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序号
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论文名称
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发表单位及时间
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完成人(﹡)
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1
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Clinical picture: herpes simplex encephalitis. (IF:18.316)
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Lancet, 2003;361:280
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Hu Zhi-ping (1)
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2
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Clinical picture: intracerebral tuberculosis. (IF:13.251)
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Lancet, 2001
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Hu Zhi-ping (1)
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3
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IL-1 receptor antagonist mediated therapeutic effect in murine myasthenia gravis is associated with suppressed serum proinflammatory cytokines, C3, and anti acetylcholine receptor IgG1. (IF: 6.387)
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J Immunol，2005
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Yang Huan (1)
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4
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Mutation analysis of the small heat-shock protein 27 gene in Chinese patients with Charcot -Marie-Tooth disease. (IF: 4.684)
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Arch Neurol, 2005, 62:1201-1207.
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Tang Bei-sha (1)
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5
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Three novel mutations of spastin gene in Chinese patients with hereditary spastic paraplegia. (IF:4.835)
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Arch Neurol, 2004,61:49-55
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Tang Bei-sha (1)
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6
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Small heat-shock protein 22 mutated in autosomal dominant Charcot-Marie-Tooth disease type 2L. (IF:4.331)
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Hum Genet, 2005;116:222-224
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Tang Bei-sha (1)
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7
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A new locus for autosomal dominant Charct-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24. (IF:4.328)
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Hum Genet, 2004;114:527-533
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Tang Bei-sha (1)
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8
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Novel compound heterozygous mutations in the PANK2 gene in a Chinese patient with atypical pantothenate kinase -associated neurodegeneration. (IF:2.83)
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Movement Disord, 2005;20(7):819-821.
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Zhang Yu-hu (1)
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9
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Catalase over-expression protects striatal neurons from transient focal cerebral ischemia. (IF:2.351)
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Neuroreport. 2004;15:413-416.
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Gu Wen-ping (1)
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10
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17β-estradiol potentiates ischemia -reperfusion injury in diabetic ovariectomized female rats. (IF:2.296)
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Brain Research. 2005;1054:192-199
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You Yong (1)
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11
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A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family. (IF:2.366)
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J Neurol Sci, 2004;221:31-34
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Tang Bei-sha (1)
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12
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Spinocerebellar ataxia type 6 in mainland China：molecular and clinical features in four families. (IF:2.035)
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J Neurol Sci, 2005;236:25-29
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Jiang Hong (1)
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13
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Incidence of cerebral hemorrhage in the Changsha community (A prospective study from 1986 to 2000). (IF:2.150)
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Cerebrovasc Dis, 2004;17:303-313
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Yang Qi-dong (1)
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14
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Apolipoprotein H gene polymorphisms and risk of primary cerebral hemorrhage in a Chinese population. (IF:2.150)
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Cerebrovasc Dis. 2004;17:197-203
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Xia Jian (1)
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15
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Clinical and genetic study on a new Chinese family with benign familial infantile seizures. (IF:2.244)
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Eur J Neurol, 2005;12:344-349
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Xiao Bo (1)
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16
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Acute dystonia induced by lamivudine. (IF:1.89)
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Clin Neuropharmacol, 2005;28(4):193-194
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Song Xing-wang (1)
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17
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Effects of problem-oriented willed-movement therapy on motor abilities for people with poststroke cognitive deficits. (IF:1.672)
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Phy Ther. 2005;85(10):1020-1032
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Tang Qing-ping (1)
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18
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Triptergium wilfordil multiglucosidetreated case of sensory perineuritis. (IF:2.000)
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Eur J Neurol, 2003;10:188-190
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Yang Qi-dong (1)
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19
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Analysis of gene expression in genetic epilepsy-prone rat using cDNA expression array. (IF:1.399)
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Seizure, 2002;11:418-422
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Xiao Bo (1)
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20
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Betal nut indulgence as a cause of epilepsy. (IF:1.102)
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Seizure, 2003;12:406-408
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Huang Zhi-ling (1)
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21
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Aetiology of epilepsy in surgically treated patients in China. (IF:1.482)
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Seizure, 2004;13:322-327
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Xiao Bo (1)
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22
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Cerebral infarction due to giant cell arteritis three case reports. (IF:1.031)
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Angiology, 2004;55:527-531
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Hu Zhi-ping (1)
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23
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Frequency analysis of autosomal dominant spinocerebellar ataxias in mainland Chinese patients and clinical and molecular characterization of spinocerebellar ataxia tyoe 6. (IF:0.561)
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Chin Med J, 2005;118(10):837-843
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Jiang Hong (1)
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24
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Clincal features of hereditary spastic paraplegia with thin corpus callosum:report of 5 Chinese cases. (IF:0.459)
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Chin Med J, 2004;117(7):1002-1005
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Tang Bei-sha (1)
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25
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Modified graeb criteria for predicting the post-hemorrhagic hydrocephalus in intraventricular hemorrhage. (IF:0.459)
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Chin Med J, 2004;19:138-142
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Song Zhi (1)
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26
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Activation of endogenous neural stem cells in experimental intracerebral hemorrhagic rat brains. (IF:0.459)
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Chin Med J (2004;117(9):1342-47
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Tang Tao(1)
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27
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Clinical and genetic analysis of two Chinese families with benign familial neonatal convulsions. (IF:0.444)
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Prog Nat Sci, 2005;15(8):757-760
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Li Hai-yan (1)
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28
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Cx32 gene mutation associated with X-linked recessive Charcot-Marie-Tooth disease. (IF:0.335)
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Prog Nat Sci, 2003;13:475-477
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Tang Bei-sha (1)
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29
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Characterization of proteolipid protein -specific CD4+ T cell of experimental allergic encephalomyelitis in Biozzi AB/H mice. (IF:0.182)
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Chin Med J, 2002;115:524-529
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Peng Yong (1)
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30
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Effect of thinking on intracranial blood flow velocities. (IF:0.108)
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Chin Med J, 2001;114:1211-1212
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Tian Fa-fa (1)
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31
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The cross-reactivity of I-Ag-7 and I-Ad tetramer. (IF:0.108)
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Chin Med J, 2001;115:1579-1581
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Peng Yong (1)
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32
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MHC tetramer: directly detected autoreactive T cells in autoimmune disease. (IF:0.108)
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Chin Med J, 2001;114:
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Peng Yong (1)
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33
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GAD and IDDM. (IF:0.108)
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Chin Med J, 2001;114
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Peng Yong (1)
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| 34
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Frequemcy of SCA1, SCA2, SCA3/MJD, SCA6, SCA7, and DRPLA CAG trinucleotide repeat expansiom in patients With hereditary spinocerebellar ataxia from Chinese kindreds.
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Arch Neuol, 2000;57:540-544.
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Tang Bei-sha (1)
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| 35
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Temporal arteritis and fever report of a case and clinical reanalysis of 360 cases.
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Angiology, 2000;51:953-958.
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Hu Zhi-ping (1)
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| 36
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Quality of life and personality in adults with epilepsy.
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Epilepsia, 1998;39:1208-1212.
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Zhu Dan-tong(1)
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| 37
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Mutations in the gene encoding gap junction protein β-3 associated with antosomal dominant hearing impairment.
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Nat Genet, 1998;20:370-373.
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Tang Bei-sha (3)
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| 38
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Spinocerebellar ataxia type 2 in China: molecular analysis and genotype-phenotype correlation in nine families.
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Neurology, 1998;51:595-598
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Tang Bei-sha (3)
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| 38
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Mutation analysis of the ATM gene in two Chinese patients With ataxia telangiectasia
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Journal of theNeurological Scie，2006，241：1-6
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Jiang Hong (1)
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| 40
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No association of C-1019G promoter polymorphism of 5-HT1A receptor gene with migraine
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European Journal of Neurology，2006,13:533-535
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X.S.Yang
(1)
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| 41
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Human serum paraoxonase gene polymorphisms, Q192R and L55M, are not associated
with the risk of cerebral infarction in Chinese Han population.
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Neurological Research，2006，28（5）：549
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Huang Q
(1)
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| 42
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Association of PINK1 and DJ-1 confers digenic inheritance of early-onset Parkinson’s disease
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Human Molecular Gentics, 2006,15(11):1816-1826
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Tang Bei-sha (1)
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