@ARTICLE{
author={Zschiedrich Katja,Koenig Inke R,Bruggemann Norbert,Kock Norman,Kasten Meike,Leenders Klaus L,Kostic Vladimir S,Vieregge Peter,Ziegler Andreas,Klein Christine,Lohmann Katja},
year={2009},
title={MDR1 variants and risk of Parkinson disease},
journal={JOURNAL OF NEUROLOGY},
volume={256},
number={1},
pages={115-120},
document_type={Article},
} 

@ARTICLE{
author={Kostic Vladimir S,Svetel Marina V,Kabakci Kemal,Ristic Aleksandar J,Petrovic Igor N,Schule B,Kock Norman,Djarmati Ana,Romac Stanka P,Klein Christine},
year={2006},
title={Intrafamilial phenotypic and genetic heterogeneity of dystonia},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={250},
number={1-2},
pages={92-96},
document_type={Article},
} 

@ARTICLE{
author={Lovicu Mario,Dessi Valentina,Lepori Maria Barbara,Zappu Antonietta,Zancan Lucia,GiacchiIorio Raffaeleno Raffaella,Marazzi MG,Iorio Raffaele,Vegnente A,Vajro Pietro,Maggiore Giuseppe,Marcellini Matilde,Barbera Cristiana,Kostic Vladimir S,Farci Anna Maria Giulia,Solinas Antonello,Altuntas B,Yuce A,Kock Norman,Tsezou A,De Virgiliis Stefano,Cao Antonio},
year={2006},
title={The canine copper toxicosis gene MURR1 is not implicated in the pathogenesis of Wilson disease},
journal={JOURNAL OF GASTROENTEROLOGY},
volume={41},
number={6},
pages={582-587},
document_type={Article},
} 

@ARTICLE{
author={Hedrich Katja,Hagenah Johann M,Djarmati Ana,Hiller A,Lohnau T,Lasek K,Grunewald RA,Hilker R,Steinlechner S,Boston H,Kock Norman,Schneider-Gold C,Kress W,Siebner Hartwig R,Binkofski Ferdinand,Lencer R,Munchau A,Klein Christine},
year={2006},
title={Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease  Role of a single hit?},
journal={ARCHIVES OF NEUROLOGY},
volume={63},
number={6},
pages={833-838},
document_type={Article},
} 

@ARTICLE{
author={Dragasevic Natasa T,Culjkovic Biljana,Klein Christine,Ristic Aleksandar J,Keckarevic Milica,Topisirovic Ivan,Vukosavic Slobodanka N,Svetel Marina V,Kock Norman,Stefanova Elka D,Romac Stanka P,Kostic Vladimir S},
year={2006},
title={Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients},
journal={MOVEMENT DISORDERS},
volume={21},
number={2},
pages={187-191},
document_type={Article},
} 

@ARTICLE{
author={Klein Christine,Djarmati Ana,Hedrich Katja,Schafer N,Scaglione C,Marchese R,Kock Norman,Schule B,Hiller A,Lohnau T,Winkler Susan,Wiegers K,Hering R,Bauer P,Riess O,Abbruzzese G,Martinelli P,Pramstaller Peter P},
year={2005},
title={PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={13},
number={9},
pages={1086-1093},
document_type={Article},
} 

@ARTICLE{
author={Schule B,Kock Norman,Svetel Marina V,Dragasevic Natasa T,Hedrich Katja,Aguiar PD,Liu L,Kabakci Kemal,Garrels J,Meyer EM,Berisavac Ivana I,Schwinger E,Kramer PL,Ozelius LJ,Klein Christine,Kostic Vladimir S},
year={2004},
title={Genetic heterogeneity in ten families with myoclonus-dystonia},
journal={JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY},
volume={75},
number={8},
pages={1181-1185},
document_type={Article},
} 

@ARTICLE{
author={Muller B,Hedrich Katja,Kock Norman,Dragasevic Natasa T,Svetel Marina V,Garrels J,Landt O,Nitschke M,Pramstaller Peter P,Reik W,Schwinger E,Sperner J,Ozelius LJ,Kostic Vladimir S,Klein Christine},
year={2002},
title={Evidence that paternal expression of the epsilon-Sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={71},
number={6},
pages={1303-1311},
document_type={Article},
} 

@ARTICLE{
author={Kock Norman,Muller B,Vieregge Peter,Pramstaller Peter P,Marder K,Abbruzzese G,Martinelli P,Lang Anthony E,Jacobs H,Hagenah Johann M,Harris J,Meija-Santana H,Fahn S,Hedrich Katja,Kann M,Gehlken U,Culjkovic Biljana,Schwinger E,Wszolek ZK,Zuhlke C,Klein Christine},
year={2002},
title={Role of SC42 mutations in early- and late-onset dopa-responsive parkinsonism},
journal={ANNALS OF NEUROLOGY},
volume={52},
number={2},
pages={257-258},
document_type={Letter},
} 

@ARTICLE{
author={Kock Norman,Culjkovic Biljana,Maniak S,Schilling Klaus,Muller B,Zuhlke C,Ozelius L,Klein Christine,Pramstaller Peter P,Kramer PL},
year={2002},
title={Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={71},
number={1},
pages={A205-208},
document_type={Letter},
}