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2012
Mark Friedreich's ataxia in patients with FXN p.R165P point mutation
Ygland, E. ^LU ; Taroni, Franco ; Gellera, Cinzia ; Duno, M ; Johnels, P. ^LU ; Soller, M. ^LU and Puschmann, A. ^LU (2012) 16th Congress of the European-Federation-of-Neurological-Societies (EFNS) In European Journal of Neurology 19(Suppl 1). p.727-727
- Contribution to journal › Published meeting abstract
Mark Novel PRRT2 mutation in an African-American family with paroxysmal kinesigenic dyskinesia
Hedera, Peter ; Xiao, Jianfeng ; Puschmann, Andreas ^LU ; Momcilovic, Dragana ; Wu, Steve W. and LeDoux, Mark S. (2012) In BMC Neurology 12(93).
- Contribution to journal › Article
2011
Mark Independent and Joint Effects of the MAPT and SNCA Genes in Parkinson Disease
Elbaz, Alexis ; Ross, Owen A. ; Ioannidis, John P. A. ; Soto-Ortolaza, Alexandra I. ; Moisan, Frederic ; Aasly, Jan ; Annesi, Grazia ; Bozi, Maria ; Brighina, Laura and Chartier-Harlin, Marie-Christine , et al. (2011) In Annals of Neurology 69(5). p.778-792
- Contribution to journal › Article
Mark Heredity in Parkinson's disease. From rare mutations to common genetic risk factors.
Puschmann, Andreas ^LU (2011) In Lund University Faculty of Medicine Doctoral Dissertation Series 2011:95.
- Thesis › Doctoral thesis (compilation)
Mark Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study
Ross, Owen A. ; Soto-Ortolaza, Alexandra I. ; Heckman, Michael G. ; Aasly, Jan O. ; Abahuni, Nadine ; Annesi, Grazia ; Bacon, Justin A. ; Bardien, Soraya ; Bozi, Maria and Brice, Alexis , et al. (2011) In Lancet Neurology 10(10). p.898-908
- Contribution to journal › Article
Mark VPS35 Mutations in Parkinson Disease
Vilarino-Gueell, Carles ; Wider, Christian ; Ross, Owen A. ; Dachsel, Justus C. ; Kachergus, Jennifer M. ; Lincoln, Sarah J. ; Soto-Ortolaza, Alexandra I. ; Cobb, Stephanie A. ; Wilhoite, Greggory J. and Bacon, Justin A. , et al. (2011) In American Journal of Human Genetics 89(1). p.162-167
- Contribution to journal › Article
Mark Human leukocyte antigen variation and Parkinson's disease.
Puschmann, Andreas ^LU ; Verbeeck, Christophe ; Heckman, Michael G ; Soto-Ortolaza, Alexandra I ; Lynch, Timothy ; Jasinska-Myga, Barbara ; Opala, Grzegorz ; Krygowska-Wajs, Anna ; Barcikowska, Maria and Uitti, Ryan J , et al. (2011) In Parkinsonism & Related Disorders 17. p.376-378
- Contribution to journal › Article
Mark An African-American family with dystonia.
Puschmann, Andreas ^LU ; Xiao, Jianfeng ; Bastian, Robert W ; Searcy, Jill A ; Ledoux, Mark S and Wszolek, Zbigniew K (2011) In Parkinsonism & Related Disorders 17. p.547-550
- Contribution to journal › Article
Mark A family with parkinsonism, essential tremor, restless legs syndrome, and depression
Puschmann, Andreas ^LU ; Pfeiffer, R. F. ; Stoessl, A. J. ; Kuriakose, R. ; Lash, J. L. ; Searcy, J. A. ; Strongosky, A. J. ; Vilarino-Gueell, C. ; Farrer, M. J. and Ross, O. A. , et al. (2011) In Neurology 76(19). p.1623-1630
- Contribution to journal › Article
Mark A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
Krüger, Rejko ; Sharma, Manu ; Riess, Olaf ; Gasser, Thomas ; Van Broeckhoven, Christine ; Theuns, Jessie ; Aasly, Jan ; Annesi, Grazia ; Bentivoglio, Anna Rita and Brice, Alexis , et al. (2011) In Neurobiology of Aging 32(3). p.9-548
- Contribution to journal › Article

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