研修医・長期短期専修医募集

業 績


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■ Neuro-Tokushima achievements 2012

 

1.論文・ 著書など (アルファベット順または五十音順)

1A 英文

1A-a. 原著

 

Fujita K, Harada M, Sasaki M, Yuasa T, Sakai K, Hamaguchi T, Sanjo N, Shiga Y, Satoh K, Atarashi R, Shirabe S, Nagata K, Maeda T, Murayama S, Izumi Y, Kaji R, Yamada M, Mizusawa H. Multicentre multiobserver study of diffusion-weighted and fluid-attenuated inversion recovery MRI for the diagnosis of sporadic Creutzfeldt-Jakob disease: a reliability and agreement study. BMJ Open 2012; 2(1): e000649

PubMed  Journal

  

Fujita K, Yuasa T, Takahashi Y, Tanaka K, Hashiguchi S, Adachi K, Izumi Y, Kaji R. Detection of anti-glutamate receptor ε2 and anti-N-methyl-D-aspartate receptor antibodies in a patient with sporadic Creutzfeldt-Jakob disease. J Neurol 2012; 259(5): 985-988

PubMed  Journal

 

Fujita K, Yuasa T, Takahashi Y, Tanaka K, Sako W, Koizumi H, Iwasaki Y, Yoshida M, Izumi Y, Kaji R. Antibodies to N-methyl-D-aspartate glutamate receptors in Creutzfeldt-Jakob disease patients. J Neuroimmunol 2012; 251(1-2): 90-93

PubMed  Journal

 

Fujita K, Yuasa T, Watanabe O, Takahashi Y, Hashiguchi S, Adachi K, Izumi Y, Kaji R. Voltage-gated potassium channel complex antibodies in Creutzfeldt-Jakob disease. J Neurol 2012; 259(10): 2249-2250

PubMed   Journal

 

Ishiura H, Sako W, Yoshida M, Kawarai T, Tanabe O, Goto J, Takahashi Y, Date H, Mitsui J, Ahsan B, Ichikawa Y, Iwata A, Yoshino H, Izumi Y, Fujita K, Maeda K, Goto S, Koizumi H, Morigaki R, Ikemura M, Yamauchi N, Murayama S, Nicholson GA, Ito H, Sobue G, Nakagawa M, Kaji R, Tsuji S. The TRK-Fused Gene Is Mutated in Hereditary Motor and Sensory Neuropathy with Proximal Dominant Involvement. Am J Hum Genet 2012; 91(2): 320-329

PubMed  Journal

   

Kuroda Y, Sako W, Goto S, Sawada T, Uchida D, Izumi Y, Takahashi T, Kagawa N, Matsumoto M, Matsumoto M, Takahashi R, Kaji R, Mitsui T. Parkin interacts with Klokin1 for mitochondrial import and maintenance of membrane potential. Hum Mol Genet 2012; 21(5): 991-1003

PubMed  Journal

 

Mezaki T, Kaji R. Reduced serum ceruloplasmin levels in cervical dystonia. Eur Neurol 2012; 67(4): 256

PubMed  Journal

 

Miyamoto R, Goto S, Sako W, Miyashiro A, Kim I, Escande F, Harada M, Morigaki R, Asanuma K, Mizobuchi Y, Nagahiro S, Izumi Y, Kaji R. Generalized dystonia in a patient with a novel mutation in the GLUD1 gene. Mov Disord 2012; 27(9): 1198-1199

PubMed  Journal

 

Miyamoto R, Ohta E, Kawarai T, Koizumi H, Sako W, Izumi Y, Obata F, Kaji R. Broad spectrum of dystonia associated with a novel thanatosis-associated protein domain-containing apoptosis-associated protein 1 mutation in a Japanese family with dystonia 6, torsion. Mov Disord 2012; 27(10): 1324-1325

PubMed  Journal

 

Miyazaki Y, Sako W, Asanuma K, Izumi Y, Miki T, Kaji R. Efficacy of zolpidem for dystonia: a study among different subtypes. Front Neurol 2012; 3: 58

PubMed  Journal

 

Nodera H, Rutkove SB. Long-term nerve excitability changes by persistent Na+ current blocker ranolazine. Neurosci Lett 2012; 524(2): 101-106

PubMed   Journal

  

Obayashi M, Ishikawa K, Izumi Y, Takahashi M, Niimi Y, Sato N, Onodera O, Kaji R, Nishizawa M, Mizusawa H. Prevalence of inositol 1, 4, 5-triphosphate receptor type 1 gene deletion, the mutation for spinocerebellar ataxia type 15, in Japan screened by gene dosage. J Hum Genet 2012; 57(3): 202-206

PubMed  Journal

 

Ogaki K, Li Y, Atsuta N, Tomiyama H, Funayama M, Watanabe H, Nakamura R, Yoshino H, Yato S, Tamura A, Naito Y, Taniguchi A, Fujita K, Izumi Y, Kaji R, Hattori N, Sobue G; Japanese Consortium for Amyotrophic Lateral Sclerosis research (JaCALS). Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis. Neurobiol Aging 2012; 33(10): 2527.e11-16

PubMed  Journal

 

Okita S, Morigaki R, Koizumi H, Kaji R, Nagahiro S, Goto S. Cell type-specific localization of optineurin in the striatal neurons of mice: implications for neuronal vulnerability in Huntington's disease. Neuroscience 2012; 202: 363-370

PubMed  Journal

 

Sako W, Ito H, Yoshida M, Koizumi H, Kamada M, Fujita K, Hashizume Y, Izumi Y, Kaji R. Nuclear factor κ B expression in patients with sporadic amyotrophic lateral sclerosis and hereditary amyotrophic lateral sclerosis with optineurin mutations. Clin Neuropathol 2012; 31(6): 418-423

PubMed  Journal

 

Sugihara K, Maruyama H, Morino H, Miyamoto R, Ueno H, Matsumoto M, Kaji R, Kitaguchi H, Yukitake M, Higashi Y, Nishinaka K, Oda M, Izumi Y, Kawakami H. The clinical characteristics of spinocerebellar ataxia 36: A study of 2121 Japanese ataxia patients. Mov Disord 2012; 27(9): 1158-1163

PubMed  Journal

 

Terasawa Y, Fujita K, Izumi Y, Kaji R. Early detection of familial Creutzfeldt-Jakob disease on diffusion-weighted imaging before symptom onset. J Neurol Sci 2012; 319(1-2): 130-132

PubMed  Journal

 

1A-b. 総説

 

Kaji R, Izumi Y, Adachi Y, Kuzuhara S. ALS-parkinsonism-dementia complex of Kii and other related diseases in Japan. Parkinsonism Relat Disord 2012; 18 Suppl 1: S190-191

PubMed  Journal