Publications

Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers.

Weissbach A, König IR, Hückelheim K, Pramstaller PP, Werner E, Brüggemann N, Tadic V, Lohmann K, Bäumer T, Münchau A, Kasten M, Klein C.
Parkinsonism Relat Disord. 2017 Jul 8. pii: S1353-8020(17)30236-5. doi: 10.1016/j.parkreldis.2017.07.003. [Epub ahead of print]
https://www.ncbi.nlm.nih.gov/pubmed/28716427

Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia

Lohmann K, Redin C, Tönnies H, Bressman SB, Subero JIM, Wiegers K, Hinrichs F, Hellenbroich Y, Rakovic A, Raymond D, Ozelius LJ, Schwinger E, Siebert R, Talkowski ME, Saunders-Pullman R, Klein C.
JAMA Neurol. 2017 Jul 1;74(7):806-812. doi: 10.1001/jamaneurol.2017.0666.
https://www.ncbi.nlm.nih.gov/pubmed/?term=28558098

Genetic risk variants in Parkinson’s disease and other movement disorders

Brockmann K, Lohmann K.
Nervenarzt. 2017 Jul;88(7):713-719. doi: 10.1007/s00115-017-0348-5.
https://www.ncbi.nlm.nih.gov/pubmed/28536875

Epidemiology and causes of Parkinson’s disease

Lill C, Klein C.
Nervenarzt. 2017 Apr;88(4):345-355. doi: 10.1007/s00115-017-0288-0.
https://www.ncbi.nlm.nih.gov/pubmed/28289797

Evaluating the role of TMEM230 variants in Parkinson’s disease

Baumann H, Wolff S, Münchau A, Hagenah JM, Lohmann K, Klein C.
Parkinsonism Relat Disord. 2017 Feb;35:100-101. doi: 10.1016/j.parkreldis.2016.12.015. Epub 2016 Dec 20.
https://www.ncbi.nlm.nih.gov/pubmed/28017548