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

Year Number of Results
2010 1
2011 4
2012 2
2014 2
2015 5
2016 5
2017 5
2018 3
2019 4
2020 7
2021 14
2022 9
2023 7
2024 1

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59 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: herzog r. 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.
Complex dystonias: an update on diagnosis and care.
Herzog R, Weissbach A, Bäumer T, Münchau A. Herzog R, et al. J Neural Transm (Vienna). 2021 Apr;128(4):431-445. doi: 10.1007/s00702-020-02275-y. Epub 2020 Nov 13. J Neural Transm (Vienna). 2021. PMID: 33185802 Free PMC article. Review.
Monitoring Daily Ultrafiltration in Automated Peritoneal Dialysis.
Eibensteiner F, Flores KO, Unterwurzacher M, Herzog R, Kratochwill K, Alper SL, Aufricht C, König F, Vychytil A. Eibensteiner F, et al. Among authors: herzog r. Clin J Am Soc Nephrol. 2022 Jan;17(1):107-110. doi: 10.2215/CJN.08180621. Epub 2021 Dec 10. Clin J Am Soc Nephrol. 2022. PMID: 34893504 Free PMC article. No abstract available.
Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14.
Jackson A, Lin SJ, Jones EA, Chandler KE, Orr D, Moss C, Haider Z, Ryan G, Holden S, Harrison M, Burrows N, Jones WD, Loveless M, Petree C, Stewart H, Low K, Donnelly D, Lovell S, Drosou K; Genomics England Research Consortium; Solve-RD consortium; Varshney GK, Banka S. Jackson A, et al. HGG Adv. 2023 Mar 3;4(2):100186. doi: 10.1016/j.xhgg.2023.100186. eCollection 2023 Apr 13. HGG Adv. 2023. PMID: 37009414 Free PMC article.
Solving unsolved rare neurological diseases-a Solve-RD viewpoint.
Schüle R, Timmann D, Erasmus CE, Reichbauer J, Wayand M; Solve-RD-DITF-RND; van de Warrenburg B, Schöls L, Wilke C, Bevot A, Zuchner S, Beltran S, Laurie S, Matalonga L, Graessner H, Synofzik M; Solve-RD Consortium. Schüle R, et al. Eur J Hum Genet. 2021 Sep;29(9):1332-1336. doi: 10.1038/s41431-021-00901-1. Epub 2021 May 10. Eur J Hum Genet. 2021. PMID: 33972714 Free PMC article. No abstract available.
59 results