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1

Effect of an enhanced recovery after surgery protocol in patients undergoing pancreaticoduodenectomy: A randomized controlled trial

Takagi, Kosei, Yoshida, Ryuichi, Yagi, Takahito, Umeda, Yuzo, Nobuoka, Daisuke, Kuise, Takashi, Hinotsu, Shiro, Matsusaki, Takashi, Morimatsu, Hiroshi, Eguchi, Jun, Wada, Jun, Senda, Masuo, Fujiwara,

Journal:

Clinical Nutrition

Year:

2018

Language:

english

File:

PDF, 1.53 MB

english, 2018

2

Interferon-γ Plays Protective Roles in Sodium Arsenite-Induced Renal Injury by Up-Regulating Intrarenal Multidrug Resistance-Associated Protein 1 Expression

Akihiko Kimura, Yuko Ishida, Takahito Hayashi, Takashi Wada, Hitoshi Yokoyama, Takeshi Sugaya, Naofumi Mukaida, Toshikazu Kondo

Journal:

The American Journal of Pathology

Year:

2006

Language:

english

File:

PDF, 1.58 MB

english, 2006

3

An Analysis Of The Underwater Gliding Motion And Dolphin Kick In The Competitive Swimming

Wada, Tadashi, Sato, Takayuki, Yamamoto, Noriyuki, Tago, Takahito, Izumi, Toshiro, Matsumoto, Takaaki, Shintaku, Yukinori, Isaka, Tadao

Journal:

Medicine & Science in Sports & Exercise

Year:

2010

Language:

english

File:

PDF, 53 KB

english, 2010

4

Intracranial Hemorrhage and Tortuosity of Veins Detected on Susceptibility-weighted Imaging of a Child with a Type IV Collagen α1 Mutation and Schizencephaly

NIWA, Tetsu, AIDA, Noriko, OSAKA, Hitoshi, WADA, Takahito, SAITSU, Hirotomo, IMAI, Yutaka

Journal:

Magnetic Resonance in Medical Sciences

Year:

2015

Language:

english

File:

PDF, 620 KB

english, 2015

5

Deformation Microstructure Developed by Nanoindentation of a MAX Phase Ti2AlC

Wada, Yusuke, Sekido, Nobuaki, Ohmura, Takahito, Yoshimi, Kyosuke

Journal:

MATERIALS TRANSACTIONS

Year:

2018

Language:

english

File:

PDF, 6.15 MB

english, 2018

6

Molecular genetic study of Japanese patients with X-linked α-thalassemia/mental retardation syndrome (ATR-X)

Takahito Wada, Takeo Kubota, Yoshimitsu Fukushima, Shinji Saitoh

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 1.34 MB

english, 2000

7

A novel mutation of KCNQ3 (c.925T→C) in a Japanese family with benign familial neonatal convulsions

Shinichi Hirose, Fumiko Zenri, Hidetaka Akiyoshi, Goryu Fukuma, Hiromi Iwata, Takahito Inoue, Minako Yonetani, Makoto Tsutsumi, Hideki Muranaka, Toru Kurokawa, Toshio Hanai, Kazumaru Wada, Sunao Kanek

Journal:

Annals of Neurology

Year:

2000

Language:

english

File:

PDF, 6.74 MB

english, 2000

8

A woman with 46,XX,dup(16)(p13.11 p13.3) and the ATR-X phenotype

Keiko Akahoshi, Hirohumi Ohashi, Yukio Hattori, Shinji Saitoh, Yoshimitsu Fukushima, Takahito Wada

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 200 KB

english, 2005

9

Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked α-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-X

Takahito Wada, Hideo Sugie, Yoshimitsu Fukushima, Shinji Saitoh

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 60 KB

english, 2005

10

A new detection method for ATRX gene mutations using a mismatch-specific endonuclease

Takahito Wada, Yoshimitsu Fukushima, Shinji Saitoh

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 176 KB

english, 2006

11

Mandibuloacral dysplasia and a novel LMNA mutation in a woman with severe progressive skeletal changes

Tomoki Kosho, Jun Takahashi, Takashige Momose, Akinori Nakamura, Akihiro Sakurai, Takahito Wada, Kunihiro Yoshida, Keiko Wakui, Takefumi Suzuki, Kazuo Kasuga, Gen Nishimura, Hiroyuki Kato, Yoshimitsu

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 242 KB

english, 2007

12

Bilateral perisylvian polymicrogyria, periventricular nodular heterotopia, and left ventricular noncompaction in a girl with 10.5–11.1 Mb terminal deletion of 1p36

Shoji Saito, Rie Kawamura, Tomoki Kosho, Takashi Shimizu, Koki Aoyama, Kenichi Koike, Takahito Wada, Naomichi Matsumoto, Mitsuhiro Kato, Keiko Wakui, Yoshimitsu Fukushima

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 206 KB

english, 2008

13

A de novo direct duplication of 16q22.1 → q23.1 in a boy with midface hypoplasia and mental retardation

Tomoharu Tokutomi, Takahito Wada, Eiji Nakagawa, Shinji Saitoh, Masayuki Sasaki

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 121 KB

english, 2009

14

Germline mosaicism of a novel mutation in lysosome-associated membrane protein-2 deficiency (Danon disease)

Maki Takahashi, Ayaka Yamamoto, Kyoko Takano, Akira Sudo, Takahito Wada, Yu-Ichi Goto, Ichizo Nishino, Shinji Saitoh

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 2.95 MB

english, 2002

15

A fourth-order Cartesian local mesh refinement method for the computational fluid dynamics of physiological flow in multi-generation branched vessels

Takahito Miki, Yohsuke Imai, Takuji Ishikawa, Shigeo Wada, Takayuki Aoki, Takami Yamaguchi

Journal:

International Journal for Numerical Methods in Biomedical Engineering

Year:

2011

Language:

english

File:

PDF, 443 KB

english, 2011

16

Mutations in the chromatin-associated protein ATRX

Richard J. Gibbons, Takahito Wada, Christopher A. Fisher, Nicola Malik, Matthew J. Mitson, David P. Steensma, Alan Fryer, David R. Goudie, Ian D. Krantz, Joanne Traeger-Synodinos

Journal:

Year:

2008

Language:

english

File:

PDF, 302 KB

english, 2008

17

Clinical characteristics of Angelman syndrome patients with a non-IC-deleted imprinting mutation

Shinji Saitoh, Takahito Wada, Tateo Kuno, Kyoung Chang Kim, Hirofumi Ohashi, Katsuyo Hashimoto, Norio Niikawa

Journal:

Clinical Genetics

Year:

1999

Language:

english

File:

PDF, 97 KB

english, 1999

18

Detection of lymphocytes and granulocytes expressing the mutant WASP message in carriers of Wiskott-Aldrich syndrome

Tadashi Ariga, Masafumi Yamada, Takahito Wada, Shinji Saitoh, Yukio Sakiyama

Journal:

British Journal of Haematology

Year:

1999

Language:

english

File:

PDF, 391 KB

english, 1999

19

An alternatively spliced gene encoding a Y-box protein showing maternal expression and tissue-specific zygotic expression in the ascidian embryo

Michiko R. Wada, Yoshiaki Ohtani, Yumiko Shibata, Kimio J. Tanaka, Naomi Tanimoto, Takahito Nishikata

Journal:

Development, Growth & Differentiation

Year:

1998

File:

PDF, 1.36 MB

1998

20

Interactions between cytoskeletal components during myoplasm rearrangement in ascidian eggs

Shota Chiba, Yuko Miki, Kazunori Ashida, Michiko R. Wada, Kimio J. Tanaka, Yumiko Shibata, Rinna Nakamori, Takahito Nishikata

Journal:

Development, Growth & Differentiation

Year:

1999

Language:

english

File:

PDF, 400 KB

english, 1999

21

Downbeat positioning nystagmus is a common clinical feature despite variable phenotypes in an FHM1 family

Ichiro Yabe, Mayumi Kitagawa, Yashio Suzuki, Keishi Fujiwara, Takahito Wada, Takashi Tsubuku, Norihito Takeichi, Ken Sakushima, Hiroyuki Soma, Sachiko Tsuji, Masaaki Niino, Shinji Saitoh, Hidenao Sasa

Journal:

Journal of Neurology

Year:

2008

Language:

english

File:

PDF, 184 KB

english, 2008

22

Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan

Kunihiro Yoshida, Takahito Wada, Akihiro Sakurai, Keiko Wakui, Shu-ichi Ikeda, Yoshimitsu Fukushima

Journal:

Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 196 KB

english, 2007

23

Non-chromosome 15 marker chromosome in a Prader-Willi syndrome patient with uniparental disomy

MIZUHO ICHIKAWA, MAKI OKAJIMA, TAKAHITO WADA, YUMI GOKAN, HIROMI SHIMAKAGE, HIDEFUMI TONOKI, SHINJI SAITOH

Journal:

Pediatrics International

Year:

2006

Language:

english

File:

PDF, 63 KB

english, 2006

24

New mutation of CACNA1A gene in episodic ataxia type 2

Koki Nikaido, Nobutada Tachi, Kazuhiro Ohya, Takahito Wada, Hiroyuki Tsutsumi

Journal:

Pediatrics International

Year:

2011

Language:

english

File:

PDF, 194 KB

english, 2011

25

Molecular Genetic Study on Angelman Syndrome Patients without a Chromosomal Deletion

Shinji Saitoh, Takahito Wada, Taeko Sakai, Norio Kobayashi

Journal:

Year:

2000

Language:

english

File:

PDF, 313 KB

english, 2000

26

Dynamics of dissolved O2, CO2, CH4, and N2O in a tropical coastal swamp in southern Thailand

Shingo Ueda, Chun-Sim U. Go, Takahito Yoshioka, Naohiro Yoshida* ast, , Eitaro Wada, Toshihiro Miyajima* ast ast, , Atsuko Sugimoto, Narin Boontanon, Pisoot Vijarnsorn, Suporn Boonprakub

Journal:

Biogeochemistry

Year:

2000

Language:

english

File:

PDF, 168 KB

english, 2000

27

Stable isotope and radiocarbon compositions of methane emitted from tropical rice paddies and swamps in Southern Thailand

Fumiko Nakagawa, Naohiro Yoshida, Atsuko Sugimoto, Eitaro Wada, Takahito Yoshioka, Shingo Ueda, Pisoot Vijarnsorn

Journal:

Biogeochemistry

Year:

2002

Language:

english

File:

PDF, 325 KB

english, 2002

28

A simple screening method using ion chromatography for the diagnosis of cerebral creatine deficiency syndromes

Wada, Takahito, Shimbo, Hiroko, Osaka, Hitoshi

Journal:

Year:

2012

Language:

english

File:

PDF, 285 KB

english, 2012

29

Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome

Shinji Saitoh, Takahito Wada, Maki Okajima, Kyoko Takano, Akira Sudo, Norio Niikawa

Journal:

Brain and Development

Year:

2005

Language:

english

File:

PDF, 81 KB

english, 2005

30

A novel splicing mutation of the ATRX gene in ATR-X syndrome

Takahito Wada, Masae Sakakibara, Yoshimitsu Fukushima, Shinji Saitoh

Journal:

Brain and Development

Year:

2006

Language:

english

File:

PDF, 191 KB

english, 2006

31

Autosomal dominant leukoencephalopathy with mild clinical symptoms due to cerebrovascular dysfunctions: A new disease entity?

Shinichi Hirabayashi, Takahito Wada, Yoshiaki Kondo, Kunimasa Arima

Journal:

Brain and Development

Year:

2008

Language:

english

File:

PDF, 469 KB

english, 2008

32

Genetic diagnosis and acetazolamide treatment of familial hemiplegic migraine

Taku Omata, Jun-ichi Takanashi, Takahito Wada, Hidee Arai, Yuzo Tanabe

Journal:

Brain and Development

Year:

2011

Language:

english

File:

PDF, 189 KB

english, 2011

33

Paradoxical increase in seizure frequency with valproate in nonketotic hyperglycinemia

Yu Tsuyusaki, Hiroko Shimbo, Takahito Wada, Mizue Iai, Megumi Tsuji, Sumimasa Yamashita, Noriko Aida, Shigeo Kure, Hitoshi Osaka

Journal:

Brain and Development

Year:

2012

Language:

english

File:

PDF, 456 KB

english, 2012

34

Intraischemic hypothermia during pretreatment with sublethal ischemia reduces the induction of ischemic tolerance in the gerbil hippocampus

Kojiro Wada, Takahito Miyazawa, Hiroshi Katoh, Namiko Nomura, Akiko Yano, Katsuji Shima, Hiroo Chigasaki

Journal:

Year:

1997

Language:

english

File:

PDF, 205 KB

english, 1997

35

Clonazepam augmentation therapy in a male at early adolescence with rapid cycling bipolar disorder

Takahito Sugimoto, Tetsuhito Murata, Masao Omori, Yuji Wada

Journal:

General Hospital Psychiatry

Year:

2003

Language:

english

File:

PDF, 88 KB

english, 2003

36

Clinical Course of Epilepsies with Cortical Dysplasia.

Sumimasa Yamashita, Yuko Matsushita, Takahito Wada, Shota Miyake, Michiko Yamada, Hiroko Iwamoto

Journal:

Year:

1996

Language:

english

File:

PDF, 216 KB

english, 1996

37

Temporal variations in carbon isotope ratio of phytoplankton in a eutrophic lake

Takahashi, Kazushi, Yoshioka, Takahito, Wada, Eitaro, Sakamoto, Mitsuru

Journal:

Journal of Plankton Research

Year:

1990

Language:

english

File:

PDF, 494 KB

english, 1990

38

Guinea Pig Liver Mu-Class GlutathioneS-Transferase M1-2 Cross-Reacts with Antibodies to both Rat Mu- and Theta-Class GlutathioneS-Transferases

Akira Hiratsuka, Kenichiro Ogura, Hiroyuki Fujioka, Yasuhiro Sakamoto, Haruhiro Okuda, Kouji Wada, Teruji Tanaka, Takahito Nishiyama, Tadashi Watabe

Journal:

Archives of Biochemistry and Biophysics

Year:

1998

Language:

english

File:

PDF, 671 KB

english, 1998

39

Vacuolating cytotoxin purified fromHelicobacter pyloricauses mitochondrial damage in human gastric cells

Miyuki Kimura, Shinji Goto, Akihiro Wada, Kinnosuke Yahiro, Takuro Niidome, Tomomitsu Hatakeyama, Haruhiko Aoyagi, Toshiya Hirayama, Takahito Kondo

Journal:

Microbial Pathogenesis

Year:

1999

Language:

english

File:

PDF, 357 KB

english, 1999

40

Group II phospholipase A2 activates mitogen-activated protein kinase in cultured rat mesangial cells

Toshihiro Sugiura, Akira Wada, Takahito Itoh, Hiromasa Tojo, Mitsuhiro Okamoto, Enyu Imai, Takenobu Kamada, Naohiko Ueda

Journal:

Year:

1995

Language:

english

File:

PDF, 466 KB

english, 1995

41

A severe mental retardation disease with defect in chromatin remodeling: ATR-X syndrome

Journal:

Neuroscience Research

Year:

2007

Language:

english

File:

PDF, 72 KB

english, 2007

42

Contiguous deletion of SLC6A8 and BAP31 in a patient with severe dystonia and sensorineural deafness

Hitoshi Osaka, Atsushi Takagi, Yu Tsuyusaki, Takahito Wada, Mizue Iai, Sumimasa Yamashita, Hiroko Shimbo, Hirotomo Saitsu, Gajja S. Salomons, Cornelis Jakobs, Noriko Aida, Shinka Toshihiro, Tomiko Kuh

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 736 KB

english, 2012

43

Tyrosine phosphorylation of clathrin heavy chain under oxidative stress

Yoshito Ihara, Chie Yasuoka, Kan Kageyama, Yoshinao Wada, Takahito Kondo

Journal:

Biochemical and Biophysical Research Communications

Year:

2002

Language:

english

File:

PDF, 363 KB

english, 2002

44

Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia

Takahito Wada, Norio Kobayashi, Yoshio Takahashi, Tomoko Aoki, Takako Watanabe, Shinji Saitoh

Journal:

Pediatric Neurology

Year:

2002

Language:

english

File:

PDF, 85 KB

english, 2002

45

Phenotypic variability in a family with a mitochondrial DNA T8993C mutation

Yuji Suzuki, Takahito Wada, Taeko Sakai, Yukitoshi Ishikawa, Ryoji Minami, Nobutada Tachi, Shinji Saitoh

Journal:

Pediatric Neurology

Year:

1998

Language:

english

File:

PDF, 128 KB

english, 1998

46

Parent-of-Origin Specific Histone Acetylation and Reactivation of a Key Imprinted Gene Locus in Prader-Willi Syndrome

Shinji Saitoh, Takahito Wada

Journal:

The American Journal of Human Genetics

Year:

2000

Language:

english

File:

PDF, 384 KB

english, 2000

47

Impairment of glutathione metabolism in human gastric epithelial cells treated with vacuolating cytotoxin fromHelicobacter pylori

Miyuki Kimura, Shinji Goto, Yoshito Ihara, Akihiro Wada, Kinnosuke Yahiro, Takuro Niidome, Haruhiko Aoyagi, Toshiya Hirayama, Takahito Kondo

Journal:

Microbial Pathogenesis

Year:

2001

Language:

english

File:

PDF, 124 KB

english, 2001

48

Visualization of the spatial positioning of theSNRPN,UBE3A, andGABRB3genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization

Kawamura, Rie, Tanabe, Hideyuki, Wada, Takahito, Saitoh, Shinji, Fukushima, Yoshimitsu, Wakui, Keiko

Journal:

Chromosome Research

Year:

2012

Language:

english

File:

PDF, 516 KB

english, 2012

49

Idiopathic Cranial Polyneuropathy With Unilateral IX and X and Contralateral XI Nerve Palsy in a 4-Year-Old Boy

Naoko Yoshihara, Mitsuko Okuda, Kyoko Takano, Takahito Wada, Hitoshi Osaka

Journal:

Pediatric Neurology

Year:

2012

Language:

english

File:

PDF, 202 KB

english, 2012

50

A novel P gene missense mutation in a Japanese patient with oculocutaneous albinism type II (OCA2)

Kato, Atsushi, Fukai, Kazuyoshi, Oiso, Naoki, Hosomi, Naoko, Saitoh, Shinji, Wada, Takahito, Shimizu, Hiroshi, Ishii, Masamitsu

Journal:

Journal of Dermatological Science

Year:

2003

Language:

english

File:

PDF, 232 KB

english, 2003