Publikationen

Genetic risk variants in Parkinson's disease and other movement disorders.

Brockmann K, Lohmann K.
Nervenarzt 2017, vorab online publiziert.


Screening study of TUBB4A in isolated dystonia.

Vulinovic F, Schaake S, Domingo A, Kumar KR, Defazio G, Mir P, Simonyan K, Ozelius LJ, Brüggemann N, Chung SJ, Rakovic A, Lohmann K, Klein C.
Parkinsonism Relat Disord 2017, vorab online publiziert.


Update on the Genetics of Dystonia.

Lohmann K, Klein C.
Curr Neurol Neurosci Rep 2017;17:26.


Deep brain stimulation for dystonia: a novel perspective on the value of genetic testing

Jinnah HA, Alterman R, Klein C, Krauss JK, Moro E, Vidailhet M, Raike R
J Neural Transm (Vienna). 2017 Apr;124(4):417-430. doi: 10.1007/s00702-016-1656-9. Epub 2017 Feb 3


Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans.

Lohmann K, asuho I, Patil DN, Baumann H, Hebert E, Steinrücke S, Trujillano D, Skamangas NK, Dobricic V, Hüning I, Gillessen-Kaesbach G, Westenberger A, Savic-Pavicevic D, Münchau A, Oprea G, Klein C, Rolfs A, Martemyanov KA.
Hum Mol Genet. 2017 Mar 15;26(6):1078-1086. doi: 10.1093/hmg/ddx018.


A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism

Wenzel GR, Lohmann K, Kühn AA
Parkinsonism Relat Disord. 2017 Feb 9. pii: S1353-8020(17)30043-3. doi: 10.1016/j.parkreldis.2017.02.009.


Novel GNB1 missense mutation in a patient with generalized dystonia, hypotonia, and intellectual disability.

Steinrücke S, Lohmann K, Domingo A, Rolfs A, Bäumer T, Spiegler J, Hartmann C, Münchau A.
Neurol Genet 2016;2:e106.


Tor1a+/- mice develop dystonia-like movements via a striatal dopaminergic dysregulation triggered by peripheral nerve injury.

Ip CW, Isaias IU, Kusche-Tekin BB, Klein D, Groh J, O’Leary A, Knorr S, Higuchi T, Koprich JB, Brotchie JM, Toyka KV, Reif A, Volkmann J.
Acta Neuropathol Commun. 2016 Oct 3;4(1):108