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2020
Mark Disappearance of familially aggregated paralysis agitans in subsequent generations: a 135-year follow up study
Nilsson, Karin ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism & Related Disorders 79(Suppl.1). p.27-27
- Contribution to journal › Published meeting abstract
Mark Long term outcome of Parkinson’s disease and validation of a new clinical classification system.
Ygland Rödström, Emil ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism & Related Disorders 79(Suppl.1). p.35-36
- Contribution to journal › Published meeting abstract
Mark Ataxia project in Scania, Sweden: Study outline and current status
Gorcenco, Sorina ^LU ; Karremo, Christin ^LU ; Kafantari, Efthymia ^LU and Puschmann, Andreas ^LU (2020) In Parkinsonism & Related Disorders 79(Suppl 1). p.112-112
- Contribution to journal › Published meeting abstract
2019
Mark Nationwide prevalence of primary dystonia, progressive ataxia and hereditary spastic paraplegia
Hellberg, Clara ^LU ; Alinder, Erik ; Jaraj, Daniel and Puschmann, Andreas ^LU (2019) In Parkinsonism and Related Disorders 69. p.79-84
- Contribution to journal › Article
Mark Low prevalence of known pathogenic mutations in dominant PD genes : A Swedish multicenter study
Puschmann, Andreas ^LU ; Jiménez-Ferrer, Itzia ^LU ; Lundblad-Andersson, Elin ^LU ; Mårtensson, Emma ^LU ; Hansson, Oskar ^LU ; Odin, Per ^LU ; Widner, Håkan ^LU ; Brolin, Kajsa ^LU ; Mzezewa, Ropafadzo and Kristensen, Jonas ^LU , et al. (2019) In Parkinsonism and Related Disorders 66. p.158-165
- Contribution to journal › Article
Mark Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
Gorcenco, Sorina ^LU ; Vaz, Frédéric M. ; Tracewska-Siemiatkowska, Anna ; Tranebjærg, Lisbeth ; Cremers, Frans P.M. ; Ygland, Emil ^LU ; Kicsi, Jenő ; Rendtorff, Nanna Dahl ; Möller, Claes and Kjellström, Ulrika ^LU , et al. (2019) In Parkinsonism & Related Disorders 61. p.245-247
- Contribution to journal › Letter
Mark Using global team science to identify genetic parkinson's disease worldwide
Vollstedt, Eva Juliane ; Kasten, Meike ; Klein, Christine ; Aasly, Jan ; Adler, Charles ; Ahmad-Annuar, Azlina ; Albanese, Alberto ; Alcalay, Roy N. ; Al-Mubarak, Bashayer and Alvarez, Victoria , et al. (2019) In Annals of Neurology 86(2). p.153-157
- Contribution to journal › Article
2018
Mark LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies : a genome-wide linkage and sequencing study
Quadri, Marialuisa ; Mandemakers, Wim ; Grochowska, Martyna M. ; Masius, Roy ; Geut, Hanneke ; Fabrizio, Edito ; Breedveld, Guido J. ; Kuipers, Demy ; Minneboo, Michelle and Vergouw, Leonie J.M. , et al. (2018) In The Lancet Neurology 17(7). p.597-608
- Contribution to journal › Article
Mark SAMD9 and SAMD9L in inherited predisposition to ataxia, pancytopenia, and myeloid malignancies
Davidsson, Josef ^LU ; Puschmann, Andreas ^LU ; Tedgård, Ulf ^LU ; Bryder, David ^LU ; Nilsson, Lars and Cammenga, Jörg (2018) In Leukemia 32(5). p.1106-1115
- Contribution to journal › Article
Mark Will FTLD-tau work for all when FTDP-17 retires?
Ygland, Emil ^LU ; Landqvist Waldö, Maria ^LU ; Englund, Elisabet ^LU ; Puschmann, Andreas ^LU and Nilsson, Christer ^LU (2018) In Brain : a journal of neurology 141(8). p.62-62
- Contribution to journal › Article

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