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1
Molecular pathogenesis of Parkinson disease: insights from genetic studies
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Artigo
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Molecular pathogenesis of Parkinson disease: insights from genetic studies

Gasser, Thomas

Expert reviews in molecular medicine, 2009-07, Vol.11, p.e22, Article e22 [Periódico revisado por pares]

Cambridge, UK: Cambridge University Press

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2
Mendelian forms of Parkinson's disease
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Artigo
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Mendelian forms of Parkinson's disease

Gasser, Thomas

Biochimica et biophysica acta, 2009-07, Vol.1792 (7), p.587-596 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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3
Update on the genetics of Parkinson's disease
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Artigo
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Update on the genetics of Parkinson's disease

Gasser, Thomas

Movement disorders, 2007, Vol.22 (S17), p.S343-S350 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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4
role of inflammation in sporadic and familial Parkinson’s disease
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Artigo
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role of inflammation in sporadic and familial Parkinson’s disease

Deleidi, Michela ; Gasser, Thomas

Cellular and molecular life sciences : CMLS, 2013-11, Vol.70 (22), p.4259-4273 [Periódico revisado por pares]

Basel: Springer-Verlag

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5
DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disorders
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Artigo
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DJ-1 and prevention of oxidative stress in Parkinson's disease and other age-related disorders

Kahle, Philipp J. ; Waak, Jens ; Gasser, Thomas

Free radical biology & medicine, 2009-11, Vol.47 (10), p.1354-1361 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Milestones in PD genetics
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Artigo
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Milestones in PD genetics

Gasser, Thomas ; Hardy, John ; Mizuno, Yoshikuni

Movement disorders, 2011-05, Vol.26 (6), p.1042-1048 [Periódico revisado por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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7
Reply to: “α‐Synuclein (SNCA) A30G Mutation as a Cause of a Complex Phenotype Without Parkinsonism”
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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, Thomas

Movement disorders, 2021-09, Vol.36 (9), p.2212-2213 [Periódico revisado por pares]

Hoboken, USA: John Wiley & Sons, Inc

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8
Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approach
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Artigo
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Analysis of differential DNA damage in the mitochondrial genome employing a semi-long run real-time PCR approach

Rothfuss, Oliver ; Gasser, Thomas ; Patenge, Nadja

Nucleic acids research, 2010-03, Vol.38 (4), p.e24-e24 [Periódico revisado por pares]

England: Oxford University Press

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9
iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis
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Artigo
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iPSC-derived neurons from GBA1-associated Parkinson's disease patients show autophagic defects and impaired calcium homeostasis

Schöndorf, 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, Michela

Nature communications, 2014-06, Vol.5 (1), p.4028-4028, Article 4028 [Periódico revisado por pares]

England: Nature Publishing Group

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10
Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation
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Artigo
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Absence of an Orphan Mitochondrial Protein, C19orf12, Causes a Distinct Clinical Subtype of Neurodegeneration with Brain Iron Accumulation

Hartig, 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, Holger

American journal of human genetics, 2011-10, Vol.89 (4), p.543-550 [Periódico revisado por pares]

Cambridge, MA: Elsevier Inc

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