Publications | Lund University Publications

1 – 4 of 4

show: 10
|
sort: year (new to old)

News feed Embed this list Save this search Mark all Export

Cancel

Embed this list

copy and paste the html snippet below into your own page:

<iframe src="https://lup.lub.lu.se/search/publication?embed=1&q=author%3D%22Opala%2C+G.%22+or+(documentType+any+%22bookEditor+conferenceEditor%22+and+editor%3D%22Opala%2C+G.%22)&amp;hide_pagination=1&amp;hide_info=1&amp;hide_options=1"
  width="100%"
  height="400"
  allowtransparency="true"
  frameborder="0">
</iframe>

2016
Mark Heterozygous PINK1 p.G411S mutation increases risk for Parkinson's disease (PD)
Springer, W ; Puschmann, A. ^LU ; Fiesel, Fabienne C ; Ando, Maya ; Caulfield, Thomas R ; Ogaki, K. ; Heckman, M. G. ; Hudec, Roman ; James, Elle D and Opala, G. , et al. (2016) 20th International Congress of Parkinson's Disease and Movement Disorders In Movement Disorders 31(Suppl. S2). p.282-282
- Contribution to journal › Published meeting abstract
2015
Mark DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients.
Lorenzo-Betancor, O ; Ogaki, K ; Soto-Ortolaza, A I ; Labbe, C ; Walton, R L ; Strongosky, A J ; van Gerpen, J A ; Uitti, R J ; McLean, P J and Springer, W , et al. (2015) In European Journal of Neurology 22(9). p.1323-1325
- Contribution to journal › Article
2014
Mark Global investigation and meta-analysis of the C9orf72 (G4C2)n repeat in Parkinson disease
Theuns, J. ; Verstraeten, A. ; Sleegers, K. ; Wauters, E. ; Gijselinck, I. ; Smolders, S. ; Crosiers, D. ; Corsmit, E. ; Elinck, E. and Sharma, M. , et al. (2014) In Neurology 83(21). p.13-1906
- Contribution to journal › Article
2013
Mark GWAS risk factors in Parkinson's disease : LRRK2 coding variation and genetic interaction with PARK16
Soto-Ortolaza, A. I. ; Heckman, M. G. ; Labbe, C. ; Serie, D. J. ; Puschmann, Andreas ^LU ; Rayaprolu, S. ; Strongosky, A. ; Boczarska-Jedynak, M. ; Opala, G. and Krygowska-Wajs, A. , et al. (2013) In American Journal of Neurodegenerative Disease 2(4). p.99-287
- Contribution to journal › Article