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Nobutaka Hattori
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142
Mizuno, Yoshikuni
24
Mori, Hideo
21
Yoshino, Hiroyo
18
Shimizu, Nobuyoshi
15
Matsumine, Hiroto
15
Asakawa, Shuichi
15
Tomiyama, Hiroyuki
13
Urabe, Takao
13
Minoshima, Shinsei
12
Kitada, Tohru
11
Li, Yuanzhe
11
Tanaka, Keiji
10
Sato, Kenichi
9
Sato, Shigeto
9
Shimura, Hideki
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All Publications
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2009: Asakawa Shuichi; Hattori Nobutaka; Shimizu Atsushi; Shimizu Yoshiko; Minoshima Shinsei; Mizuno Yoshikuni; Shimizu Nobuyoshi
Analysis of eighteen deletion breakpoints in the parkin gene.
Biochemical and biophysical research communications 2009;389(1):181-6.
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2009: Yatomi Kenji; Miyamoto Nobukazu; Komine-Kobayashi Miki; Liu Meizi; Oishi Hidenori; Arai Hajime; Hattori Nobutaka; Urabe Takao
Pathophysiological dual action of adiponectin after transient focal ischemia in mouse brain.
Brain research 2009;1297():169-76.
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2009: Miyamoto Nobukazu; Tanaka Ryota; Shimosawa Tatsuo; Yatomi Yutaka; Fujita Toshiro; Hattori Nobutaka; Urabe Takao
Protein kinase A-dependent suppression of reactive oxygen species in transient focal ischemia in adrenomedullin-deficient mice.
Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2009;29(11):1769-79.
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2009: Iijima M; Tomita M; Morozumi S; Kawagashira Y; Nakamura T; Koike H; Katsuno M; Hattori N; Tanaka F; Yamamoto M; Sobue G
Single nucleotide polymorphism of TAG-1 influences IVIg responsiveness of Japanese patients with CIDP.
Neurology 2009;73(17):1348-52.
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2009: Okuma Yasuyuki; Kamei Satoshi; Morita Akihiko; Yoshii Fumihito; Yamamoto Toshimasa; Hashimoto Shiori; Utsumi Hiroya; Hatano Taku; Hattori Nobutaka; Matsumura Miyuki; Takahashi Kazushi; Nogawa Shigeru; Watanabe Yuka; Miyamoto Tomoyuki; Miyamoto Masayuki; Hirata Koichi
Fatigue in Japanese patients with Parkinson's disease: a study using Parkinson fatigue scale.
Movement disorders : official journal of the Movement Disorder Society 2009;24(13):1977-83.
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2009: Nishioka Kenya; Ross Owen A; Ishii Kenji; Kachergus Jennifer M; Ishiwata Kiichi; Kitagawa Mayumi; Kono Satoshi; Obi Tomokazu; Mizoguchi Koichi; Inoue Yuichi; Imai Hisamasa; Takanashi Masashi; Mizuno Yoshikuni; Farrer Matthew J; Hattori Nobutaka
Expanding the clinical phenotype of SNCA duplication carriers.
Movement disorders : official journal of the Movement Disorder Society 2009;24(12):1811-9.
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2009: Liu M; Eguchi N; Yamasaki Y; Urade Y; Hattori N; Urabe T
Protective role of hematopoietic prostaglandin D synthase in transient focal cerebral ischemia in mice.
Neuroscience 2009;163(1):296-307.
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2009: Saiki Shinji; Ueno Yuji; Moritani Toshio; Sato Takeshi; Sekine Takeshi; Kawajiri Sumihiro; Adachi Satoshi; Yokoyama Kazumasa; Tomizawa Yuji; Motoi Yumiko; Hattori Nobutaka
Extensive hemispheric lesions with radiological evidence of blood-brain barrier integrity in a patient with neuromyelitis optica.
Journal of the neurological sciences 2009;284(1-2):217-9.
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2009: Saiki Shinji; Sekine Takeshi; Ueno Yuji; Yoshino Hiroyo; Takahashi Junko; Tani Yoshihiko; Kambe Yasunori; Motoi Yumiko; Hattori Nobutaka
[An adult-onset case of idiopathic neurodegeneration with brain iron accumulation without mutations in the PANK2 and PLA2G6 genes]
Rinsho shinkeigaku = Clinical neurology 2009;49(8):474-8.
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2009: Tatsuta Kuniaki; Yoshihara Shusuke; Hattori Nobutaka; Yoshida Shinpei; Hosokawa Seijiro
The first total synthesis of nidulalin A, a dihydroxanthone possessing multiple bioactivities.
The Journal of antibiotics 2009;62(8):469-70.
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2009: Miyamoto N; Tanaka R; Zhang N; Shimura H; Onodera M; Mochizuki H; Hattori N; Urabe T
Crucial role for Ser133-phosphorylated form of cyclic AMP-responsive element binding protein signaling in the differentiation and survival of neural progenitors under chronic cerebral hypoperfusion.
Neuroscience 2009;162(2):525-36.
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2009: Ueno Y; Zhang N; Miyamoto N; Tanaka R; Hattori N; Urabe T
Edaravone attenuates white matter lesions through endothelial protection in a rat chronic hypoperfusion model.
Neuroscience 2009;162(2):317-27.
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2009: Sasaki Kumi; Shimura Hideki; Itaya Masako; Tanaka Ryota; Mori Hideo; Mizuno Yoshikuni; Kosik Kenneth S; Tanaka Shigeki; Hattori Nobutaka
Excitatory amino acid transporter 2 associates with phosphorylated tau and is localized in neurofibrillary tangles of tauopathic brains.
FEBS letters 2009;583(13):2194-200.
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2009: Kanai Kazuaki; Asahina Masato; Arai Kimihito; Tomiyama Hiroyuki; Kuwabara Yoichi; Uchiyama Tomoyuki; Sekiguchi Yukari; Funayama Manabu; Kuwabara Satoshi; Hattori Nobutaka; Hattori Takamichi
Preserved cardiac (123)I-MIBG uptake and lack of severe autonomic dysfunction in a PARK9 patient.
Movement disorders : official journal of the Movement Disorder Society 2009;24(9):1403-4.
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2009: Pirkevi C; Lesage S; Condroyer C; Tomiyama H; Hattori N; Ertan S; Brice A; Basak A N
A LRRK2 G2019S mutation carrier from Turkey shares the Japanese haplotype.
Neurogenetics 2009;10(3):271-3.
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2009: Saiki Shinji; Hattori Nobutaka
[Molecular genetics and pathogenesis of Parkinson disease]
No shinkei geka. Neurological surgery 2009;37(6):531-41.
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2009: Shiba Kahori; Arai Takeo; Sato Shigeto; Kubo Shin-ichiro; Ohba Yusuke; Mizuno Yoshikuni; Hattori Nobutaka
Parkin stabilizes PINK1 through direct interaction.
Biochemical and biophysical research communications 2009;383(3):331-5.
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2009: Hatano T; Kubo S-I; Shimo Y; Nishioka K; Hattori N
Unmet needs of patients with Parkinson's disease: interview survey of patients and caregivers.
The Journal of international medical research 2009;37(3):717-26.
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2009: Mitsui Jun; Mizuta Ikuko; Toyoda Atsushi; Ashida Ryo; Takahashi Yuji; Goto Jun; Fukuda Yoko; Date Hidetoshi; Iwata Atsushi; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi; Tsuji Shoji
Mutations for Gaucher disease confer high susceptibility to Parkinson disease.
Archives of neurology 2009;66(5):571-6.
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2009: Tomiyama Hiroyuki; Li Yuanzhe; Yoshino Hiroyo; Mizuno Yoshikuni; Kubo Shin-Ichiro; Toda Tatsushi; Hattori Nobutaka
Mutation analysis for DJ-1 in sporadic and familial parkinsonism: screening strategy in parkinsonism.
Neuroscience letters 2009;455(3):159-61.
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2009: Natori Shihoko; Yoshimi Kenji; Takahashi Toshimitsu; Kagohashi Maki; Oyama Genko; Shimo Yasushi; Hattori Nobutaka; Kitazawa Shigeru
Subsecond reward-related dopamine release in the mouse dorsal striatum.
Neuroscience research 2009;63(4):267-72.
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2009: Urabe Takao; Watada Hirotaka; Okuma Yasuyuki; Tanaka Ryota; Ueno Yuji; Miyamoto Nobukazu; Tanaka Yasutaka; Hattori Nobutaka; Kawamori Ryuzo
Prevalence of abnormal glucose metabolism and insulin resistance among subtypes of ischemic stroke in Japanese patients.
Stroke; a journal of cerebral circulation 2009;40(4):1289-95.
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2009: Oyama Genko; Hayashi Akito; Mizuno Yoshikuni; Hattori Nobutaka
Mechanism and treatment of dropped head syndrome associated with parkinsonism.
Parkinsonism & related disorders 2009;15(3):181-6.
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2009: Fukae Jiro; Sato Shigeto; Shiba Kahori; Sato Ken-ichi; Mori Hideo; Sharp Philip A; Mizuno Yoshikuni; Hattori Nobutaka
Programmed cell death-2 isoform1 is ubiquitinated by parkin and increased in the substantia nigra of patients with autosomal recessive Parkinson's disease.
FEBS letters 2009;583(3):521-5.
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2009: Kamigaichi R; Kubo S; Ishikawa K; Yokoyama K; Ogaki K; Usui C; Hatta K; Arai H; Mochizuki H; Hattori N
Effective control of catatonia in Parkinson's disease by electroconvulsive therapy: a case report.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2009;16(2):e6.
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2009: Yasuda Toru; Nihira Tomoko; Ren Yong-Ri; Cao Xu-Qing; Wada Keiichiro; Setsuie Rieko; Kabuta Tomohiro; Wada Keiji; Hattori Nobutaka; Mizuno Yoshikuni; Mochizuki Hideki
Effects of UCH-L1 on alpha-synuclein over-expression mouse model of Parkinson's disease.
Journal of neurochemistry 2009;108(4):932-44.
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2009: Momma Kazunari; Funayama Manabu; Li Yuanzhe; Ichinose Hiroshi; Motoyoshi Kazuo; Hattori Nobutaka; Mizuno Yoshikuni; Kamakura Keiko
A new mutation in the GCH1 gene presents as early-onset Parkinsonism.
Parkinsonism & related disorders 2009;15(2):160-1.
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2009: Mellick George D; Siebert Gerhard A; Funayama Manabu; Buchanan Daniel D; Li Yuanzhe; Imamichi Yoko; Yoshino Hiroyo; Silburn Peter A; Hattori Nobutaka
Screening PARK genes for mutations in early-onset Parkinson's disease patients from Queensland, Australia.
Parkinsonism & related disorders 2009;15(2):105-9.
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2009: Ichikawa Naoki; Iwabuchi Kazuhisa; Kurihara Hidetake; Ishii Kumiko; Kobayashi Toshihide; Sasaki Takako; Hattori Nobutaka; Mizuno Yoshikuni; Hozumi Kentaro; Yamada Yoshihiko; Arikawa-Hirasawa Eri
Binding of laminin-1 to monosialoganglioside GM1 in lipid rafts is crucial for neurite outgrowth.
Journal of cell science 2009;122(Pt 2):289-99.
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2009: Miyauchi Katsumi; Takaya Norihide; Hirose Takahisa; Ikeda Fuki; Kawamori Ryuzo; Ohishi Hidenori; Yoshida Kensaku; Yamamoto Munetaka; Arai Hajime; Urabe Takao; Hattori Nobutaka; Suzuki Michimasa; Maehara Tadayuki; Sase Kazuhiro; Hatsukami Thomas S; Yuan Chun; Daida Hiroyuki
Rationale and design of the carotid plaque in human for all evaluations with aggressive rosuvastatin therapy (CHALLENGER trial): evaluation by magnetic resonance imaging.
Circulation journal : official journal of the Japanese Circulation Society 2009;73(1):111-5.
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2009: Arimura Takuro; Hayashi Yukiko K; Murakami Terumi; Oya Yasushi; Funabe Sayaka; Arikawa-Hirasawa Eri; Hattori Nobutaka; Nishino Ichizo; Kimura Akinori
Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy.
Circulation journal : official journal of the Japanese Circulation Society 2009;73(1):158-61.
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2009: Suzuki Keisuke; Miyamoto Masayuki; Miyamoto Tomoyuki; Okuma Yasuyuki; Hattori Nobutaka; Kamei Satoshi; Yoshii Fumihito; Utsumi Hiroya; Iwasaki Yasuo; Iijima Mutsumi; Hirata Koichi
Correlation between depressive symptoms and nocturnal disturbances in Japanese patients with Parkinson's disease.
Parkinsonism & related disorders 2009;15(1):15-9.
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2009: Tomizawa Yuji; Fukae Jiro; Noda Kazuyuki; Fujishima Kenji; Yokoyama Kazumasa; Hattori Nobutaka; Takahashi Toshiyuki; Okuma Yasuyuki
Linear medullary pericanal lesion with longitudinal myelitis can be diagnostic of neuromyelitis optica.
Internal medicine (Tokyo, Japan) 2009;48(3):175-6.
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2009: Yoritaka Asako; Ohizumi Hideki; Tanaka Shigeki; Hattori Nobutaka
Parkinson's disease with and without REM sleep behaviour disorder: are there any clinical differences?
European neurology 2009;61(3):164-70.
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2008: Diaz-Corrales Francisco J; Asanuma Masato; Miyazaki Ikuko; Miyoshi Ko; Hattori Nobutaka; Ogawa Norio
Dopamine induces supernumerary centrosomes and subsequent cell death through Cdk2 up-regulation in dopaminergic neuronal cells.
Neurotoxicity research 2008;14(4):295-305.
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2008: Tomiyama Hiroyuki; Kokubo Yasumasa; Sasaki Ryogen; Li Yuanzhe; Imamichi Yoko; Funayama Manabu; Mizuno Yoshikuni; Hattori Nobutaka; Kuzuhara Shigeki
Mutation analyses in amyotrophic lateral sclerosis/parkinsonism-dementia complex of the Kii peninsula, Japan.
Movement disorders : official journal of the Movement Disorder Society 2008;23(16):2344-8.
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2008: Hattori Nobutaka
[Recent progress in Parkinson's disease]
Rinsho shinkeigaku = Clinical neurology 2008;48(11):980.
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2008: Yamashita Hiroshi; Kohriyama Tatsuo; Ohshita Tomohiko; Takahashi Tetsuya; Hashikawa Kazuo; Hattori Nobutaka; Fukuyama Hidenao; Matsumoto Masayasu
[Case of a 30-year history of PARK6 --findings from functional imaging of the brain]
Rinsho shinkeigaku = Clinical neurology 2008;48(9):662-5.
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2008: Han Baek-Soo; Iacovitti Lorraine; Katano Taku; Hattori Nobutaka; Seol Wongi; Kim Kwang-Soo
Expression of the LRRK2 gene in the midbrain dopaminergic neurons of the substantia nigra.
Neuroscience letters 2008;442(3):190-4.
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2008: Mizuta Ikuko; Tsunoda Tatsuhiko; Satake Wataru; Nakabayashi Yuko; Watanabe Masahiko; Takeda Atsushi; Hasegawa Kazuko; Nakashima Kenji; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.
Human genetics 2008;124(1):89-94.
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2008: Suzuki Keisuke; Miyamoto Tomoyuki; Miyamoto Masayuki; Okuma Yasuyuki; Hattori Nobutaka; Kamei Satoshi; Yoshii Fumihito; Utsumi Hiroya; Iwasaki Yasuo; Iijima Mutsumi; Hirata Koichi
Excessive daytime sleepiness and sleep episodes in Japanese patients with Parkinson's disease.
Journal of the neurological sciences 2008;271(1-2):47-52.
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2008: Funayama Manabu; Li Yuanzhe; Tsoi Tak-Hong; Lam Ching-Wan; Ohi Takekazu; Yazawa Shogo; Uyama Eiichiro; Djaldetti Ruth; Melamed Eldad; Yoshino Hiroyo; Imamichi Yoko; Takashima Hiroshi; Nishioka Kenya; Sato Kenichi; Tomiyama Hiroyuki; Kubo Shin-Ichiro; Mizuno Yoshikuni; Hattori Nobutaka
Familial Parkinsonism with digenic parkin and PINK1 mutations.
Movement disorders : official journal of the Movement Disorder Society 2008;23(10):1461-5.
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2008: Miyamoto Nobukazu; Zhang Ning; Tanaka Ryota; Liu Meizi; Hattori Nobutaka; Urabe Takao
Neuroprotective role of angiotensin II type 2 receptor after transient focal ischemia in mice brain.
Neuroscience research 2008;61(3):249-56.
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2008: Ross Owen A; Wu Yih-Ru; Lee Mei-Ching; Funayama Manabu; Chen Meng-Ling; Soto Alexandra I; Mata Ignacio F; Lee-Chen Guey-Jen; Chen Chiung Mei; Tang Michelle; Zhao Yi; Hattori Nobutaka; Farrer Matthew J; Tan Eng-King; Wu Ruey-Meei
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease.
Annals of neurology 2008;64(1):88-92.
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2008: Ross Owen A; Braithwaite Adam T; Skipper Lisa M; Kachergus Jennifer; Hulihan Mary M; Middleton Frank A; Nishioka Kenya; Fuchs Julia; Gasser Thomas; Maraganore Demetrius M; Adler Charles H; Larvor Lydie; Chartier-Harlin Marie-Christine; Nilsson Christer; Langston J William; Gwinn Katrina; Hattori Nobutaka; Farrer Matthew J
Genomic investigation of alpha-synuclein multiplication and parkinsonism.
Annals of neurology 2008;63(6):743-50.
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2008: Kumazawa Ryuya; Tomiyama Hiroyuki; Li Yuanzhe; Imamichi Yoko; Funayama Manabu; Yoshino Hiroyo; Yokochi Fusako; Fukusako Toshihiro; Takehisa Yasushi; Kashihara Kenichi; Kondo Tomoyoshi; Elibol Bulent; Bostantjopoulou Sevasti; Toda Tatsushi; Takahashi Hirohide; Yoshii Fumihito; Mizuno Yoshikuni; Hattori Nobutaka
Mutation analysis of the PINK1 gene in 391 patients with Parkinson disease.
Archives of neurology 2008;65(6):802-8.
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2008: Shin Narae; Jeong Hyerhan; Kwon Jungsun; Heo Hye Young; Kwon Jung June; Yun Hye Jin; Kim Cy-Hyun; Han Baek Soo; Tong Youren; Shen Jie; Hatano Taku; Hattori Nobutaka; Kim Kwang-Soo; Chang Sunghoe; Seol Wongi
LRRK2 regulates synaptic vesicle endocytosis.
Experimental cell research 2008;314(10):2055-65.
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2008: Mizuno Yoshikuni; Hattori Nobutaka; Kubo Shin-Ichiro; Sato Shigeto; Nishioka Kenya; Hatano Taku; Tomiyama Hiroyuki; Funayama Manabu; Machida Yutaka; Mochizuki Hideki
Progress in the pathogenesis and genetics of Parkinson's disease.
Philosophical transactions of the Royal Society of London. Series B, Biological sciences 2008;363(1500):2215-27.
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2008: Yamashiro Kazuo; Komine-Kobayashi Miki; Hatano Taku; Urabe Takao; Mochizuki Hideki; Hattori Nobutaka; Iwama Yoshitaka; Daida Hiroyuki; Sakai Michi; Nakayama Takeo; Mizuno Yoshikuni
The frequency of cardiac valvular regurgitation in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2008;23(7):935-41.
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2008: Chan Daniel Kam Yin; Mok Vincent; Ng Ping Wing; Yeung Jonas; Kwok John B; Fang Zhi Ming; Clarke Raymond; Wong Lawrence; Schofield Peter R; Hattori Nobutaka
PARK2 mutations and clinical features in a Chinese population with early-onset Parkinson's disease.
Journal of neural transmission (Vienna, Austria : 1996) 2008;115(5):715-9.
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2008: Ning Y P; Kanai K; Tomiyama H; Li Y; Funayama M; Yoshino H; Sato S; Asahina M; Kuwabara S; Takeda A; Hattori T; Mizuno Y; Hattori N
PARK9-linked parkinsonism in eastern Asia: mutation detection in ATP13A2 and clinical phenotype.
Neurology 2008;70(16 Pt 2):1491-3.
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2008: Hirayama T; Fukae J; Noda K; Fujishima K; Yamamoto T; Mori K; Maeda M; Hattori N; Shiroma N; Tsurui S; Okuma Y
Adult-onset Alexander disease with palatal myoclonus and intraventricular tumour.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2008;15(2):e16-7.
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2008: Obi T; Nishioka K; Ross O A; Terada T; Yamazaki K; Sugiura A; Takanashi M; Mizoguchi K; Mori H; Mizuno Y; Hattori N
Clinicopathologic study of a SNCA gene duplication patient with Parkinson disease and dementia.
Neurology 2008;70(3):238-41.
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2008: Kagohashi Maki; Nakazato Taizo; Yoshimi Kenji; Moizumi Shunjiro; Hattori Nobutaka; Kitazawa Shigeru
Wireless voltammetry recording in unanesthetised behaving rats.
Neuroscience research 2008;60(1):120-7.
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2008: Tomiyama Hiroyuki; Mizuta Ikuko; Li Yuanzhe; Funayama Manabu; Yoshino Hiroyo; Li Lin; Murata Miho; Yamamoto Mitsutoshi; Kubo Shin-Ichiro; Mizuno Yoshikuni; Toda Tatsushi; Hattori Nobutaka
LRRK2 P755L variant in sporadic Parkinson's disease.
Journal of human genetics 2008;53(11-12):1012-5.
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2008: Kubo Shin-ichiro; Iwatake Akira; Ebihara Nobuyuki; Murakami Akira; Hattori Nobutaka
Visual impairment in Parkinson's disease treated with amantadine: case report and review of the literature.
Parkinsonism & related disorders 2008;14(2):166-9.
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2007: Fukae Jiro; Noda Kazuyuki; Fujishima Kenji; Wada Ryo; Yoshiike Takashi; Hattori Nobutaka; Okuma Yasuyuki
Successful treatment of relapsing neuro-Sweet's disease with corticosteroid and dapsone combination therapy.
Clinical neurology and neurosurgery 2007;109(10):910-3.
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2007: Hattori Nobutaka; Kubo Shin-ichiro
[The pathogenesis of Parkinson's disease: a hint from insights of familial Parkinson's disease]
Rinsho shinkeigaku = Clinical neurology 2007;47(11):774-8.
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2007: Suzuki Akane; Ivandini Tribidasari A; Yoshimi Kenji; Fujishima Akira; Oyama Genko; Nakazato Taizo; Hattori Nobutaka; Kitazawa Shigeru; Einaga Yasuaki
Fabrication, characterization, and application of boron-doped diamond microelectrodes for in vivo dopamine detection.
Analytical chemistry 2007;79(22):8608-15.
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2007: Hattori Nobutaka; Sato Shigeto
Animal models of Parkinson's disease: similarities and differences between the disease and models.
Neuropathology : official journal of the Japanese Society of Neuropathology 2007;27(5):479-83.
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2007: Kawajiri Sumihiro; Tani Momo; Noda Kazuyuki; Fujishima Kenji; Hattori Nobutaka; Okuma Yasuyuki
Segmental zoster paresis of limbs: report of three cases and review of literature.
The neurologist 2007;13(5):313-7.
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2007: Ueno Yuji; Kimura Kazumi; Iguchi Yasuyuki; Shibazaki Kensaku; Inoue Takeshi; Hattori Nobutaka; Urabe Takao
Mobile aortic plaques are a cause of multiple brain infarcts seen on diffusion-weighted imaging.
Stroke; a journal of cerebral circulation 2007;38(9):2470-6.
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2007: Hattori Nobutaka
[Neuromuscular disorders due to adverse effects of antiparkinson agents]
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine 2007;96(8):1614-20.
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2007: Tomiyama Hiroyuki; Hatano Taku; Hattori Nobutaka
[Clinical molecular genetics for PARK8 (LRRK2)]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(8):839-50.
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2007: Funayama Manabu; Hattori Nobutaka
[Molecular genetics of PINK1]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(8):831-8.
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2007: Nishioka Kenya; Hattori Nobutaka
[Relationship between alpha-synuclein and Parkinson's disease]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(8):825-30.
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2007: Yasuda Toru; Fukuda-Tani Momo; Nihira Tomoko; Wada Keiichiro; Hattori Nobutaka; Mizuno Yoshikuni; Mochizuki Hideki
Correlation between levels of pigment epithelium-derived factor and vascular endothelial growth factor in the striatum of patients with Parkinson's disease.
Experimental neurology 2007;206(2):308-17.
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2007: Suzuki Keisuke; Okuma Yasuyuki; Hattori Nobutaka; Kamei Satoshi; Yoshii Fumihito; Utsumi Hiroya; Iwasaki Yasuo; Iijima Mutsumi; Miyamoto Tomoyuki; Miyamoto Masayuki; Hirata Koichi
Characteristics of sleep disturbances in Japanese patients with Parkinson's disease. A study using Parkinson's disease sleep scale.
Movement disorders : official journal of the Movement Disorder Society 2007;22(9):1245-51.
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2007: Satake Wataru; Mizuta Ikuko; Suzuki Satoko; Nakabayashi Yuko; Ito Chiyomi; Watanabe Masahiko; Takeda Atsushi; Hasegawa Kazuko; Sakoda Saburo; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Fibroblast growth factor 20 gene and Parkinson's disease in the Japanese population.
Neuroreport 2007;18(9):937-40.
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2007: Yamashiro K; Liu R; Maeda M; Hattori N; Urabe T
Induction and selective accumulation of mutant ubiquitin in CA1 pyramidal neurons after transient global ischemia.
Neuroscience 2007;147(1):71-9.
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2007: Tamo Wakako; Imaizumi Tadaatsu; Tanji Kunikazu; Yoshida Hidemi; Takanashi Shingo; Wakabayashi Koichi; Takahashi Ryosuke; Hattori Nobutaka; Satoh Kei
Parkin is expressed in vascular endothelial cells.
Neuroscience letters 2007;419(3):199-201.
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2007: Saiki Misuzu; Saiki Shinji; Sakai Koichiro; Matsunari Ichiro; Higashi Kotaro; Murata Ken-Ya; Hattori Nobutaka; Hirose Genjiro
Neurological deficits are associated with increased brain calcinosis, hypoperfusion, and hypometabolism in idiopathic basal ganglia calcification.
Movement disorders : official journal of the Movement Disorder Society 2007;22(7):1027-30.
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2007: Takata Yukiko; Noda Kazuyuki; Fujishima Kenji; Hattori Nobutaka; Mizuno Yoshikuni; Okuma Yasuyuki
[A case of neuralgic amyotrophy in the lower extremity (lumbosacral radiculoplexus neuropathy)]
Brain and nerve = Shinkei kenkyu no shinpo 2007;59(4):435-8.
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2007: Saiki Shinji; Sakai Koichiro; Murata Ken-ya; Saiki Misuzu; Nakanishi Megumi; Kitagawa Yoko; Kaito Muichi; Gondo Yuichiro; Kumamoto Toshihide; Matsui Makoto; Hattori Nobutaka; Hirose Genjiro
Primary skeletal muscle involvement in chorea-acanthocytosis.
Movement disorders : official journal of the Movement Disorder Society 2007;22(6):848-52.
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2007: Hatano Taku; Kubo Shin-Ichiro; Imai Satoshi; Maeda Masahiro; Ishikawa Kiyoshi; Mizuno Yoshikuni; Hattori Nobutaka
Leucine-rich repeat kinase 2 associates with lipid rafts.
Human molecular genetics 2007;16(6):678-90.
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2007: Ephraty Lilach; Porat Omer; Israeli David; Cohen Oren S; Tunkel Olga; Yael Shinar; Hatano Yasaku; Hattori Nobutaka; Hassin-Baer Sharon
Neuropsychiatric and cognitive features in autosomal-recessive early parkinsonism due to PINK1 mutations.
Movement disorders : official journal of the Movement Disorder Society 2007;22(4):566-9.
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2007: Liu M; Eguchi N; Yamasaki Y; Urade Y; Hattori N; Urabe T
Focal cerebral ischemia/reperfusion injury in mice induces hematopoietic prostaglandin D synthase in microglia and macrophages.
Neuroscience 2007;145(2):520-9.
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2007: Funayama Manabu; Li Yuanzhe; Tomiyama Hiroyuki; Yoshino Hiroyo; Imamichi Yoko; Yamamoto Mitsutoshi; Murata Miho; Toda Tatsushi; Mizuno Yoshikuni; Hattori Nobutaka
Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.
Neuroreport 2007;18(3):273-5.
-
2007: Fukae Jiro; Mizuno Yoshikuni; Hattori Nobutaka
Mitochondrial dysfunction in Parkinson's disease.
Mitochondrion 2007;7(1-2):58-62.
-
2007: Ihara Masafumi; Yamasaki Nobuyuki; Hagiwara Akari; Tanigaki Ai; Kitano Ayumi; Hikawa Rie; Tomimoto Hidekazu; Noda Makoto; Takanashi Masashi; Mori Hideo; Hattori Nobutaka; Miyakawa Tsuyoshi; Kinoshita Makoto
Sept4, a component of presynaptic scaffold and Lewy bodies, is required for the suppression of alpha-synuclein neurotoxicity.
Neuron 2007;53(4):519-33.
-
2007: Kono Satoshi; Shirakawa Kentaro; Ouchi Yasuomi; Sakamoto Masanobu; Ida Hiroyuki; Sugiura Takeshi; Tomiyama Hiroyuki; Suzuki Hitoshi; Takahashi Yoshitomo; Miyajima Hiroaki; Hattori Nobutaka; Mizuno Yoshikuni
Dopaminergic neuronal dysfunction associated with parkinsonism in both a Gaucher disease patient and a carrier.
Journal of the neurological sciences 2007;252(2):181-4.
-
2007: Ishihara Lianna; Gibson Rachel A; Warren Liling; Amouri Rim; Lyons Kelly; Wielinski Catherine; Hunter Christine; Swartz Jina E; Elango Ramu; Akkari P Anthony; Leppert David; Surh Linda; Reeves Kevin H; Thomas Siwan; Ragone Leigh; Hattori Nobutaka; Pahwa Rajesh; Jankovic Joseph; Nance Martha; Freeman Alan; Gouider-Khouja Neziha; Kefi Mounir; Zouari Mourad; Ben Sassi Samia; Ben Yahmed Samia; El Euch-Fayeche Ghada; Middleton Lefkos; Burn David J; Watts Ray L; Hentati Faycal
Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families.
Movement disorders : official journal of the Movement Disorder Society 2007;22(1):55-61.
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2007: Mizuno Yoshikuni; Hattori Nobutaka; Mochizuki Hideki
Genetic aspects of Parkinson's disease.
Handbook of clinical neurology / edited by P.J. Vinken and G.W. Bruyn 2007;83():217-44.
-
2007: Tani Momo; Natori Shihoko; Noda Kazuyuki; Fujishima Kenji; Hattori Nobutaka; Mizuno Yoshikuni; Okuma Yasuyuki
Isolated reversible splenial lesion in adult meningitis: a case report and review of the literature.
Internal medicine (Tokyo, Japan) 2007;46(18):1597-600.
-
2006: Sato Shigeto; Chiba Tomoki; Nishiyama Shingo; Kakiuchi Takeharu; Tsukada Hideo; Hatano Taku; Fukuda Takahiro; Yasoshima Yasunobu; Kai Nobuyuki; Kobayashi Kazuto; Mizuno Yoshikuni; Tanaka Keiji; Hattori Nobutaka
Decline of striatal dopamine release in parkin-deficient mice shown by ex vivo autoradiography.
Journal of neuroscience research 2006;84(6):1350-7.
-
2006: Nakamura Atsuko; Kitami Toshiaki; Mori Hideo; Mizuno Yoshikuni; Hattori Nobutaka
Nuclear localization of the 20S proteasome subunit in Parkinson's disease.
Neuroscience letters 2006;406(1-2):43-8.
-
2006: Ishihara Lianna; Warren Liling; Gibson Rachel; Amouri Rim; Lesage Suzanne; Dürr Alexandra; Tazir Meriem; Wszolek Zbigniew K; Uitti Ryan J; Nichols William C; Griffith Alida; Hattori Nobutaka; Leppert David; Watts Ray; Zabetian Cyrus P; Foroud Tatiana M; Farrer Matthew J; Brice Alexis; Middleton Lefkos; Hentati Faycal
Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.
Archives of neurology 2006;63(9):1250-4.
-
2006: Sato Kenichi; Hatano Taku; Yamashiro Kazuo; Kagohashi Maki; Nishioka Kenya; Izawa Nana; Mochizuki Hideki; Hattori Nobutaka; Mori Hideo; Mizuno Yoshikuni;
Prognosis of Parkinson's disease: time to stage III, IV, V, and to motor fluctuations.
Movement disorders : official journal of the Movement Disorder Society 2006;21(9):1384-95.
-
2006: Maraganore Demetrius M; de Andrade Mariza; Elbaz Alexis; Farrer Matthew J; Ioannidis John P; Krüger Rejko; Rocca Walter A; Schneider Nicole K; Lesnick Timothy G; Lincoln Sarah J; Hulihan Mary M; Aasly Jan O; Ashizawa Tetsuo; Chartier-Harlin Marie-Christine; Checkoway Harvey; Ferrarese Carlo; Hadjigeorgiou Georgios; Hattori Nobutaka; Kawakami Hideshi; Lambert Jean-Charles; Lynch Timothy; Mellick George D; Papapetropoulos Spiridon; Parsian Abbas; Quattrone Aldo; Riess Olaf; Tan Eng-King; Van Broeckhoven Christine;
Collaborative analysis of alpha-synuclein gene promoter variability and Parkinson disease.
JAMA : the journal of the American Medical Association 2006;296(6):661-70.
-
2006: Arai Takeo; Fukae Jiro; Hatano Taku; Kubo Shin-ichiro; Ohtsubo Toshio; Nakabeppu Yusaku; Mori Hideo; Mizuno Yoshikuni; Hattori Nobutaka
Up-regulation of hMUTYH, a DNA repair enzyme, in the mitochondria of substantia nigra in Parkinson's disease.
Acta neuropathologica 2006;112(2):139-45.
-
2006: Tomiyama Hiroyuki; Li Yuanzhe; Funayama Manabu; Hasegawa Kazuko; Yoshino Hiroyo; Kubo Shin-Ichiro; Sato Kenichi; Hattori Tatsuya; Lu Chin-Song; Inzelberg Rivka; Djaldetti Ruth; Melamed Eldad; Amouri Rim; Gouider-Khouja Neziha; Hentati Faycal; Hatano Yasuko; Wang Mei; Imamichi Yoko; Mizoguchi Koichi; Miyajima Hiroaki; Obata Fumiya; Toda Tatsushi; Farrer Matthew J; Mizuno Yoshikuni; Hattori Nobutaka
Clinicogenetic study of mutations in LRRK2 exon 41 in Parkinson's disease patients from 18 countries.
Movement disorders : official journal of the Movement Disorder Society 2006;21(8):1102-8.
-
2006: Kubo Shin-ichiro; Hattori Nobutaka; Mizuno Yoshikuni
Recessive Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2006;21(7):885-93.
-
2006: Akagawa Mitsugu; Ito Sohei; Toyoda Kazuyo; Ishii Yoshihisa; Tatsuda Emi; Shibata Takahiro; Yamaguchi Satoru; Kawai Yoshichika; Ishino Kousuke; Kishi Yusuke; Adachi Takahiro; Tsubata Takeshi; Takasaki Yoshinari; Hattori Nobutaka; Matsuda Tsukasa; Uchida Koji
Bispecific abs against modified protein and DNA with oxidized lipids.
Proceedings of the National Academy of Sciences of the United States of America 2006;103(16):6160-5.
-
2006: Mizuta Ikuko; Satake Wataru; Nakabayashi Yuko; Ito Chiyomi; Suzuki Satoko; Momose Yoshio; Nagai Yoshitaka; Oka Akira; Inoko Hidetoshi; Fukae Jiro; Saito Yuko; Sawabe Motoji; Murayama Shigeo; Yamamoto Mitsutoshi; Hattori Nobutaka; Murata Miho; Toda Tatsushi
Multiple candidate gene analysis identifies alpha-synuclein as a susceptibility gene for sporadic Parkinson's disease.
Human molecular genetics 2006;15(7):1151-8.
-
2006: Yamamoto Shoji; Fukae Jiro; Mori Hideo; Mizuno Yoshikuni; Hattori Nobutaka
Positive immunoreactivity for vesicular monoamine transporter 2 in Lewy bodies and Lewy neurites in substantia nigra.
Neuroscience letters 2006;396(3):187-91.
-
2006: Atsumi Masahiko; Li Yuanzhe; Tomiyama Hiroyuki; Sato Kenichi; Hattori Nobutaka
[A 62-year-old woman with early-onset Parkinson's disease associated with the PINKi gene deletion]
Rinsho shinkeigaku = Clinical neurology 2006;46(3):199-202.
-
2006: Nishioka Kenya; Hayashi Shin; Farrer Matthew J; Singleton Andrew B; Yoshino Hiroyo; Imai Hisamasa; Kitami Toshiaki; Sato Kenichi; Kuroda Ryu; Tomiyama Hiroyuki; Mizoguchi Koichi; Murata Miho; Toda Tatsushi; Imoto Issei; Inazawa Johji; Mizuno Yoshikuni; Hattori Nobutaka
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's disease.
Annals of neurology 2006;59(2):298-309.
-
2006: Matsuda Noriyuki; Kitami Toshiaki; Suzuki Toshiaki; Mizuno Yoshikuni; Hattori Nobutaka; Tanaka Keiji
Diverse effects of pathogenic mutations of Parkin that catalyze multiple monoubiquitylation in vitro.
The Journal of biological chemistry 2006;281(6):3204-9.
-
2006: Kitami Makiko-Iijima; Kitami Toshiaki; Nagahama Masami; Tagaya Mitsuo; Hori Seiji; Kakizuka Akira; Mizuno Yoshikuni; Hattori Nobutaka
Dominant-negative effect of mutant valosin-containing protein in aggresome formation.
FEBS letters 2006;580(2):474-8.
-
2006: Sato Shigeto; Chiba Tomoki; Sakata Eri; Kato Koichi; Mizuno Yoshikuni; Hattori Nobutaka; Tanaka Keiji
14-3-3eta is a novel regulator of parkin ubiquitin ligase.
The EMBO journal 2006;25(1):211-21.
-
2006: Hattori N; Machida Y; Sato S; Noda K; Iijima-Kitami M; Kubo S; Mizuno Y
Molecular mechanisms of nigral neurodegeneration in Park2 and regulation of parkin protein by other proteins.
Journal of neural transmission. Supplementum 2006;(70):205-8.
-
2006: Mizuno Y; Hattori N; Yoshino H; Hatano Y; Satoh K; Tomiyama H; Li Y
Progress in familial Parkinson's disease.
Journal of neural transmission. Supplementum 2006;(70):191-204.
-
2005: Shimura Hideki; Mori Hideo; Komatsuzaki Yasuko; Nakamura Kazuhiro; Takanashi Masashi; Hattori Nobutaka; Mizuno Yoshikuni
[A 54-year-old man with familial parkinsonism, gaze palsy, and dementia]
No to shinkei = Brain and nerve 2005;57(12):1104-12.
-
2005: Inzelberg Rivka; Hattori Nobutaka; Mizuno Yoshikuni
Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.
Neurology 2005;65(11):1843.
-
2005: Li Xiaobing; Kitami Toshiaki; Wang Mei; Mizuno Yoshikuni; Hattori Nobutaka
Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease.
Parkinsonism & related disorders 2005;11(8):485-91.
-
2005: Lu Chin-Song; Simons Erik J; Wu-Chou Yah-Huei; Fonzo Alessio Di; Chang Hsiu-Chen; Chen Rou-Shayn; Weng Yi-Hsin; Rohé Christan F; Breedveld Guido J; Hattori Nobutaka; Gasser Thomas; Oostra Ben A; Bonifati Vincenzo
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease.
Parkinsonism & related disorders 2005;11(8):521-2.
-
2005: Hattori Nobutaka; Machida Yutaka; Noda Kazuyuki
[Pathogenesis of Parkinson's disease: a common pathway between alpha-synuclein and parkin and the mechanism of Lewy bodies formation]
Rinsho shinkeigaku = Clinical neurology 2005;45(11):905-7.
-
2005: Hatano Taku; Takanashi Masashi; Sumino Teiko; Liu Ying; Mori Hideo; Hattori Nobutaka; Mizuno Yoshikuni
[A 73-year-old woman with depression, dementia, and parkinsonism]
No to shinkei = Brain and nerve 2005;57(10):907-14.
-
2005: Ide Masayuki; Yamada Kazuo; Toyota Tomoko; Iwayama Yoshimi; Ishitsuka Yuichi; Minabe Yoshio; Nakamura Kazuhiko; Hattori Nobutaka; Asada Takashi; Mizuno Yoshikuni; Mori Norio; Yoshikawa Takeo
Genetic association analyses of PHOX2B and ASCL1 in neuropsychiatric disorders: evidence for association of ASCL1 with Parkinson's disease.
Human genetics 2005;117(6):520-7.
-
2005: Orimo Satoshi; Amino Takeshi; Yokochi Masayuki; Kojo Tohru; Uchihara Toshiki; Takahashi Atsushi; Wakabayashi Koichi; Takahashi Hitoshi; Hattori Nobutaka; Mizuno Yoshikuni
Preserved cardiac sympathetic nerve accounts for normal cardiac uptake of MIBG in PARK2.
Movement disorders : official journal of the Movement Disorder Society 2005;20(10):1350-3.
-
2005: Kubo Shin-ichiro; Nemani Venu M; Chalkley Robert J; Anthony Malcolm D; Hattori Nobutaka; Mizuno Yoshikuni; Edwards Robert H; Fortin Doris L
A combinatorial code for the interaction of alpha-synuclein with membranes.
The Journal of biological chemistry 2005;280(36):31664-72.
-
2005: Machida Yuh; Lijima Makiko; Nakamura Kazuhiro; Ota Satoshi; Hattori Nobutaka; Mizuno Yoshikuni
[A 60-year-old man with intention tremor as an initial symptom followed by cerebellar ataxia, peripheral neuropathy and dementia]
No to shinkei = Brain and nerve 2005;57(8):710-9.
-
2005: Clarimon Jordi; Johnson Janel; Djaldetti Ruth; Hernandez Dena; Hattori Nobutaka; Sroka Hava; Barhom Yael; Singleton Andrew
Mutation of the Parkin gene in a Persian family: clinical progression over a 40-year period.
Movement disorders : official journal of the Movement Disorder Society 2005;20(7):887-90.
-
2005: Fukae Jiro; Kubo Shin-Ichiro; Hattori Nobutaka; Komatsu Kaoru; Kato Masaaki; Aoki Masashi; Mizuno Yoshikuni
Hoarseness due to bilateral vocal cord paralysis as an initial manifestation of familial amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis and other motor neuron disorders : official publication of the World Federation of Neurology, Research Group on Motor Neuron Diseases 2005;6(2):122-4.
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2005: Li Y; Tomiyama H; Sato K; Hatano Y; Yoshino H; Atsumi M; Kitaguchi M; Sasaki S; Kawaguchi S; Miyajima H; Toda T; Mizuno Y; Hattori N
Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.
Neurology 2005;64(11):1955-7.
-
2005: Machida Yutaka; Chiba Tomoki; Takayanagi Atsushi; Tanaka Yoshikazu; Asanuma Masato; Ogawa Norio; Koyama Akihiko; Iwatsubo Takeshi; Ito Shosuke; Jansen Poul Hening; Shimizu Nobuyoshi; Tanaka Keiji; Mizuno Yoshikuni; Hattori Nobutaka
Common anti-apoptotic roles of parkin and alpha-synuclein in human dopaminergic cells.
Biochemical and biophysical research communications 2005;332(1):233-40.
-
2005: Noda Kazuyuki; Kitami Toshiaki; Gai Wei Ping; Chegini Fariba; Jensen Poul Henning; Fujimura Tsutomu; Murayama Kimie; Tanaka Keiji; Mizuno Yoshikuni; Hattori Nobutaka
Phosphorylated IkappaBalpha is a component of Lewy body of Parkinson's disease.
Biochemical and biophysical research communications 2005;331(1):309-17.
-
2005: Suzuki Masahiko; Hattori Nobutaka; Orimo Satoshi; Fukumitsu Nobuyoshi; Abo Masahiro; Kono Yu; Sengoku Renpei; Kurita Akira; Honda Hidehiko; Inoue Kiyoharu
Preserved myocardial [123I]metaiodobenzylguanidine uptake in autosomal recessive juvenile parkinsonism: first case report.
Movement disorders : official journal of the Movement Disorder Society 2005;20(5):634-6.
-
2005: Hatano Yasuko; Ri Gyohyo; Hattori Nobutaka; Mizuno Yoshikuni
[Gene abnormalities in Parkinson disease]
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine 2005;94(4):775-81.
-
2005: Fukae Jiro; Takanashi Masashi; Kubo Shin-ichiro; Nishioka Ken-ichi; Nakabeppu Yusaku; Mori Hideo; Mizuno Yoshikuni; Hattori Nobutaka
Expression of 8-oxoguanine DNA glycosylase (OGG1) in Parkinson's disease and related neurodegenerative disorders.
Acta neuropathologica 2005;109(3):256-62.
-
2005: Sato Shigeto; Mizuno Yoshikuni; Hattori Nobutaka
Urinary 8-hydroxydeoxyguanosine levels as a biomarker for progression of Parkinson disease.
Neurology 2005;64(6):1081-3.
-
2005: Moore Darren J; Zhang Li; Troncoso Juan; Lee Michael K; Hattori Nobutaka; Mizuno Yoshikuni; Dawson Ted M; Dawson Valina L
Association of DJ-1 and parkin mediated by pathogenic DJ-1 mutations and oxidative stress.
Human molecular genetics 2005;14(1):71-84.
-
2004: Namihira Tomoo; Hattori Nobutaka; Shiroma Seigo; Miyazato Yoshikazu
Autosomal recessive juvenile Parkinson's disease with partial trisomy of chromosome 6q syndrome: a case report.
Psychiatry and clinical neurosciences 2004;58(6):672-3.
-
2004: Hattori Nobutaka
[The gene products for familial Parkinson's disease provide us hints to elucidate the mechanisms of nigral degeneration]
Rinsho shinkeigaku = Clinical neurology 2004;44(11):821-3.
-
2004: Tanaka Keiji; Suzuki Toshiaki; Hattori Nobutaka; Mizuno Yoshikuni
Ubiquitin, proteasome and parkin.
Biochimica et biophysica acta 2004;1695(1-3):235-47.
-
2004: Hatano Y; Sato K; Elibol B; Yoshino H; Yamamura Y; Bonifati V; Shinotoh H; Asahina M; Kobayashi S; Ng A R; Rosales R L; Hassin-Baer S; Shinar Y; Lu C S; Chang H C; Wu-Chou Y H; Ataç F B; Kobayashi T; Toda T; Mizuno Y; Hattori N
PARK6-linked autosomal recessive early-onset parkinsonism in Asian populations.
Neurology 2004;63(8):1482-5.
-
2004: Tanaka Masashi; Cabrera Vicente M; González Ana M; Larruga José M; Takeyasu Takeshi; Fuku Noriyuki; Guo Li-Jun; Hirose Raita; Fujita Yasunori; Kurata Miyuki; Shinoda Ken-ichi; Umetsu Kazuo; Yamada Yoshiji; Oshida Yoshiharu; Sato Yuzo; Hattori Nobutaka; Mizuno Yoshikuni; Arai Yasumichi; Hirose Nobuyoshi; Ohta Shigeo; Ogawa Osamu; Tanaka Yasushi; Kawamori Ryuzo; Shamoto-Nagai Masayo; Maruyama Wakako; Shimokata Hiroshi; Suzuki Ryota; Shimodaira Hidetoshi
Mitochondrial genome variation in eastern Asia and the peopling of Japan.
Genome research 2004;14(10A):1832-50.
-
2004: Shiba Kahori; Hattori Nobutaka
[Molecular biology for familial Parkinson's disease]
Nippon rinsho. Japanese journal of clinical medicine 2004;62(9):1617-22.
-
2004: Hatano Yasuko; Li Yuanzhe; Sato Kenichi; Asakawa Shuichi; Yamamura Yasuhiro; Tomiyama Hiroyuki; Yoshino Hiroyo; Asahina Masato; Kobayashi Susumu; Hassin-Baer Sharon; Lu Chin-Song; Ng Arlene R; Rosales Raymond L; Shimizu Nobuyoshi; Toda Tatsushi; Mizuno Yoshikuni; Hattori Nobutaka
Novel PINK1 mutations in early-onset parkinsonism.
Annals of neurology 2004;56(3):424-7.
-
2004: Hattori Nobutaka; Mizuno Yoshikuni
Pathogenetic mechanisms of parkin in Parkinson's disease.
Lancet 2004;364(9435):722-4.
-
2004: Higashi Youichirou; Asanuma Masato; Miyazaki Ikuko; Hattori Nobutaka; Mizuno Yoshikuni; Ogawa Norio
Parkin attenuates manganese-induced dopaminergic cell death.
Journal of neurochemistry 2004;89(6):1490-7.
-
2004: Hattori Nobutaka
[Etiology and pathogenesis of Parkinson's disease: from mitochondrial dysfunctions to familial Parkinson's disease]
Rinsho shinkeigaku = Clinical neurology 2004;44(4-5):241-62.
-
2004: Nomiyama Takashi; Tanaka Yasushi; Piao Lianshan; Hattori Nobutaka; Uchino Hiroshi; Watada Hirotaka; Kawamori Ryuzo; Ohta Shigeo
Accumulation of somatic mutation in mitochondrial DNA and atherosclerosis in diabetic patients.
Annals of the New York Academy of Sciences 2004;1011():193-204.
-
2004: Maraganore Demetrius M; Lesnick Timothy G; Elbaz Alexis; Chartier-Harlin Marie-Christine; Gasser Thomas; Krüger Rejko; Hattori Nobutaka; Mellick George D; Quattrone Aldo; Satoh Jun-Ichi; Toda Tatsushi; Wang Jian; Ioannidis John P A; de Andrade Mariza; Rocca Walter A;
UCHL1 is a Parkinson's disease susceptibility gene.
Annals of neurology 2004;55(4):512-21.
-
2003: Hattori Nobutaka
Appropriate dosing of pergolide in monotherapy and adjunctive therapy in Parkinson's disease.
Current opinion in neurology 2003;16 Suppl 1():S21-5.
-
2003: Nagano Yoshito; Yamashita Hiroshi; Takahashi Tetsuya; Kishida Shosei; Nakamura Takeshi; Iseki Eizo; Hattori Nobutaka; Mizuno Yoshikuni; Kikuchi Akira; Matsumoto Masayasu
Siah-1 facilitates ubiquitination and degradation of synphilin-1.
The Journal of biological chemistry 2003;278(51):51504-14.
-
2003: Toda Tatsushi; Momose Yoshio; Murata Miho; Tamiya Gen; Yamamoto Mitsutoshi; Hattori Nobutaka; Inoko Hidetoshi
Toward identification of susceptibility genes for sporadic Parkinson's disease.
Journal of neurology 2003;250 Suppl 3():III40-3.
-
2003: Hattori Nobutaka; Kobayashi Hirokazu; Sasaki-Hatano Yasuko; Sato Kenichi; Mizuno Yoshikuni
Familial Parkinson's disease: a hint to elucidate the mechanisms of nigral degeneration.
Journal of neurology 2003;250 Suppl 3():III2-10.
-
2003: Kim Se Jung; Sung Jee Young; Um Ji Won; Hattori Nobutaka; Mizuno Yoshikuni; Tanaka Keiji; Paik Seung R; Kim Jongsun; Chung Kwang Chul
Parkin cleaves intracellular alpha-synuclein inclusions via the activation of calpain.
The Journal of biological chemistry 2003;278(43):41890-9.
-
2003: Hattori Nobutaka; Hatano Yasuko; Sato Kenichi; Mizuno Yoshikuni
[Juvenile parkinsonism]
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine 2003;92(8):1406-13.
-
2003: Takahashi Ryosuke; Imai Yuzuru; Hattori Nobutaka; Mizuno Yoshikuni
Parkin and endoplasmic reticulum stress.
Annals of the New York Academy of Sciences 2003;991():101-6.
-
2003: Okuma Yasuyuki; Hattori Nobutaka; Mizuno Yoshikuni
Sensory neuropathy in autosomal recessive juvenile parkinsonism (PARK2).
Parkinsonism & related disorders 2003;9(5):313-4.
-
2003: Gouider-Khouja Neziha; Larnaout Abdelmajid; Amouri Rim; Sfar Sana; Belal Samir; Ben Hamida Christiane; Ben Hamida Mongi; Hattori Nobutaka; Mizuno Yoshikuni; Hentati Fayçal
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Parkinsonism & related disorders 2003;9(5):247-51.
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2003: Inzelberg R; Hattori N; Nisipeanu P; Abo Mouch S; Blumen S C; Carasso R L; Mizuno Y
Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutation.
Neurology 2003;60(8):1393-4.
-
2003: Rawal N; Periquet M; Lohmann E; Lücking C B; Teive H A; Ambrosio G; Raskin S; Lincoln S; Hattori N; Guimaraes J; Horstink M W I M; Dos Santos Bele W; Brousolle E; Destée A; Mizuno Y; Farrer M; Deleuze J-F; De Michele G; Agid Y; Dürr A; Brice A;
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism.
Neurology 2003;60(8):1378-81.
-
2003: Mori Hideo; Hattori Nobutaka; Mizuno Yoshikuni
Genotype-phenotype correlation: familial Parkinson disease.
Neuropathology : official journal of the Japanese Society of Neuropathology 2003;23(1):90-4.
-
2003: Sakata Eri; Yamaguchi Yoshiki; Kurimoto Eiji; Kikuchi Jun; Yokoyama Shigeyuki; Yamada Shingo; Kawahara Hiroyuki; Yokosawa Hideyoshi; Hattori Nobutaka; Mizuno Yoshikuni; Tanaka Keiji; Kato Koichi
Parkin binds the Rpn10 subunit of 26S proteasomes through its ubiquitin-like domain.
EMBO reports 2003;4(3):301-6.
-
2003: Kobayashi Tomonori; Matsumine Hiroto; Zhang JiaLin; Imamichi Yoko; Mizuno Yoshikuni; Hattori Nobutaka
Pseudo-autosomal dominant inheritance of PARK2: two families with parkin gene mutations.
Journal of the neurological sciences 2003;207(1-2):11-7.
-
2003: Furuya Tsuyoshi; Namihira Tomoo; Yamazaki Shigetaka; Mori Hideo; Hattori Nobutaka; Mizuno Yoshikuni
[A 65-year-old woman with progressive loss of vision and visual field defects]
No to shinkei = Brain and nerve 2003;55(1):87-96.
-
2003: Kobayashi Hirokazu; Krüger Rejko; Markopoulou Katerina; Wszolek Zbigniew; Chase Bruce; Taka Hikaru; Mineki Reiko; Murayama Kimie; Riess Olaf; Mizuno Yoshikuni; Hattori Nobutaka
Haploinsufficiency at the alpha-synuclein gene underlies phenotypic severity in familial Parkinson's disease.
Brain : a journal of neurology 2003;126(Pt 1):32-42.
-
2002: Hattori Nobutaka
[Parkin gene: its mutations and function]
Rinsho shinkeigaku = Clinical neurology 2002;42(11):1077-81.
-
2002: Nomiyama T; Tanaka Y; Hattori N; Nishimaki K; Nagasaka K; Kawamori R; Ohta S
Accumulation of somatic mutation in mitochondrial DNA extracted from peripheral blood cells in diabetic patients.
Diabetologia 2002;45(11):1577-83.
-
2002: Tanaka Masashi; Fuku Noriyuki; Takeyasu Takeshi; Guo Li-Jun; Hirose Raita; Kurata Miyuki; Borgeld Harm-Jan W; Yamada Yoshiji; Maruyama Wakako; Arai Yasumichi; Hirose Nobuyoshi; Oshida Yoshiharu; Sato Yuzo; Hattori Nobutaka; Mizuno Yoshikuni; Iwata So; Yagi Kunio
Golden mean to longevity: rareness of mitochondrial cytochrome b variants in centenarians but not in patients with Parkinson's disease.
Journal of neuroscience research 2002;70(3):347-55.
-
2002: Takanashi Masashi; Mori Hideo; Arima Kunimasa; Mizuno Yoshikuni; Hattori Nobutaka
Expression patterns of tau mRNA isoforms correlate with susceptible lesions in progressive supranuclear palsy and corticobasal degeneration.
Brain research. Molecular brain research 2002;104(2):210-9.
-
2002: Hyun Dong-Hoon; Lee MoonHee; Hattori Nobutaka; Kubo Shin-Ichiro; Mizuno Yoshikuni; Halliwell Barry; Jenner Peter
Effect of wild-type or mutant Parkin on oxidative damage, nitric oxide, antioxidant defenses, and the proteasome.
The Journal of biological chemistry 2002;277(32):28572-7.
-
2002: Schlossmacher Michael G; Frosch Matthew P; Gai Wei Ping; Medina Miguel; Sharma Nutan; Forno Lysia; Ochiishi Tomoyo; Shimura Hideki; Sharon Ronit; Hattori Nobutaka; Langston J William; Mizuno Yoshikuni; Hyman Bradley T; Selkoe Dennis J; Kosik Kenneth S
Parkin localizes to the Lewy bodies of Parkinson disease and dementia with Lewy bodies.
The American journal of pathology 2002;160(5):1655-67.
-
2002: Hattori Nobutaka; Mizuno Yoshikuni
[Mitochondrial dysfunction in Parkinson's disease]
Nippon rinsho. Japanese journal of clinical medicine 2002;60 Suppl 4():406-11.
-
2002: Sato Kenichi; Hattori Nobutaka; Mizuno Yoshikuni
[Malignant migraine]
Nippon rinsho. Japanese journal of clinical medicine 2002;60 Suppl 4():278-81.
-
2002: Nomiyama Takashi; Kawamori Ryuzo; Hattori Nobutaka
[Pathogenesis and contribution of mitochondria to diabetes or deafness]
Nippon rinsho. Japanese journal of clinical medicine 2002;60 Suppl 4():273-7.
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2001: Suzuki A; Ikebe S; Komatsuzaki Y; Takanashi M; Mori H; Hattori N; Mizuno Y
[A 64-year-old man with parkinsonism as an initial symptom followed by dementia associated with marked abnormal behaviours]
No to shinkei = Brain and nerve 2001;53(11):1075-87.
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2001: Tanaka K; Suzuki T; Chiba T; Shimura H; Hattori N; Mizuno Y
Parkin is linked to the ubiquitin pathway.
Journal of molecular medicine (Berlin, Germany) 2001;79(9):482-94.
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2001: Mizuno Y; Hattori N; Mori H; Suzuki T; Tanaka K
Parkin and Parkinson's disease.
Current opinion in neurology 2001;14(4):477-82.
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2001: Shimo-Nakanishi Y; Urabe T; Hattori N; Watanabe Y; Nagao T; Yokochi M; Hamamoto M; Mizuno Y
Polymorphism of the lipoprotein lipase gene and risk of atherothrombotic cerebral infarction in the Japanese.
Stroke; a journal of cerebral circulation 2001;32(7):1481-6.
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2001: Kubo S I; Kitami T; Noda S; Shimura H; Uchiyama Y; Asakawa S; Minoshima S; Shimizu N; Mizuno Y; Hattori N
Parkin is associated with cellular vesicles.
Journal of neurochemistry 2001;78(1):42-54.
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2001: Shimura H; Schlossmacher M G; Hattori N; Frosch M P; Trockenbacher A; Schneider R; Mizuno Y; Kosik K S; Selkoe D J
Ubiquitination of a new form of alpha-synuclein by parkin from human brain: implications for Parkinson's disease.
Science (New York, N.Y.) 2001;293(5528):263-9.
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2001: Imai Y; Soda M; Inoue H; Hattori N; Mizuno Y; Takahashi R
An unfolded putative transmembrane polypeptide, which can lead to endoplasmic reticulum stress, is a substrate of Parkin.
Cell 2001;105(7):891-902.
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2001: Wang M; Suzuki T; Kitada T; Asakawa S; Minoshima S; Shimizu N; Tanaka K; Mizuno Y; Hattori N
Developmental changes in the expression of parkin and UbcR7, a parkin-interacting and ubiquitin-conjugating enzyme, in rat brain.
Journal of neurochemistry 2001;77(6):1561-8.
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2001: Jeon B S; Kim J M; Lee D S; Hattori N; Mizuno Y
An apparently sporadic case with parkin gene mutation in a Korean woman.
Archives of neurology 2001;58(6):988-9.
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2001: Nisipeanu P; Inzelberg R; Abo Mouch S; Carasso R L; Blumen S C; Zhang J; Matsumine H; Hattori N; Mizuno Y
Parkin gene causing benign autosomal recessive juvenile parkinsonism.
Neurology 2001;56(11):1573-5.
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2001: Lu C S; Wu J C; Tsai C H; Chen R S; Chou Y H; Hattori N; Yoshino H; Mizuno Y
Clinical and genetic studies on familial parkinsonism: the first report on a parkin gene mutation in a Taiwanese family.
Movement disorders : official journal of the Movement Disorder Society 2001;16(1):164-6.
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2001: Mizuno Y; Hattori N; Kitada T; Matsumine H; Mori H; Shimura H; Kubo S; Kobayashi H; Asakawa S; Minoshima S; Shimizu N
Familial Parkinson's disease. Alpha-synuclein and parkin.
Advances in neurology 2001;86():13-21.
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2000: Hattori N; Shimura H; Kubo S; Suzuki T; Tanaka K; Mizuno Y
[Autosomal recessive juvenile parkinsonism: its pathogenesis is involved in the ubiquitin-proteasome pathway]
Rinsho shinkeigaku = Clinical neurology 2000;40(12):1293-6.
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2000: Kubo S; Hattori T; Takanashi M; Mori H; Mizutani Y; Suda K; Hattori N; Mizuno Y
[A 57-year-old woman with progressive disturbance of gait and mental deterioration]
No to shinkei = Brain and nerve 2000;52(11):1035-44.
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2000: Mizuno Y; Hattori N
[Progress in studies of Parkinson's disease]
Nihon Naika Gakkai zasshi. The Journal of the Japanese Society of Internal Medicine 2000;89(9):1970-6.
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2000: Hattori N; Shimura H; Kubo S; Kitada T; Wang M; Asakawa S; Minashima S; Shimizu N; Suzuki T; Tanaka K; Mizuno Y
Autosomal recessive juvenile parkinsonism: a key to understanding nigral degeneration in sporadic Parkinson's disease.
Neuropathology : official journal of the Japanese Society of Neuropathology 2000;20 Suppl():S85-90.
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2000: Yamamura Y; Hattori N; Matsumine H; Kuzuhara S; Mizuno Y
Autosomal recessive early-onset parkinsonism with diurnal fluctuation: clinicopathologic characteristics and molecular genetic identification.
Brain & development 2000;22 Suppl 1():S87-91.
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2000: Shimura H; Hattori N; Kubo S i; Mizuno Y; Asakawa S; Minoshima S; Shimizu N; Iwai K; Chiba T; Tanaka K; Suzuki T
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.
Nature genetics 2000;25(3):302-5.
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2000: Kitada T; Asakawa S; Matsumine H; Hattori N; Shimura H; Minoshima S; Shimizu N; Mizuno Y
Progress in the clinical and molecular genetics of familial parkinsonism.
Neurogenetics 2000;2(4):207-18.
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2000: Hattori N; Shimura H; Kubo S; Wang M; Shimizu N; Tanaka K; Mizuno Y
Importance of familial Parkinson's disease and parkinsonism to the understanding of nigral degeneration in sporadic Parkinson's disease.
Journal of neural transmission. Supplementum 2000;(60):101-16.
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2000: Shimizu N; Asakawa S; Minoshima S; Kitada T; Hattori N; Matsumine H; Yokochi M; Yamamura Y; Mizuno Y
PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.
Journal of neural transmission. Supplementum 2000;(58):19-30.
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2000: Urabe T; Yamasaki Y; Hattori N; Yoshikawa M; Uchida K; Mizuno Y
Accumulation of 4-hydroxynonenal-modified proteins in hippocampal CA1 pyramidal neurons precedes delayed neuronal damage in the gerbil brain.
Neuroscience 2000;100(2):241-50.
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1999: Kitada T; Asakawa S; Matsumine H; Hattori N; Minoshima S; Shimizu N; Mizuno Y
Positional cloning of the autosomal recessive juvenile parkinsonism (AR-JP) gene and its diversity in deletion mutations.
Parkinsonism & related disorders 1999;5(4):163-8.
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1999: Hattori N; Mizuno Y
[Parkin gene and its function; a key to understand nigral degeneration]
Rinsho shinkeigaku = Clinical neurology 1999;39(12):1259-61.
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1999: Shimura-Miura H; Hattori N; Kang D; Miyako K; Nakabeppu Y; Mizuno Y
Increased 8-oxo-dGTPase in the mitochondria of substantia nigral neurons in Parkinson's disease.
Annals of neurology 1999;46(6):920-4.
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1999: Nisipeanu P; Inzelberg R; Blumen S C; Carasso R L; Hattori N; Matsumine H; Mizuno Y
Autosomal-recessive juvenile parkinsonism in a Jewish Yemenite kindred: mutation of Parkin gene.
Neurology 1999;53(7):1602-4.
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1999: Hattori N; Sumino S; Takanashi M; Mori H; Wakiya M; Shirai T; Sugita H; Mizuno Y
[An 80-year-old woman with parkinsonism and progressive dementia]
No to shinkei = Brain and nerve 1999;51(6):541-50.
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1999: Hattori N; Mizuno Y
[The Parkin gene and its product in AR-JP]
No to shinkei = Brain and nerve 1999;51(6):493-500.
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1999: Shimura H; Hattori N; Kubo S; Yoshikawa M; Kitada T; Matsumine H; Asakawa S; Minoshima S; Yamamura Y; Shimizu N; Mizuno Y
Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.
Annals of neurology 1999;45(5):668-72.
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1999: Wang M; Hattori N; Matsumine H; Kobayashi T; Yoshino H; Morioka A; Kitada T; Asakawa S; Minoshima S; Shimizu N; Mizuno Y
Polymorphism in the parkin gene in sporadic Parkinson's disease.
Annals of neurology 1999;45(5):655-8.
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1999: Mizuno Y; Hattori N; Mori H
Genetics of Parkinson's disease.
Biomedicine & pharmacotherapy = Biomédecine & pharmacothérapie 1999;53(3):109-16.
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1999: Yoritaka A; Nakagawa-Hattori Y; Hattori N; Kitahara A; Mizuno Y
A large Japanese family with Machado-Joseph disease: clinical and genetic analysis.
Acta neurologica Scandinavica 1999;99(4):241-4.
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1999: Mizuno Y; Shimoda-Matsubayashi S; Matsumine H; Morikawa N; Hattori N; Kondo T
Genetic and environmental factors in the pathogenesis of Parkinson's disease.
Advances in neurology 1999;80():171-9.
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1998: Hattori N; Kitada T; Matsumine H; Asakawa S; Yamamura Y; Yoshino H; Kobayashi T; Yokochi M; Wang M; Yoritaka A; Kondo T; Kuzuhara S; Nakamura S; Shimizu N; Mizuno Y
Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.
Annals of neurology 1998;44(6):935-41.
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1998: Mizuno Y; Yoshino H; Ikebe S; Hattori N; Kobayashi T; Shimoda-Matsubayashi S; Matsumine H; Kondo T
Mitochondrial dysfunction in Parkinson's disease.
Annals of neurology 1998;44(3 Suppl 1):S99-109.
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1998: Mizuno Y; Hattori N; Matsumine H
Neurochemical and neurogenetic correlates of Parkinson's disease.
Journal of neurochemistry 1998;71(3):893-902.
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1998: Hattori N; Matsumine H; Asakawa S; Kitada T; Yoshino H; Elibol B; Brookes A J; Yamamura Y; Kobayashi T; Wang M; Yoritaka A; Minoshima S; Shimizu N; Mizuno Y
Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.
Biochemical and biophysical research communications 1998;249(3):754-8.
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1998: Okuma Y; Hattori N; Nobukawa B; Mori H; Suda K; Takubo H; Mizuno Y
[A 74-year-old woman with parkinsonism and dementia who died four years after the onset]
No to shinkei = Brain and nerve 1998;50(7):671-82.
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1998: Urabe T; Hattori N; Yoshikawa M; Yoshino H; Uchida K; Mizuno Y
Colocalization of Bcl-2 and 4-hydroxynonenal modified proteins in microglial cells and neurons of rat brain following transient focal ischemia.
Neuroscience letters 1998;247(2-3):159-62.
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1998: Takubo H; Hattori N; Irie S; Mizutani Y; Mori H; Suda K; Kondo T; Oshimi K; Mizuno Y
[A 45-year-old man with peripheral monocytosis and right hemiparesis]
No to shinkei = Brain and nerve 1998;50(5):481-9.
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1998: Matsumine H; Yamamura Y; Hattori N; Kobayashi T; Kitada T; Yoritaka A; Mizuno Y
A microdeletion of D6S305 in a family of autosomal recessive juvenile parkinsonism (PARK2).
Genomics 1998;49(1):143-6.
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1998: Hattori N; Yoshino H; Tanaka M; Suzuki H; Mizuno Y
Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease.
Genomics 1998;49(1):52-8.
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1998: Kitada T; Asakawa S; Hattori N; Matsumine H; Yamamura Y; Minoshima S; Yokochi M; Mizuno Y; Shimizu N
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.
Nature 1998;392(6676):605-8.
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1998: Sato S; Hattori N; Matsumine H; Imai H; Mizuno Y
[A patient with focal bi-parietal atrophy presenting motor clumsiness and cortical sensory loss]
Rinsho shinkeigaku = Clinical neurology 1998;38(3):246-51.
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1997: Yoshino H; Hattori N; Urabe T; Uchida K; Tanaka M; Mizuno Y
Postischemic accumulation of lipid peroxidation products in the rat brain: immunohistochemical detection of 4-hydroxy-2-nonenal modified proteins.
Brain research 1997;767(1):81-6.
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1997: Yoritaka A; Hattori N; Mori H; Kato K; Mizuno Y
An immunohistochemical study on manganese superoxide dismutase in Parkinson's disease.
Journal of the neurological sciences 1997;148(2):181-6.
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1997: Yoritaka A; Hattori N; Yoshino H; Mizuno Y
Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication.
Journal of neural transmission (Vienna, Austria : 1996) 1997;104(11-12):1313-7.
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1996: Hattori N; Goto K; Mori H; Tominaga I; Kondo T; Mizuno Y
[A 46-year-old man with right-side dominant parkinsonism, who suffered a sudden death]
No to shinkei = Brain and nerve 1996;48(11):1059-67.
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1996: Nakamura N; Hattori N; Tanaka M; Mizuno Y
Specific detection of deleted mitochondrial DNA by in situ hybridization using a chimera probe.
Biochimica et biophysica acta 1996;1308(3):215-21.
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1996: Urabe T; Hattori N; Nagamatsu S; Sawa H; Mizuno Y
Expression of glucose transporters in rat brain following transient focal ischemic injury.
Journal of neurochemistry 1996;67(1):265-71.
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1996: Yoritaka A; Hattori N; Uchida K; Tanaka M; Stadtman E R; Mizuno Y
Immunohistochemical detection of 4-hydroxynonenal protein adducts in Parkinson disease.
Proceedings of the National Academy of Sciences of the United States of America 1996;93(7):2696-701.
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1995: Hattori N; Suzuki H; Wang Y; Minoshima S; Shimizu N; Yoshino H; Kurashima R; Tanaka M; Ozawa T; Mizuno Y
Structural organization and chromosomal localization of the human nuclear gene (NDUFV2) for the 24-kDa iron-sulfur subunit of complex I in mitochondrial respiratory chain.
Biochemical and biophysical research communications 1995;216(3):771-7.
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1995: Hattori N; Sugano K; Wakiya M; Mori H; Shirai T; Mizuno Y
[A 56-year-old woman with parkinsonism and dementia with the age of onset at 41 years]
No to shinkei = Brain and nerve 1995;47(9):911-9.
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1995: Mizuno Y; Ikebe S; Hattori N; Nakagawa-Hattori Y; Mochizuki H; Tanaka M; Ozawa T
Role of mitochondria in the etiology and pathogenesis of Parkinson's disease.
Biochimica et biophysica acta 1995;1271(1):265-74.
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1994: Mizuno Y; Ikebe S; Hattori N; Mochizuki H; Nakagawa-Hattori Y; Kondo T
Studies on the pathogenesis of Parkinson's disease in Japan.
Archives of gerontology and geriatrics 1994;19(2):105-21.
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1994: Mizuno Y; Matuda S; Yoshino H; Mori H; Hattori N; Ikebe S
An immunohistochemical study on alpha-ketoglutarate dehydrogenase complex in Parkinson's disease.
Annals of neurology 1994;35(2):204-10.
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1994: Mochizuki H; Imai H; Endo K; Yokomizo K; Murata Y; Hattori N; Mizuno Y
Iron accumulation in the substantia nigra of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced hemiparkinsonian monkeys.
Neuroscience letters 1994;168(1-2):251-3.
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1993: Mizuno Y; Ikebe S; Hattori N; Kondo T; Tanaka M; Ozawa T
Mitochondrial energy crisis in Parkinson's disease.
Advances in neurology 1993;60():282-7.
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1993: Hattori N; Ikebe S; Tanaka M; Ozawa T; Mizuno Y
Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease.
Advances in neurology 1993;60():292-6.
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1991: Hattori N; Tanaka M; Ozawa T; Mizuno Y
Immunohistochemical studies on complexes I, II, III, and IV of mitochondria in Parkinson's disease.
Annals of neurology 1991;30(4):563-71.
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1990: Shimoda-Matsubayashi S; Kuru Y; Sumie H; Ito T; Hattori N; Okuma Y; Mizuno Y
MRI findings in the mild type of mucopolysaccharidosis II (Hunter's syndrome).
Neuroradiology 1990;32(4):328-30.
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