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Items: 11

1.

Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review.

Kasten M, Hartmann C, Hampf J, Schaake S, Westenberger A, Vollstedt EJ, Balck A, Domingo A, Vulinovic F, Dulovic M, Zorn I, Madoev H, Zehnle H, Lembeck CM, Schawe L, Reginold J, Huang J, König IR, Bertram L, Marras C, Lohmann K, Lill CM, Klein C.

Mov Disord. 2018 May;33(5):730-741. doi: 10.1002/mds.27352. Epub 2018 Apr 11. Review.

PMID:
29644727
2.

Age- and sex-related heterogeneity in prodromal Parkinson's disease.

Heinzel S, Kasten M, Behnke S, Vollstedt EJ, Klein C, Hagenah J, Pausch C, Heilmann R, Brockmann K, Suenkel U, Yilmaz R, Liepelt-Scarfone I, Walter U, Berg D.

Mov Disord. 2018 Jul;33(6):1025-1027. doi: 10.1002/mds.27349. Epub 2018 Mar 23. No abstract available.

PMID:
29570852
3.

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.

Genes (Basel). 2017 Oct 18;8(10). pii: E276. doi: 10.3390/genes8100276. Review.

4.

Analysis of blood-based gene expression in idiopathic Parkinson disease.

Shamir R, Klein C, Amar D, Vollstedt EJ, Bonin M, Usenovic M, Wong YC, Maver A, Poths S, Safer H, Corvol JC, Lesage S, Lavi O, Deuschl G, Kuhlenbaeumer G, Pawlack H, Ulitsky I, Kasten M, Riess O, Brice A, Peterlin B, Krainc D.

Neurology. 2017 Oct 17;89(16):1676-1683. doi: 10.1212/WNL.0000000000004516. Epub 2017 Sep 15.

PMID:
28916538
5.

Non-motor symptoms and quality of life in subjects with mild parkinsonian signs.

Prasuhn J, Piskol L, Vollstedt EJ, Graf J, Schmidt A, Tadic V, Tunc S, Hampf J, Warrlich E, Bibergeil C, Hagenah J, Klein C, Kasten M, Brüggemann N.

Acta Neurol Scand. 2017 Nov;136(5):495-500. doi: 10.1111/ane.12760. Epub 2017 Mar 27.

PMID:
28345787
6.

Validation of conversion between mini-mental state examination and montreal cognitive assessment.

Lawton M, Kasten M, May MT, Mollenhauer B, Schaumburg M, Liepelt-Scarfone I, Maetzler W, Vollstedt EJ, Hu MT, Berg D, Ben-Shlomo Y.

Mov Disord. 2016 Apr;31(4):593-6. doi: 10.1002/mds.26498. Epub 2016 Feb 10.

7.

RAB39B mutations are a rare finding in Parkinson disease patients.

Löchte T, Brüggemann N, Vollstedt EJ, Krause P, Domingo A, Rosales R, Lee LV, Hopfner F, Westenberger A, Kühn A, Klein C, Lohmann K.

Parkinsonism Relat Disord. 2016 Feb;23:116-7. doi: 10.1016/j.parkreldis.2015.12.014. Epub 2015 Dec 22. No abstract available.

PMID:
26739247
8.

Qualitative Characteristics of Depression in Parkinson's Patients and Controls.

Kritzinger C, Vollstedt EJ, Hückelheim K, Lorwin A, Graf J, Tunc S, Klein C, Kasten M.

Behav Neurol. 2015;2015:961372. doi: 10.1155/2015/961372. Epub 2015 Aug 16.

9.

A population-based study on combined markers for early Parkinson's disease.

Tunc S, Graf J, Tadic V, Brüggemann N, Schmidt A, Al-Khaled M, Wolff S, Vollstedt EJ, Lorwin A, Hampf J, Piskol L, Klein C, Hagenah J, Kasten M.

Mov Disord. 2015 Apr;30(4):531-7. doi: 10.1002/mds.26100. Epub 2014 Dec 27.

PMID:
25546094
10.

The recurrent mutation Arg258Gln in SYNJ1 (PARK20) is not a common cause of Parkinson's disease.

Winkler S, Vollstedt EJ, Kasten M, Alvarez-Fischer D, Klein C, Lohmann K.

J Neurol. 2014 Apr;261(4):833-4. doi: 10.1007/s00415-014-7306-y. Epub 2014 Mar 9. No abstract available.

PMID:
24609975
11.

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.

Int J Epidemiol. 2013 Feb;42(1):128-128k. doi: 10.1093/ije/dys202. Epub 2012 Dec 19.

PMID:
23257687

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