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Oosterloo, Mayke; Touze, Alexiane; Byrne, Lauren M; Achenbach, Jannis; Aksoy, Hande; Coleman, Annabelle; Lammert, Dawn; Nance, Martha; Nopoulos, Peggy; Reilmann, Ralf; Saft, Carsten; Santini, Helen; Squitieri, Ferdinando; Tabrizi, Sarah; Burgunder, Jean-Marc; Quarrell, Oliver (2024). Clinical Review of Juvenile Huntington's Disease. Journal of Huntington's disease, 13(2), pp. 149-161. IOS Press 10.3233/JHD-231523
Xia, Jie-Qiang; Cheng, Yang-Fan; Zhang, Si-Rui; Ma, Yuan-Zheng; Fu, Jia-Jia; Yang, Tian-Mi; Zhang, Ling-Yu; Burgunder, Jean-Marc; Shang, Hui-Fang (2024). The characteristic and prognostic role of blood inflammatory markers in patients with Huntington's disease from China. Frontiers in neurology, 15(1374365) Frontiers Media S.A. 10.3389/fneur.2024.1374365
Saft, Carsten; Burgunder, Jean-Marc; Dose, Matthias; Jung, Hans Heinrich; Katzenschlager, Regina; Priller, Josef; Nguyen, Huu Phuc; Reetz, Kathrin; Reilmann, Ralf; Seppi, Klaus; Landwehrmeyer, Georg Bernhard (2023). Differential diagnosis of chorea (guidelines of the German Neurological Society). Neurological research and practice, 5(1), p. 63. BioMed Central 10.1186/s42466-023-00292-2
Saft, Carsten; Burgunder, Jean-Marc; Dose, Matthias; Jung, Hans Heinrich; Katzenschlager, Regina; Priller, Josef; Nguyen, Huu Phuc; Reetz, Kathrin; Reilmann, Ralf; Seppi, Klaus; Landwehrmeyer, Georg Bernhard (2023). Symptomatic treatment options for Huntington's disease (guidelines of the German Neurological Society). Neurological research and practice, 5(1), p. 61. BioMed Central 10.1186/s42466-023-00285-1
Cheng, Yang-Fan; Liu, Kun-Cheng; Yang, Tian-Mi; Xiao, Yi; Jiang, Qi-Rui; Huang, Jing-Xuan; Zhang, Sirui; Wei, Qian-Qian; Ou, Ru-Wei; Li, Chun-Yu; Gu, Xiao-Jing; Burgunder, Jean-Marc; Shang, Hui-Fang (2023). Factors influencing cognitive function in patients with Huntington's disease from China: A cross-sectional clinical study. Brain and Behavior, 13(11), e3258. Wiley 10.1002/brb3.3258
Cheng, Yangfan; Gu, Xiaojing; Liu, Kuncheng; Yang, Tianmi; Xiao, Yi; Jiang, Qirui; Huang, Jingxuan; Lin, Junyu; Wei, Qianqian; Ou, Ruwei; Hou, Yanbing; Zhang, Lingyu; Li, Chunyu; Burgunder, Jean-Marc; Shang, Huifang (2022). The Comprehensive Analysis of Motor and Neuropsychiatric Symptoms in Patients with Huntington's Disease from China: A Cross-Sectional Study. Journal of clinical medicine, 12(1) MDPI 10.3390/jcm12010206
Li, Xiao-Yan; Bao, Yu-Feng; Xie, Juan-Juan; Qian, Shu-Xia; Gao, Bin; Xu, Miao; Dong, Yi; Burgunder, Jean-Marc; Wu, Zhi-Ying (2022). The Chinese Version of UHDRS in Huntington's Disease: Reliability and Validity Assessment. Journal of Huntington's disease, 11(4), pp. 407-413. IOS Press 10.3233/JHD-220542
Burgunder, Jean-Marc (2022). Chorea: An Update on Genetics. European neurology, 85(5), pp. 342-348. Karger 10.1159/000526237
Aleksovska, Katina; Kobulashvili, Teia; Costa, Joao; Zimmermann, Georg; Ritchie, Karen; Reinhard, Carola; Vignatelli, Luca; Fanciulli, Alessandra; Damian, Maxwel; Pavlakova, Lucia; Burgunder, Jean-Marc; Kopishinskaya, Svetlana; Rakusa, Martin; Kovacs, Norbert; Erdogan, Fusun Ferda; Linton, Lori Renna; Copetti, Massimiliano; Lamperti, Costanza; Servidei, Serenella; Evangelista, Theresina; ... (2022). European Academy of Neurology guidance for developing and reporting clinical practice guidelines on rare neurological diseases. European journal of neurology, 29(6), pp. 1571-1586. Wiley 10.1111/ene.15267
Nguyen, Quang Tuan Rémy; Ortigoza Escobar, Juan Dario; Burgunder, Jean-Marc; Mariotti, Caterina; Saft, Carsten; Hjermind, Lena Elisabeth; Youssov, Katia; Landwehrmeyer, G Bernhard; Bachoud-Lévi, Anne-Catherine (2022). Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy. Frontiers in neurology, 13, p. 891800. Frontiers Media S.A. 10.3389/fneur.2022.891800
Ferreira, Joaquim J; Rodrigues, Filipe B; Duarte, Gonçalo S; Mestre, Tiago A; Bachoud-Levi, Anne-Catherine; Bentivoglio, Anna Rita; Burgunder, Jean-Marc; Cardoso, Francisco; Claassen, Daniel O; Landwehrmeyer, G Bernard; Kulisevsky, Jaime; Nirenberg, Melissa J; Rosser, Anne; Roth, Jan; Seppi, Klaus; Slawek, Jaroslaw; Furr-Stimming, Erin; Tabrizi, Sarah J; Walker, Francis O; Vandenberghe, Wim; ... (2022). A MDS Evidence-Based Review on Treatments for Huntington's Disease. Movement disorders, 37(1), pp. 25-35. Wiley-Blackwell 10.1002/mds.28855
Nguyen, Quang Tuan Rémy; Ortigoza Escobar, Juan Dario; Burgunder, Jean-Marc; Mariotti, Caterina; Saft, Carsten; Hjermind, Lena Elisabeth; Youssov, Katia; Landwehrmeyer, G Bernhard; Bachoud-Lévi, Anne-Catherine (2022). Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy. Frontiers in neurology, 13, p. 817753. Frontiers Media S.A. 10.3389/fneur.2022.817753
Guttman, Mark; Pedrazzoli, Marco; Ponomareva, Marina; Pelletier, Marsha; Townson, Louisa; Mukelabai, Kopano; Levine, Aaron; Nordström, Anna-Lena; Reilmann, Ralf; Burgunder, Jean-Marc (2021). The Impact of Upcoming Treatments in Huntington's Disease: Resource Capacity Limitations and Access to Care Implications. Journal of Huntington's disease, 10(2), pp. 303-311. IOS Press 10.3233/JHD-200462
You, Huajing; Wu, Tengteng; Du, Gang; Huang, Yue; Zeng, Yixuan; Lin, Lishan; Chen, Dingbang; Wu, Chao; Li, Xunhua; Burgunder, Jean-Marc; Pei, Zhong (2021). Evaluation of Blood Glial Fibrillary Acidic Protein as a Potential Marker in Huntington's Disease. Frontiers in neurology, 12, p. 779890. Frontiers Media S.A. 10.3389/fneur.2021.779890
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
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