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Potential utility of metagenomic sequencing for improving etiologic diagnosis of infective endocarditis.

Chan WS, Au CH, Leung HC, Ho DN, Li D, Chan TL, Lam TW, Ma ES, Tang BS.

Future Cardiol. 2019 Nov;15(6):411-424. doi: 10.2217/fca-2018-0088. Epub 2019 Nov 6.


Analysis of Salivary Microbiome in Patients with Alzheimer's Disease.

Liu XX, Jiao B, Liao XX, Guo LN, Yuan ZH, Wang X, Xiao XW, Zhang XY, Tang BS, Shen L.

J Alzheimers Dis. 2019 Oct 3. doi: 10.3233/JAD-190587. [Epub ahead of print]


Preliminary study of hsa-miR-626 change in the cerebrospinal fluid of Parkinson's disease patients.

Qin LX, Tan JQ, Zhang HN, Tang JG, Jiang B, Shen XM, Tang BS, Wang CY.

J Clin Neurosci. 2019 Dec;70:198-201. doi: 10.1016/j.jocn.2019.08.082. Epub 2019 Sep 3.


Clinical effect and safety of dendritic cell-cytokine-induced killer cell immunotherapy for pancreatic cancer: a systematic review and meta-analysis.

Liu YL, Yang LX, Zhang F, Tang BS, Zhao LT, Zhu JR, Jin QY, Wang RX, Li YM.

Cytotherapy. 2019 Oct;21(10):1064-1080. doi: 10.1016/j.jcyt.2019.07.006. Epub 2019 Aug 26.


Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease.

Sun SC, Ma D, Li MY, Zhang RX, Huang C, Huang HJ, Xie YZ, Wang ZJ, Liu J, Cai DC, Liu CX, Yang Q, Bao FX, Gong XL, Li JR, Hui Z, Wei XF, Zhong JM, Zhou WJ, Shang X, Zhang C, Liu XG, Tang BS, Xiong F, Xu XM.

Brain. 2019 Aug 1;142(8):2215-2229. doi: 10.1093/brain/awz151.


Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders.

Tian Y, Wang JL, Huang W, Zeng S, Jiao B, Liu Z, Chen Z, Li Y, Wang Y, Min HX, Wang XJ, You Y, Zhang RX, Chen XY, Yi F, Zhou YF, Long HY, Zhou CJ, Hou X, Wang JP, Xie B, Liang F, Yang ZY, Sun QY, Allen EG, Shafik AM, Kong HE, Guo JF, Yan XX, Hu ZM, Xia K, Jiang H, Xu HW, Duan RH, Jin P, Tang BS, Shen L.

Am J Hum Genet. 2019 Jul 3;105(1):166-176. doi: 10.1016/j.ajhg.2019.05.013. Epub 2019 Jun 6.


Examining the causal role of leptin in bone mineral density: A Mendelian randomization study.

Meng XH, Tan LJ, Xiao HM, Tang BS, Deng HW.

Bone. 2019 Aug;125:25-29. doi: 10.1016/j.bone.2019.05.006. Epub 2019 May 8.


Clinical Features and Correlates of Excessive Daytime Sleepiness in Parkinson's Disease.

Xiang YQ, Xu Q, Sun QY, Wang ZQ, Tian Y, Fang LJ, Yang Y, Tan JQ, Yan XX, Tang BS, Guo JF.

Front Neurol. 2019 Feb 19;10:121. doi: 10.3389/fneur.2019.00121. eCollection 2019.


Impaired iPLA2╬▓ activity affects iron uptake and storage without iron accumulation: An in vitro study excluding decreased iPLA2╬▓ activity as the cause of iron deposition in PLAN.

Guo YP, Tang BS, Liu HL, Huang JJ, Xu Q, Sun QY, Yan XX, Guo JF.

Brain Res. 2019 Jun 1;1712:25-33. doi: 10.1016/j.brainres.2019.01.036. Epub 2019 Jan 29.


PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes.

Guo YP, Tang BS, Guo JF.

Front Neurol. 2018 Dec 18;9:1100. doi: 10.3389/fneur.2018.01100. eCollection 2018. Review.


Draft Genome Sequence of Helicobacter cinaedi, Compiled by Direct Whole-Genome Sequencing of a Blood Culture-Positive Isolate in Hong Kong.

Chan WS, Au CH, Leung HC, Ho DN, Chan TL, Lam TW, Ma ES, Tang BS.

Microbiol Resour Announc. 2018 Nov 8;7(18). pii: e01263-18. doi: 10.1128/MRA.01263-18. eCollection 2018 Nov.


[Comparative analysis of two hybrid technique in treating multilevel cervical spondylotic myelopathy via anterior approach].

Tang BS, Yan C, Zhang XK, Liu YB, Wang C, Wei B.

Zhongguo Gu Shang. 2018 Nov 25;31(11):1034-1040. doi: 10.3969/j.issn.1003-0034.2018.11.010. Chinese.


Coding mutations in NUS1 contribute to Parkinson's disease.

Guo JF, Zhang L, Li K, Mei JP, Xue J, Chen J, Tang X, Shen L, Jiang H, Chen C, Guo H, Wu XL, Sun SL, Xu Q, Sun QY, Chan P, Shang HF, Wang T, Zhao GH, Liu JY, Xie XF, Jiang YQ, Liu ZH, Zhao YW, Zhu ZB, Li JD, Hu ZM, Yan XX, Fang XD, Wang GH, Zhang FY, Xia K, Liu CY, Zhu XW, Yue ZY, Li SC, Cai HB, Zhang ZH, Duan RH, Tang BS.

Proc Natl Acad Sci U S A. 2018 Nov 6;115(45):11567-11572. doi: 10.1073/pnas.1809969115. Epub 2018 Oct 22.


Identifying mild-moderate Parkinson's disease using whole-brain functional connectivity.

Tang Y, Liu B, Yang Y, Wang CM, Meng L, Tang BS, Guo JF.

Clin Neurophysiol. 2018 Dec;129(12):2507-2516. doi: 10.1016/j.clinph.2018.09.006. Epub 2018 Sep 24.


Comparative evaluation of a laboratory-developed real-time PCR assay and RealStar® Adenovirus PCR Kit for quantitative detection of human adenovirus.

Wong SSY, Yip CCY, Sridhar S, Leung KH, Cheng AKW, Fung AMY, Lam HY, Chan KH, Chan JFW, Cheng VCC, Tang BSF, Yuen KY.

Virol J. 2018 Sep 27;15(1):149. doi: 10.1186/s12985-018-1059-7.


Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy.

Zeng S, Zhang MY, Wang XJ, Hu ZM, Li JC, Li N, Wang JL, Liang F, Yang Q, Liu Q, Fang L, Hao JW, Shi FD, Ding XB, Teng JF, Yin XM, Jiang H, Liao WP, Liu JY, Wang K, Xia K, Tang BS.

J Med Genet. 2019 Apr;56(4):265-270. doi: 10.1136/jmedgenet-2018-105484. Epub 2018 Sep 7.


Prevalence of pre-diagnostic symptoms did not differ between LRRK2-related, GBA-related and idiopathic patients with Parkinson's disease.

Liu SY, Zheng Z, Gu ZQ, Wang CD, Tang BS, Xu YM, Ma JH, Zhou YT, Feng T, Chen SD, Chan P; Chinese Parkinson Study Group.

Parkinsonism Relat Disord. 2018 Dec;57:72-76. doi: 10.1016/j.parkreldis.2018.08.007. Epub 2018 Aug 14.


Alzheimer's disease susceptibility genes modify the risk of Parkinson disease and Parkinson's disease-associated cognitive impairment.

Fang L, Tang BS, Fan K, Wan CM, Yan XX, Guo JF.

Neurosci Lett. 2018 Jun 11;677:55-59. doi: 10.1016/j.neulet.2018.04.042. Epub 2018 Apr 24.


Prospective study on human fecal carriage of Enterobacteriaceae possessing mcr-1 and mcr-2 genes in a regional hospital in Hong Kong.

Chan WS, Au CH, Ho DN, Chan TL, Ma ES, Tang BS.

BMC Infect Dis. 2018 Feb 13;18(1):81. doi: 10.1186/s12879-018-2987-y.


Proline-rich transmembrane protein 2-negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients.

Tian WT, Huang XJ, Mao X, Liu Q, Liu XL, Zeng S, Guo XN, Shen JY, Xu YQ, Tang HD, Yin XM, Zhang M, Tang WG, Liu XR, Tang BS, Chen SD, Cao L.

Mov Disord. 2018 Mar;33(3):459-467. doi: 10.1002/mds.27274. Epub 2018 Jan 22.


Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS.

Hum Mol Genet. 2018 Feb 15;27(4):757-758. doi: 10.1093/hmg/ddy025. No abstract available.


Screening for SH3TC2, PMP2, and BSCL2 Variants in a Cohort of Chinese Patients with Charcot-Marie-Tooth.

Zhao X, Jiang MM, Yan YZ, Liu L, Xie YZ, Li XB, Hu ZM, Zi XH, Xia K, Tang BS, Zhang RX.

Chin Med J (Engl). 2018 Jan 20;131(2):151-155. doi: 10.4103/0366-6999.222331.


Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 gene.

Yin XM, Lin JH, Cao L, Zhang TM, Zeng S, Zhang KL, Tian WT, Hu ZM, Li N, Wang JL, Guo JF, Wang RX, Xia K, Zhang ZH, Yin F, Peng J, Liao WP, Yi YH, Liu JY, Yang ZX, Chen Z, Mao X, Yan XX, Jiang H, Shen L, Chen SD, Zhang LM, Tang BS.

Hum Mol Genet. 2018 Feb 15;27(4):625-637. doi: 10.1093/hmg/ddx430. Erratum in: Hum Mol Genet. 2018 Feb 15;27(4):757-758.


Evaluation of the molecular Xpert Xpress Flu/RSV assay vs. Alere i Influenza A & B assay for rapid detection of influenza viruses.

Chen JH, Lam HY, Yip CC, Cheng VC, Chan JF, Leung TH, Sridhar S, Chan KH, Tang BS, Yuen KY.

Diagn Microbiol Infect Dis. 2018 Mar;90(3):177-180. doi: 10.1016/j.diagmicrobio.2017.11.010. Epub 2017 Nov 24.


PiT2 regulates neuronal outgrowth through interaction with microtubule-associated protein 1B.

Ma XX, Li X, Yi P, Wang C, Weng J, Zhang L, Xu X, Sun H, Feng S, Liu K, Chen R, Du S, Mao X, Zeng X, Zhang LY, Liu M, Tang BS, Zhu X, Jin S, Liu JY.

Sci Rep. 2017 Dec 19;7(1):17850. doi: 10.1038/s41598-017-17953-3.


Identification of Ser465 as a novel PINK1 autophosphorylation site.

Guo JF, Yao LY, Sun QY, Cui YT, Yang Y, Xu Q, Yan XX, Tang BS.

Transl Neurodegener. 2017 Dec 14;6:34. doi: 10.1186/s40035-017-0103-7. eCollection 2017.


Altered Functional Brain Connectomes between Sporadic and Familial Parkinson's Patients.

Tang Y, Xiao X, Xie H, Wan CM, Meng L, Liu ZH, Liao WH, Tang BS, Guo JF.

Front Neuroanat. 2017 Nov 6;11:99. doi: 10.3389/fnana.2017.00099. eCollection 2017.


Identification of novel SPG11 mutations in a cohort of Chinese families with hereditary spastic paraplegia.

Du J, Hu YC, Tang BS, Jiang H, Shen L.

Int J Neurosci. 2018 Feb;128(2):146-150. doi: 10.1080/00207454.2017.1378878. Epub 2017 Oct 5.


Can brain impermeable BACE1 inhibitors serve as anti-CAA medicine?

Li JM, Huang LL, Liu F, Tang BS, Yan XX.

BMC Neurol. 2017 Aug 25;17(1):163. doi: 10.1186/s12883-017-0942-y.


Microglial Activation in the Pathogenesis of Huntington's Disease.

Yang HM, Yang S, Huang SS, Tang BS, Guo JF.

Front Aging Neurosci. 2017 Jun 19;9:193. doi: 10.3389/fnagi.2017.00193. eCollection 2017. Review.


Sortilin Fragments Deposit at Senile Plaques in Human Cerebrum.

Hu X, Hu ZL, Li Z, Ruan CS, Qiu WY, Pan A, Li CQ, Cai Y, Shen L, Chu Y, Tang BS, Cai H, Zhou XF, Ma C, Yan XX.

Front Neuroanat. 2017 Jun 7;11:45. doi: 10.3389/fnana.2017.00045. eCollection 2017.


BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage.

Qin LX, Tan JQ, Zhang HN, Rizwana K, Lu JH, Tang JG, Jiang B, Shen XM, Guo JF, Tang BS, Tan LM, Wang CY.

Oxid Med Cell Longev. 2017;2017:5094934. doi: 10.1155/2017/5094934. Epub 2017 Mar 2.


Identifying the presence of Parkinson's disease using low-frequency fluctuations in BOLD signals.

Tang Y, Meng L, Wan CM, Liu ZH, Liao WH, Yan XX, Wang XY, Tang BS, Guo JF.

Neurosci Lett. 2017 Apr 3;645:1-6. doi: 10.1016/j.neulet.2017.02.056. Epub 2017 Feb 27.


Parkinson's Disease and Cognitive Impairment.

Yang Y, Tang BS, Guo JF.

Parkinsons Dis. 2016;2016:6734678. doi: 10.1155/2016/6734678. Epub 2016 Dec 12. Review.


In Vitro Activity of Posaconazole against Talaromyces marneffei by Broth Microdilution and Etest Methods and Comparison to Itraconazole, Voriconazole, and Anidulafungin.

Lau SK, Lo GC, Lam CS, Chow WN, Ngan AH, Wu AK, Tsang DN, Tse CW, Que TL, Tang BS, Woo PC.

Antimicrob Agents Chemother. 2017 Feb 23;61(3). pii: e01480-16. doi: 10.1128/AAC.01480-16. Print 2017 Mar.


Phenotypes and cellular effects of GJB1 mutations causing CMT1X in a cohort of 226 Chinese CMT families.

Liu L, Li XB, Hu ZHM, Zi XH, Zhao X, Xie YZ, Huang SHX, Xia K, Tang BS, Zhang RX.

Clin Genet. 2017 Jun;91(6):881-891. doi: 10.1111/cge.12913. Epub 2017 Mar 8.


RAB39B gene mutations are not linked to familial Parkinson's disease in China.

Kang JF, Luo Y, Tang BS, Wan CM, Yang Y, Li K, Liu ZH, Sun QY, Xu Q, Yan XX, Guo JF.

Sci Rep. 2016 Oct 3;6:34502. doi: 10.1038/srep34502.


SPG46 and SPG56 are rare causes of hereditary spastic paraplegia in China.

Yang YJ, Zhou ZF, Liao XX, Luo YY, Zhan ZX, Huang MF, Zhou L, Tang BS, Shen L, Du J.

J Neurol. 2016 Oct;263(10):2136-8. doi: 10.1007/s00415-016-8256-3. Epub 2016 Aug 23. No abstract available.


Genome-wide comparison of AP2/ERF superfamily genes between Gossypium arboreum and G. raimondii.

Lei ZP, He DH, Xing HY, Tang BS, Lu BX.

Genet Mol Res. 2016 Jul 29;15(3). doi: 10.4238/gmr.15038211.


Paroxysmal hypnogenic dyskinesia is associated with mutations in the PRRT2 gene.

Liu XR, Huang D, Wang J, Wang YF, Sun H, Tang B, Li W, Lai JX, He N, Wu M, Su T, Meng H, Shi YW, Li BM, Tang BS, Liao WP.

Neurol Genet. 2016 Mar 22;2(2):e66. doi: 10.1212/NXG.0000000000000066. eCollection 2016 Apr.


Clinical Evaluation of the New High-Throughput Luminex NxTAG Respiratory Pathogen Panel Assay for Multiplex Respiratory Pathogen Detection.

Chen JHK, Lam HY, Yip CCY, Wong SCY, Chan JFW, Ma ESK, Cheng VCC, Tang BSF, Yuen KY.

J Clin Microbiol. 2016 Jul;54(7):1820-1825. doi: 10.1128/JCM.00517-16. Epub 2016 Apr 27.


Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia.

To KK, Lee KC, Wong SS, Sze KH, Ke YH, Lui YM, Tang BS, Li IW, Lau SK, Hung IF, Law CY, Lam CW, Yuen KY.

Diagn Microbiol Infect Dis. 2016 Jun;85(2):249-54. doi: 10.1016/j.diagmicrobio.2016.03.012. Epub 2016 Mar 14.


Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants.

Tang BS.

Chin Med J (Engl). 2016 May 5;129(9):1009-10. doi: 10.4103/0366-6999.180531. No abstract available.


The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients.

Fan K, Tang BS, Wang YQ, Kang JF, Li K, Liu ZH, Sun QY, Xu Q, Yan XX, Guo JF.

Neurosci Lett. 2016 May 16;621:133-136. doi: 10.1016/j.neulet.2016.04.014. Epub 2016 Apr 13.


Prevalence and phylogenetic characterization of human enterovirus D68 among children with respiratory infection in Hong Kong.

Lam HY, Wong AT, Tsao YC, Tang BS.

Diagn Microbiol Infect Dis. 2016 Jun;85(2):174-6. doi: 10.1016/j.diagmicrobio.2016.02.024. Epub 2016 Mar 3.


Safety and efficacy of valproic acid treatment in SCA3/MJD patients.

Lei LF, Yang GP, Wang JL, Chuang DM, Song WH, Tang BS, Jiang H.

Parkinsonism Relat Disord. 2016 May;26:55-61. doi: 10.1016/j.parkreldis.2016.03.005. Epub 2016 Mar 12.


Matrix-assisted laser desorption ionization time-of-flight mass spectrometry for rapid identification of mold and yeast cultures of Penicillium marneffei.

Lau SK, Lam CS, Ngan AH, Chow WN, Wu AK, Tsang DN, Tse CW, Que TL, Tang BS, Woo PC.

BMC Microbiol. 2016 Mar 10;16:36. doi: 10.1186/s12866-016-0656-0.


Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

Che XQ, Sun ZF, Mao X, Xia K, Yan XX, Jiang H, Shen L, Li N, Tang BS.

Int J Neurosci. 2017 Jan;127(1):10-13. Epub 2016 Apr 6.


A novel hemizygous SACS mutation identified by whole exome sequencing and SNP array analysis in a Chinese ARSACS patient.

Liu L, Li XB, Zi XH, Shen L, Hu ZhM, Huang ShX, Yu DL, Li HB, Xia K, Tang BS, Zhang RX.

J Neurol Sci. 2016 Mar 15;362:111-4. doi: 10.1016/j.jns.2016.01.026. Epub 2016 Jan 18.


The Progress of Induced Pluripotent Stem Cells as Models of Parkinson's Disease.

Kang JF, Tang BS, Guo JF.

Stem Cells Int. 2016;2016:4126214. doi: 10.1155/2016/4126214. Epub 2016 Jan 6. Review.

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