Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1953 1
1956 1
1957 2
1960 3
1961 2
1964 1
1969 1
1972 1
1974 1
1975 1
1976 1
1977 1
1979 1
1980 1
1982 1
1985 1
1986 1
1987 2
1989 1
1990 2
1991 2
1993 4
1994 3
1995 3
1996 5
1998 4
1999 3
2000 4
2001 2
2002 2
2003 7
2004 6
2005 4
2006 3
2007 5
2008 12
2009 11
2010 19
2011 21
2012 23
2013 22
2014 20
2015 22
2016 20
2017 26
2018 24
2019 24
2020 26
2021 28
2022 26
2023 30
2024 6

Text availability

Article attribute

Article type

Publication date

Search Results

402 results

Results by year

Filters applied: . Clear all
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: lohmann k. 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.
An intronic GAA repeat expansion in FGF14 causes the autosomal-dominant adult-onset ataxia SCA50/ATX-FGF14.
Rafehi H, Read J, Szmulewicz DJ, Davies KC, Snell P, Fearnley LG, Scott L, Thomsen M, Gillies G, Pope K, Bennett MF, Munro JE, Ngo KJ, Chen L, Wallis MJ, Butler EG, Kumar KR, Wu KH, Tomlinson SE, Tisch S, Malhotra A, Lee-Archer M, Dolzhenko E, Eberle MA, Roberts LJ, Fogel BL, Brüggemann N, Lohmann K, Delatycki MB, Bahlo M, Lockhart PJ. Rafehi H, et al. Among authors: lohmann k. Am J Hum Genet. 2023 Jan 5;110(1):105-119. doi: 10.1016/j.ajhg.2022.11.015. Epub 2022 Dec 8. Am J Hum Genet. 2023. PMID: 36493768 Free PMC article.
Nomenclature of Genetic Movement Disorders: Recommendations of the International Parkinson and Movement Disorder Society Task Force - An Update.
Lange LM, Gonzalez-Latapi P, Rajalingam R, Tijssen MAJ, Ebrahimi-Fakhari D, Gabbert C, Ganos C, Ghosh R, Kumar KR, Lang AE, Rossi M, van der Veen S, van de Warrenburg B, Warner T, Lohmann K, Klein C, Marras C; on behalf of the Task Force on Genetic Nomenclature in Movement Disorders. Lange LM, et al. Among authors: lohmann k. Mov Disord. 2022 May;37(5):905-935. doi: 10.1002/mds.28982. Epub 2022 Apr 28. Mov Disord. 2022. PMID: 35481685 Review.
Genetics and Pathogenesis of Dystonia.
Thomsen M, Lange LM, Zech M, Lohmann K. Thomsen M, et al. Among authors: lohmann k. Annu Rev Pathol. 2024 Jan 24;19:99-131. doi: 10.1146/annurev-pathmechdis-051122-110756. Epub 2023 Sep 22. Annu Rev Pathol. 2024. PMID: 37738511 Free article. Review.
Hereditary Dystonia Overview.
Klein C, Lohmann K, Marras C, Münchau A. Klein C, et al. Among authors: lohmann k. 2003 Oct 28 [updated 2017 Jun 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2003 Oct 28 [updated 2017 Jun 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301334 Free Books & Documents. Review.
Animal migration research takes wing.
Lohmann KJ. Lohmann KJ. Curr Biol. 2018 Sep 10;28(17):R952-R955. doi: 10.1016/j.cub.2018.08.016. Curr Biol. 2018. PMID: 30205070 Free article.
Update on the Genetics of Dystonia.
Lohmann K, Klein C. Lohmann K, et al. Curr Neurol Neurosci Rep. 2017 Mar;17(3):26. doi: 10.1007/s11910-017-0735-0. Curr Neurol Neurosci Rep. 2017. PMID: 28283962 Review.
Magnetic maps in animal navigation.
Lohmann KJ, Goforth KM, Mackiewicz AG, Lim DS, Lohmann CMF. Lohmann KJ, et al. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2022 Jan;208(1):41-67. doi: 10.1007/s00359-021-01529-8. Epub 2022 Jan 9. J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2022. PMID: 34999936 Free PMC article. Review.
Animal navigation: a noisy magnetic sense?
Johnsen S, Lohmann KJ, Warrant EJ. Johnsen S, et al. Among authors: lohmann kj. J Exp Biol. 2020 Sep 23;223(Pt 18):jeb164921. doi: 10.1242/jeb.164921. J Exp Biol. 2020. PMID: 32967977 Review.
Genotype-Phenotype Correlations for ATX-TBP (SCA17): MDSGene Systematic Review.
Rossi M, Hamed M, Rodríguez-Antigüedad J, Cornejo-Olivas M, Breza M, Lohmann K, Klein C, Rajalingam R, Marras C, van de Warrenburg BP. Rossi M, et al. Among authors: lohmann k. Mov Disord. 2023 Mar;38(3):368-377. doi: 10.1002/mds.29278. Epub 2022 Nov 14. Mov Disord. 2023. PMID: 36374860 Review.
402 results