Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients
Duindam, H.B., Mengel, D., Kox, M., Göpfert, J.C., Kessels, R.P.C., Synofzik, M., Pickkers, P., Abdo, W.F.
Published in Brain, behavior, and immunity (01.03.2024)
Published in Brain, behavior, and immunity (01.03.2024)
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Intensive coordinative training improves motor performance in degenerative cerebellar disease
Ilg, W, Synofzik, M, Brötz, D, Burkard, S, Giese, M A, Schöls, L
Published in Neurology (01.12.2009)
Published in Neurology (01.12.2009)
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Corrigendum to “Systemic inflammation relates to neuroaxonal damage associated with long-term cognitive dysfunction in COVID-19 patients” [Brain Behav. Immun. 117 (2024) 510–520]
Duindam, H.B., Mengel, D., Kox, M., Göpfert, J.C., Kessels, R.P.C., Synofzik, M., Pickkers, P., Abdo, W.F.
Published in Brain, behavior, and immunity (01.08.2024)
Published in Brain, behavior, and immunity (01.08.2024)
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CHIP mutations affect the heat shock response differently in human fibroblasts and iPSC-derived neurons
Schuster, S, Heuten, E, Velic, A, Admard, J, Synofzik, M, Ossowski, S, Macek, B, Hauser, S, Schöls, L
Published in Disease models & mechanisms (01.10.2020)
Published in Disease models & mechanisms (01.10.2020)
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Consensus Paper: Management of Degenerative Cerebellar Disorders
Ilg, W., Bastian, A. J., Boesch, S., Burciu, R. G., Celnik, P., Claaßen, J., Feil, K., Kalla, R., Miyai, I., Nachbauer, W., Schöls, L., Strupp, M., Synofzik, M., Teufel, J., Timmann, D.
Published in Cerebellum (London, England) (01.04.2014)
Published in Cerebellum (London, England) (01.04.2014)
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Antisense oligonucleotide therapy for splicing defects in OPA1‐related dominant optic atrophy
Wissinger, B., Synofzik, M., Schöls, L., Bonifert, T.
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
Published in Acta ophthalmologica (Oxford, England) (01.09.2017)
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Boucher–Neuhäuser syndrome: cerebellar degeneration, chorioretinal dystrophy and hypogonadotropic hypogonadism: two novel cases and a review of 40 cases from the literature
Tarnutzer, A. A., Gerth-Kahlert, C., Timmann, D., Chang, D. I., Harmuth, F., Bauer, P., Straumann, D., Synofzik, M.
Published in Journal of neurology (2015)
Published in Journal of neurology (2015)
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SARAspeech—Feasibility of automated assessment of ataxic speech disturbance
Grobe-Einsler, M., Faber, J., Taheri, A., Kybelka, J., Raue, J., Volkening, J., Helmhold, F., Synofzik, M., Klockgether, T.
Published in NPJ digital medicine (16.03.2023)
Published in NPJ digital medicine (16.03.2023)
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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
Anheim, M., Monga, B., Fleury, M., Charles, P., Barbot, C., Salih, M., Delaunoy, J. P., Fritsch, M., Arning, L., Synofzik, M., Schöls, L., Sequeiros, J., Goizet, C., Marelli, C., Le Ber, I., Koht, J., Gazulla, J., De Bleecker, J., Mukhtar, M., Drouot, N., Ali-Pacha, L., Benhassine, T., Chbicheb, M., M’Zahem, A., Hamri, A., Chabrol, B., Pouget, J., Murphy, R., Watanabe, M., Coutinho, P., Tazir, M., Durr, A., Brice, A., Tranchant, C., Koenig, M.
Published in Brain (London, England : 1878) (01.10.2009)
Published in Brain (London, England : 1878) (01.10.2009)
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Phenotypic differences of amyotrophic lateral sclerosis (ALS) in China and Germany
Rosenbohm, Angela, Liu, Mingsheng, Nagel, Gabriele, Peter, Raphael S., Cui, Bo, Li, Xiaoguang, Kassubek, Jan, Rothenbacher, Dietrich, Lulé, Dorothée, Cui, Liying, Ludolph, Albert C.
Published in Journal of neurology (01.04.2018)
Published in Journal of neurology (01.04.2018)
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Slowly progressive LGI1 encephalitis with isolated late-onset cognitive dysfunction: a treatable mimic of Alzheimer's disease
Marquetand, J., van Lessen, M., Bender, B., Reimold, M., Elsen, G., Stoecker, W., Synofzik, M.
Published in European journal of neurology (01.05.2016)
Published in European journal of neurology (01.05.2016)
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Frequency and phenotype of SPG11 and SPG15 in complicated hereditary spastic paraplegia
Schüle, R, Schlipf, N, Synofzik, M, Klebe, S, Klimpe, S, Hehr, U, Winner, B, Lindig, T, Dotzer, A, Rieß, O, Winkler, J, Schöls, L, Bauer, P
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.12.2009)
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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia
Ozes, B., Karagoz, N., Schüle, R., Rebelo, A., Sobrido, M.‐J., Harmuth, F., Synofzik, M., Pascual, S.I.P., Colak, M., Ciftci‐Kavaklioglu, B., Kara, B., Ordóñez‐Ugalde, A., Quintáns, B., Gonzalez, M.A., Soysal, A., Zuchner, S., Battaloglu, E.
Published in Clinical genetics (01.11.2017)
Published in Clinical genetics (01.11.2017)
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Expanding the phenotype of DNAJC3 mutations: A case with hypothyroidism additionally to diabetes mellitus and multisystemic neurodegeneration
Bublitz, S.K., Alhaddad, B., Synofzik, M., Kuhl, V., Lindner, A., Freiberg, C., Schmidt, H., Strom, T.M., Haack, T.B., Deschauer, M.
Published in Clinical genetics (01.11.2017)
Published in Clinical genetics (01.11.2017)
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A clinical diagnostic algorithm for early onset cerebellar ataxia
Brandsma, R., Verschuuren-Bemelmans, C.C., Amrom, D., Barisic, N., Baxter, P., Bertini, E., Blumkin, L., Brankovic-Sreckovic, V., Brouwer, O.F., Bürk, K., Catsman-Berrevoets, C.E., Craiu, D., de Coo, I.F.M., Gburek, J., Kennedy, C., de Koning, T.J., Kremer, H.P.H., Kumar, R., Macaya, A., Micalizzi, A., Mirabelli-Badenier, M., Nemeth, A., Nuovo, S., Poll-The, B., Lerman-Sagie, T., Steinlin, M., Synofzik, M., Tijssen, M.A.J., Vasco, G., Willemsen, M.A.A.P., Zanni, G., Valente, E.M., Boltshauser, E., Sival, D.A.
Published in European journal of paediatric neurology (01.09.2019)
Published in European journal of paediatric neurology (01.09.2019)
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