Burgunder, Jean-Marc

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Kaelin-Lang, Alain; You, Hana; Burgunder, Jean-Marc; Lönnfors-Weitze, Tarja; Loher, Thomas J.; Taub, Ethan; Isaias, Ioannis U; Krauss, Joachim K; Schüpbach, W. M. Michael (2020). Bilateral pallidal stimulation improves cervical dystonia for more than a decade. Parkinsonism & related disorders, 81, pp. 78-81. Elsevier 10.1016/j.parkreldis.2020.10.028

Nef, Tobias; Chesham, Alvin; Schütz, Narayan; Botros, Angela Amira; Vanbellingen, Tim; Burgunder, Jean-Marc; Müllner, Julia; Müri, René Martin; Urwyler, Prabitha (2020). Development and Evaluation of Maze-Like Puzzle Games to Assess Cognitive and Motor Function in Aging and Neurodegenerative Diseases. Frontiers in aging neuroscience, 12(87), p. 87. Frontiers Research Foundation 10.3389/fnagi.2020.00087

Li, X-Y; Li, H-L; Dong, Y; Gao, B; Cheng, H-R; Ni, W; Gan, S-R; Liu, Z-J; Burgunder, Jean-Marc; Wu, Z-Y (2020). Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease. European journal of neurology, 27(2), pp. 273-279. Wiley 10.1111/ene.14072


Li, Hong-Lei; Li, Xiao-Yan; Dong, Yi; Zhang, Yan-Bin; Cheng, Hong-Rong; Gan, Shi-Rui; Liu, Zhi-Jun; Ni, Wang; Burgunder, Jean-Marc; Yang, X William; Wu, Zhi-Ying (2019). Clinical and Genetic Profiles in Chinese Patients with Huntington's Disease: A Ten-year Multicenter Study in China. Aging and disease, 10(5), pp. 1003-1011. Aging and Disease 10.14336/AD.2018.0911

Lachenmayer, Lenard; Bettschen, Cindy; Bernasconi, Corrado; Petermann, Katrin; Debove, Ines; Müllner, Julia; Michelis, Joan Philipp; Burgunder, Jean-Marc; Krauss, J K; Oertel, M F; Pollo, C; Kaelin-Lang, A; Schüpbach, Michael (2019). Stimulation of the globus pallidus internus in the treatment of Parkinson's disease: Long-term results of a monocentric cohort. Parkinsonism & related disorders, 64, pp. 118-123. Elsevier 10.1016/j.parkreldis.2019.03.009

Ho, Aileen K; Horton, Mike C; Landwehrmeyer, G Bernhard; Burgunder, Jean-Marc; Tennant, Alan (2019). Meaningful and Measurable Health Domains in Huntington's Disease: Large-Scale Validation of the Huntington's Disease Health-Related Quality of Life Questionnaire Across Severity Stages. Value in health, 22(6), pp. 712-720. Elsevier 10.1016/j.jval.2019.01.016

Quarrell, Oliver W J; Nance, Martha A; Nopoulos, Peg; Reilmann, Ralf; Oosterloo, Mayke; Tabrizi, Sarah J; Furby, Hannah; Saft, Carsten; Roos, Raymund A C; Squitieri, Ferdinando; Landwehrmeyer, G Bernhard; Burgunder, Jean-Marc (2019). Defining pediatric huntington disease: Time to abandon the term Juvenile Huntington Disease? Movement disorders, 34(4), pp. 584-585. Wiley-Blackwell 10.1002/mds.27640

Bachoud-Lévi, Anne-Catherine; Ferreira, Joaquim; Massart, Renaud; Youssov, Katia; Rosser, Anne; Busse, Monica; Craufurd, David; Reilmann, Ralf; De Michele, Giuseppe; Rae, Daniela; Squitieri, Ferdinando; Seppi, Klaus; Perrine, Charles; Scherer-Gagou, Clarisse; Audrey, Olivier; Verny, Christophe; Burgunder, Jean-Marc (2019). International Guidelines for the Treatment of Huntington's Disease. Frontiers in neurology, 10(710), p. 710. Frontiers Media S.A. 10.3389/fneur.2019.00710

Horton, Mike C; Nopoulos, Peggy; Nance, Martha; Landwehrmyer, G Bernhard; Barker, Roger A; Squitieri, Ferdinando; Burgunder, Jean-Marc; Quarrell, Oliver (2019). Assessment of the Performance of a Modified Motor Scale as Applied to Juvenile Onset Huntington's Disease. Journal of Huntington's disease, 8(2), pp. 181-193. IOS Press 10.3233/JHD-180306


Vez, S.; Kohli, J.; Frey, B.; Magezi, D. A.; Annoni, J. M.; Burgunder, Jean-Marc (2018). Auditory time perception in Huntington's disease. Neuropsychologia, 119, pp. 247-252. Elsevier 10.1016/j.neuropsychologia.2018.08.018

Finsterer, Josef; Mancuso, Michelangelo; Pareyson, Davide; Burgunder, Jean-Marc; Klopstock, Thomas (2018). Mitochondrial disorders of the retinal ganglion cells and the optic nerve. Mitochondrion, 42, pp. 1-10. Elsevier 10.1016/j.mito.2017.10.003

Mestre, T. A.; Busse, M.; Davis, A. M.; Quinn, L.; Rodrigues, F. B.; Burgunder, Jean-Marc; Carlozzi, N. E.; Walker, F.; Ho, A. K.; Sampaio, C.; Goetz, C. G.; Cubo, E.; Martinez-Martin, P.; Stebbins, G. T. (2018). Rating Scales and Performance-based Measures for Assessment of Functional Ability in Huntington's Disease: Critique and Recommendations. Movement disorders clinical practice, 5(4), pp. 361-372. Wiley 10.1002/mdc3.12617

Winder, J. Y.; Roos, R. A. C.; Burgunder, Jean-Marc; Marinus, J.; Reilmann, R. (2018). Interrater Reliability of the Unified Huntington's Disease Rating Scale-Total Motor Score Certification. Movement disorders clinical practice, 5(3), pp. 290-295. Wiley 10.1002/mdc3.12618

Mestre, T. A.; Carlozzi, N. E.; Ho, A. K.; Burgunder, Jean-Marc; Walker, F.; Davis, A. M.; Busse, M.; Quinn, L.; Rodrigues, F. B.; Sampaio, C.; Goetz, C. G.; Cubo, E.; Martinez-Martin, P.; Stebbins, G. T. (2018). Quality of Life in Huntington's Disease: Critique and Recommendations for Measures Assessing Patient Health-Related Quality of Life and Caregiver Quality of Life. Movement disorders, 33(5), pp. 742-749. Wiley-Blackwell 10.1002/mds.27317

Aubry, Emilie; Aeberhard, Carla; Bally, Lia; Nuoffer, Jean-Marc; Risch, Lorenz; Mühlebach, Stefan; Burgunder, Jean-Marc; Stanga, Zeno (2018). Are patients affected by mitochondrial disorders at nutritional risk? Nutrition, 47, pp. 56-62. Elsevier 10.1016/j.nut.2017.09.011

Neuhaus, M; Bagutti, S; Yaldizli, Ö; Zwahlen, D; Schaub, S; Frey, B; Fischer-Barnicol, B; Burgunder, Jean-Marc; Martory, M-D; Pöttgen, J; Annoni, J-M; Penner, I-K (2018). Characterization of social cognition impairment in multiple sclerosis. European journal of neurology, 25(1), pp. 90-96. Wiley-Blackwell 10.1111/ene.13457


Frese, Sebastian; Petersen, Jens A; Ligon-Auer, Maria; Mueller, Sandro Manuel; Mihaylova, Violeta; Gehrig, Saskia M; Kana, Veronika; Rushing, Elisabeth J; Unterburger, Evelyn; Kägi, Georg; Burgunder, Jean-Marc; Toigo, Marco; Jung, Hans H (2017). Exercise effects in Huntington disease. Journal of neurology, 264(1), pp. 32-39. Springer-Medizin-Verlag 10.1007/s00415-016-8310-1

Kübel, Stefanie; Stegmayer, Katharina; Vanbellingen, Tim; Pastore-Wapp, Manuela; Bertschi, Manuel; Burgunder, Jean-Marc; Abela, Eugenio; Weder, Bruno; Walther, Sebastian; Bohlhalter, Stephan (2017). Altered praxis network underlying limb kinetic apraxia in Parkinson's disease - an fMRI study. NeuroImage: Clinical, 16, pp. 88-97. Elsevier 10.1016/j.nicl.2017.07.007

Wiest, Roland; Burgunder, Jean-Marc; Kiefer, Claus (2017). Model-Based Magnetization Transfer Imaging Markers to Characterize Patients and Asymptomatic Gene Carriers in Huntington's Disease. Frontiers in neurology, 8(465), p. 465. Frontiers Media S.A. 10.3389/fneur.2017.00465


Liu, Wanglin; Yang, Jing; Burgunder, Jean-Marc; Cheng, Bochao; Shang, Huifang (2016). Diffusion imaging studies of Huntington's disease: A meta-analysis. Parkinsonism & related disorders, 32, pp. 94-101. Elsevier 10.1016/j.parkreldis.2016.09.005

Yang, Jing; Chen, Ke; Wei, Qianqian; Chen, Yongping; Cao, Bei; Burgunder, Jean-Marc; Shang, Hui-Fang (2016). Clinical and genetic characteristics in patients with Huntington's disease from China. Neurological research, 38(10), pp. 916-920. Maney 10.1080/01616412.2016.1214555

Lachenmayer, Lenard; Bettschen, C.; Debove, Ines; Müllner, Julia Nicole Maria; Bernasconi, Corrado Angelo; Burgunder, Jean-Marc; Krauss, J. K.; Oertel, Markus Florian; Kaelin, Alain; Pollo, Claudio; Schüpbach, Michael (2016). Stimulation of the globus pallidus internus in the treatment of Parkinson`s disease: Long-term results of a monocentric follow-up. Movement disorders, 31(Suppl 2), p. 19. Wiley-Blackwell


Metzger, Silke; Walter, Carolin; Riess, Olaf; Roos, Raymund A. C.; Nielsen, Jørgen E.; Craufurd, David; European Huntington's Disease Network, REGISTRY Investigators of the; Nguyen, Huu Phuc; Burgunder, Jean-Marc; Kaelin, Alain; Schüpbach, Michael (2013). The V471A polymorphism in autophagy-related gene ATG7 modifies age at onset specifically in Italian Huntington disease patients. PLoS ONE, 8(7), e68951. Public Library of Science 10.1371/journal.pone.0068951


Chen, Yongping; Chen, Ke; Burgunder, Jean-Marc; Song, Wei; Huang, Rui; Zhao, Bi; Cao, Bei; Chen, Xueping; Jiang, Yi; Shang, Hui-Fang (2012). Association of rs1182 polymorphism of the DYT1 gene with primary dystonia in Chinese population. Journal of the neurological sciences, 323(1-2), pp. 228-31. Amsterdam: Elsevier 10.1016/j.jns.2012.09.025

Zheng, Zhenzhen; Burgunder, Jean-Marc; Shang, Huifang; Guo, Xiaoyan (2012). Huntington's like conditions in China, A review of published Chinese cases. PLoS currents, 4, RRN1302. Lawrence, Kans.: Public Library of Science

Shang, Huifang; Danek, Adrian; Landwehrmeyer, Bernhard; Burgunder, Jean-Marc (2012). Huntington's disease: new aspects on phenotype and genotype. Parkinsonism & related disorders, 18 Suppl 1, S107-S109. Oxford: Elsevier

Chen, Y; Burgunder, J-M; Song, W; Huang, R; Shang, H-F (2012). Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort. European journal of neurology, 19(6), pp. 924-6. Oxford: Blackwell Science 10.1111/j.1468-1331.2011.03582.x

Li, Peng; Huang, Rui; Song, Wei; Ji, Jie; Burgunder, Jean-Marc; Wang, Xing; Zhong, Qi; Kaelin-Lang, Alain; Wang, Wei; Shang, Hui-Fang (2012). Deep brain stimulation of the globus pallidus internal improves symptoms of chorea-acanthocytosis. Neurological sciences, 33(2), pp. 269-74. Milano: Springer 10.1007/s10072-011-0741-y


Isaias, Ioannis U; Volkmann, Jens; Kupsch, Andreas; Burgunder, Jean-Marc; Ostrem, Jill L; Alterman, Ron L; Mehdorn, Hubertus Maximilian; Schönecker, Thomas; Krauss, Joachim K; Starr, Philip; Reese, Rene; Kühn, Andrea A; Schüpbach, W M Michael; Tagliati, Michele (2011). Factors predicting protracted improvement after pallidal DBS for primary dystonia: the role of age and disease duration. Journal of neurology, 258(8), pp. 1469-76. Heidelberg: Springer-Medizin-Verlag 10.1007/s00415-011-5961-9

Chang, Xue-Li; Mao, Xue-Ye; Li, Hui-Hua; Zhang, Jin-Hong; Li, Nan-Nan; Burgunder, Jean-Marc; Peng, Rong; Tan, Eng-King (2011). Association of GWAS loci with PD in China. American journal of medical genetics. Part B - Neuropsychiatric genetics, 156B(3), pp. 334-9. Hoboken, N.J.: Wiley-Liss 10.1002/ajmg.b.31167

Chang, Xue-Li; Mao, Xue-Ye; Li, Hui-Hua; Zhang, Jin-Hong; Li, Nan-Nan; Burgunder, Jean-Marc; Peng, Rong; Tan, Eng-King (2011). Functional parkin promoter polymorphism in Parkinson's disease: new data and meta-analysis. Journal of the neurological sciences, 302(1-2), pp. 68-71. Amsterdam: Elsevier 10.1016/j.jns.2010.11.023


Tan, Eng-King; Peng, Rong; Teo, Yik-Ying; Tan, Louis C; Angeles, Dario; Ho, Patrick; Chen, Meng-Ling; Lin, Chin-Hsien; Mao, Xue-Ye; Chang, Xue-Li; Prakash, Kumar M; Liu, Jian-Jun; Au, Wing-Lok; Le, Wei-Dong; Jankovic, Joseph; Burgunder, Jean-Marc; Zhao, Yi; Wu, Ruey-Meei (2010). Multiple LRRK2 variants modulate risk of Parkinson disease: a Chinese multicenter study. Human mutation, 31(5), pp. 561-8. Hoboken, N.J.: Wiley-Blackwell 10.1002/humu.21225


Burgunder, Jean-Marc; Huifang, Shang; Beguin, Pascal; Baur, Roland; Eng, Chew Soh; Seet, Raymond C S; Lim, Erle C H; Ong, Benjamin K C; Hunziker, Walter; Sigel, Erwin (2008). Novel chloride channel mutations leading to mild myotonia among Chinese. Neuromuscular disorders, 18(8), pp. 633-40. Amsterdam: Elsevier 10.1016/j.nmd.2008.05.007

Chen, Qin; Lui, Su; Wang, Jian-Gang; Ou-Yang, Luo; Zhou, Dong; Burgunder, Jean-Marc; Gong, Qi-Yong; Shang, Hui-Fang (2008). Diffusion tensor imaging of two unrelated Chinese men with hereditary spastic paraplegia associated with thin corpus callosum. Neuroscience letters, 441(1), pp. 21-4. Amsterdam: Elsevier 10.1016/j.neulet.2008.05.114

Chen, Xue-Ping; Zhang, Yang-Wei; Zhang, Shu-Shan; Chen, Qin; Burgunder, Jean-Marc; Wu, Shu-Hui; Yang, Yuan; Luo, Zu-Ming; Shang, Hui-Fang (2008). A novel mutation of the epsilon-sarcoglycan gene in a Chinese family with myoclonus-dystonia syndrome. Movement disorders, 23(10), pp. 1472-5. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.22008

Galimanis, Aekaterini; Glutz, Louis; Spiegel, Roland; Burgunder, Jean-Marc; Kaelin-Lang, Alain (2008). Very-late-onset Friedreich ataxia with disturbing head tremor and without spinal atrophy--a case report. Movement disorders, 23(7), pp. 1058-9. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21946

Chan, Yee-Cheun; Burgunder, Jean-Marc; Wilder-Smith, Einar; Chew, Soh-Eng; Lam-Mok-Sing, Karen M J; Sharma, Vijay; Ong, Benjamin K C (2008). Electroencephalographic changes and seizures in familial hemiplegic migraine patients with the CACNA1A gene S218L mutation. Journal of clinical neuroscience, 15(8), pp. 891-4. Amsterdam: Elsevier 10.1016/j.jocn.2007.01.013

Chen, Qin; Chen, Xue-Ping; Zou, Ling; Zhou, Dong; Gong, Qi-Yong; Burgunder, Jean-Marc; Shang, Hui-Fang (2008). High brain iron level in asymptomatic carriers of heterozygous ceruloplasmin gene mutations. Movement disorders, 23(6), pp. 916-7. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21980

Zhang, Shu-Shan; Chen, Qin; Chen, Xue-Ping; Wang, Jian-Gang; Burgunder, Jean-Marc; Shang, Hui-Fang (2008). Two novel mutations in the SPG11 gene causing hereditary spastic paraplegia associated with thin corpus callosum. Movement disorders, 23(6), pp. 917-9. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21942

Loher, T J; Capelle, H-H; Kaelin-Lang, A; Weber, S; Weigel, R; Burgunder, J M; Krauss, J K (2008). Deep brain stimulation for dystonia: outcome at long-term follow-up. Journal of neurology, 255(6), pp. 881-4. Heidelberg: Springer-Medizin-Verlag 10.1007/s00415-008-0798-6

Petitprez, S; Tiab, L; Chen, Lie; Kappeler, Liliane; Rösler, Kai Michael; Schorderet, D; Abriel, Hugues; Burgunder, Jean-Marc (2008). A novel dominant mutation of the Nav1.4 {alpha}-subunit domain I leading to sodium channel myotonia. Neurology, 71(21), pp. 1669-1675. Hagerstown, Md.: Lippincott Williams & Wilkins 10.1212/01.wnl.0000335168.86248.55


Schüpbach, W; Vadday, K; Schaller, A; Brekenfeld, C; Kappeler, L; Benoist, JF; Xuan-Huong, C; Burgunder, J; Seibold, F; Gallati, S; Mattle, H (2007). Mitochondrial neurogastrointestinal encephalomyopathy in three siblings: clinical, genetic and neuroradiological features. Journal of neurology, 254(2), pp. 146-53. Heidelberg: Steinkopff-Verlag; www.steinkopff.springer.de 10.1007/s00415-006-0255-3

Lee, Li-Yen; Ong, Wei-Yi; Farooqui, Akhlaq A; Burgunder, Jean-Marc (2007). Role of calcium-independent phospholipase A2 in cortex striatum thalamus cortex circuitry-enzyme inhibition causes vacuous chewing movements in rats. Psychopharmacology, 195(3), pp. 387-95. Berlin: Springer 10.1007/s00213-007-0912-y

Chang, S Y; Yong, T F; Yu, C Y; Liang, M C; Pletnikova, O; Troncoso, J; Burgunder, J-M; Soong, T W (2007). Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand. Neuroscience, 145(3), pp. 1026-36. Oxford: Elsevier 10.1016/j.neuroscience.2006.12.054


Ramelli, Gian Paolo; Gallati, Sabina; Weis, Joachim; Krähenbühl, Stephan; Burgunder, Jean-Marc (2006). Point mutation tRNA(Ser(UCN)) in a child with hearing loss and myoclonus epilepsy. Journal of child neurology, 21(3), pp. 253-5. Hamilton, Ontario: Decker 10.2310/7010.2006.00047

Shang, Hui-Fang; Jiang, Xiao-Feng; Burgunder, Jean-Marc; Chen, Qin; Zhou, Dong (2006). Novel mutation in the ceruloplasmin gene causing a cognitive and movement disorder with diabetes mellitus. Movement disorders, 21(12), pp. 2217-20. Hoboken, N.J.: Wiley-Blackwell 10.1002/mds.21121

Ma, Dong Liang; Chia, Shwn Chin; Tang, Yong Cheng; Chang, May Ling Joyce; Probst, Alphonse; Burgunder, Jean-Marc; Tang, Feng Ru (2006). Spastin in the human and mouse central nervous system with special reference to its expression in the hippocampus of mouse pilocarpine model of status epilepticus and temporal lobe epilepsy. Neurochemistry international, 49(7), pp. 651-64. Amsterdam: Elsevier 10.1016/j.neuint.2006.05.008

Ramelli, G P; Joncourt, F; Luetschg, J; Weis, J; Tolnay, M; Burgunder, J M (2006). Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss medical weekly, 136(11-12), pp. 189-93. Muttenz: EMH Schweizerischer Ärzteverlag

Ramelli, Gian Paolo; Joncourt, Franziska; Gasperini, Marcella; Tonin, Paola; Burgunder, Jean Marc (2006). Rather mild phenotype in a patient with homozygous null mutations in the alpha-sarcoglycan gene. Swiss medical weekly, 136(5-6), pp. 96-7. Muttenz: EMH Schweizerischer Ärzteverlag

Jamora, Roland Dominic G; Tan, Eng-King; Liu, Chun-Ping; Kathirvel, Paramasivam; Burgunder, Jean-Marc; Tan, Louis C S (2006). DYT1 mutations amongst adult primary dystonia patients in Singapore with review of literature comparing East and West. Journal of the neurological sciences, 247(1), pp. 35-7. Amsterdam: Elsevier 10.1016/j.jns.2006.03.009

Ma, Dong Liang; Tang, Yong Cheng; Chen, Peng Min; Chia, Shwn Chin; Jiang, Feng Li; Burgunder, Jean-Marc; Lee, Wei Ling; Tang, Feng Ru (2006). Reorganization of CA3 area of the mouse hippocampus after pilocarpine induced temporal lobe epilepsy with special reference to the CA3-septum pathway. Journal of neuroscience research, 83(2), pp. 318-31. New York, N.Y.: Wiley-Liss 10.1002/jnr.20731


Capper-Loup, Christine; Burgunder, Jean-Marc; Kaelin-Lang, Alain (2005). Modulation of parvalbumin expression in the motor cortex of parkinsonian rats. Experimental neurology, 193(1), pp. 234-7. San Diego, Calif.: Elsevier 10.1016/j.expneurol.2004.12.007


Chen, Lie; Schaerer, Martin; Lu, Zen H; Lang, Doris; Joncourt, Franziska; Weis, Joachim; Fritschi, Juerg; Kappeler, Lilianne; Gallati, Sabina; Sigel, Erwin; Burgunder, Jean-Marc (2004). Exon 17 skipping in CLCN1 leads to recessive myotonia congenita. Muscle & nerve, 29(5), pp. 670-6. New York, N.Y.: John Wiley & Sons 10.1002/mus.20005

Shang, Huifang; Lang, Doris; Jean-Marc, Burgunder; Kaelin-Lang, Alain (2004). Localization of DJ-1 mRNA in the mouse brain. Neuroscience letters, 367(3), pp. 273-7. Amsterdam: Elsevier 10.1016/j.neulet.2004.06.002


Loher, Thomas J; Gutbrod, Klemens; Fravi, Nina L; Pohle, Thomas; Burgunder, Jean-Marc; Krauss, Joachim K (2003). Thalamic stimulation for tremor. Subtle changes in episodic memory are related to stimulation per se and not to a microthalamotomy effect. Journal of neurology, 250(6), pp. 707-13. Heidelberg: Springer-Medizin-Verlag 10.1007/s00415-003-1067-3

Krauss, Joachim K; Loher, Thomas J; Weigel, Ralf; Capelle, H Holger; Weber, Sabine; Burgunder, Jean-Marc (2003). Chronic stimulation of the globus pallidus internus for treatment of non-dYT1 generalized dystonia and choreoathetosis: 2-year follow up. Journal of neurosurgery, 98(4), pp. 785-92. Charlottesville, Va.: American Association of Neurological Surgeons 10.3171/jns.2003.98.4.0785


Loher, Thomas J; Burgunder, Jean-Marc; Pohle, Thomas; Weber, Sabine; Sommerhalder, Regine; Krauss, Joachim K (2002). Long-term pallidal deep brain stimulation in patients with advanced Parkinson disease: 1-year follow-up study. Journal of neurosurgery, 96(5), pp. 844-53. Charlottesville, Va.: American Association of Neurological Surgeons 10.3171/jns.2002.96.5.0844

Loher, Thomas J; Krauss, Joachim K; Wielepp, Johannes P; Weber, Sabine; Burgunder, Jean-Marc (2002). Pallidal deep brain stimulation in a parkinsonian patient with late-life dementia: sustained benefit in motor symptoms but not in functional disability. European neurology, 47(2), pp. 122-3. Basel: Karger 10.1159/000047964

Serrien, Deborah J; Nirkko, Arto C; Loher, Thomas J; Lövblad, Karl-Olof; Burgunder, Jean-Marc; Wiesendanger, Mario (2002). Movement control of manipulative tasks in patients with Gilles de la Tourette syndrome. Brain, 125(Pt 2), pp. 290-300. Oxford: Oxford University Press 10.1093/brain/awf024

Serrien, Deborah J.; Burgunder, Jean-Marc; Wiesendanger, Mario (2002). Control of manipulative forces during unimanual and bimanual tasks in patients with Huntington’s disease. Experimental brain research, 143(3), pp. 328-334. Springer 10.1007/s00221-001-0992-6


Brockington, Martin; Yuva, Yeliz; Prandini, Paola; Brown, Susan C.; Torelli, Silvia; Benson, Matthew A.; Herrmann, Ralf; Anderson, Louise V.B.; Bashir, Rumaisa; Burgunder, Jean-Marc; Fallet, Shari; Romero, Norma; Fardeau, Michel; Straub, Volker; Storey, Gillian; Pollitt, Christine; Richard, Isabelle; Sewry, Caroline A.; Bushby, Kate; Voit, Thomas; ... (2001). Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Human molecular genetics, 10(25), pp. 2851-2859. Oxford University Press 10.1093/hmg/10.25.2851


Dürr, A.; Davoine, C.-S.; Paternotte, C.; Von Fellenberg, J.; Cogilnicean, S.; Coutinho, P.; Lamy, C.; Bourgeois, S.; Prud'Homme, J.-F.; Penet, C.; Mas, J.-L.; Burgunder, J.-M.; Hazan, J.; Weissenbach, J.; Brice, A.; Fontaine, B. (1996). Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2. Brain, 119(5), pp. 1487-1496. Oxford University Press 10.1093/brain/119.5.1487

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