Matsukawa Takashi

Research keywords (5)： Leukodystrophy , Multiple system atrophy , Genetics , Neurology , Adrenoleukodystrophy

Papers (9)：

Takamichi Kanbayashi, Fumiaki Saito, Takashi Matsukawa, Hiroshi Oba, Keiichi Hokkoku, Yuki Hatanaka, Shoji Tsuji, Masahiro Sonoo. Adult-onset vanishing white matter disease with novel missense mutations in a subunit of translational regulator, EIF2B4. CLINICAL GENETICS. 2015. 88. 4. 401-403
Jun Mitsui, Takashi Matsukawa, Hidenao Sasaki, Ichiro Yabe, Masaaki Matsushima, Alexandra Duerr, Alexis Brice, Hiroshi Takashima, Akio Kikuchi, Masashi Aoki, et al. Variants associated with Gaucher disease in multiple system atrophy. ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. 2015. 2. 4. 417-426
Ryo Ohtomo, Takashi Matsukawa, Shoji Tsuji, Atsushi Iwata. Abadie's sign in adrenomyeloneuropathy. JOURNAL OF THE NEUROLOGICAL SCIENCES. 2014. 340. 1-2. 245-246
Yuji Takahashi, Yoko Fukuda, Jun Yoshimura, Atsushi Toyoda, Kari Kurppa, Hiroyoko Moritoyo, Veronique V. Belzil, Patrick A. Dion, Koichiro Higasa, Koichiro Doi, et al. ERBB4 Mutations that Disrupt the Neuregulin-ErbB4 Pathway Cause Amyotrophic Lateral Sclerosis Type 19. AMERICAN JOURNAL OF HUMAN GENETICS. 2013. 93. 5. 900-905
Jun Mitsui, Takashi Matsukawa, Hiroyuki Ishiura, Koichiro Higasa, Jun Yoshimura, Taro L. Saito, Budrul Ahsan, Yuji Takahashi, Jun Goto, Atsushi Iwata, et al. CSF1R Mutations Identified in Three Families With Autosomal Dominantly Inherited Leukoencephalopathy. AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2012. 159B. 8. 951-957

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MISC (13)：

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Work history (9)：

2014 - 2015 日本学術振興会特別研究員(PD)
2015 - The University of Tokyo Faculty of Medicine University Hospital, Department of Neurology
2013 - 2014 日本学術振興会特別研究員(DC2)
2010 - 2014 東京大学大学院医学系研究科脳神経医学専攻神経内科博士課程大学院生
2009 - 2010 The University of Tokyo Faculty of Medicine University Hospital, Department of Neurology

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