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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2013 1
2014 1
2015 2
2016 6
2017 8
2018 4
2019 2
2020 4
2021 4
2022 7
2023 5
2024 2

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41 results

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Page 1
De Novo and Dominantly Inherited SPTAN1 Mutations Cause Spastic Paraplegia and Cerebellar Ataxia.
Van de Vondel L, De Winter J, Beijer D, Coarelli G, Wayand M, Palvadeau R, Pauly MG, Klein K, Rautenberg M, Guillot-Noël L, Deconinck T, Vural A, Ertan S, Dogu O, Uysal H, Brankovic V, Herzog R, Brice A, Durr A, Klebe S, Stock F, Bischoff AT, Rattay TW, Sobrido MJ, De Michele G, De Jonghe P, Klopstock T, Lohmann K, Zanni G, Santorelli FM, Timmerman V, Haack TB, Züchner S; PREPARE Consortium; Schüle R, Stevanin G, Synofzik M, Basak AN, Baets J. Van de Vondel L, et al. Among authors: rattay tw. Mov Disord. 2022 Jun;37(6):1175-1186. doi: 10.1002/mds.28959. Epub 2022 Feb 12. Mov Disord. 2022. PMID: 35150594 Free PMC article.
Freezing of Swallowing.
Maetzler W, Rattay TW, Hobert MA, Synofzik M, Bader A, Berg D, Schaeffer E, Rommel N, Devos D, Bloem BR, Bender B. Maetzler W, et al. Among authors: rattay tw. Mov Disord Clin Pract. 2016 Jan 18;3(5):490-493. doi: 10.1002/mdc3.12314. eCollection 2016 Sep-Oct. Mov Disord Clin Pract. 2016. PMID: 30868092 Free PMC article.
Face pareidolia in schizophrenia.
Rolf R, Sokolov AN, Rattay TW, Fallgatter AJ, Pavlova MA. Rolf R, et al. Among authors: rattay tw. Schizophr Res. 2020 Apr;218:138-145. doi: 10.1016/j.schres.2020.01.019. Epub 2020 Feb 10. Schizophr Res. 2020. PMID: 32057538
Amantadine for NeuroenhaNcement in acutE patients Study - a protocol for a prospective pilot proof of concept phase IIb study in intensive and intermediate care unit patients (ANNES).
Hofmann A, Blum C, Single C, Adeyemi K, Schwarz P, Siokas V, Rattay TW, Häberle HA, Riessen R, Brendel B, Haug I, Bösel R, Zago M, Martus P, Ziemann U, Mengel A, Feil K. Hofmann A, et al. Among authors: rattay tw. BMC Neurol. 2023 Aug 22;23(1):308. doi: 10.1186/s12883-023-03345-w. BMC Neurol. 2023. PMID: 37608315 Free PMC article.
FAHN/SPG35: a narrow phenotypic spectrum across disease classifications.
Rattay TW, Lindig T, Baets J, Smets K, Deconinck T, Söhn AS, Hörtnagel K, Eckstein KN, Wiethoff S, Reichbauer J, Döbler-Neumann M, Krägeloh-Mann I, Auer-Grumbach M, Plecko B, Münchau A, Wilken B, Janauschek M, Giese AK, De Bleecker JL, Ortibus E, Debyser M, Lopez de Munain A, Pujol A, Bassi MT, D'Angelo MG, De Jonghe P, Züchner S, Bauer P, Schöls L, Schüle R. Rattay TW, et al. Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102. Brain. 2019. PMID: 31135052 Free PMC article.
Reply: POLR3A variants in hereditary spastic paraplegia and ataxia.
Minnerop M, Kurzwelly D, Rattay TW, Timmann D, Hengel H, Synofzik M, Stendel C, Horvath R, Schüle R, Ramirez A. Minnerop M, et al. Among authors: rattay tw. Brain. 2018 Jan 1;141(1):e2. doi: 10.1093/brain/awx291. Brain. 2018. PMID: 29236946 Free PMC article. No abstract available.
41 results