Movement Disorders (revue) - Exploration (Accueil)

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List of bibliographic references indexed by Asian Continental Ancestry Group

Number of relevant bibliographic references: 39.
[0-20] [0 - 20][0 - 39][20-38][20-40]
Ident.Authors (with country if any)Title
000627 (2014) Fu-Bo Cheng [République populaire de Chine] ; Jia-Chun Feng ; Ling-Yan Ma ; Jing Miao ; Thomas Ott ; Xin-Hua Wan ; Kathrin GrundmannCombined occurrence of a novel TOR1A and a THAP1 mutation in primary dystonia.
000866 (2013) Chang-He Shi ; Shi-Lei Sun ; Jun-Ling Wang ; Ai-Qin Liu ; Wang Miao ; Chandra Avinash ; Xiao Mao ; Bei-Sha Tang ; Yu-Ming XuPRRT2 gene mutations in familial and sporadic paroxysmal kinesigenic dyskinesia cases.
000B59 (2012) Maya Ando [Japon] ; Manabu Funayama ; Yuanzhe Li ; Kenichi Kashihara ; Yoshitake Murakami ; Nobutaka Ishizu ; Chizuko Toyoda ; Katsuhiko Noguchi ; Takashi Hashimoto ; Naoki Nakano ; Ryogen Sasaki ; Yasumasa Kokubo ; Shigeki Kuzuhara ; Kotaro Ogaki ; Chikara Yamashita ; Hiroyo Yoshino ; Taku Hatano ; Hiroyuki Tomiyama ; Nobutaka HattoriVPS35 mutation in Japanese patients with typical Parkinson's disease.
000B80 (2012) Tamara Pringsheim [Canada] ; Katie Wiltshire ; Lundy Day ; Jonathan Dykeman ; Thomas Steeves ; Nathalie JetteThe incidence and prevalence of Huntington's disease: a systematic review and meta-analysis.
000B85 (2012) Katsunobu Sugihara [Japon] ; Hirofumi Maruyama ; Hiroyuki Morino ; Ryosuke Miyamoto ; Hiroki Ueno ; Masayasu Matsumoto ; Ryuji Kaji ; Hiroshi Kitaguchi ; Motohiro Yukitake ; Yasuto Higashi ; Kazuto Nishinaka ; Masaya Oda ; Yuishin Izumi ; Hideshi KawakamiThe clinical characteristics of spinocerebellar ataxia 36: a study of 2121 Japanese ataxia patients.
000E21 (2012) Paolo Aridon ; Patrizia Tarantino ; Paolo Ragonese ; Marco D'Amelio ; Antono Cinturino ; Giuseppe Salemi ; Monica Gagliardi ; Vincenzina Lo Re ; Antonio Scarpitta ; Antonio Gambardella ; Aldo Quattrone ; Grazia Annesi ; Giovanni SavettieriDentatorubral-pallidoluysian atrophy: haplotype of Asian origin in 2 Italian families.
000E64 (2012) Ryosuke Miyamoto ; Etsuro Ohta ; Toshitaka Kawarai ; Hidetaka Koizumi ; Wataru Sako ; Yuishin Izumi ; Fumiya Obata ; Ryuji KajiBroad 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.
001439 (2011) Jennifer G. Goldman [États-Unis] ; Darcy Marr [Canada] ; Lili Zhou [États-Unis] ; Bichun Ouyang [États-Unis] ; Sue E. Leurgans [États-Unis] ; Elizabeth Berry-Kravis [États-Unis] ; Christopher G. Goetz [États-Unis]Racial differences may influence the role of cholecystokinin polymorphisms in Parkinson's disease hallucinations
001768 (2011) Morinobu Seki [Japon] ; Kazushi Takahashi [Japon] ; Atsuo Koto [Japon] ; Ban Mihara [Japon] ; Yoko Morita [Japon] ; Kazuo Isozumi [Japon] ; Kouichi Ohta [Japon] ; Kazuhiro Muramatsu [Japon] ; Jun Gotoh [Japon] ; Keiji Yamaguchi [Japon] ; Yutaka Tomita [Japon] ; Hideki Sato [Japon] ; Yoshihiro Nihei [Japon] ; Satoko Iwasawa [Japon] ; Norihiro Suzuki [Japon]Camptocormia in Japanese patients with Parkinson's disease: A multicenter study
001A66 (2010) Manabu Funayama [Japon] ; Hiroyuki Tomiyama [Japon] ; Ruey-Meei Wu [Taïwan] ; Kotaro Ogaki [Japon] ; Hiroyo Yoshino [Japon] ; Yoshikuni Mizuno [Japon] ; Nobutaka Hattori [Japon]Rapid screening of ATP13A2 variant with high‐resolution melting analysis
001B41 (2010) Tomoyuki Miyamoto [Japon] ; Masayuki Miyamoto [Japon] ; Masaoki Iwanami [Japon] ; Koichi Hirata [Japon]Olfactory dysfunction in Japanese patients with idiopathic REM sleep behavior disorder: Comparison of data using the university of Pennsylvania smell identification test and odor stick identification test for Japanese
001B49 (2010) Huijuan Li [République populaire de Chine] ; Meifen Zhang [République populaire de Chine] ; Ling Chen [République populaire de Chine] ; June Zhang [République populaire de Chine] ; Zhong Pei [République populaire de Chine] ; Ailing Hu [République populaire de Chine] ; Qing Wang [République populaire de Chine]Nonmotor symptoms are independently associated with impaired health‐related quality of life in Chinese patients with Parkinson's disease
001C65 (2010) Qi-Ying Sun [République populaire de Chine] ; Ji-Feng Guo [République populaire de Chine] ; Lei Wang [République populaire de Chine] ; Ren-He Yu [République populaire de Chine] ; Xing Zuo [République populaire de Chine] ; Ling-Yan Yao [République populaire de Chine] ; Qian Pan [République populaire de Chine] ; Kun Xia [République populaire de Chine] ; Bei-Sha Tang [République populaire de Chine]Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
001C73 (2010) Xin Liu [République populaire de Chine] ; Shu-Shan Zhang [République populaire de Chine] ; Deng-Fu Fang [République populaire de Chine] ; Ming-Yi Ma [République populaire de Chine] ; Xiao-Yan Guo [République populaire de Chine] ; Yuan Yang [République populaire de Chine] ; Hui-Fang Shang [République populaire de Chine]GCH1 mutation and clinical study of Chinese patients with dopa‐responsive dystonia
001C82 (2010) Li Cao [République populaire de Chine] ; Lan Zheng [République populaire de Chine] ; Wei-Guo Tang [République populaire de Chine] ; Qin Xiao [République populaire de Chine] ; Ting Zhang [République populaire de Chine] ; Hui-Dong Tang [République populaire de Chine] ; Song-Bin He [République populaire de Chine] ; Xi-Jin Wang [République populaire de Chine] ; Jian-Qing Ding [République populaire de Chine] ; Sheng-Di Chen [République populaire de Chine]Four novel mutations in the GCH1 gene of Chinese patients with dopa‐responsive dystonia
001D95 (2010) Takeshi Sekine [Japon] ; Hajime Kagaya [Japon] ; Manabu Funayama [Japon] ; Yuanzhe Li [Japon] ; Hiroyo Yoshino [Japon] ; Hiroyuki Tomiyama [Japon] ; Nobutaka Hattori [Japon]Clinical course of the first Asian family with Parkinsonism related to SNCA triplication
001E95 (2010) Joo-Hyun Seo [Corée du Sud] ; Seok Woo Yong [Corée du Sud] ; Sook K. Song [Corée du Sud] ; Ji E. Lee [Corée du Sud] ; Young H. Sohn [Corée du Sud] ; Phil Hyu Lee [Corée du Sud]A case–control study of multiple system atrophy in Korean patients
002239 (2009) Zijuan Zhang [République populaire de Chine] ; Jean-Marc Burgunder [République populaire de Chine, Suisse, Singapour] ; Xingkai An [République populaire de Chine] ; Yan Wu [République populaire de Chine] ; Wenjun Chen [République populaire de Chine] ; Jinhong Zhang [République populaire de Chine] ; Yingcheng Wang [République populaire de Chine] ; Yanming Xu [République populaire de Chine] ; Yingru Gou [République populaire de Chine] ; Guanggu Yuan [République populaire de Chine] ; Xueye Mao [République populaire de Chine] ; Rong Peng [République populaire de Chine]LRRK2 R1628P variant is a risk factor of Parkinson's disease among Han‐Chinese from mainland China
002289 (2009) Ming-Jen Lee [Taïwan] ; Ignacio F. Mata [États-Unis] ; Chin-Hsien Lin [Taïwan] ; Kai-Yuan Tzen [Taïwan] ; Sarah J. Lincoln [États-Unis] ; Rebecca Bounds [États-Unis] ; Paul J. Lockhart [Australie] ; Mary M. Hulihan [États-Unis] ; Matthew J. Farrer [États-Unis] ; Ruey-Meei Wu [Taïwan]Genotype–phenotype correlates in Taiwanese patients with early‐onset recessive parkinsonism
002476 (2009) Akatsuki Kubota [Japon] ; Ayumi Hida [Japon] ; Yaeko Ichikawa [Japon] ; Yoshio Momose [Japon] ; Jun Goto [Japon] ; Yukifusa Igeta [Japon] ; Hideji Hashida [Japon] ; Kunihiro Yoshida [Japon] ; Syu-Ichi Ikeda [Japon] ; Ichiro Kanazawa [Japon] ; Shoji Tsuji [Japon]A novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: Description of clinical features and implications for genotype–phenotype correlations
002700 (2008) Eng-King Tan [Singapour] ; Hui-Qin Lim [Singapour] ; Yih Yuen [Singapour] ; Yi Zhao [Singapour]Pathogenicity of LRRK2 P755L variant in Parkinson's disease

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