EFNS/ENS Consensus on the diagnosis and management of chronic ataxias in adulthood von van de Warrenburg, B. P. C., van Gaalen, J., Boesch, S., Burgunder, J.-M., Dürr, A., Giunti, P., Klockgether, T., Mariotti, C., Pandolfo, M., Riess, O.

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Characterization of social cognition impairment in multiple sclerosis von Neuhaus, M., Bagutti, S., Yaldizli, Ö., Zwahlen, D., Schaub, S., Frey, B., Fischer‐Barnicol, B., Burgunder, J.‐M., Martory, M.‐D., Pöttgen, J., Annoni, J.‐M., Penner, I.‐K.

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Haplotype analysis encompassing HTT gene in Chinese patients with Huntington's disease von Li, X.‐Y., Li, H.‐L., Dong, Y., Gao, B., Cheng, H.‐R., Ni, W., Gan, S.‐R., Liu, Z.‐J., Burgunder, J.‐M., Wu, Z.‐Y.

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Auditory time perception in Huntington's disease von Vez, S., Köhli, J., Frey, B., Magezi, D.A., Annoni, J.-M., Burgunder, J.-M.

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Deep brain stimulation for dystonia: outcome at long-term follow-up von Loher, T. J., Capelle, H.-H., Kaelin-Lang, A., Weber, S., Weigel, R., Burgunder, J. M., Krauss, J. K.

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Association between GBA L444P mutation and sporadic Parkinson's disease from Mainland China von Mao, X.-Y., Burgunder, J.-M., Zhang, Z.-J., An, X.-K., Zhang, J.-H., Yang, Y., Li, T., Wang, Y.-C., Chang, X.-L., Peng, R.

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EFNS guidelines for the molecular diagnosis of neurogenetic disorders: motoneuron, peripheral nerve and muscle disorders von Burgunder, J.-M., Schöls, L., Baets, J., Andersen, P., Gasser, T., Szolnoki, Z., Fontaine, B., Van Broeckhoven, C., Di Donato, S., De Jonghe, P., Lynch, T., Mariotti, C., Spinazzola, A., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Harbo, H. F., Finsterer, J.

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PRRT2 mutation screening in patients with paroxysmal kinesigenic dyskinesia from Southwest China von Chen, Y. P., Song, W., Yang, J., Zheng, Z.-Z., Huang, R., Chen, K., Zhao, B., Chen, X. P., Burgunder, J.-M., Shang, H.-F.

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EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias von Harbo, H. F., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Burgunder, J.-M., Gasser, T.

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia von Heilig, Roland, Dürr, Alexandra, Brottier, Philippe, Fontaine, Bertrand, Weissenbach, Jean, Burgunder, Jean-Marc, Paternotte, Caroline, Fonknechten, Nùria, Samson, Delphine, Cruaud, Corinne, Wincker, Patrick, Davoine, Claire-Sophie, Brice, Alexis, Hazan, Jamilé, Cattolico, Laurence, Mavel, Delphine, Artiguenave, François, Barbe, Valérie, Prud'homme, Jean-François

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LRRK2 Gly2385Arg variant is a risk factor of Parkinson's disease among Han-Chinese from mainland China von An, X.-K., Peng, R., Li, T., Burgunder, J.-M., Wu, Y., Chen, W.-J., Zhang, J.-H., Wang, Y.-C., Xu, Y.-M., Gou, Y.-R., Yuan, G.-G., Zhang, Z.-J.

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EFNS guidelines on the molecular diagnosis of mitochondrial disorders von Finsterer, J., Harbo, H. F., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C. M. E., Zeviani, M., Burgunder, J.-M., Gasser, T.

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Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls von Jiang, H., Sun, Y. M., Hao, Y., Yan, Y. P., Chen, K., Xin, S. H., Tang, Y. P., Li, X. H., Jun, T., Chen, Y. Y., Liu, Z. J., Wang, C. R., Li, H., Pei, Z., Shang, H. F., Zhang, B. R., Gu, W. H., Wu, Z. Y., Tang, B. S., Burgunder, J.-M.

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Circadian patterns of neurotransmitter related gene expression in motor regions of the rat brain von Weber, M., Lauterburg, T., Tobler, I., Burgunder, J.-M.

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Bilateral stimulation of globus pallidus internus for treatment of cervical dystonia von Krauss, Joachim K, Pohle, Thomas, Weber, Sabine, Ozdoba, Christoph, Burgunder, Jean-Marc

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Assessment of D216H DYT1 polymorphism in a Chinese primary dystonia patient cohort von Chen, Y., Burgunder, J.-M., Song, W., Huang, R., Shang, H.-F.

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EFNS guidelines on the molecular diagnosis of ataxias and spastic paraplegias von Gasser, T., Finsterer, J., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C.M.E., Zeviani, M., Burgunder, J-M., Harbo, H. F.

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Pallidal deep brain stimulation in patients with cervical dystonia and severe cervical dyskinesias with cervical myelopathy von Krauss, J K, Loher, T J, Pohle, T, Weber, S, Taub, E, Bärlocher, C B, Burgunder, J-M

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Clinical feature and DYT1 mutation screening in primary dystonia patients from South-West China von Zhang, S.-S., Fang, D.-F., Hu, X.-H., Burgunder, J.-M., Chen, X.-P., Zhang, Y.-W., Shang, H.-F.

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Age and gender-dependent alternative splicing of P/Q-type calcium channel EF-hand von Chang, S.Y, Yong, T.F, Yu, C.Y, Liang, M.C, Pletnikova, O, Troncoso, J, Burgunder, J.-M, Soong, T.W

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