Movement Disorders (revue) - Checkpoint (Ncbi)

Index « Mesh.i » - entrée « Asian Continental Ancestry Group »
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List of bibliographic references

Number of relevant bibliographic references: 39.
[0-20] [0 - 20][0 - 39][20-38][20-40]
Ident.Authors (with country if any)Title
000405 (2000) J. Wang [République populaire de Chine] ; Z. LiuNo association between paraoxonase 1 (PON1) gene polymorphisms and susceptibility to Parkinson's disease in a Chinese population.
000406 (2000) J. Wang [République populaire de Chine] ; Z. Liu ; P. ChanLack of association between cytochrome P450 2E1 gene polymorphisms and Parkinson's disease in a Chinese population.
000529 (2001) E K Tan [Singapour] ; A. Seah ; S J See ; E. Lim ; M C Wong ; K K KohRestless legs syndrome in an Asian population: A study in Singapore.
000825 (2002) Ruey-Meei Wu [République populaire de Chine] ; Din-E Shan ; Chen-Ming Sun ; Ren-Shyan Liu ; Wuh-Liang Hwu ; Chun-Hwei Tai ; Jennifer Hussey ; Andrew West ; Katrina Gwinn-Hardy ; John Hardy ; Judy Chen ; Matt Farrer ; Sarah LincolnClinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations.
000838 (2002) Jian Wang [République populaire de Chine] ; Chun-Ying Zhao ; Yan-Mei Si ; Zhuo-Lin Liu ; Biao Chen ; Long YuACT and UCH-L1 polymorphisms in Parkinson's disease and age of onset.
001186 (2005) Yu-Hu Zhang [République populaire de Chine] ; Bei-Sha Tang [République populaire de Chine] ; Ai-Ling Zhao [République populaire de Chine] ; Kun Xia [République populaire de Chine] ; Zhi-Gao Long [République populaire de Chine] ; Ji-Feng Guo [République populaire de Chine] ; Shawn K. Westaway [États-Unis] ; Susan J. Hayflick [États-Unis]Novel Compound Heterozygous Mutations in the PANK2 Gene in a Chinese Patient With Atypical Pantothenate Kinase-Associated Neurodegeneration
001405 (2006) Louis C S. Tan [Singapour] ; Puay-Ngoh Lau ; Roland Dominic G. Jamora ; Edwin S Y. ChanUse of complementary therapies in patients with Parkinson's disease in Singapore.
001478 (2006) Takashi Nomura [Japon] ; Yuichi Inoue ; Masahiro Miyake ; Kenichi Yasui ; Kenji NakashimaPrevalence and clinical characteristics of restless legs syndrome in Japanese patients with Parkinson's disease.
001576 (2006) Eng-King Tan [Singapour] ; Kenneth Yew ; Eva Chua ; K. Puvan ; Hui Shen ; Esther Lee ; Kim-Yoong Puong ; Yi Zhao ; Ratnagopal Pavanni ; Meng-Cheong Wong ; Dominic Jamora ; Deidre De Silva ; Kyaw-Thu Moe ; Fung-Peng Woon ; Yih Yuen ; Louis TanPINK1 mutations in sporadic early-onset Parkinson's disease.
001933 (2007) Eng-King Tan [Singapour] ; Lisa Skipper ; Louis Tan ; Jian-Jun LiuLRRK2 G2019S founder haplotype in the Chinese population.
001935 (2007) Zbigniew K. Wszolek ; Laura A. BrownPrevalence and clinical characteristics of restless legs syndrome in Japanese patients with Parkinson's disease.
001B53 (2007) Eun Joo Chung ; Won Yong Lee ; Ji-Youn Kim ; Jong-Hun Kim ; Gyeong-Moon Kim ; Chang Seok Ki ; In-Suk KimNovel SGCE gene mutation in a Korean patient with myoclonus-dystonia with unique phenotype mimicking Moya-Moya disease.
001B93 (2007) Masato Kanazawa ; Kazuhiro Sanpei ; Yasuko Toyoshima ; Izumi Kawachi ; Yoshiaki Honma ; Hitoshi TakahashiAn autopsy case of dementia with Lewy bodies showing autonomic failure and dementia as the initial symptoms.
001D49 (2007) Ji Youn Kim [Corée du Sud] ; Seong Tae Kim ; Seong Hee Jeon ; Won Yong LeeMidbrain transcranial sonography in Korean patients with Parkinson's disease.
001F17 (2008) Kimiyoshi Arimura [Japon] ; Yumiko Arimura ; Yoshiharu Takata ; Tomonori Nakamura ; Ryuji KajiComparative electrophysiological study of response to botulinum toxin type B in Japanese and Caucasians.
002005 (2008) Hoon-Chul Kang [Corée du Sud] ; Su Jeong You ; Myung Jae Chey ; Jong Sam Baik ; Jong-Won Kim ; Chang-Seok KiIdentification of a de novo Lys304Gln mutation in the glycine receptor alpha-1 subunit gene in a Korean infant with hyperekplexia.
002040 (2008) Eng-King Tan [Singapour] ; Hui-Qin Lim ; Yih Yuen ; Yi ZhaoPathogenicity of LRRK2 P755L variant in Parkinson's disease.
002325 (2008) Ji-Feng Guo [République populaire de Chine] ; Bin Xiao ; Bing Liao ; Xue-Wei Zhang ; Li-Luo Nie ; Yu-Hu Zhang ; Lu Shen ; Hong Jiang ; Kun Xia ; Qian Pan ; Xin-Xiang Yan ; Bei-Sha TangMutation analysis of Parkin, PINK1, DJ-1 and ATP13A2 genes in Chinese patients with autosomal recessive early-onset Parkinsonism.
002437 (2009) Ming-Jen Lee [Taïwan] ; Ignacio F. Mata ; Chin-Hsien Lin ; Kai-Yuan Tzen ; Sarah J. Lincoln ; Rebecca Bounds ; Paul J. Lockhart ; Mary M. Hulihan ; Matthew J. Farrer ; Ruey-Meei WuGenotype-phenotype correlates in Taiwanese patients with early-onset recessive Parkinsonism.
002472 (2009) Akatsuki Kubota [Japon] ; Ayumi Hida ; Yaeko Ichikawa ; Yoshio Momose ; Jun Goto ; Yukifusa Igeta ; Hideji Hashida ; Kunihiro Yoshida ; Syu-Ichi Ikeda ; Ichiro Kanazawa ; Shoji TsujiA novel ferritin light chain gene mutation in a Japanese family with neuroferritinopathy: description of clinical features and implications for genotype-phenotype correlations.
002773 (2009) Zijuan Zhang [République populaire de Chine] ; Jean-Marc Burgunder ; Xingkai An ; Yan Wu ; Wenjun Chen ; Jinhong Zhang ; Yingcheng Wang ; Yanming Xu ; Yingru Gou ; Guanggu Yuan ; Xueye Mao ; Rong PengLRRK2 R1628P variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China.

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