Works matching AU Kasten, Meike

Results: 77
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    Mutations in GNAL.

    Published in:
    JAMA Neurology, 2014, v. 71, n. 4, p. 490, doi. 10.1001/jamaneurol.2013.4677
    By:
    • Kumar, Kishore R.;
    • Lohmann, Katja;
    • Masuho, Ikuo;
    • Miyamoto, Ryosuke;
    • Ferbert, Andreas;
    • Lohnau, Thora;
    • Kasten, Meike;
    • Hagenah, Johann;
    • Brüggemann, Norbert;
    • Graf, Julia;
    • Münchau, Alexander;
    • Kostic, Vladimir S.;
    • Sue, Carolyn M.;
    • Domingo, Aloysius R.;
    • Rosales, Raymond L.;
    • Lee, Lilian V.;
    • Freimann, Karen;
    • Westenberger, Ana;
    • Mukai, Youhei;
    • Kawarai, Toshitaka
    Publication type:
    Article
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    Prodromal Markers in Parkinson's Disease: Limitations in Longitudinal Studies and Lessons Learned.

    Published in:
    Frontiers in Aging Neuroscience, 2016, p. 1, doi. 10.3389/fnagi.2016.00147
    By:
    • Heinzel, Sebastian;
    • Roeben, Benjamin;
    • Ben-Shlomo, Yoav;
    • Lerche, Stefanie;
    • Alves, Guido;
    • Barone, Paolo;
    • Behnke, Stefanie;
    • Berendse, Henk W.;
    • Bloem, Bastiaan R.;
    • Burn, David;
    • Dodel, Richard;
    • Grosset, Donald G.;
    • Hu, Michele;
    • Kasten, Meike;
    • Krüger, Rejko;
    • Moccia, Marcello;
    • Mollenhauer, Brit;
    • Oertel, Wolfgang;
    • Suenkel, Ulrike;
    • Walter, Uwe
    Publication type:
    Article
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    Aiming for Study Comparability in Parkinson's Disease: Proposal for a Modular Set of Biomarker Assessments to be Used in Longitudinal Studies.

    Published in:
    Frontiers in Aging Neuroscience, 2016, p. 1, doi. 10.3389/fnagi.2016.00121
    By:
    • Lerche, Stefanie;
    • Heinzel, Sebastian;
    • Alves, Guido W.;
    • Barone, Paolo;
    • Behnke, Stefanie;
    • Ben-Shlomo, Yoav;
    • Berendse, Henk;
    • Bloem, Bastiaan R.;
    • Burn, David;
    • Dodel, Richard;
    • Grosset, Donald G.;
    • Hipp, Geraldine;
    • Hu, Michele T.;
    • Kasten, Meike;
    • Krüger, Rejko;
    • Liepelt-Scarfone, Inga;
    • Maetzler, Walter;
    • Moccia, Marcello;
    • Mollenhauer, Brit;
    • Oertel, Wolfgang
    Publication type:
    Article
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    Using global team science to identify genetic parkinson's disease worldwide.

    Published in:
    2019
    By:
    • Vollstedt, Eva‐Juliane;
    • Kasten, Meike;
    • Klein, Christine;
    • Aasly, Jan;
    • Adler, Charles;
    • Ahmad‐Annuar, Azlina;
    • Albanese, Alberto;
    • Alcalay, Roy N.;
    • Al‐Mubarak, Bashayer;
    • Alvarez, Victoria;
    • Andree‐Muñoz, Brennie;
    • Annesi, Grazia;
    • Appel‐Cresswell, Silke;
    • Arkadir, David;
    • Armasu, Sebastian;
    • Barber, Thomas R.;
    • Bardien, Soraya;
    • Barkhuizen, Melinda;
    • Barrett, Matthew J.;
    • Başak, A. Nazlı
    Publication type:
    Editorial
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    Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.

    Published in:
    Annals of Neurology, 2013, v. 73, n. 4, p. 537, doi. 10.1002/ana.23829
    By:
    • Lohmann, Katja;
    • Wilcox, Robert A.;
    • Winkler, Susen;
    • Ramirez, Alfredo;
    • Rakovic, Aleksandar;
    • Park, Jin ‐ Sung;
    • Arns, Björn;
    • Lohnau, Thora;
    • Groen, Justus;
    • Kasten, Meike;
    • Brüggemann, Norbert;
    • Hagenah, Johann;
    • Schmidt, Alexander;
    • Kaiser, Frank J.;
    • Kumar, Kishore R.;
    • Zschiedrich, Katja;
    • Alvarez ‐ Fischer, Daniel;
    • Altenmüller, Eckart;
    • Ferbert, Andreas;
    • Lang, Anthony E.
    Publication type:
    Article
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    Solvent exposures and parkinson disease risk in twins.

    Published in:
    Annals of Neurology, 2012, v. 71, n. 6, p. 776, doi. 10.1002/ana.22629
    By:
    • Goldman, Samuel M.;
    • Quinlan, Patricia J.;
    • Ross, G. Webster;
    • Marras, Connie;
    • Meng, Cheryl;
    • Bhudhikanok, Grace S.;
    • Comyns, Kathleen;
    • Korell, Monica;
    • Chade, Anabel R.;
    • Kasten, Meike;
    • Priestley, Benjamin;
    • Chou, Kelvin L.;
    • Fernandez, Hubert H.;
    • Cambi, Franca;
    • Langston, J. William;
    • Tanner, Caroline M.
    Publication type:
    Article
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    Rotenone, Paraquat, and Parkinson's Disease.

    Published in:
    Environmental Health Perspectives, 2011, v. 119, n. 6, p. 866, doi. 10.1289/ehp.1002839
    By:
    • Tanner, Caroline M.;
    • Kamel, Freya;
    • Ross, G. Webster;
    • Hoppin, Jane A.;
    • Goldman, Samuel M.;
    • Korell, Monica;
    • Marras, Connie;
    • Bhudhikanok, Grace S.;
    • Kasten, Meike;
    • Chade, Anabel R.;
    • Comyns, Kathleen;
    • Richards, Marie Barber;
    • Meng, Cheryl;
    • Priestley, Benjamin;
    • Fernandez, Hubert H.;
    • Cambi, Franca;
    • Umbach, David M.;
    • Blair, Aaron;
    • Sandler, Dale P.;
    • Langston, J. William
    Publication type:
    Article
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    Large‐Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.

    Published in:
    Movement Disorders, 2024, v. 39, n. 3, p. 526, doi. 10.1002/mds.29693
    By:
    • Thomsen, Mirja;
    • Marth, Katrin;
    • Loens, Sebastian;
    • Everding, Judith;
    • Junker, Johanna;
    • Borngräber, Friederike;
    • Ott, Fabian;
    • Jesús, Silvia;
    • Gelderblom, Mathias;
    • Odorfer, Thorsten;
    • Kuhlenbäumer, Gregor;
    • Kim, Han‐Joon;
    • Schaeffer, Eva;
    • Becktepe, Jos;
    • Kasten, Meike;
    • Brüggemann, Norbert;
    • Pfister, Robert;
    • Kollewe, Katja;
    • Krauss, Joachim K.;
    • Lohmann, Ebba
    Publication type:
    Article
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    Embracing Monogenic Parkinson's Disease: The MJFF Global Genetic PD Cohort.

    Published in:
    Movement Disorders, 2023, v. 38, n. 2, p. 286, doi. 10.1002/mds.29288
    By:
    • Vollstedt, Eva‐Juliane;
    • Schaake, Susen;
    • Lohmann, Katja;
    • Padmanabhan, Shalini;
    • Brice, Alexis;
    • Lesage, Suzanne;
    • Tesson, Christelle;
    • Vidailhet, Marie;
    • Wurster, Isabel;
    • Hentati, Faycel;
    • Mirelman, Anat;
    • Giladi, Nir;
    • Marder, Karen;
    • Waters, Cheryl;
    • Fahn, Stanley;
    • Kasten, Meike;
    • Brüggemann, Norbert;
    • Borsche, Max;
    • Foroud, Tatiana;
    • Tolosa, Eduardo
    Publication type:
    Article
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    Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review.

    Published in:
    Movement Disorders, 2021, v. 36, n. 5, p. 1086, doi. 10.1002/mds.28485
    By:
    • Lange, Lara M.;
    • Junker, Johanna;
    • Loens, Sebastian;
    • Baumann, Hauke;
    • Olschewski, Luisa;
    • Schaake, Susen;
    • Madoev, Harutyun;
    • Petkovic, Sonja;
    • Kuhnke, Neele;
    • Kasten, Meike;
    • Westenberger, Ana;
    • Domingo, Aloysius;
    • Marras, Connie;
    • König, Inke R.;
    • Camargos, Sarah;
    • Ozelius, Laurie J.;
    • Klein, Christine;
    • Lohmann, Katja
    Publication type:
    Article
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    The Rostock International Parkinson's Disease (ROPAD) Study: Protocol and Initial Findings.

    Published in:
    Movement Disorders, 2021, v. 36, n. 4, p. 1005, doi. 10.1002/mds.28416
    By:
    • Skrahina, Volha;
    • Gaber, Hanaa;
    • Vollstedt, Eva‐Juliane;
    • Förster, Toni M.;
    • Usnich, Tatiana;
    • Curado, Filipa;
    • Brüggemann, Norbert;
    • Paul, Jefri;
    • Bogdanovic, Xenia;
    • Zülbahar, Selen;
    • Olmedillas, Maria;
    • Skobalj, Snezana;
    • Ameziane, Najim;
    • Bauer, Peter;
    • Csoti, Ilona;
    • Koleva‐Alazeh, Natalia;
    • Grittner, Ulrike;
    • Westenberger, Ana;
    • Kasten, Meike;
    • Beetz, Christian
    Publication type:
    Article
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    Rare Variants in Specific Lysosomal Genes Are Associated With Parkinson's Disease.

    Published in:
    2020
    By:
    • Hopfner, Franziska;
    • Mueller, Stefanie H.;
    • Szymczak, Silke;
    • Junge, Olaf;
    • Tittmann, Lukas;
    • May, Sandra;
    • Lohmann, Katja;
    • Grallert, Harald;
    • Lieb, Wolfgang;
    • Strauch, Konstantin;
    • Müller‐Nurasyid, Martina;
    • Berger, Klaus;
    • Schormair, Barbara;
    • Winkelmann, Juliane;
    • Mollenhauer, Brit;
    • Trenkwalder, Claudia;
    • Maetzler, Walter;
    • Berg, Daniela;
    • Kasten, Meike;
    • Klein, Christine
    Publication type:
    journal article
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    Utility and implications of exome sequencing in early-onset Parkinson's disease.

    Published in:
    2019
    By:
    • Trinh, Joanne;
    • Lohmann, Katja;
    • Baumann, Hauke;
    • Balck, Alexander;
    • Borsche, Max;
    • Brüggemann, Norbert;
    • Dure, Leon;
    • Dean, Marissa;
    • Volkmann, Jens;
    • Tunc, Sinem;
    • Prasuhn, Jannik;
    • Pawlack, Heike;
    • Imhoff, Sophie;
    • Lill, Christina M.;
    • Kasten, Meike;
    • Bauer, Peter;
    • Rolfs, Arndt;
    • Klein, Christine;
    • International Parkinson's Disease Genomics Consortium (IPDGC)
    Publication type:
    journal article
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    Age- and sex-related heterogeneity in prodromal Parkinson's disease.

    Published in:
    2018
    By:
    • Heinzel, Sebastian;
    • Kasten, Meike;
    • Behnke, Stefanie;
    • Vollstedt, Eva‐Juliane;
    • Klein, Christine;
    • Hagenah, Johann;
    • Pausch, Christoph;
    • Heilmann, Robert;
    • Brockmann, Kathrin;
    • Suenkel, Ulrike;
    • Yilmaz, Rezzak;
    • Liepelt‐Scarfone, Inga;
    • Walter, Uwe;
    • Berg, Daniela;
    • Vollstedt, Eva-Juliane;
    • Liepelt-Scarfone, Inga
    Publication type:
    Letter
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    Clustering of motor and nonmotor traits in leucine-rich repeat kinase 2 G2019S Parkinson's disease nonparkinsonian relatives: A multicenter family study.

    Published in:
    2018
    By:
    • Mestre, Tiago A.;
    • Pont‐Sunyer, Claustre;
    • Kausar, Farah;
    • Visanji, Naomi P.;
    • Ghate, Taneera;
    • Connolly, Barbara S.;
    • Gasca‐Salas, Carmen;
    • Kern, Drew S.;
    • Jain, Jennifer;
    • Slow, Elizabeth J.;
    • Faust‐Socher, Achinoam;
    • Kasten, Meike;
    • Wadia, Pettarusp M.;
    • Zadikoff, Cindy;
    • Kumar, Prakash;
    • de Bie, Ronald M.;
    • Thomsen, Teri;
    • Lang, Anthony E.;
    • Schüle, Birgitt;
    • Klein, Christine
    Publication type:
    journal article
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    A population-based study on combined markers for early Parkinson's disease.

    Published in:
    Movement Disorders, 2015, v. 30, n. 4, p. 531, doi. 10.1002/mds.26100
    By:
    • Tunc, Sinem;
    • Graf, Julia;
    • Tadic, Vera;
    • Brüggemann, Norbert;
    • Schmidt, Alexander;
    • Al‐Khaled, Mohamed;
    • Wolff, Simone;
    • Vollstedt, Eva‐Juliane;
    • Lorwin, Anne;
    • Hampf, Jennie;
    • Piskol, Linda;
    • Klein, Christine;
    • Hagenah, Johann;
    • Kasten, Meike
    Publication type:
    Article
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    Assessment of Olfactory Function in MAPT-Associated Neurodegenerative Disease Reveals Odor-Identification Irreproducibility as a Non-Disease-Specific, General Characteristic of Olfactory Dysfunction.

    Published in:
    PLoS ONE, 2016, v. 11, n. 11, p. 1, doi. 10.1371/journal.pone.0165112
    By:
    • Markopoulou, Katerina;
    • Chase, Bruce A.;
    • Robowski, Piotr;
    • Strongosky, Audrey;
    • Narożańska, Ewa;
    • Sitek, Emilia J.;
    • Berdynski, Mariusz;
    • Barcikowska, Maria;
    • Baker, Matt C.;
    • Rademakers, Rosa;
    • Sławek, Jarosław;
    • Klein, Christine;
    • Hückelheim, Katja;
    • Kasten, Meike;
    • Wszolek, Zbigniew K.
    Publication type:
    Article
    40

    ApoE polymorphisms in narcolepsy.

    Published in:
    BMC Medical Genetics, 2001, v. 2, p. 1
    By:
    • Gencik, Martin;
    • Dahmen, Norbert;
    • Wieczorek, Stefan;
    • Kasten, Meike;
    • Gencikova, Alexandra;
    • Epplen, Jorg T.
    Publication type:
    Article
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    Recessive dystonia-ataxia syndrome in a Turkish family caused by a COX20 ( FAM36A) mutation.

    Published in:
    Journal of Neurology, 2014, v. 261, n. 1, p. 207, doi. 10.1007/s00415-013-7177-7
    By:
    • Doss, Sarah;
    • Lohmann, Katja;
    • Seibler, Philip;
    • Arns, Björn;
    • Klopstock, Thomas;
    • Zühlke, Christine;
    • Freimann, Karen;
    • Winkler, Susen;
    • Lohnau, Thora;
    • Drungowski, Mario;
    • Nürnberg, Peter;
    • Wiegers, Karin;
    • Lohmann, Ebba;
    • Naz, Sadaf;
    • Kasten, Meike;
    • Bohner, Georg;
    • Ramirez, Alfredo;
    • Endres, Matthias;
    • Klein, Christine
    Publication type:
    Article
    45

    MDR1 variants and risk of Parkinson disease.

    Published in:
    Journal of Neurology, 2009, v. 256, n. 1, p. 115, doi. 10.1007/s00415-009-0089-x
    By:
    • Zschiedrich, Katja;
    • König, Inke R.;
    • Brüggemann, Norbert;
    • Kock, Norman;
    • Kasten, Meike;
    • Leenders, Klaus L.;
    • Kostić, Vladimir;
    • Vieregge, Peter;
    • Ziegler, Andreas;
    • Klein, Christine;
    • Lohmann, Katja
    Publication type:
    Article
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    Exome sequencing in a family with restless legs syndrome.

    Published in:
    Movement Disorders, 2012, v. 27, n. 13, p. 1686, doi. 10.1002/mds.25191
    By:
    • Weissbach, Anne;
    • Siegesmund, Katharina;
    • Brüggemann, Norbert;
    • Schmidt, Alexander;
    • Kasten, Meike;
    • Pichler, Irene;
    • Muhle, Hiltrud;
    • Lohmann, Ebba;
    • Lohnau, Thora;
    • Schwinger, Eberhard;
    • Hagenah, Johann;
    • Stephani, Ulrich;
    • Pramstaller, Peter P.;
    • Klein, Christine;
    • Lohmann, Katja
    Publication type:
    Article