Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Molecular pathogenesis of Parkinson disease: insights from genetic studiesGasser, ThomasExpert reviews in molecular medicine, 2009-07, Vol.11, p.e22, Article e22 [Periódico revisado por pares]Cambridge, UK: Cambridge University PressTexto completo disponível |
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2 |
Material Type: Artigo
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Mendelian forms of Parkinson's diseaseGasser, ThomasBiochimica et biophysica acta, 2009-07, Vol.1792 (7), p.587-596 [Periódico revisado por pares]Netherlands: Elsevier B.VTexto completo disponível |
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3 |
Material Type: Artigo
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Update on the genetics of Parkinson's diseaseGasser, ThomasMovement disorders, 2007, Vol.22 (S17), p.S343-S350 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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4 |
Material Type: Artigo
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role of inflammation in sporadic and familial Parkinson’s diseaseDeleidi, Michela ; Gasser, ThomasCellular and molecular life sciences : CMLS, 2013-11, Vol.70 (22), p.4259-4273 [Periódico revisado por pares]Basel: Springer-VerlagTexto completo disponível |
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5 |
Material Type: Artigo
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DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disordersKahle, Philipp J. ; Waak, Jens ; Gasser, ThomasFree radical biology & medicine, 2009-11, Vol.47 (10), p.1354-1361 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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6 |
Material Type: Artigo
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Milestones in PD geneticsGasser, Thomas ; Hardy, John ; Mizuno, YoshikuniMovement disorders, 2011-05, Vol.26 (6), p.1042-1048 [Periódico revisado por pares]Hoboken: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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7 |
Material Type: Artigo
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Reply to: “α‐Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism”Liu, Hui ; Koros, Christos ; Stefanis, Leonidas ; Gasser, ThomasMovement disorders, 2021-09, Vol.36 (9), p.2212-2213 [Periódico revisado por pares]Hoboken, USA: John Wiley & Sons, IncTexto completo disponível |
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8 |
Material Type: Artigo
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Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approachRothfuss, Oliver ; Gasser, Thomas ; Patenge, NadjaNucleic acids research, 2010-03, Vol.38 (4), p.e24-e24 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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9 |
Material Type: Artigo
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iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasisSchöndorf, David C ; Aureli, Massimo ; McAllister, Fiona E ; Hindley, Christopher J ; Mayer, Florian ; Schmid, Benjamin ; Sardi, S Pablo ; Valsecchi, Manuela ; Hoffmann, Susanna ; Schwarz, Lukas Kristoffer ; Hedrich, Ulrike ; Berg, Daniela ; Shihabuddin, Lamya S ; Hu, Jing ; Pruszak, Jan ; Gygi, Steven P ; Sonnino, Sandro ; Gasser, Thomas ; Deleidi, MichelaNature communications, 2014-06, Vol.5 (1), p.4028-4028, Article 4028 [Periódico revisado por pares]England: Nature Publishing GroupTexto completo disponível |
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10 |
Material Type: Artigo
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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron AccumulationHartig, Monika B. ; Iuso, Arcangela ; Haack, Tobias ; Kmiec, Tomasz ; Jurkiewicz, Elzbieta ; Heim, Katharina ; Roeber, Sigrun ; Tarabin, Victoria ; Dusi, Sabrina ; Krajewska-Walasek, Malgorzata ; Jozwiak, Sergiusz ; Hempel, Maja ; Winkelmann, Juliane ; Elstner, Matthias ; Oexle, Konrad ; Klopstock, Thomas ; Mueller-Felber, Wolfgang ; Gasser, Thomas ; Trenkwalder, Claudia ; Tiranti, Valeria ; Kretzschmar, Hans ; Schmitz, Gerd ; Strom, Tim M. ; Meitinger, Thomas ; Prokisch, HolgerAmerican journal of human genetics, 2011-10, Vol.89 (4), p.543-550 [Periódico revisado por pares]Cambridge, MA: Elsevier IncTexto completo disponível |