Volgen
Kenya Nishioka
Kenya Nishioka
Juntendo University School of Medicine
Geverifieerd e-mailadres voor juntendo.ac.jp
Titel
Geciteerd door
Geciteerd door
Jaar
Genomic investigation of α‐synuclein multiplication and parkinsonism
OA Ross, AT Braithwaite, LM Skipper, J Kachergus, MM Hulihan, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
3982008
Translation initiator EIF4G1 mutations in familial Parkinson disease
MC Chartier-Harlin, JC Dachsel, C Vilariño-Güell, SJ Lincoln, F Leprêtre, ...
The American Journal of Human Genetics 89 (3), 398-406, 2011
3942011
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease
K Nishioka, S Hayashi, MJ Farrer, AB Singleton, H Yoshino, H Imai, ...
Annals of Neurology: Official Journal of the American Neurological …, 2006
3932006
CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study
M Funayama, K Ohe, T Amo, N Furuya, J Yamaguchi, S Saiki, Y Li, ...
The Lancet Neurology 14 (3), 274-282, 2015
3622015
LRRK2 knockout mice have an intact dopaminergic system but display alterations in exploratory and motor co-ordination behaviors
KM Hinkle, M Yue, B Behrouz, JC Dächsel, SJ Lincoln, EE Bowles, ...
Molecular neurodegeneration 7, 1-17, 2012
2102012
Progress in the pathogenesis and genetics of Parkinson's disease
Y Mizuno, N Hattori, S Kubo, S Sato, K Nishioka, T Hatano, H Tomiyama, ...
Philosophical Transactions of the Royal Society B: Biological Sciences 363 …, 2008
1572008
Prognosis of Parkinson's disease: time to stage III, IV, V, and to motor fluctuations
K Sato, T Hatano, K Yamashiro, M Kagohashi, K Nishioka, N Izawa, ...
Movement disorders: official journal of the Movement Disorder Society 21 (9 …, 2006
1532006
Expanding the clinical phenotype of SNCA duplication carriers
K Nishioka, OA Ross, K Ishii, JM Kachergus, K Ishiwata, M Kitagawa, ...
Movement disorders 24 (12), 1811-1819, 2009
1482009
Homozygous alpha-synuclein p. A53V in familial Parkinson's disease
H Yoshino, M Hirano, AJ Stoessl, Y Imamichi, A Ikeda, Y Li, M Funayama, ...
Neurobiology of aging 57, 248. e7-248. e12, 2017
1142017
CLINICOPATHOLOGIC STUDY OF A SNCA GENE DUPLICATION PATIENT WITH PARKINSON DISEASE AND DEMENTIA
T Obi, K Nishioka, OA Ross, T Terada, K Yamazaki, A Sugiura, ...
Neurology 70 (3), 238-241, 2008
932008
Clinicogenetic study of GBA mutations in patients with familial Parkinson's disease
Y Li, T Sekine, M Funayama, L Li, H Yoshino, K Nishioka, H Tomiyama, ...
Neurobiology of aging 35 (4), 935. e3-935. e8, 2014
872014
An epidemiologic internet survey of fibromyalgia and chronic pain in Japan
I Nakamura, K Nishioka, C Usui, K Osada, H Ichibayashi, M Ishida, ...
Arthritis care & research 66 (7), 1093-1101, 2014
862014
Association of α-, β-, and γ-synuclein with diffuse Lewy body disease
K Nishioka, C Wider, C Vilarino-Güell, AI Soto-Ortolaza, SJ Lincoln, ...
Archives of neurology 67 (8), 970-975, 2010
852010
Variants in saposin D domain of prosaposin gene linked to Parkinson’s disease
Y Oji, T Hatano, SI Ueno, M Funayama, K Ishikawa, A Okuzumi, S Noda, ...
Brain 143 (4), 1190-1205, 2020
802020
The E3 ligase synoviolin controls body weight and mitochondrial biogenesis through negative regulation of PGC‐1β
H Fujita, N Yagishita, S Aratani, T Saito‐Fujita, S Morota, Y Yamano, ...
The EMBO journal 34 (8), 1042-1055, 2015
772015
DNAJC12 and dopa‐responsive nonprogressive parkinsonism
L Straniero, I Guella, R Cilia, L Parkkinen, V Rimoldi, A Young, R Asselta, ...
Annals of neurology 82 (4), 640-646, 2017
682017
Molecular genetics of Parkinson’s disease: Contributions and global trends
M Funayama, K Nishioka, Y Li, N Hattori
Journal of human genetics 68 (3), 125-130, 2023
672023
Familial Parkinsonism with digenic parkin and PINK1 mutations
M Funayama, Y Li, TH Tsoi, CW Lam, T Ohi, S Yazawa, E Uyama, ...
Movement disorders: official journal of the Movement Disorder Society 23 (10 …, 2008
652008
Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders
K Ogaki, S Koga, MG Heckman, FC Fiesel, M Ando, C Labbé, ...
Neurology 85 (23), 2016-2025, 2015
642015
FBXO7 mutations in Parkinson's disease and multiple system atrophy
S Conedera, H Apaydin, Y Li, H Yoshino, A Ikeda, T Matsushima, ...
Neurobiology of aging 40, 192. e1-192. e5, 2016
622016
Het systeem kan de bewerking nu niet uitvoeren. Probeer het later opnieuw.
Artikelen 1–20