Profile

Baorong,Zhang, M.D ，Department of Neurology
Chair of Department of Neurology
Kiel University,Germany
Zhejiang University, School of Medicine, Hangzhou
Zhejiang
Academic Rank
Professor of Neurology
Research interests：
Molecular genetics in Parkinson’s disease ;Alzhmeimer’s disease, the gene mapping and identification in Neuro-genetics disease.Focusing on the function study for IT15 gene in Huntington’s disease
Main Publications
1. Yin XZ,Ding MP, Zhang BR,etal. Report of two Chinese families and a review of Mainland Chinese CADASIL patients. J Neurolo Sci 2009 Apr 15;279(1-2):88-92.
2. Wang S, Hu HT, Wen SQ, Wang ZJ, Zhang BR, Ding MP.An insulinoma with clinical and electroencephalographic features resembling complex partial seizures. J Zhejiang Univ Sci B 2008 Jun;9(6):496-9.
3. Liu Z, Ding Y, Du A, Zhang BR etal. Mol Vis .A novel Twinkle (PEO1) gene mutation in a Chinese family with adPEO.2008;14:1995.
4. Zhao G, Ding M, Zhang BR etal.. Clinical manifestations and management of acute thallium poisoning.Eur Neurol. 2008;60(6):292.
5. Zhang BR, Liu Z, Zhao G etal. Novel mutations of the FRMD7 gene in X-linked congenital motor nystagmus.Mol Vis. 2007；13;13:1674.
6. Zhang BR, Liu Z, Zhao G.Novel human pathological mutations. Gene symbol: FRMD7. Disease: congenital motor nystagmus.Hum genet.2007;122(3-4):414.
7. BR Zhang, jun Tian,wei Luo,Kun Xia. Protective effect of sodium butyrate on the cell culture model of Huntington disease Prog Nat sci,2007,17(7),785
8. BR Zhang ,Song Fei,Yin Xin-Zhen,etal.IT15 gene analysis in two pedigrees of Huntington’s Disease.HEREDITAS(Beijing),2006,28(11):1345
9．Zhang BR , Xia K, Ding M etal. Confirmation and refinement of a genetic locus of congenital motor nystagmus in Xq26.3-q27.1 in a Chinese family.Hum Genet. 2005;116(1-2):128.
11. BR Zhang , Li J.The clinical study in spinal vascular malformation following DSA confirmation. Chin J Neurol, 2005, 38(7):453-454.
13. BR Zhang , XZ Yin, X kun,Bao YY, ZM HU,Liu ZR, JH Xia.The clinical tomography and gene mutation analysis in Huntington’s disease .Chin J Neurol 2005,38(11):686-689.
14.Liu Z, BR Zhang , M Ding,X kun, ZM HU, H Deng,JH Xia.Mapping of pedigree with congenital nystagmus, Hereditas (Beijing), 2004, 26(4):437-440.
15. BR Zhang , Jin Y, Feng MY, Huang JZ. Severe dementia and tumor-like manifestation in multi-sclerosis. Chin J Neurol, 2004，37（1）:76.
16.Wenzelburger R, Kopper F，BR Zhang etal。Subthalamic Nucleus Stimulation for Parkinson’s disease Preferentially Improves Akinesia of Proximal Arm Movements Compared to Finger Movements.Move Disord，2003，18（10），1162-9.
17.Wenzelburger R, BR Zhang, Deuschl G et al. Force overflow and levodopa-induced dyskinesias in Parkinson’s disease. Brain,2002,125（Pt4）:871-9.
18.Wenzelburger R, BR Zhang, Deuschl G et al. Dyskinesias and stimulation of the subthalamic nucleus. Ann Neurol, 2002, 52(2):240-3.
19. BR Zhang , Ying ZL, JH Xia, Zheng YS, PAN J, TONG XY, Ke LY, YU WE. The gene mutation study in spinal cerebellar ataxia with SCA3 by DNA sequence. Chin J Neurol,2000，33(3):162-164
20. BR Zhang etal. The Gene Mutation Research in Machado-Joseph Disease by DNA Sequencing. Chinese Journal of Neurology, 2000，33（3），162-164.
21.Xia JH, Liu CY, Tang BS, Pan Q, Huang L, Dai HP, Zhang BR, Xie W, Hu DX, Zheng D, Shi XL, Wang DA, Xia K, Yu KP, Liao XD, Feng Y, Yang YF, Xiao JY, Xie DH, Huang JZ.. Mutation in the gene encoding gap junction proteinβ3 associated with autosomal dominant hearing impairment. Nat. genet. 1998，20（4），370.