Rinsho Shinkeigaku (Clinical Neurology)

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Vol.56 No.6 contents

Review

Autosomal recessive spinocerebellar ataxias in Japan

Fumiaki Tanaka, M.D., Ph.D.1), Hiroshi Doi, M.D., Ph.D.1) and Misako Kunii, M.D., Ph.D.1)

CLINICA NEUROL, 56: 395|399, 2016

Original Article

[123I]-Ioflupane SPECT in combination with MIBG myocardial scintigraphy in Parkinson's disease: a case series study

Akane Yamada, M.D.1), Takenobu Murakami, M.D., Ph.D.1)2)3), Yongjin Kang, M.D., Ph.D.4), Yoichiro Iikuni, M.D.1), Akeshi Morimatsu, M.D.1), Akiko Shirata, M.D., Ph.D.1), Hiroshi Ito, M.D., Ph.D.3), Yoshikazu Ugawa, M.D., Ph.D.2) and Kiyomi Yamane, M.D., Ph.D.1)

CLINICA NEUROL, 56: 400|406, 2016

Original Article

Survey on genetic counseling and health management for symptomatic and asymptomatic female dystrophinopathy carriers in Japan today

Michio Kobayashi, M.D., Ph.D.1), Masatoshi Ishizaki, M.D., Ph.D.2), Katsuhito Adachi, M.D., Ph.D.3), Naohiro Yonemoto, M.P.H.4), Tsuyoshi Matsumura, M.D., Ph.D.5), Itaru Toyoshima, M.D., Ph.D.1) and En Kimura, M.D., Ph.D.4)

CLINICA NEUROL, 56: 407|412, 2016

Case Report

A case considered gluten ataxia with anti-TG6 IgA antibodies

Kenji Sato, M.D.1)3), Makiko Kobayashi, M.D.2), Yuki Ueta, M.D.3), Nobuyuki Tanaka, M.D.3) and Kazunori Nanri, M.D.3)

CLINICA NEUROL, 56: 413|417, 2016

Case Report

Dementia with Lewy bodies presenting marked tongue protrusion and bite due to lingual dystonia: A case report

Yuji Shiga, M.D.1), Yuhei Kanaya, M.D.1), Ryuhei Kono, M.D.1)2), Shinichi Takeshima, M.D.1), Yutaka Shimoe, M.D., Ph.D.1) and Masaru Kuriyama, M.D., Ph.D.1)

CLINICA NEUROL, 56: 418|423, 2016

Case Report

A case of variant biochemical phenotype of Niemann-Pick disease type C accompanying savant syndrome

Mio Hamatani, M.D.1), Naoto Jingami, M.D.1), Kengo Uemura, M.D., Ph.D.1)2), Naoe Nakasone3), Hisanori Kinoshita, M.D.1), Hodaka Yamakado, M.D., Ph.D.1), Haruaki Ninomiya, M.D., Ph.D.3) and Ryosuke Takahashi, M.D., Ph.D.1)

CLINICA NEUROL, 56: 424|429, 2016

Case Report

Familial amyloid polyneuropathy involving a homozygous Val30Met mutation in the amyloidogenic transthyretin gene presenting with superficial siderosis: a case report

Yuta Maetani, M.D.1), Dai Agari, M.D.1), Eiichi Nomura, M.D., Ph.D.1), Mitsuharu Ueda, M.D., Ph.D.2), Yukio Ando, M.D., Ph.D.2) and Takemori Yamawaki, M.D., Ph.D.1)

CLINICA NEUROL, 56: 430|434, 2016

Brief Clinical Note

Herpes simplex encephalitis without cerebrospinal fluid pleocytosis in a patient with bullous pemphigoid: a case report

Yoshitsugu Nakamura, M.D.1), Kensuke Kakiuti, M.D.1), Hiroki Tani, M.D.1), Hideto Nakajima, M.D.1), Fumiharu Kimura, M.D.1) and Toshiaki Hanafusa, M.D.1)

CLINICA NEUROL, 56: 435|438, 2016

Brief Clinical Note

Sporadic adult-onset neuronal intranuclear inclusion disease with the main presentation of repeated cerebellar ataxia: a case study

Takeo Sakurai, M.D.1), Seiko Harada, M.D.1), Kenji Wakida, M.D.1), Mari Yoshida, M.D.2) and Hiroshi Nishida, M.D.1)

CLINICA NEUROL, 56: 439|443, 2016

The Proceedings of the 2015 Hokkaido Regional Post Graduate Education Meeting

CLINICA NEUROL, 56: 444|446, 2016

The Proceedings of the 98th Hokkaido Regional Meeting of the Japanese Society of Neurology

CLINICA NEUROL, 56: 447|453, 2016

Notice for Members

CLINICA NEUROL, 56: 454|454, 2016

Editor's Note

CLINICA NEUROL, 56: 455|455, 2016