Resultados de búsqueda - Mathias Toft

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  1. 1
    Surgical Site Infections after Deep Brain Stimulation Surgery: Frequency, Characteristics and Management in a 10-Year Period

    Surgical Site Infections after Deep Brain Stimulation Surgery: Frequency, Characteristics and Management in a 10-Year Period por Silje Bjerknes, Inger Marie Skogseid, Terje Sæhle, Espen Dietrichs, Mathias Toft

    Publicado 2014
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  2. 2
    Multiple<i>alpha-synuclein</i>gene polymorphisms are associated with Parkinson’s disease in a Norwegian population

    Multiple<i>alpha-synuclein</i>gene polymorphisms are associated with Parkinson’s disease in a Norwegian population por Ronny Myhre, Mathias Toft, Jennifer M. Kachergus, Mary Hulihan, Jan Aasly, Helge Klungland, Matthew J. Farrer

    Publicado 2008
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  3. 3
    Long-term follow-up of thalamic deep brain stimulation for essential tremor – patient satisfaction and mortality

    Long-term follow-up of thalamic deep brain stimulation for essential tremor – patient satisfaction and mortality por Mari Naumann Børretzen, Silje Bjerknes, Terje Sæhle, Mona Skjelland, Inger Marie Skogseid, Mathias Toft, Espen Dietrichs

    Publicado 2014
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  4. 4
    The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal

    The GBA variant E326K is associated with Parkinson's disease and explains a genome-wide association signal por Victoria Berge‐Seidl, Lasse Pihlstrøm, Jodi Maple‐Grødem, Lars Forsgren, Jan Linder, Jan Larsen, Ole‐Bjørn Tysnes, Mathias Toft

    Publicado 2017
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  5. 5
    Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia

    Targeted high throughput sequencing in hereditary ataxia and spastic paraplegia por Zafar Iqbal, Siri Lynne Rydning, Iselin Marie Wedding, Jeanette Koht, Lasse Pihlstrøm, Aina Rengmark, Sandra Pilar Henriksen, Chantal Tallaksen, Mathias Toft

    Publicado 2017
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  6. 6
    Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes

    Transcriptomic profiling of Parkinson's disease brains reveals disease stage specific gene expression changes por Chiara Cappelletti, Sandra Pilar Henriksen, Hanneke Geut, Annemieke J.M. Rozemüller, Wilma D.J. van de Berg, Lasse Pihlstrøm, Mathias Toft

    Publicado 2023
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  7. 7
    Linkage Disequilibrium and Association of MAPT H1 in Parkinson Disease

    Linkage Disequilibrium and Association of MAPT H1 in Parkinson Disease por Lisa Skipper, Kristen Wilkes, Mathias Toft, Matthew Baker, Sarah Lincoln, Mary Hulihan, Owen A. Ross, Mike Hutton, Jan Aasly, Matthew J. Farrer

    Publicado 2004
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  8. 8
    APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease

    APOE and MAPT Are Associated With Dementia in Neuropathologically Confirmed Parkinson's Disease por Jon-Anders Tunold, Hanneke Geut, Annemieke J.M. Rozemüller, Sandra Pilar Henriksen, Mathias Toft, Wilma D.J. van de Berg, Lasse Pihlstrøm

    Publicado 2021
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  9. 9
    Missense mutations in DYT-TOR1A dystonia

    Missense mutations in DYT-TOR1A dystonia por Zafar Iqbal, Jeanette Koht, Lasse Pihlstrøm, Sandra Pilar Henriksen, Chiara Cappelletti, Michael Bjørn Russel, Osmar Norberto de Souza, Inger Marie Skogseid, Mathias Toft

    Publicado 2019
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  10. 10
    Personality Changes after Deep Brain Stimulation in Parkinson’s Disease

    Personality Changes after Deep Brain Stimulation in Parkinson’s Disease por 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

    Publicado 2015
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  11. 11
    Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease

    Fine mapping and resequencing of the PARK16 locus in Parkinson’s disease por 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

    Publicado 2015
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  12. 12
    Prehospital screening of acute stroke with the National Institutes of Health Stroke Scale (ParaNASPP): a stepped-wedge, cluster-randomised controlled trial

    Prehospital screening of acute stroke with the National Institutes of Health Stroke Scale (ParaNASPP): a stepped-wedge, cluster-randomised controlled trial por 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

    Publicado 2023
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  13. 13
    Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease

    Supportive evidence for 11 loci from genome-wide association studies in Parkinson's disease por 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

    Publicado 2012
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  14. 14
    A comprehensive analysis of <i>SNCA</i>‐related genetic risk in sporadic parkinson disease

    A comprehensive analysis of <i>SNCA</i>‐related genetic risk in sporadic parkinson disease por 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

    Publicado 2018
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  15. 15
    Impulse control and correlation to dopamine agonist serum concentrations in people with Parkinson's disease

    Impulse control and correlation to dopamine agonist serum concentrations in people with Parkinson's disease por 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

    Publicado 2025
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  16. 16
    Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology

    Epigenome-wide association study of human frontal cortex identifies differential methylation in Lewy body pathology por 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

    Publicado 2022
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  17. 17
    Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations

    Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations por 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

    Publicado 2005
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  18. 18
    Fine mapping of the HLA locus in Parkinson’s disease in Europeans

    Fine mapping of the HLA locus in Parkinson’s disease in Europeans por 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

    Publicado 2021
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  19. 19
    Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease

    Lysosomal polygenic risk is associated with the severity of neuropathology in Lewy body disease por 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

    Publicado 2023
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  20. 20
    Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease

    Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease por 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

    Publicado 2010
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