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

Year Number of Results
2001 1
2002 1
2003 1
2004 1
2010 2
2011 1
2012 2
2013 3
2014 8
2015 6
2016 3
2017 5
2018 7
2019 8
2020 5
2021 13
2022 9
2023 5

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70 results

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Page 1
'Atypical' Parkinson's disease - genetic.
Weissbach A, Wittke C, Kasten M, Klein C. Weissbach A, et al. Among authors: kasten m. Int Rev Neurobiol. 2019;149:207-235. doi: 10.1016/bs.irn.2019.10.011. Epub 2019 Nov 25. Int Rev Neurobiol. 2019. PMID: 31779813 Review.
Genetic atypical Parkinson's disease (PD) describes monogenic forms of PD that resemble idiopathic PD but feature prominent atypical clinical signs and symptoms and can be sub-grouped into i) atypical monogenic forms caused by mutations in the ATP13A2, DNAJC6, FBXO7, SYNJ1 …
Genetic atypical Parkinson's disease (PD) describes monogenic forms of PD that resemble idiopathic PD but feature prominent atypical …
Using global team science to identify genetic parkinson's disease worldwide.
Vollstedt EJ, Kasten M, Klein C; MJFF Global Genetic Parkinson's Disease Study Group. Vollstedt EJ, et al. Among authors: kasten m. Ann Neurol. 2019 Aug;86(2):153-157. doi: 10.1002/ana.25514. Epub 2019 Jun 26. Ann Neurol. 2019. PMID: 31155756 Free PMC article. No abstract available.
Genotype-Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.
Lange LM, Junker J, Loens S, Baumann H, Olschewski L, Schaake S, Madoev H, Petkovic S, Kuhnke N, Kasten M, Westenberger A, Domingo A, Marras C, König IR, Camargos S, Ozelius LJ, Klein C, Lohmann K. Lange LM, et al. Among authors: kasten m. Mov Disord. 2021 May;36(5):1086-1103. doi: 10.1002/mds.28485. Epub 2021 Jan 27. Mov Disord. 2021. PMID: 33502045 Review.
This comprehensive MDSGene review is devoted to 7 genes - TOR1A, THAP1, GNAL, ANO3, PRKRA, KMT2B, and HPCA - mutations in which may cause isolated dystonia. It followed MDSGene's standardized data extraction protocol and screened a total of ~1200 citations. ...
This comprehensive MDSGene review is devoted to 7 genes - TOR1A, THAP1, GNAL, ANO3, PRKRA, KMT2B, and HPCA - mutations in which may cause is …
Pronounced Orthostatic Hypotension in GBA-Related Parkinson's Disease.
Usnich T, Hanssen H, Lohmann K, Lohse C, Klein C, Kasten M, Brüggemann N; EPIPARK Study Group. Usnich T, et al. Among authors: kasten m. J Parkinsons Dis. 2022;12(5):1539-1544. doi: 10.3233/JPD-223197. J Parkinsons Dis. 2022. PMID: 35491800
Patients with Parkinson's disease (PD) carrying variants in the Glucocerebrosidase (GBA) gene (GBA-PD) suffer from orthostatic symptoms more frequently than idiopathic PD patients (IPD). ...
Patients with Parkinson's disease (PD) carrying variants in the Glucocerebrosidase (GBA) gene (GBA-PD) suffer from orthostatic sympto …
[Positioning the hand to act-Validation of the 8-point reaching range test].
Krupp S, Petersen T, Balck F, Kasten M, Willkomm M, Kasper J. Krupp S, et al. Among authors: kasten m. Z Gerontol Geriatr. 2022 Mar;55(2):93-98. doi: 10.1007/s00391-022-02029-3. Epub 2022 Feb 24. Z Gerontol Geriatr. 2022. PMID: 35201394 Free PMC article. Review. German.
On the individual level a ceiling effect (both sides score 8) occurred in 4.1% (n = 3) but no floor effect was observed. The internal consistency (Cronbach's alpha) of the two-factorial test according to factor analysis was 0.78 (right) and 0.76 (left). ...
On the individual level a ceiling effect (both sides score 8) occurred in 4.1% (n = 3) but no floor effect was observed. The internal consis …
Functional Characterization of Rare RAB12 Variants and Their Role in Musician's and Other Dystonias.
Hebert E, Borngräber F, Schmidt A, Rakovic A, Brænne I, Weissbach A, Hampf J, Vollstedt EJ, Größer L, Schaake S, Müller M, Manzoor H, Jabusch HC, Alvarez-Fischer D, Kasten M, Kostic VS, Gasser T, Zeuner KE, Kim HJ, Jeon B, Bauer P, Altenmüller E, Klein C, Lohmann K. Hebert E, et al. Among authors: kasten m. Genes (Basel). 2017 Oct 18;8(10):276. doi: 10.3390/genes8100276. Genes (Basel). 2017. PMID: 29057844 Free PMC article. Review.
Mutations in RAB (member of the Ras superfamily) genes are increasingly recognized as cause of a variety of disorders including neurological conditions. While musician's dystonia (MD) and writer's dystonia (WD) are task-specific movement disorders, other dystonias p …
Mutations in RAB (member of the Ras superfamily) genes are increasingly recognized as cause of a variety of disorders including neurological …
Cohort Profile: a population-based cohort to study non-motor symptoms in parkinsonism (EPIPARK).
Kasten M, Hagenah J, Graf J, Lorwin A, Vollstedt EJ, Peters E, Katalinic A, Raspe H, Klein C. Kasten M, et al. Int J Epidemiol. 2013 Feb;42(1):128-128k. doi: 10.1093/ije/dys202. Epub 2012 Dec 19. Int J Epidemiol. 2013. PMID: 23257687
Parkinson's disease is increasingly viewed as a complex disorder including a range of typical non-motor symptoms in addition to the cardinal motor signs. This cohort was set up in 2010 to investigate the specificity of non-motor symptoms for Parkinson's disease. For …
Parkinson's disease is increasingly viewed as a complex disorder including a range of typical non-motor symptoms in addition to the c …
Lifestyle factors and clinical severity of Parkinson's disease.
Gabbert C, König IR, Lüth T, Kasten M, Grünewald A, Klein C, Trinh J. Gabbert C, et al. Among authors: kasten m. Sci Rep. 2023 Jun 12;13(1):9537. doi: 10.1038/s41598-023-31531-w. Sci Rep. 2023. PMID: 37308498 Free PMC article.
70 results