Publications by authors named "Xi-Ru Wu"

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Novel collagen VI mutations identified in Chinese patients with Ullrich congenital muscular dystrophy.
Yan-Zhi Zhang, Dan-Hua Zhao, Hai-Po Yang, Ai-Jie Liu, Xing-Zhi Chang, Xi-Ru Wu

World J Pediatr· May 2014

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[Clinical and genetic characteristics of glucose transporter type 1 deficiency syndrome].
Yan-yan Liu, Xin-hua Bao, Shuang Wang, Na Fu, Xiao-yan Liu, Ye Wu, Jian-xin Wu, Yu-wu Jiang, Xi-ru Wu

Zhonghua Er Ke Za Zhi· June 2013

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[Clinical, pathological and molecular biological characteristics of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episode in children].
Xiao-li Liu, Xin-hua Bao, Yi-nan Ma, Xing-zhi Chang, Jiong Qin, Xi-ru Wu

Zhonghua Er Ke Za Zhi· February 2013

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[Genetic and phenotypic characteristics of SCN1A mutations in Dravet syndrome].
Xiao-jing Xu, Yue-hua Zhang, Hui-hui Sun, Xiao-yan Liu, Yu-wu Jiang, Xi-ru Wu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2012

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[Analysis of HEPACAM mutations in a Chinese family with megalencephalic leukoencephalopathy with subcortical cysts].
Mang-mang Guo, Yu-wu Jiang, Han Xie, Ye Wu, Jing Shang, Xi-ru Wu

Zhonghua Er Ke Za Zhi· December 2012

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[Phenotype and SCN1A gene mutation screening in 39 families with generalized epilepsy with febrile seizures plus].
Xiao-jing Xu, Yue-hua Zhang, Hui-hui Sun, Xiao-yan Liu, Hu-sheng Wu, Xi-ru Wu

Zhonghua Er Ke Za Zhi· August 2012

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[Effects on oligodendrocytic function resulting from proteolipid protein 1 gene mutations].
Jing-Min Wang, Yu-Wu Jiang, Xi-Ru Wu

Sheng Li Ke Xue Jin Zhan· August 2012

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Genotype/phenotype of 6 Chinese cases with Niemann-Pick disease type C.
Hui Xiong, Katsumi Higaki, Cui-Jie Wei, Xin-Hua Bao, Yue-Hua Zhang, Xi-Ru Wu

Gene· May 2012

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[Clinical and genetic study of twelve Chinese patients with Alexander disease].
Li-li Zang, Ye Wu, Jing-min Wang, Qiang Gu, Yu-wu Jiang, Xi-ru Wu

Zhonghua Er Ke Za Zhi· May 2012

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Niemann-Pick disease type C: analysis of 7 patients.
Hui Xiong, Xin-Hua Bao, Yue-Hua Zhang, You-Ning Xu, Jiong Qin, Xi-Ru Wu

World J Pediatr· February 2012

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Long-term effects of recurrent neonatal seizures on neurobehavioral function and related gene expression and its intervention by inhibitor of cathepsin B.
Hong Ni, Jian-Zhen Yan, Le-Ling Zhang, Xing Feng, Xi-Ru Wu

Neurochem Res· January 2012

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Acute phase expression pattern of ZnTs, LC3, and beclin-1 in rat Hippocampus and its regulation by 3-methyladenine following recurrent neonatal seizures.
Hong Ni, Xing Feng, Yong Gong, Lu-Yang Tao, Xi-Ru Wu

Biol Trace Elem Res· October 2011

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[Clinical and mutation analysis of a Chinese family with muscle eye brain disease].
Hui Jiao, Hui Xiong, Yan-zhi Zhang, Shuo Wang, Yan-ling Yang, Xi-ru Wu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2011

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[Electroclinical features of myoclonic-atonic epilepsy].
Jie Deng, Yue-hua Zhang, Xiao-yan Liu, Zhi-xian Yang, Hui Xiong, Yu-wu Jiang, Xi-ru Wu

Zhonghua Er Ke Za Zhi· August 2011

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[Association of genetic polymorphisms in methionine metabolism genes with X-linked adrenoleukodystrophy].
Guang-na Cao, Xin-hua Bao, Hui Xiong, Ye Wu, Xi-ru Wu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· June 2011

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[Clinical characteristics and follow-up management of 135 children with myasthenia gravis].
Zhi-xiao Yang, Hui Xiong, Yue-hua Zhang, Xin-Hua Bao, Yu-wu Jiang, Ye Wu, Xi-ru Wu

Beijing Da Xue Xue Bao Yi Xue Ban· June 2011

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[Clinical characteristics of Huntington disease in two pedigrees and analysis of expanded CAG trinucleotide repeat].
Guang-na Cao, Xin-hua Bao, Hong-mei Lu, Jing-jing Zhang, Yi-nan Ma, Xi-ru Wu

Beijing Da Xue Xue Bao Yi Xue Ban· April 2011

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[Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy].
Yan-zhi Zhang, Hui Xiong, Xiao-zhu Wang, Shuo Wang, Jing Luo, Yu-wu Jiang, Xi-ru Wu

Beijing Da Xue Xue Bao Yi Xue Ban· December 2010

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Dynamic pattern of gene expression of ZnT-1, ZnT-3 and PRG-1 in rat brain following flurothyl-induced recurrent neonatal seizures.
Hong Ni, Yu-wu Jiang, Zhuo-jun Xiao, Lu-yang Tao, Mei-fang Jin, Xi-ru Wu

Toxicol Lett· May 2010

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[Analysis of the parental origin of MECP2 mutations in patients with Rett syndrome].
Jing-jing Zhang, Xin-hua Bao, Guang-na Cao, Sheng-ling Jiang, Xing-wang Zhu, Xi-ru Wu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· April 2010

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[Effects on astrocytic function from MLC1 gene mutation with megalencephalic leukoencephalopathy with subcortical cysts].
Jing-Min Wang, Yu-Wu Jiang, Xi-Ru Wu

Sheng Li Ke Xue Jin Zhan· February 2010

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[Multiplex ligation-dependent probe amplification analysis of subtelomeric chromosome rearrangements in children with idiopathic mental retardation].
Mei-rong Li, Xiao-zhu Wang, Yan-ling Yang, Yue-hua Zhang, Hui Xiong, Xi-ru Wu

Zhonghua Yi Xue Za Zhi· November 2009

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[Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome].
Xing-wang Zhu, Hong Pan, Mei-rong Li, Xin-hua Bao, Jing-jing Zhang, Xi-ru Wu

Zhonghua Er Ke Za Zhi· August 2009

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[Epigenetics and neurodevelopmental diseases].
Xi-ru Wu

Zhonghua Er Ke Za Zhi· June 2009

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[Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome].
Mei-rong Li, Hong Pan, Xin-hua Bao, Xing-wang Zhu, Guang-na Cao, Xi-ru Wu

Zhonghua Er Ke Za Zhi· February 2009

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