Works matching AU Tsuji, Shoji

Results: 337

The incidence and risk factors of asymptomatic primary spontaneous pneumothorax detected during health check-ups.

Published in:

2017

By:

Akihisa Mitani;
Yukichika Hakamata;
Megumi Hosoi;
Masafumi Horie;
Yoko Murano;
Akira Saito;
Shintaro Yanagimoto;
Shoji Tsuji;
Kazuhiko Yamamoto;
Takahide Nagase;
Mitani, Akihisa;
Hakamata, Yukichika;
Hosoi, Megumi;
Horie, Masafumi;
Murano, Yoko;
Saito, Akira;
Yanagimoto, Shintaro;
Tsuji, Shoji;
Yamamoto, Kazuhiko;
Nagase, Takahide

Publication type:

journal article

Polymyositis associated with focal mesangial proliferative glomerulonephritis with depositions of immune complexes.

Published in:

2007

By:

Takizawa, Yasunobu;
Kanda, Hiroko;
Sato, Kojiro;
Kawahata, Kimito;
Yamaguchi, Akihiro;
Uozaki, Hiroshi;
Shimizu, Jun;
Tsuji, Shoji;
Misaki, Yoshikata;
Yamamoto, Kazuhiko

Publication type:

Report

Churg-Strauss syndrome and the leukotriene receptor antagonist pranlukast.

Published in:

Clinical Rheumatology, 2005, v. 24, n. 6, p. 661, doi. 10.1007/s10067-004-1035-z

By:

Shimbo, Junsuke;
Onodera, Osamu;
Tanaka, Keiko;
Tsuji, Shoji

Publication type:

Article

Diffusion tensor tract-specific analysis of the uncinate fasciculus in patients with amyotrophic lateral sclerosis.

Published in:

Neuroradiology, 2010, v. 52, n. 8, p. 729, doi. 10.1007/s00234-010-0653-1

By:

Sato, Kanako;
Aoki, Shigeki;
Iwata, Nobue;
Masutani, Yoshitaka;
Watadani, Takeyuki;
Nakata, Yasuhiro;
Yoshida, Mariko;
Terao, Yasuo;
Abe, Osamu;
Ohtomo, Kuni;
Tsuji, Shoji

Publication type:

Article

A Japanese Family with a Novel Pathogenic Variant in KIF1A Presenting with Spastic Paraparesis, Cerebellar Ataxia, and Intellectual Disability.

Published in:

Cerebellum, 2025, v. 24, n. 1, p. 1, doi. 10.1007/s12311-024-01782-y

By:

Mitsutake, Akihiko;
Kawai, Mizuho;
Orimo, Kenta;
Matsukawa, Takashi;
Ishiura, Hiroyuki;
Mitsui, Jun;
Nakajima, Hideki;
Murai, Hiroyuki;
Tsuji, Shoji;
Goto, Jun;
Iwata, Nobue K.

Publication type:

Article

New Horizon of Multiple System Atrophy Research.

Published in:

Cerebellum, 2024, v. 23, n. 1, p. 1, doi. 10.1007/s12311-024-01667-0

By:

Tsuji, Shoji;
Wenning, Gregor

Publication type:

Article

Clinical and Genetic Features of Multiplex Families with Multiple System Atrophy and Parkinson's Disease.

Published in:

Cerebellum, 2024, v. 23, n. 1, p. 22, doi. 10.1007/s12311-022-01426-z

By:

Matsukawa, Takashi;
Porto, Kristine Joyce L.;
Mitsui, Jun;
Chikada, Ayaka;
Ishiura, Hiroyuki;
Takahashi, Yuji;
Nakamoto, Fumiko Kusunoki;
Seki, Tomonari;
Shiio, Yasushi;
Toda, Tatsushi;
Tsuji, Shoji

Publication type:

Article

Correction: A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity.

Published in:

2023

By:

Hama, Yuka;
Date, Hidetoshi;
Fujimoto, Akiko;
Matsui, Ayano;
Ishiura, Hiroyuki;
Mitsui, Jun;
Yamamoto, Toshiyuki;
Tsuji, Shoji;
Mizusawa, Hidehiro;
Takahashi, Yuji

Publication type:

Correction Notice

A Novel de novo KIF1A Mutation in a Patient with Ataxia, Intellectual Disability and Mild Foot Deformity.

Published in:

2023

By:

Hama, Yuka;
Date, Hidetoshi;
Fujimoto, Akiko;
Matsui, Ayano;
Ishiura, Hiroyuki;
Mitsui, Jun;
Yamamoto, Toshiyuki;
Tsuji, Shoji;
Mizusawa, Hidehiro;
Takahashi, Yuji

Publication type:

Case Study

Frequency of FMR1 Premutation Alleles in Patients with Undiagnosed Cerebellar Ataxia and Multiple System Atrophy in the Japanese Population.

Published in:

Cerebellum, 2022, v. 21, n. 6, p. 954, doi. 10.1007/s12311-021-01329-5

By:

Almansour, Asem;
Ishiura, Hiroyuki;
Mitsui, Jun;
Matsukawa, Takashi;
Matsukawa, Miho Kawabe;
Shimizu, Hideaki;
Sugiyama, Atsuhiko;
Toda, Tatsushi;
Tsuji, Shoji

Publication type:

Article

Quantitative Evaluation of Cerebellar Function in Multiple System Atrophy with Transcranial Magnetic Stimulation.

Published in:

Cerebellum, 2022, v. 21, n. 2, p. 219, doi. 10.1007/s12311-021-01293-0

By:

Shirota, Yuichiro;
Hanajima, Ritsuko;
Shimizu, Takahiro;
Terao, Yasuo;
Tsuji, Shoji;
Ugawa, Yoshikazu

Publication type:

Article

The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force.

Published in:

Cerebellum, 2019, v. 18, n. 6, p. 1098, doi. 10.1007/s12311-019-01052-2

By:

Beaudin, Marie;
Matilla-Dueñas, Antoni;
Soong, Bing-Weng;
Pedroso, Jose Luiz;
Barsottini, Orlando G.;
Mitoma, Hiroshi;
Tsuji, Shoji;
Schmahmann, Jeremy D.;
Manto, Mario;
Rouleau, Guy A;
Klein, Christopher;
Dupre, Nicolas

Publication type:

Article

Novel De Novo <italic>KCND3</italic> Mutation in a Japanese Patient with Intellectual Disability, Cerebellar Ataxia, Myoclonus, and Dystonia.

Published in:

Cerebellum, 2018, v. 17, n. 2, p. 237, doi. 10.1007/s12311-017-0883-4

By:

Kurihara, Masanori;
Ishiura, Hiroyuki;
Sasaki, Takuya;
Otsuka, Juuri;
Hayashi, Toshihiro;
Terao, Yasuo;
Matsukawa, Takashi;
Mitsui, Jun;
Kaneko, Juntaro;
Nishiyama, Kazutoshi;
Doi, Koichiro;
Yoshimura, Jun;
Morishita, Shinichi;
Shimizu, Jun;
Tsuji, Shoji

Publication type:

Article

Three-Year Follow-Up of High-Dose Ubiquinol Supplementation in a Case of Familial Multiple System Atrophy with Compound Heterozygous COQ2 Mutations.

Published in:

Cerebellum, 2017, v. 16, n. 3, p. 664, doi. 10.1007/s12311-017-0846-9

By:

Mitsui, Jun;
Koguchi, Ken;
Momose, Toshimitsu;
Takahashi, Miwako;
Matsukawa, Takashi;
Yasuda, Tsutomu;
Tokushige, Shin-ichi;
Ishiura, Hiroyuki;
Goto, Jun;
Nakazaki, Shigeaki;
Kondo, Tomoyoshi;
Ito, Hidefumi;
Yamamoto, Yorihiro;
Tsuji, Shoji

Publication type:

Article

Visual Scanning Area is Abnormally Enlarged in Hereditary Pure Cerebellar Ataxia.

Published in:

Cerebellum, 2015, v. 14, n. 2, p. 63, doi. 10.1007/s12311-014-0600-5

By:

Matsuda, Shunichi;
Matsumoto, Hideyuki;
Furubayashi, Toshiaki;
Fukuda, Hideki;
Hanajima, Ritsuko;
Tsuji, Shoji;
Ugawa, Yoshikazu;
Terao, Yasuo

Publication type:

Article

Sporadic ataxias in Japan – a population-based epidemiological study.

Published in:

Cerebellum, 2008, v. 7, n. 2, p. 189, doi. 10.1007/s12311-008-0028-x

By:

Tsuji, Shoji;
Onodera, Osamu;
Goto, Jun;
Nishizawa, Masatoyo

Publication type:

Article

International Workshop on multiple system atrophy (MSA)2 November 2006, Kyoto, Japan.

Published in:

Cerebellum, 2007, v. 6, n. 4, p. 335, doi. 10.1080/14734220701200071

By:

Nishizawa, Masatoyo;
Wenning, Gregor K.;
Tsuji, Shoji

Publication type:

Article

Spinocerebellar ataxia type 15.

Published in:

Cerebellum, 2005, v. 4, n. 1, p. 47, doi. 10.1080/14734220410019029

By:

McKinlay Gardner, R. J.;
Knight, Melanie A.;
Hara, Kenju;
Tsuji, Shoji;
Forrest, Susan M.;
Storey, Elsdon

Publication type:

Article

Late-onset spastic ataxia phenotype in a patient with a homozygous DDHD2 mutation.

Published in:

Scientific Reports, 2014, p. 1, doi. 10.1038/srep07132

By:

Hiroshi Doi;
Masao Ushiyama;
Takashi Baba;
Katsuko Tani;
Masaaki Shiina;
Kazuhiro Ogata;
Satoko Miyatake;
Yoko Fukuda-Yuzawa;
Shoji Tsuji;
Mitsuko Nakashima;
Yoshinori Tsurusaki;
Noriko Miyake;
Hirotomo Saitsu;
Shu-ichi Ikeda;
Fumiaki Tanaka;
Naomichi Matsumoto;
Kunihiro Yoshida

Publication type:

Article

Dysbiosis of the gut microbiota as a susceptibility factor for Kawasaki disease.

Published in:

Frontiers in Immunology, 2023, p. 1, doi. 10.3389/fimmu.2023.1268453

By:

Yoshiki Teramoto;
Shohei Akagawa;
Shin-ichiro Hori;
Shoji Tsuji;
Koichiro Higasa;
Kazunari Kaneko

Publication type:

Article

Elevated Serum Uric Acid Levels Are Related to Cognitive Deterioration in an Elderly Japanese Population.

Published in:

Dementia & Geriatric Cognitive Disorders Extra, 2016, v. 6, n. 3, p. 580, doi. 10.1159/000454660

By:

Kazushi Suzuki;
Daisuke Koide;
Kurumi Fujii;
Tsutomu Yamazaki;
Shoji Tsuji;
Atsushi Iwata

Publication type:

Article

Genetics of familial adult myoclonus epilepsy: From linkage studies to noncoding repeat expansions.

Published in:

Epilepsia (Series 4), 2023, v. 64, p. S14, doi. 10.1111/epi.17610

By:

Corbett, Mark A.;
Depienne, Christel;
Veneziano, Liana;
Klein, Karl Martin;
Brancati, Francesco;
Guerrini, Renzo;
Zara, Federico;
Tsuji, Shoji;
Gecz, Jozef

Publication type:

Article

History of familial adult myoclonus epilepsy/benign adult familial myoclonic epilepsy around the world.

Published in:

Epilepsia (Series 4), 2023, v. 64, p. S3, doi. 10.1111/epi.17519

By:

Berkovic, Samuel F.;
Striano, Pasquale;
Tsuji, Shoji

Publication type:

Article

Insights into familial adult myoclonus epilepsy pathogenesis: How the same repeat expansion in six unrelated genes may lead to cortical excitability.

Published in:

Epilepsia (Series 4), 2023, v. 64, p. S31, doi. 10.1111/epi.17504

By:

Depienne, Christel;
van den Maagdenberg, Arn M. J. M.;
Kühnel, Theresa;
Ishiura, Hiroyuki;
Corbett, Mark A.;
Tsuji, Shoji

Publication type:

Article

A Role of Aging in the Progression of Cortical Excitability in Benign Adult Familial Myoclonus Epilepsy type 1 Patients.

Published in:

2021

By:

Neshige, Shuichiro;
Hitomi, Takefumi;
Tojima, Maya;
Oi, Kazuki;
Kobayashi, Katsuya;
Matsuhashi, Masao;
Shimotake, Akihiro;
Matsumoto, Riki;
Kanda, Masutaro;
Maruyama, Hirofumi;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Takahashi, Ryosuke;
Ikeda, Akio

Publication type:

Letter

Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement Disorders.

Published in:

Movement Disorders, 2021, v. 36, n. 1, p. 251, doi. 10.1002/mds.28302

By:

Yau, Wai Yan;
Vandrovcova, Jana;
Sullivan, Roisin;
Chen, Zhongbo;
Zecchinelli, Anna;
Cilia, Roberto;
Stefano, Duga;
Murray, Malgorzata;
Carmona, Susana;
Chelban, Viorica;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Jaunmuktane, Zane;
Turner, Chris;
Wood, Nicholas W.;
Houlden, Henry

Publication type:

Article

Cerebellar dysfunction in progressive supranuclear palsy: A transcranial magnetic stimulation study.

Published in:

Movement Disorders, 2010, v. 25, n. 14, p. 2413, doi. 10.1002/mds.23298

By:

Shirota, Yuichiro;
Hamada, Masashi;
Hanajima, Ritsuko;
Terao, Yasuo;
Matsumoto, Hideyuki;
Ohminami, Shinya;
Tsuji, Shoji;
Ugawa, Yoshikazu

Publication type:

Article

Postural tremor in X-linked spinal and bulbar muscular atrophy.

Published in:

Movement Disorders, 2009, v. 24, n. 14, p. 2063, doi. 10.1002/mds.22566

By:

Hanajima, Ritsuko;
Terao, Yasuo;
Nakatani-Enomoto, Setsu;
Hamada, Masashi;
Yugeta, Akihiro;
Matsumoto, Hideyuki;
Yamamoto, Tomotaka;
Tsuji, Shoji;
Ugawa, Yoshikazu

Publication type:

Article

A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype-phenotype correlations.

Published in:

Movement Disorders, 2009, v. 24, n. 3, p. 441, doi. 10.1002/mds.22435

By:

Kubota, Akatsuki;
Hida, Ayumi;
Ichikawa, Yaeko;
Momose, Yoshio;
Goto, Jun;
Igeta, Yukifusa;
Hashida, Hideji;
Yoshida, Kunihiro;
Ikeda, Syu-Ichi;
Kanazawa, Ichiro;
Tsuji, Shoji

Publication type:

Article

Severe hypokinesis caused by paraneoplastic anti-Ma2 encephalitis associated with bilateral intratubular germ-cell neoplasm of the testes.

Published in:

2007

By:

Matsumoto, Lumine;
Yamamoto, Tomotaka;
Higashihara, Mana;
Sugimoto, Izumi;
Kowa, Hisatomo;
Shibahara, Junji;
Nakamura, Koichiro;
Shimizu, Jun;
Ugawa, Yoshikazu;
Goto, Jun;
Dalmau, Josep;
Tsuji, Shoji

Publication type:

journal article

An immigrant family with Kii amyotrophic lateral sclerosis/parkinsonism-dementia complex.

Published in:

2022

By:

Kokubo, Yasumasa;
Morimoto, Satoru;
Sasaki, Ryogen;
Hasegawa, Masato;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Yoshida, Mari;
Yamazoe, Naohisa;
Miyazaki, Mitsukazu;
Kuzuhara, Shigeki

Publication type:

journal article

Comprehensive Genetic Analyses of Inherited Peripheral Neuropathies in Japan: Making Early Diagnosis Possible.

Published in:

Biomedicines, 2022, v. 10, n. 7, p. N.PAG, doi. 10.3390/biomedicines10071546

By:

Ando, Masahiro;
Higuchi, Yujiro;
Yuan, Junhui;
Yoshimura, Akiko;
Taniguchi, Takaki;
Kojima, Fumikazu;
Noguchi, Yutaka;
Hobara, Takahiro;
Takeuchi, Mika;
Takei, Jun;
Hiramatsu, Yu;
Sakiyama, Yusuke;
Hashiguchi, Akihiro;
Okamoto, Yuji;
Mitsui, Jun;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Takashima, Hiroshi

Publication type:

Article

Clinicopathologic Features of Oculopharyngodistal Myopathy With LRP12 CGG Repeat Expansions Compared With Other Oculopharyngodistal Myopathy Subtypes.

Published in:

JAMA Neurology, 2021, v. 78, n. 7, p. 853, doi. 10.1001/jamaneurol.2021.1509

By:

Kumutpongpanich, Theerawat;
Ogasawara, Masashi;
Ozaki, Ayami;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Minami, Narihiro;
Hayashi, Shinichiro;
Noguchi, Satoru;
Iida, Aritoshi;
Nishino, Ichizo;
Mori-Yoshimura, Madoka;
Oya, Yasushi;
Ono, Kenjiro;
Shimizu, Toshio;
Kawata, Akihiro;
Shimohama, Shun;
Toyooka, Keiko;
Endo, Kaoru;
Toru, Shuta;
Sasaki, Oga

Publication type:

Article

Plasma Coenzyme Q10 Levels and Multiple System Atrophy.

Published in:

JAMA Neurology, 2016, v. 73, n. 12, p. 1499, doi. 10.1001/jamaneurol.2016.4133

By:

Jun Mitsui;
Shoji Tsuji

Publication type:

Article

Plasma Coenzyme Q10 Levels in Patients With Multiple System Atrophy.

Published in:

JAMA Neurology, 2016, v. 73, n. 8, p. 977, doi. 10.1001/jamaneurol.2016.1325

By:

Jun Mitsui;
Takashi Matsukawa;
Tsutomu Yasuda;
Hiroyuki Ishiura;
Shoji Tsuji

Publication type:

Article

An autopsy case of G<sub>M1</sub> gangliosidosis type II in a patient who survived a long duration with artificial respiratory support.

Published in:

Neuropathology, 2020, v. 40, n. 4, p. 379, doi. 10.1111/neup.12651

By:

Uchino, Akiko;
Nagai, Makiko;
Kanazawa, Naomi;
Ichinoe, Masaaki;
Yanagisawa, Nobuyuki;
Adachi, Kaori;
Nanba, Eiji;
Ishiura, Hiroyuki;
Mitsui, Jun;
Tsuji, Shoji;
Suzuki, Kinuko;
Murayama, Shigeo;
Nishiyama, Kazutoshi

Publication type:

Article

A 52-year-old man with hypohidrosis.

Published in:

2006

By:

Shimizu, Jun;
Hashimoto, Meiko;
Murayama, Shigeo;
Tsuji, Shoji

Publication type:

Other

Polyglutamine disease: Recent advances in the neuropathology of dentatorubral-pallidoluysian atrophy.

Published in:

2006

By:

Yamada, Mitsunori;
Shimohata, Mitsuteru;
Sato, Toshiya;
Tsuji, Shoji;
Takahashi, Hitoshi

Publication type:

Other

Association of subclinical carotid atherosclerosis with immediate memory and other cognitive functions.

Published in:

Geriatrics & Gerontology International, 2018, v. 18, n. 1, p. 65, doi. 10.1111/ggi.13142

By:

Tsuji, Shoji;
Iwata, Atsushi;
Matsumoto, Lumine;
Suzuki, Kazushi;
Mizuno, Yoshiko;
Ohike, Yumiko;
Ozeki, Atsuko;
Ono, Satoshi;
Takanashi, Mikio;
Sawaki, Daigo;
Suzuki, Toru;
Yamazaki, Tsutomu

Publication type:

Article

Novel mutations in the PNPLA6 gene in Boucher-Neuhäuser syndrome.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 4, p. 217, doi. 10.1038/jhg.2015.3

By:

Koh, Kishin;
Kobayashi, Fumikazu;
Miwa, Michiaki;
Shindo, Kazumasa;
Isozaki, Eiji;
Ishiura, Hiroyuki;
Tsuji, Shoji;
Takiyama, Yoshihisa

Publication type:

Article

Molecular epidemiology and clinical spectrum of hereditary spastic paraplegia in the Japanese population based on comprehensive mutational analyses.

Published in:

Journal of Human Genetics, 2014, v. 59, n. 3, p. 163, doi. 10.1038/jhg.2013.139

By:

Ishiura, Hiroyuki;
Takahashi, Yuji;
Hayashi, Toshihiro;
Saito, Kayoko;
Furuya, Hirokazu;
Watanabe, Mitsunori;
Murata, Miho;
Suzuki, Mikiya;
Sugiura, Akira;
Sawai, Setsu;
Shibuya, Kazumoto;
Ueda, Naohisa;
Ichikawa, Yaeko;
Kanazawa, Ichiro;
Goto, Jun;
Tsuji, Shoji

Publication type:

Article

Comprehensive mutational analysis of LRRK2 reveals variants supporting association with autosomal dominant Parkinson's disease.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 9, p. 671, doi. 10.1038/jhg.2011.79

By:

Seki, Naomi;
Takahashi, Yuji;
Tomiyama, Hiroyuki;
Rogaeva, Ekaterina;
Murayama, Shigeo;
Mizuno, Yoshikuni;
Hattori, Nobutaka;
Marras, Connie;
Lang, Anthony E;
George-Hyslop, Peter St;
Goto, Jun;
Tsuji, Shoji

Publication type:

Article

Multiplexed resequencing analysis to identify rare variants in pooled DNA with barcode indexing using next-generation sequencer.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 7, p. 448, doi. 10.1038/jhg.2010.46

By:

Mitsui, Jun;
Fukuda, Yoko;
Azuma, Kyo;
Tozaki, Hirokazu;
Ishiura, Hiroyuki;
Takahashi, Yuji;
Goto, Jun;
Tsuji, Shoji

Publication type:

Article

Genome-wide association database developed in the Japanese Integrated Database Project.

Published in:

Journal of Human Genetics, 2009, v. 54, n. 9, p. 543, doi. 10.1038/jhg.2009.68

By:

Koike, Asako;
Nishida, Nao;
Inoue, Ituro;
Tsuji, Shoji;
Tokunaga, Katsushi

Publication type:

Article

Appropriate data cleaning methods for genome-wide association study.

Published in:

Journal of Human Genetics, 2008, v. 53, n. 10, p. 886, doi. 10.1007/s10038-008-0322-y

By:

Miyagawa, Taku;
Nishida, Nao;
Ohashi, Jun;
Kimura, Ryosuke;
Fujimoto, Akihiro;
Kawashima, Minae;
Koike, Asako;
Sasaki, Tsukasa;
Tanii, Hisashi;
Otowa, Takeshi;
Momose, Yoshio;
Nakahara, Yasuo;
Gotoh, Jun;
Okazaki, Yuji;
Tsuji, Shoji;
Tokunaga, Katsushi

Publication type:

Article

Aprataxin, causative gene product for EAOH/AOA1, repairs DNA single-strand breaks with damaged 3′-phosphate and 3′-phosphoglycolate ends.

Published in:

Nucleic Acids Research, 2007, v. 35, n. 11, p. 3797, doi. 10.1093/nar/gkm158

By:

Takahashi, Tetsuya;
Tada, Masayoshi;
Igarashi, Shuichi;
Koyama, Akihide;
Date, Hidetoshi;
Yokoseki, Akio;
Shiga, Atsushi;
Yoshida, Yutaka;
Tsuji, Shoji;
Nishizawa, Masatoyo;
Onodera, Osamu

Publication type:

Article

Genetic spectrum of Charcot–Marie–Tooth disease associated with myelin protein zero gene variants in Japan.

Published in:

Clinical Genetics, 2021, v. 99, n. 3, p. 359, doi. 10.1111/cge.13881

By:

Taniguchi, Takaki;
Ando, Masahiro;
Okamoto, Yuji;
Yoshimura, Akiko;
Higuchi, Yujiro;
Hashiguchi, Akihiro;
Shiga, Kensuke;
Hayashida, Arisa;
Hatano, Taku;
Ishiura, Hiroyuki;
Mitsui, Jun;
Hattori, Nobutaka;
Mizuno, Toshiki;
Nakagawa, Masanori;
Tsuji, Shoji;
Takashima, Hiroshi

Publication type:

Article

Adult-onset vanishing white matter disease with novel missense mutations in a subunit of translational regulator, EIF2B4.

Published in:

Clinical Genetics, 2015, v. 88, n. 4, p. 401, doi. 10.1111/cge.12554

By:

Kanbayashi, Takamichi;
Saito, Fumiaki;
Matsukawa, Takashi;
Oba, Hiroshi;
Hokkoku, Keiichi;
Hatanaka, Yuki;
Tsuji, Shoji;
Sonoo, Masahiro

Publication type:

Article

Regular Article Transmission disequilibrium test and haplotype analysis of the NOTCH4 gene in Japanese patients with schizophrenia.

Published in:

Psychiatry & Clinical Neurosciences, 2004, v. 58, n. 2, p. 199, doi. 10.1111/j.1440-1819.2003.01217.x

By:

KANEKO, NAOSHI;
MURATAKE, TATSUYUKI;
AMAGANE, HIDEKI;
SAKURAI, MIKI;
TANAKA, TOSHIHISA;
TSUJI, SHOJI;
SOMEYA, TOSHIYUKI

Publication type:

Article

Dysbiosis of the gut microbiota in children with severe motor and intellectual disabilities receiving enteral nutrition: A pilot study.

Published in:

JPEN Journal of Parenteral & Enteral Nutrition, 2023, v. 47, n. 1, p. 67, doi. 10.1002/jpen.2435

By:

Nakai, Yoko;
Akagawa, Shohei;
Fujishiro, Sadayuki;
Akagawa, Yuko;
Yamagishi, Mitsuru;
Yamanouchi, Sohsaku;
Kimata, Takahisa;
Ohashi, Atsushi;
Hashiyada, Masaki;
Akane, Atsushi;
Tsuji, Shoji;
Kaneko, Kazunari

Publication type:

Article