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2023
Mark Substitution of PINK1 Gly411 modulates substrate receptivity and turnover
Fiesel, Fabienne C. ; Fričová, Dominika ; Hayes, Caleb S. ; Coban, Mathew A. ; Hudec, Roman ; Bredenberg, Jenny M. ; Broadway, Benjamin J. ; Markham, Briana N. ; Yan, Tingxiang and Boneski, Paige K. , et al. (2023) In Autophagy 19(6). p.1711-1732
- Contribution to journal › Article
2022
Mark Tau and neurofilament light-chain as fluid biomarkers in spinocerebellar ataxia type 3
Garcia-Moreno, Hector ; Prudencio, Mercedes ; Thomas-Black, Gilbert ; Solanky, Nita ; Jansen-West, Karen R ; Hanna Al-Shaikh, Rana ; Heslegrave, Amanda ; Zetterberg, Henrik ^LU ; Santana, Magda M and Pereira de Almeida, Luis , et al. (2022) In European Journal of Neurology 29(8). p.2439-2452
- Contribution to journal › Article
2020
Mark Toward allele-specific targeting therapy and pharmacodynamic marker for spinocerebellar ataxia type 3
Prudencio, Mercedes ; Garcia-Moreno, Hector ; Jansen-West, Karen R ; Al-Shaikh, Rana Hanna ; Gendron, Tania F ; Heckman, Michael G ; Spiegel, Matthew R ; Carlomagno, Yari ; Daughrity, Lillian M and Song, Yuping , et al. (2020) In Science Translational Medicine 12(566).
- Contribution to journal › Article
2018
Mark Slowly progressive dementia caused by MAPT R406W mutations : Longitudinal report on a new kindred and systematic review
Ygland, Emil ^LU ; Van Westen, Danielle ^LU ; Englund, Elisabet ^LU ; Rademakers, Rosa ; Wszolek, Zbigniew K. ; Nilsson, Karin ^LU ; Nilsson, Christer ^LU ; Landqvist Waldö, Maria ^LU ; Alafuzoff, Irina and Hansson, Oskar ^LU , et al. (2018) In Alzheimer's Research and Therapy 10(1).
- Contribution to journal › Article
2017
Mark PBB3 imaging in Parkinsonian disorders : Evidence for binding to tau and other proteins
Perez-Soriano, Alexandra ; Arena, Julieta E ; Dinelle, Katie ; Miao, Qing ; McKenzie, Jessamyn ; Neilson, Nicole ; Puschmann, Andreas ^LU ; Schaffer, Paul ; Shinotoh, Hitoshi and Smith-Forrester, Jenna , et al. (2017) In Movement Disorders 32(7). p.1016-1024
- Contribution to journal › Article
Mark Heterozygous PINK1 p.G411S increases risk of Parkinson's disease via a dominant-negative mechanism
Puschmann, Andreas ^LU ; Fiesel, Fabienne C ; Caulfield, Thomas R ; Hudec, Roman ; Ando, Maya ; Truban, Dominika ; Hou, Xu ; Ogaki, Kotaro ; Heckman, Michael G. and James, Elle D , et al. (2017) In Brain 140(1). p.98-117
- Contribution to journal › Article
Mark Reply: Heterozygous PINK1 p.G411S in rapid eye movement sleep behaviour disorder
Puschmann, Andreas ^LU ; Fiesel, Fabienne C ; Caulfield, Thomas R ; Hudec, Roman ; Ando, Maya ; Truban, Dominika ; Hou, Xu ; Ogaki, Kotaro ; Heckman, Michael G. and James, Elle D , et al. (2017) In Brain 140(6). p.33-33
- Contribution to journal › Letter
2016
Mark Autosomal dominant Parkinson's disease caused by SNCA duplications.
Konno, Takuya ; Ross, Owen A ; Puschmann, Andreas ^LU ; Dickson, Dennis W and Wszolek, Zbigniew K (2016) In Parkinsonism & Related Disorders 22(sep 3). p.1-6
- Contribution to journal › Article
2015
Mark CHCHD2 and Parkinson's disease
Puschmann, Andreas ^LU ; Dickson, Dennis W ; Englund, Elisabet ^LU ; Wszolek, Zbigniew K and Ross, Owen A (2015) In Lancet Neurology 14(7). p.679-679
- Contribution to journal › Letter
Mark Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders.
Ogaki, Kotaro ; Koga, Shunsuke ; Heckman, Michael G ; Fiesel, Fabienne C ; Ando, Maya ; Labbé, Catherine ; Lorenzo-Betancor, Oswaldo ; Moussaud-Lamodière, Elisabeth L ; Soto-Ortolaza, Alexandra I and Walton, Ronald L , et al. (2015) In Neurology
- Contribution to journal › Article

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