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Hong-Fu Li

Showing results (11-20 of 70) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2022
Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A VariantsYu-Lan Chen, Dian-Fu Chen, Hong-Fu Li, et al.
Biomedical Reports|July 23, 2016
Novel homozygous <i>PANK2</i> mutation identified in a consanguineous Chinese pedigree with pantothenate kinase-associated neurodegenerationYan-Fang Li, Hong-Fu Li, Yan-Bin Zhang, et al.
Neuroscience Letters|February 5, 2008
Reactive oxygen species mediate ERK activation through different Raf-1-dependent signaling pathways following cerebral ischemiaHui-wen Wu, Hong-fu Li, Xiang-yang Wu, et al.
Multiple Sclerosis and Related Disorders|June 14, 2020
Characteristic of gut microbiota in southeastern Chinese patients with neuromyelitis optica spectrum disordersJuan Zhang, Yong-Feng Xu, Lei Wu, et al.
CNS Neuroscience & Therapeutics|November 27, 2012
PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesiaHong-Fu Li, Wang Ni, Zhi-Qi Xiong, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
(E)-2-{4-[1-(Hydroxyimino)ethyl]phenyl-iminomethyl}-6-methoxyphenol mono-hydrateJun-Feng Tong, Su-Xia Gao, Wen-Kui Dong, et al.
CNS Neuroscience & Therapeutics|September 7, 2021
Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndromeYan-Yan Xue, Xue-Rong Huang, Hai-Lin Dong, et al.
CNS Neuroscience & Therapeutics|July 13, 2022
Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populationsWang Ni, Yi Zhang, Liang Zhang, et al.
Chinese Medical Journal|April 22, 2016
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia PatientsHong-Xia Wang, Hong-Fu Li, Gong-Lu Liu, et al.
CNS Neuroscience & Therapeutics|June 23, 2015
Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System AtrophyXiao-Dan Wen, Hong-Fu Li, Hong-Xia Wang, et al.
Pageof 7

Showing results (11-20 of 70) with videos related to

Sort By:
Pageof 7
Movement Disorders : Official Journal of the Movement Disorder Society|January 27, 2022
Features Differ Between Paroxysmal Kinesigenic Dyskinesia Patients with PRRT2 and TMEM151A VariantsYu-Lan Chen, Dian-Fu Chen, Hong-Fu Li, et al.
Biomedical Reports|July 23, 2016
Novel homozygous <i>PANK2</i> mutation identified in a consanguineous Chinese pedigree with pantothenate kinase-associated neurodegenerationYan-Fang Li, Hong-Fu Li, Yan-Bin Zhang, et al.
Neuroscience Letters|February 5, 2008
Reactive oxygen species mediate ERK activation through different Raf-1-dependent signaling pathways following cerebral ischemiaHui-wen Wu, Hong-fu Li, Xiang-yang Wu, et al.
Multiple Sclerosis and Related Disorders|June 14, 2020
Characteristic of gut microbiota in southeastern Chinese patients with neuromyelitis optica spectrum disordersJuan Zhang, Yong-Feng Xu, Lei Wu, et al.
CNS Neuroscience & Therapeutics|November 27, 2012
PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesiaHong-Fu Li, Wang Ni, Zhi-Qi Xiong, et al.
Acta Crystallographica. Section E, Structure Reports Online|May 18, 2011
(E)-2-{4-[1-(Hydroxyimino)ethyl]phenyl-iminomethyl}-6-methoxyphenol mono-hydrateJun-Feng Tong, Su-Xia Gao, Wen-Kui Dong, et al.
CNS Neuroscience & Therapeutics|September 7, 2021
Identification of a large homozygous SPG21 deletion in a Chinese patient with Mast syndromeYan-Yan Xue, Xue-Rong Huang, Hai-Lin Dong, et al.
CNS Neuroscience & Therapeutics|July 13, 2022
Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populationsWang Ni, Yi Zhang, Liang Zhang, et al.
Chinese Medical Journal|April 22, 2016
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia PatientsHong-Xia Wang, Hong-Fu Li, Gong-Lu Liu, et al.
CNS Neuroscience & Therapeutics|June 23, 2015
Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System AtrophyXiao-Dan Wen, Hong-Fu Li, Hong-Xia Wang, et al.
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