P P Pramstaller

32-channel time-correlated-single-photon-counting system for high-throughput lifetime imaging.

I Rech, M Ghioni, G Acconcia, 2017, The Review of scientific instruments.

On the use of dense SNP marker data for the identification of distant relative pairs.

N A Sheehan, T Egeland, P P Pramstaller, 2016, Theoretical population biology.

Motor reorganization in asymptomatic carriers of a single mutant Parkin allele: a human model for presymptomatic parkinsonism.

C Büchel, P P Pramstaller, T van Eimeren, 2005, Brain : a journal of neurology.

Distinguishing early-onset PD from dopa-responsive dystonia with transcranial sonography

B Becker, P P Pramstaller, P. Pramstaller, 2006, Neurology.

Absence of previously reported variants in the SCNA (G88C and G209A), NR4A2 (T291D and T245G) and the DJ‐1 (T497C) genes in familial Parkinson's disease from the GenePD study

Mark Guttman, R H Myers, P P Pramstaller, 2005, Movement disorders : official journal of the Movement Disorder Society.

Positron emission tomographic analysis of the nigrostriatal dopaminergic system in familial Parkinsonism associated with mutations in the Parkin gene

W D Heiss, P P Pramstaller, K. Herholz, 2001, Annals of neurology.

Morphometric fingerprint of asymptomatic Parkin and PINK1 mutation carriers in the basal ganglia

C Büchel, P P Pramstaller, T van Eimeren, 2007, Neurology.