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

Year Number of Results
1993 1
1997 2
1999 4
2000 9
2001 7
2002 6
2003 9
2004 7
2005 7
2006 10
2007 12
2008 11
2009 14
2010 11
2011 15
2012 26
2013 21
2014 29
2015 19
2016 21
2017 28
2018 20
2019 24
2020 18
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287 results
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Page 1
Movement Disorders in Treatable Inborn Errors of Metabolism.
Ebrahimi-Fakhari D, Van Karnebeek C, Münchau A. Ebrahimi-Fakhari D, et al. Among authors: munchau a. Mov Disord. 2019 May;34(5):598-613. doi: 10.1002/mds.27568. Epub 2018 Dec 17. Mov Disord. 2019. PMID: 30557456 Review.
Treatable inherited rare movement disorders.
Jinnah HA, Albanese A, Bhatia KP, Cardoso F, Da Prat G, de Koning TJ, Espay AJ, Fung V, Garcia-Ruiz PJ, Gershanik O, Jankovic J, Kaji R, Kotschet K, Marras C, Miyasaki JM, Morgante F, Munchau A, Pal PK, Rodriguez Oroz MC, Rodríguez-Violante M, Schöls L, Stamelou M, Tijssen M, Uribe Roca C, de la Cerda A, Gatto EM; International Parkinson's Disease Movement Disorders Society Task Force on Rare Movement Disorders. Jinnah HA, et al. Among authors: munchau a. Mov Disord. 2018 Jan;33(1):21-35. doi: 10.1002/mds.27140. Epub 2017 Sep 1. Mov Disord. 2018. PMID: 28861905 Free PMC article. Review.
Mutations in VPS13D lead to a new recessive ataxia with spasticity and mitochondrial defects.
Seong E, Insolera R, Dulovic M, Kamsteeg EJ, Trinh J, Brüggemann N, Sandford E, Li S, Ozel AB, Li JZ, Jewett T, Kievit AJA, Münchau A, Shakkottai V, Klein C, Collins CA, Lohmann K, van de Warrenburg BP, Burmeister M. Seong E, et al. Among authors: munchau a. Ann Neurol. 2018 Jun;83(6):1075-1088. doi: 10.1002/ana.25220. Epub 2018 Jun 30. Ann Neurol. 2018. PMID: 29604224 Free PMC article.
A special issue on childhood-onset movement disorders.
Ebrahimi-Fakhari D, Münchau A, Stamelou M. Ebrahimi-Fakhari D, et al. Among authors: munchau a. Mov Disord. 2019 May;34(5):595-597. doi: 10.1002/mds.27663. Epub 2019 Apr 2. Mov Disord. 2019. PMID: 30938852 No abstract available.
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. Among authors: munchau a. Brain. 2019 Jun 1;142(6):1561-1572. doi: 10.1093/brain/awz102. Brain. 2019. PMID: 31135052 Free PMC article.
Hereditary Dystonia Overview.
Klein C, Lohmann K, Marras C, Münchau A. Klein C, et al. Among authors: munchau a. 2003 Oct 28 [updated 2017 Jun 22]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Stephens K, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2020. GeneReviews®. 1993–2020. PMID: 20301334 Free Books & Documents. Review.
Safety and efficacy of epigallocatechin gallate in multiple system atrophy (PROMESA): a randomised, double-blind, placebo-controlled trial.
Levin J, Maaß S, Schuberth M, Giese A, Oertel WH, Poewe W, Trenkwalder C, Wenning GK, Mansmann U, Südmeyer M, Eggert K, Mollenhauer B, Lipp A, Löhle M, Classen J, Münchau A, Kassubek J, Gandor F, Berg D, Egert-Schwender S, Eberhardt C, Paul F, Bötzel K, Ertl-Wagner B, Huppertz HJ, Ricard I, Höglinger GU; PROMESA Study Group. Levin J, et al. Among authors: munchau a. Lancet Neurol. 2019 Aug;18(8):724-735. doi: 10.1016/S1474-4422(19)30141-3. Epub 2019 Jul 2. Lancet Neurol. 2019. PMID: 31278067 Clinical Trial.
Iron overload is accompanied by mitochondrial and lysosomal dysfunction in WDR45 mutant cells.
Seibler P, Burbulla LF, Dulovic M, Zittel S, Heine J, Schmidt T, Rudolph F, Westenberger A, Rakovic A, Münchau A, Krainc D, Klein C. Seibler P, et al. Among authors: munchau a. Brain. 2018 Oct 1;141(10):3052-3064. doi: 10.1093/brain/awy230. Brain. 2018. PMID: 30169597 Free PMC article.
[Neuronal plasticity and neuromodulation in pediatric neurology].
Jung NH, Münchau A, Mall V. Jung NH, et al. Among authors: munchau a. Nervenarzt. 2018 Oct;89(10):1131-1139. doi: 10.1007/s00115-018-0586-1. Nervenarzt. 2018. PMID: 30141068 Review. German.
Striatal Microstructure and Its Relevance for Cognitive Control.
Beste C, Moll CKE, Pötter-Nerger M, Münchau A. Beste C, et al. Among authors: munchau a. Trends Cogn Sci. 2018 Sep;22(9):747-751. doi: 10.1016/j.tics.2018.06.007. Epub 2018 Jul 14. Trends Cogn Sci. 2018. PMID: 30017252 Review.
287 results
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