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

Year Number of Results
1990 1
1992 1
1993 1
1994 1
1995 4
1996 5
1997 3
1998 3
1999 3
2000 8
2001 3
2002 10
2003 5
2004 17
2005 17
2006 12
2007 20
2008 20
2009 15
2010 20
2011 10
2012 15
2013 17
2014 19
2015 17
2016 15
2017 12
2018 9
2019 17
2020 10
2021 11
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284 results
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Page 1
Consensus Paper: Experimental Neurostimulation of the Cerebellum.
Miterko LN, Baker KB, Beckinghausen J, Bradnam LV, Cheng MY, Cooperrider J, DeLong MR, Gornati SV, Hallett M, Heck DH, Hoebeek FE, Kouzani AZ, Kuo SH, Louis ED, Machado A, Manto M, McCambridge AB, Nitsche MA, Taib NOB, Popa T, Tanaka M, Timmann D, Steinberg GK, Wang EH, Wichmann T, Xie T, Sillitoe RV. Miterko LN, et al. Among authors: timmann d. Cerebellum. 2019 Dec;18(6):1064-1097. doi: 10.1007/s12311-019-01041-5. Cerebellum. 2019. PMID: 31165428 Free PMC article. Review.
Consensus Paper: Revisiting the Symptoms and Signs of Cerebellar Syndrome.
Bodranghien F, Bastian A, Casali C, Hallett M, Louis ED, Manto M, Mariën P, Nowak DA, Schmahmann JD, Serrao M, Steiner KM, Strupp M, Tilikete C, Timmann D, van Dun K. Bodranghien F, et al. Among authors: timmann d. Cerebellum. 2016 Jun;15(3):369-91. doi: 10.1007/s12311-015-0687-3. Cerebellum. 2016. PMID: 26105056 Free PMC article. Review.
Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmüller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brüstle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schöls L, Nürnberg P, Zuchner S, Klockgether T, Ramirez A, Schüle R. Minnerop M, et al. Among authors: timmann d. Brain. 2017 Jun 1;140(6):1561-1578. doi: 10.1093/brain/awx095. Brain. 2017. PMID: 28459997 Free PMC article.
Endocrine and Growth Abnormalities in 4H Leukodystrophy Caused by Variants in POLR3A, POLR3B, and POLR1C.
Pelletier F, Perrier S, Cayami FK, Mirchi A, Saikali S, Tran LT, Ulrick N, Guerrero K, Rampakakis E, van Spaendonk RML, Naidu S, Pohl D, Gibson WT, Demos M, Goizet C, Tejera-Martin I, Potic A, Fogel BL, Brais B, Sylvain M, Sébire G, Lourenço CM, Bonkowsky JL, Catsman-Berrevoets C, Pinto PS, Tirupathi S, Strømme P, de Grauw T, Gieruszczak-Bialek D, Krägeloh-Mann I, Mierzewska H, Philippi H, Rankin J, Atik T, Banwell B, Benko WS, Blaschek A, Bley A, Boltshauser E, Bratkovic D, Brozova K, Cimas I, Clough C, Corenblum B, Dinopoulos A, Dolan G, Faletra F, Fernandez R, Fletcher J, Garcia Garcia ME, Gasparini P, Gburek-Augustat J, Gonzalez Moron D, Hamati A, Harting I, Hertzberg C, Hill A, Hobson GM, Innes AM, Kauffman M, Kirwin SM, Kluger G, Kolditz P, Kotzaeridou U, La Piana R, Liston E, McClintock W, McEntagart M, McKenzie F, Melançon S, Misbahuddin A, Suri M, Monton FI, Moutton S, Murphy RPJ, Nickel M, Onay H, Orcesi S, Özkınay F, Patzer S, Pedro H, Pekic S, Pineda Marfa M, Pizzino A, Plecko B, Poll-The BT, Popovic V, Rating D, Rioux MF, Rodriguez Espinosa N, Ronan A, Ostergaard JR, Rossignol E, Sanchez-Carpintero R, Schossig A, Senbil N, Sønderberg Roos LK, Stevens CA, Synofzik M, Sztriha L, Tibussek D, Timmann D, Tonduti D, van de Warrenburg BP, Vázquez-López M, Venkateswaran S, Wasling P, Wassmer E, Webster RI, Wiegand G, Yoon G, Rotteveel J, Schiffmann R, van der Knaap MS, Vanderver A, Martos-Moreno GÁ, Polychronakos C, Wolf NI, Bernard G. Pelletier F, et al. Among authors: timmann d. J Clin Endocrinol Metab. 2021 Jan 23;106(2):e660-e674. doi: 10.1210/clinem/dgaa700. J Clin Endocrinol Metab. 2021. PMID: 33005949 Free PMC article.
Cerebellar mutism.
Küper M, Timmann D. Küper M, et al. Among authors: timmann d. Brain Lang. 2013 Dec;127(3):327-33. doi: 10.1016/j.bandl.2013.01.001. Epub 2013 Feb 9. Brain Lang. 2013. PMID: 23398780 Review.
[Genetics of movement disorders-rare but important].
Klebe S, Timmann D. Klebe S, et al. Among authors: timmann d. Nervenarzt. 2019 Feb;90(2):197-210. doi: 10.1007/s00115-018-0659-1. Nervenarzt. 2019. PMID: 30645659 Review. German.
Probabilistic 3D MRI atlas of the human cerebellar dentate/interposed nuclei.
Dimitrova A, Zeljko D, Schwarze F, Maschke M, Gerwig M, Frings M, Beck A, Aurich V, Forsting M, Timmann D. Dimitrova A, et al. Among authors: timmann d. Neuroimage. 2006 Mar;30(1):12-25. doi: 10.1016/j.neuroimage.2005.09.020. Epub 2005 Oct 27. Neuroimage. 2006. PMID: 16257240
[Contribution of the cerebellum to cognition].
Timmann D. Timmann D. Fortschr Neurol Psychiatr. 2012 Jan;80(1):44-52. doi: 10.1055/s-0031-1282022. Epub 2012 Jan 10. Fortschr Neurol Psychiatr. 2012. PMID: 22234815 Review. German.
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