ando, Shoichiro;
Kato, Taisuke;
Tokunaga, Jun;
Ito, Gaku;
Miyahara, Hiroaki;
Toyoshima, Yasuko;
Yokoseki, Akio;
Ozawa, Tetsutaro;
Akazawa, Kohei;
Onodera, Osamu;
Kakita, Akiyoshi

Publication type:

Correction Notice

A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.

Published in:

2021

By:

Sainouchi, Makoto;
Hatano, Yuya;
Tada, Mari;
Ishihara, Tomohiko;
Ando, Shoichiro;
Kato, Taisuke;
Tokunaga, Jun;
Ito, Gaku;
Miyahara, Hiroaki;
Toyoshima, Yasuko;
Yokoseki, Akio;
Ozawa, Tetsutaro;
Akazawa, Kohei;
Onodera, Osamu;
Kakita, Akiyoshi

Publication type:

Letter

A novel splicing variant of ANXA11 in a patient with amyotrophic lateral sclerosis: histologic and biochemical features.

Published in:

2021

By:

Sainouchi, Makoto;
Hatano, Yuya;
Tada, Mari;
Ishihara, Tomohiko;
Ando, Shoichiro;
Kato, Taisuke;
Tokunaga, Jun;
Ito, Gaku;
Miyahara, Hiroaki;
Toyoshima, Yasuko;
Yokoseki, Akio;
Ozawa, Tetsutaro;
Akazawa, Kohei;
Onodera, Osamu;
Kakita, Akiyoshi

Publication type:

Letter

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

Published in:

2020

By:

Saito, Rie;
Hara, Norikazu;
Tada, Mari;
Honma, Yoshiaki;
Miyashita, Akinori;
Onodera, Osamu;
Ikeuchi, Takeshi;
Kakita, Akiyoshi

Publication type:

Letter

Stem cell transplantation for pediatric patients with adrenoleukodystrophy: A nationwide retrospective analysis in Japan.

Published in:

Pediatric Transplantation, 2022, v. 26, n. 1, p. 1, doi. 10.1111/petr.14125

By:

Kato, Koji;
Yabe, Hiromasa;
Shimozawa, Nobuyuki;
Adachi, Souichi;
Kurokawa, Mineo;
Hashii, Yoshiko;
Sato, Atsushi;
Yoshida, Nao;
Kaga, Makiko;
Onodera, Osamu;
Kato, Shunichi;
Atsuta, Yoshiko;
Morio, Tomohiro

Publication type:

Article

Case report: Progressive multifocal leukoencephalopathy co-occurring with neurosarcoidosis: early brain biopsy and appropriate therapy for PML resulted in a favorable prognosis.

Published in:

Frontiers in Immunology, 2024, p. 1, doi. 10.3389/fimmu.2024.1447992

By:

Qiannan Wang;
Shintaro Tsuboguchi;
Kouichirou Okamoto;
Mari Tada;
Akiyoshi Kakita;
Kazuo Nakamichi;
Makoto Oishi;
Masato Kanazawa;
Osamu Onodera

Publication type:

Article

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

Published in:

Neuropathology & Applied Neurobiology, 2025, v. 51, n. 1, p. 1, doi. 10.1111/nan.70006

By:

Hongo, Shoko;
Ikeda, Tetsuhiko;
Tada, Mari;
Aida, Rina;
Ozawa, Tetsuo;
Hara, Norikazu;
Miyashita, Akinori;
Nakajima, Takashi;
Onodera, Osamu;
Ikeuchi, Takeshi;
Ichinose, Hiroshi;
Kakita, Akiyoshi

Publication type:

Article

Slow disease progression and characteristic TDP‐43 inclusions in a patient with familial amyotrophic lateral sclerosis carrying a TARDBP G357S variant.

Published in:

Neuropathology & Applied Neurobiology, 2024, v. 50, n. 1, p. 1, doi. 10.1111/nan.12966

By:

Sainouchi, Makoto;
Oginezawa, Shinya;
Tada, Mari;
Ishihara, Tomohiko;
Onodera, Osamu;
Kakita, Akiyoshi

Publication type:

Article

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

Published in:

Neuropathology & Applied Neurobiology, 2022, v. 48, n. 3, p. 1, doi. 10.1111/nan.12786

By:

Sainouchi, Makoto;
Tada, Mari;
Fitrah, Yusran Ady;
Hara, Norikazu;
Tanaka, Kou;
Idezuka, Jiro;
Aida, Izumi;
Nakajima, Takashi;
Miyashita, Akinori;
Akazawa, Kohei;
Ikeuchi, Takeshi;
Onodera, Osamu;
Kakita, Akiyoshi

Publication type:

Article

Stroke incidence and chronic kidney disease: A hospital‐based prospective cohort study.

Published in:

Nephrology, 2022, v. 27, n. 7, p. 577, doi. 10.1111/nep.14049

By:

Wakasugi, Minako;
Yokoseki, Akio;
Wada, Masakazu;
Sanpei, Kazuhiro;
Momotsu, Takeshi;
Sato, Kenji;
Kawashima, Hiroyuki;
Nakamura, Kazutoshi;
Onodera, Osamu;
Narita, Ichiei

Publication type:

Article

HTRA1 Mutations Identified in Symptomatic Carriers Have the Property of Interfering the Trimer-Dependent Activation Cascade.

Published in:

Frontiers in Neurology, 2019, p. N.PAG, doi. 10.3389/fneur.2019.00693

By:

Uemura, Masahiro;
Nozaki, Hiroaki;
Koyama, Akihide;
Sakai, Naoko;
Ando, Shoichiro;
Kanazawa, Masato;
Kato, Taisuke;
Onodera, Osamu

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Article

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

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PLoS ONE, 2012, v. 7, n. 8, p. 1, doi. 10.1371/journal.pone.0043120

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Shiga, Atsushi;
Ishihara, Tomohiko;
Miyashita, Akinori;
Kuwabara, Misaki;
Kato, Taisuke;
Watanabe, Norihiro;
Yamahira, Akie;
Kondo, Chigusa;
Yokoseki, Akio;
Takahashi, Masuhiro;
Kuwano, Ryozo;
Kakita, Akiyoshi;
Nishizawa, Masatoyo;
Takahashi, Hitoshi;
Onodera, Osamu;
Nagai, Yoshitaka

Publication type:

Article