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Results of search for 'au:"Li, Hong-fu"', page 1 of 2
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Authors
Chen, Cong-Xin
Chen, Mei-Jiao
Chen, Sheng
Chen, Wan-Jin
Dong, Hai-Lin
Dong, Yi
Li, Hong-Fu
Li, Li-Xi
Liu, Gong-Lu
Liu, Zhi-Jun
Lu, Cong
Ni, Wang
Tan, Guo-He
Tao, Qing-Qing
Wang, Hong-Xia
Wang, Ning
Wei, Qiao
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Xiong, Zhi-Qi
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1.
Genotype-phenotype correlations of amyotrophic lateral sclerosis.
[electronic resource]
by
Li, Hong-Fu
Wu, Zhi-Ying
Producer:
20160204
In:
Translational neurodegeneration
vol. 5
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2.
Trigeminal Autonomic Cephalalgias Manifested As The Only Initial Symptom Of Ehlers-Danlos Syndrome Type IV.
[electronic resource]
by
Chen, Mei-Jiao
Li, Hong-Fu
Mao, Shanying
Publication details:
Journal of pain research
2019
In:
Journal of pain research
vol. 12
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3.
N-methyl-D-aspartate receptors mediate diphosphorylation of extracellular signal-regulated kinases through Src family tyrosine kinases and Ca2+/calmodulin-dependent protein kinase II in rat hippocampus after cerebral ischemia.
[electronic resource]
by
Wu, Hui-Wen
Li, Hong-Fu
Guo, Jun
Producer:
20070809
In:
Neuroscience bulletin
vol. 23
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4.
Identification of novel senataxin mutations in Chinese patients with autosomal recessive cerebellar ataxias by targeted next-generation sequencing.
[electronic resource]
by
Lu, Cong
Zheng, Yi-Cen
Dong, Yi
Li, Hong-Fu
Producer:
20161219
In:
BMC neurology
vol. 16
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5.
Paroxysmal kinesigenic dyskinesia and myotonia congenita in the same family: coexistence of a PRRT2 mutation and two CLCN1 mutations.
[electronic resource]
by
Li, Hong-Fu
Chen, Wan-Jin
Ni, Wang
Wu, Zhi-Ying
Producer:
20150724
In:
Neuroscience bulletin
vol. 30
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6.
FTL mutation in a Chinese pedigree with neuroferritinopathy.
[electronic resource]
by
Ni, Wang
Li, Hong-Fu
Zheng, Yi-Cen
Wu, Zhi-Ying
Producer:
20160509
In:
Neurology. Genetics
vol. 2
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7.
Novel homozygous
[electronic resource]
by
Li, Yan-Fang
Li, Hong-Fu
Zhang, Yan-Bin
Wu, Ji-Min
Publication details:
Biomedical reports
Aug 2016
In:
Biomedical reports
vol. 5
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8.
Unilateral versus bilateral stent insertion for malignant hilar biliary obstruction.
[electronic resource]
by
Chang, Gang
Xia, Feng-Fei
Li, Hong-Fu
Niu, Su
Xu, Yuan-Shun
Producer:
20180314
In:
Abdominal radiology (New York)
vol. 42
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9.
Reactive oxygen species mediate ERK activation through different Raf-1-dependent signaling pathways following cerebral ischemia.
[electronic resource]
by
Wu, Hui-wen
Li, Hong-fu
Wu, Xiang-yang
Zhao, Jie
Guo, Jun
Producer:
20080602
In:
Neuroscience letters
vol. 432
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10.
PRRT2 c.649dupC mutation derived from de novo in paroxysmal kinesigenic dyskinesia.
[electronic resource]
by
Li, Hong-Fu
Ni, Wang
Xiong, Zhi-Qi
Xu, Jianfeng
Wu, Zhi-Ying
Producer:
20130530
In:
CNS neuroscience & therapeutics
vol. 19
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11.
(E)-2-{4-[1-(Hydroxyimino)ethyl]phenyl-iminomethyl}-6-methoxyphenol mono-hydrate.
[electronic resource]
by
Tong, Jun-Feng
Gao, Su-Xia
Dong, Wen-Kui
Li, Hong-Fu
Wu, Jian-Chao
Producer:
20110714
In:
Acta crystallographica. Section E, Structure reports online
vol. 65
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12.
Mutation Analysis of MR-1, SLC2A1, and CLCN1 in 28 PRRT2-negative Paroxysmal Kinesigenic Dyskinesia Patients.
[electronic resource]
by
Wang, Hong-Xia
Li, Hong-Fu
Liu, Gong-Lu
Wen, Xiao-Dan
Wu, Zhi-Ying
Producer:
20170307
In:
Chinese medical journal
vol. 129
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13.
Mutation Analysis of COQ2 in Chinese Patients with Cerebellar Subtype of Multiple System Atrophy.
[electronic resource]
by
Wen, Xiao-Dan
Li, Hong-Fu
Wang, Hong-Xia
Ni, Wang
Dong, Yi
Wu, Zhi-Ying
Producer:
20160419
In:
CNS neuroscience & therapeutics
vol. 21
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14.
Spastic paraplegia as the predominant phenotype in a cohort of Chinese patients with adrenoleukodystrophy.
[electronic resource]
by
Luo, Wen-Jiao
Wei, Qiao
Dong, Hai-Lin
Yan, Yang-Tian
Chen, Mei-Jiao
Li, Hong-Fu
Producer:
20210326
In:
Molecular genetics & genomic medicine
vol. 8
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15.
The association of XRCC1 polymorphism with osteosarcoma risk, clinicopathologic features, and prognosis in a Chinese Han population.
[electronic resource]
by
Wu, Ying-Guang
Li, Hong-Fu
Ren, Yan-Jun
Zou, De-Bo
Zhang, Kai-Ning
Xiao, Xing
Publication details:
Cancer management and research
2018
In:
Cancer management and research
vol. 10
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16.
Genetic spectrum of MCM3AP and its relationship with phenotype of Charcot-Marie-Tooth disease.
[electronic resource]
by
Dong, Hai-Lin
Wei, Qiao
Li, Jia-Qi
Li, Hong-Fu
Bai, Ge
Ma, Huan
Wu, Zhi-Ying
Producer:
20210601
In:
Journal of the peripheral nervous system : JPNS
vol. 25
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17.
Urine-derived induced pluripotent stem cells as a modeling tool for paroxysmal kinesigenic dyskinesia.
[electronic resource]
by
Zhang, Shu-Zhen
Li, Hong-Fu
Ma, Li-Xiang
Qian, Wen-Jing
Wang, Zhong-Feng
Wu, Zhi-Ying
Producer:
20151217
In:
Biology open
vol. 4
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18.
Improving molecular diagnosis of Chinese patients with Charcot-Marie-Tooth by targeted next-generation sequencing and functional analysis.
[electronic resource]
by
Li, Li-Xi
Zhao, Shao-Yun
Liu, Zhi-Jun
Ni, Wang
Li, Hong-Fu
Xiao, Bao-Guo
Wu, Zhi-Ying
Producer:
20180115
In:
Oncotarget
vol. 7
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19.
Systematic screening and characterization of prototype constituents and metabolites of total astragalosides using HPLC-ESI-IT-TOF-MS
[electronic resource]
by
Li, Hong-Fu
Xu, Feng
Yang, Ping
Liu, Guang-Xue
Shang, Ming-Ying
Wang, Xuan
Yin, Jun
Cai, Shao-Qing
Producer:
20180119
In:
Journal of pharmaceutical and biomedical analysis
vol. 142
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20.
Novel PLA2G6 mutations and clinical heterogeneity in Chinese cases with phospholipase A2-associated neurodegeneration.
[electronic resource]
by
Chen, Yi-Jun
Chen, Yu-Chao
Dong, Hai-Lin
Li, Li-Xi
Ni, Wang
Li, Hong-Fu
Wu, Zhi-Ying
Producer:
20190523
In:
Parkinsonism & related disorders
vol. 49
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