医療者向けTOP
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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
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
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
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
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
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
Mezaki T, Kaji R. Reduced serum ceruloplasmin levels in cervical
dystonia. Eur Neurol 2012; 67(4): 256
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
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
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
Nodera
H, Rutkove SB. Long-term nerve excitability
changes by persistent Na+ current blocker ranolazine. Neurosci Lett 2012;
524(2): 101-106
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
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
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
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
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
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
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