Sökresultat - Mathias Toft
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Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes av Chiara Cappelletti, Sandra Pilar Henriksen, Hanneke Geut, Annemieke J.M. Rozemüller, Wilma D.J. van de Berg, Lasse Pihlstrøm, Mathias Toft
Publicerad 2023Artigo -
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Personality Changes after Deep Brain Stimulation in Parkinson’s Disease av Uyen Pham, Anne‐Kristin Solbakk, Inger-Marie Skogseid, Mathias Toft, Are Hugo Pripp, Ane Konglund, Stein Andersson, Ira Haraldsen, Dag Aarsland, Espen Dietrichs, Ulrik Fredrik Malt
Publicerad 2015Artigo -
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Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease av Lasse Pihlstrøm, Aina Rengmark, Kari Anne Bjørnarå, Nil Dizdar, Camilla Fardell, Lars Forsgren, Björn Holmberg, Jan Larsen, Jan Linder, Hans Nissbrandt, Ole‐Bjørn Tysnes, Espen Dietrichs, Mathias Toft
Publicerad 2015Artigo -
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Prehospital screening of acute stroke with the National Institutes of Health Stroke Scale (ParaNASPP): a stepped-wedge, cluster-randomised controlled trial av Mona Guterud, Helge Fagerheim Bugge, Jo R⊘islien, Jo Kramer‐Johansen, Mathias Toft, Hege Ihle‐Hansen, Kristi G. Bache, Karianne Larsen, Anne‐Cathrine Braarud, Else Charlotte Sandset, Maren Ranhoff Hov
Publicerad 2023Artigo -
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Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease av Lasse Pihlstrøm, Gunnar Axelsson, Kari Anne Bjørnarå, Nil Dizdar, Camilla Fardell, Lars Forsgren, Björn Holmberg, Jan Larsen, Jan Linder, Hans Nissbrandt, Ole‐Bjørn Tysnes, E. Wallin Öhman, Espen Dietrichs, Mathias Toft
Publicerad 2012Artigo -
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A comprehensive analysis of <i>SNCA</i>‐related genetic risk in sporadic parkinson disease av Lasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, Victoria Berge‐Seidl, Margrete Langmyhr, Sandra Pilar Henriksen, Wilma D.J. van de Berg, J. Raphael Gibbs, Mark Cookson, Andrew Singleton, Mike A. Nalls, Mathias Toft
Publicerad 2018Artigo -
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Impulse control and correlation to dopamine agonist serum concentrations in people with Parkinson's disease av Sara C. Staubo, Ole‐Martin Fuskevåg, Mathias Toft, Ingeborg Haugesag Lie, Kirsti M. J. Alvik, Pål Jostad, Stein H. Tingvoll, Hallvard Lilleng, Kristina Rosqvist, Elisabet Størset, Per Odin, Espen Dietrichs, Erik Sveberg Dietrichs
Publicerad 2025Artigo -
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Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology av Lasse Pihlstrøm, Gemma Shireby, Hanneke Geut, Sandra Pilar Henriksen, Annemieke J.M. Rozemüller, Jon‐Anders Tunold, Eilís Hannon, Paul T. Francis, Alan Thomas, Seth Love, Jonathan Mill, Wilma D.J. van de Berg, Mathias Toft
Publicerad 2022Revisão -
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Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations av Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan, Julie P. Taylor, Sarah Lincoln, Jan Aasly, Jonathan Gibson, Owen A. Ross, Timothy Lynch, Joseph Wiley, Haydeh Payami, John G. Nutt, Demetrius M. Maraganore, K Czyźewski, Maria Styczyńska, Zbigniew K. Wszołek, Matthew J. Farrer, Mathias Toft
Publicerad 2005Artigo -
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Fine mapping of the HLA locus in Parkinson’s disease in Europeans av Eric Yu, Aditya Ambati, Maren Stolp Andersen, Lynne Krohn, Mehrdad A. Estiar, Prabhjyot Saini, Konstantin Senkevich, Yuri L. Sosero, Ashwin Ashok Kumar Sreelatha, Jennifer A. Ruskey, Farnaz Asayesh, Dan Spiegelman, Mathias Toft, Marte K. Viken, Manu Sharma, Cornelis Blauwendraat, Lasse Pihlstrøm, Emmanuel Mignot, Ziv Gan‐Or
Publicerad 2021Artigo -
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Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease av Jon‐Anders Tunold, Manuela Tan, Shunsuke Koga, Hanneke Geut, Annemieke J.M. Rozemüller, Rebecca R. Valentino, Hiroaki Sekiya, Nicholas B. Martin, Michael G. Heckman, José Brás, Rita Guerreiro, Dennis W. Dickson, Mathias Toft, Wilma D.J. van de Berg, Owen A. Ross, Lasse Pihlstrøm
Publicerad 2023Artigo -
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Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease av Jan Aasly, Carles Vilariño‐Güell, Justus C. Dächsel, Philip J. Webber, Andrew B. West, Kristoffer Haugarvoll, Krisztina K. Johansen, Mathias Toft, John G. Nutt, Haydeh Payami, Jennifer M. Kachergus, Sarah Lincoln, Amela Felic, Christian Wider, Alexandra I. Soto‐Ortolaza, Stephanie A. Cobb, Linda R. White, Owen A. Ross, Matthew J. Farrer
Publicerad 2010Artigo
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Medicine
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Biology
Genetics
Internal medicine
Gene
Parkinson's disease
Genotype
Single-nucleotide polymorphism
Genetic association
Genome-wide association study
Psychology
Dementia
Allele
Haplotype
LRRK2
Pathology
Locus (genetics)
Odds ratio
Neuroscience
Psychiatry
Linkage disequilibrium
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Confidence interval
Dementia with Lewy bodies
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