Ichizo NISHINO


Ichizo NISHINO

J-GLOBAL         Last updated: Jun 3, 2019 at 16:38
 
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Name
Ichizo NISHINO
E-mail
nishinoncnp.go.jp
URL
http://scholar.google.com/citations?hl=en&user=uBzKcR0AAAAJ
Affiliation
National Center of Neurology and Psychiatry
Section
National Institute of Neuroscience, Ncnp, Department of Neuromuscular Research
Job title
Director
Degree
M.D., Ph.D.(Kyoto University)
Other affiliation
Waseda UniversityYamanashi University School of MedicineNational Chiao Tung University
ORCID ID
0000-0001-9452-112X

Research Areas

 
 

Academic & Professional Experience

 
2013
 - 
Today
Visiting Professor, College of Biological Science and Technology, National Chiao Tung University
 
2012
 - 
Today
Director, Department of Clinical Development, Translational Medical Center, National Center of Neurology and Psychiatry
 
2011
 - 
Today
Guest Professor, Yamanashi University School of Medicine
 
2004
 - 
Today
Guest Professor, Faculty of Science and Engineering, Waseda University
 
2001
 - 
Today
Director, Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry
 

Education

 
1983
 - 
1989
Faculty of Medicine, Kyoto University
 

Committee Memberships

 
2011
 - 
Today
TREAT-NMD Alliance  Executive Committee
 
2007
 - 
Today
World Muscle Society  Executive Board
 
2002
 - 
Today
Japanese Society of Neurology  Executive Board
 
2000
 - 
Today
Asian and Oceanian Myology Center  Executive Board, Secretary
 

Awards & Honors

 
2009
Japanese Society of Neurology Award
 
2001
Uchida Award
 

Published Papers

 
GNE myopathy in Chinese population: hotspot and novel mutations.
Chen Y, Xi J, Zhu W, Lin J, Luo S, Yue D, Cai S, Sun C, Zhao C, Mitsuhashi S, Nishino I, Xu M, Lu J
J Hum Genet.   64(1) 11-16   Jan 2019   [Refereed]
Three novel MTM1 pathogenic variants identified in Japanese patients with X-linked myotubular myopathy.
Nishikawa A, Iida A, Hayashi S, Okubo M, Oya Y, Yamanaka G, Takahashi I, Nonaka I, Noguchi S, Nishino I
Mol Genet Genomic Med.   7(5) e621   May 2019   [Refereed]
RNA sequencing solved the most common but unrecognized NEB pathogenic variant in Japanese nemaline myopathy.
Hamanaka K, Miyatake S, Koshimizu E, Tsurusaki Y, Mitsuhashi S, Iwama K, Alkanaq AN, Fujita A, Imagawa E, Uchiyama Y, Tawara N, Ando Y, Mitsumi Y, Okubo M, Nakashima M, Mizuguchi T, Takata A, Miyake N, Saitsu H, Iida A, Nishino I
Genet Med.   Epub ahead of print   2019   [Refereed]
Absence of sarcoplasmic MxA expression in antisynthetase syndrome in cohort of 194 cases.
Inoue M, Tanboon J, Okubo M, Theerawat K, Saito Y, Ogasawara M, Indrawati LA, Uruha A, Okiyama N, Fujimoto M, Suzuki S, Nishino I
Neuropathol Appl Neurobiol.   Epub Ahead of print   2019   [Refereed]
Three novel recessive DYSF mutations identified in three patients with muscular dystrophy, limb-girdle, type 2B.
Okubo M, Iida A, Hayashi S, Mori-Yoshimura M, Oya Y, Watanabe A, Arahata H, El Sherif R, Noguchi S, Nishino I
J Neurol Sci.   15(395) 169-171   Dec 2018   [Refereed]
Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation.
Tadokoro K, Ohta Y, Sasaki R, Takahashi Y, Sato K, Shang J, Takemoto M, Hishikawa N, Yamashita T, Nakamura K, Nishino I
J Neurol Sci.   393(2018) 142-144   Oct 2018   [Refereed]
A novel LMNA mutation identified in a Japanese patient with LMNA-associated congenital muscular dystrophy.
Ishiyama A, Iida A, Hayashi S, Komaki H, Sasaki M, Nonaka I, Noguchi S, Nishino I
Hum Genome Var.   2018(5) 19,ecollection   Jul 2018   [Refereed]
Two novel VCP missense variants identified in Japanese patients with multisystem proteinopathy.
Inoue M, Iida A, Hayashi S, Mori-Yoshimura M, Nagaoka A, Yoshimura S, Shiraishi H, Tsujino A, Takahashi Y, Nonaka I, Hayashi YK, Noguchi S, Nishino I
Hum Genome Var.   (5:9) eCllection   May 2018   [Refereed]
Transient swelling in the globus pallidus and substantia nigra in childhood suggests SENDA/ BPAN.
Ishiyama A, Kimura Y, Iida A, Saito Y, Miyamoto Y, Okada M, Sato N, Nishino I, Sasaki M
Neurology.   90(21) 974-976   May 2018   [Refereed]
10. Zhu W, Eto M, Mitsuhashi S, Takata K, Beck G, Sumi-Akamaru H, Mochizuki H, Sakoda S, Takahashi MP, Nishino I
Neuromuscul Disord   28(2) 154-157   Feb 2018   [Refereed]

Misc

 
Shi Z, Hayashi YK, Mitsuhashi S, Goto K, Kaneda D, Choi YC, Toyoda C, Hieda S, Kamiyama T, Sato H, Wada M, Noguchi S, Nonaka I, Nishino I
European journal of neurology : the official journal of the European Federation of Neurological Societies   19 501-509   Mar 2012   [Refereed]
Suzuki S, Hayashi YK, Kuwana M, Tsuburaya R, Suzuki N, Nishino I
Archives of neurology      Feb 2012   [Refereed]
Hattori A, Komaki H, Kawatani M, Sakuma H, Saito Y, Nakagawa E, Sugai K, Sasaki M, Hayashi YK, Nonaka I, Nishino I
Neuromuscular disorders : NMD   22 149-151   Feb 2012   [Refereed]
Malicdan MC, Noguchi S, Tokutomi T, Goto Y, Nonaka I, Hayashi YK, Nishino I
The Journal of biological chemistry   287 2689-2705   Jan 2012   [Refereed]
Matsuura T, Minami N, Arahata H, Ohno K, Abe K, Hayashi YK, Nishino I
Journal of human genetics      Jan 2012   [Refereed]

Conference Activities & Talks

 
GNE myopathy.
Ichizo NISHINO
4th International Neuromuscular Congress of Iran   26 Sep 2018   
New histological classification of idiopathic inflammatory myopathies.
Ichizo NISHINO
4th International Neuromuscular Congress of Iran   26 Sep 2018   
Muscle pathology in the era of NGS.
Ichizo NISHINO
19th International Congress of Neuropathology   23 Sep 2018   
Mouse and zebra fish models.
Ichizo NISHINO
237th ENMC International Workshop: GNE myopathy   15 Sep 2018   
GNE cohort and natural history study in Japan.
Ichizo NISHINO
237th ENMC International Workshop: GNE myopathy   14 Sep 2018   

Research Grants & Projects

 
Elucidation of pathomechanism of and development of therapy of hereditary muscle diseases
Development of therapy of distal myopathy with rimmed vacuoles/hereditary inclusion body myopathy
Elucidation of pathomechanism of and development of therapy of lysosomal muscle diseases