Altered resting state brain networks in Parkinson's disease von Göttlich, Martin, Münte, Thomas F, Heldmann, Marcus, Kasten, Meike, Hagenah, Johann, Krämer, Ulrike M

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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene von 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., Münchau, Alexander, Kostic, Vladimir, Simonyan, Kristina, Agzarian, Marc, Ozelius, Laurie J., Langeveld, Antonius P. M., Sue, Carolyn M., Tijssen, Marina A. J., Klein, Christine

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Evaluating the role of TMEM230 variants in Parkinson's disease von Baumann, Hauke, Wolff, Simone, Münchau, Alexander, Hagenah, Johann M, Lohmann, Katja, Klein, Christine

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Mutations in THAP1 ( DYT6 ) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study von Djarmati, Ana, PhD, Schneider, Susanne A, MD, Lohmann, Katja, PhD, Winkler, Susen, BSc, Pawlack, Heike, BSc, Hagenah, Johann, MD, Brüggemann, Norbert, MD, Zittel, Simone, MD, Fuchs, Tania, PhD, Raković, Aleksandar, MSc, Schmidt, Alexander, MD, Jabusch, Hans-Christian, MD, Wilcox, Robert, MD, Kostić, Vladimir S, MD, Siebner, Hartwig, MD, Altenmüller, Eckart, MD, Münchau, Alexander, MD, Ozelius, Laurie J, PhD, Klein, Christine, MD

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Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization von Saunders-Pullman, Rachel, Hagenah, Johann, Dhawan, Vijay, Stanley, Kaili, Pastores, Gregory, Sathe, Swati, Tagliati, Michele, Condefer, Kelly, Palmese, Christina, Brüggemann, Norbert, Klein, Christine, Roe, AM, Kornreich, Ruth, Ozelius, Laurie, Bressman, Susan

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Substantia nigra hyperechogenicity correlates with clinical status and number of Parkin mutated alleles von HAGENAH, Johann M, KÖNIG, Inke R, BECKER, Björn, HILKER, Rüdiger, KASTEN, Meike, HEDRICH, Katja, PRAMSTALLER, Peter P, KLEIN, Christine, SEIDEL, Günter

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Impaired sense of smell and color discrimination in monogenic and idiopathic Parkinson's disease von Kertelge, Lena, Brüggemann, Norbert, Schmidt, Alexander, Tadic, Vera, Wisse, Claudia, Dankert, Sylwia, Drude, Laura, van der Vegt, Joyce, Siebner, Hartwig, Pawlack, Heike, Pramstaller, Peter P., Behrens, Maria Isabel, Ramirez, Alfredo, Reichel, Dirk, Buhmann, Carsten, Hagenah, Johann, Klein, Christine, Lohmann, Katja, Kasten, Meike

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Structural imaging in the presymptomatic stage of genetically determined parkinsonism von Reetz, Kathrin, Tadic, Vera, Kasten, Meike, Brüggemann, Norbert, Schmidt, Alexander, Hagenah, Johann, Pramstaller, Peter P, Ramirez, Alfredo, Behrens, Maria I, Siebner, Hartwig R, Klein, Christine, Binkofski, Ferdinand

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ATP13A2 variants in early-onset Parkinson's disease patients and controls von Djarmati, Ana, Hagenah, Johann, Reetz, Kathrin, Winkler, Susen, Behrens, Maria Isabel, Pawlack, Heike, Lohmann, Katja, Ramirez, Alfredo, Tadić, Vera, Brüggemann, Norbert, Berg, Daniela, Siebner, Hartwig R., Lang, Anthony E., Pramstaller, Peter P., Binkofski, Ferdinand, Kostić, Vladimir S., Volkmann, Jens, Gasser, Thomas, Klein, Christine

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Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease von Kasten, Meike, Kertelge, Lena, Tadic, Vera, Brüggemann, Norbert, Schmidt, Alexander, van der Vegt, Joyce, Siebner, Hartwig, Buhmann, Carsten, Lencer, Rebekka, Kumar, Kishore R., Lohmann, Katja, Hagenah, Johann, Klein, Christine

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Focal dystonia as a presenting sign of spinocerebellar ataxia 17 von Hagenah, Johann M., Zühlke, Christine, Hellenbroich, Yorck, Heide, Wolfgang, Klein, Christine

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Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease von Facheris, Maurizio F., Hicks, Andrew A., Minelli, Cosetta, Hagenah, Johann M., Kostic, Vladimir, Campbell, Susan, Hayward, Caroline, Volpato, Claudia B., Pattaro, Cristian, Vitart, Veronique, Wright, Alan, Campbell, Harry, Klein, Christine, Pramstaller, Peter P.

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The bioenergetic status relates to dopamine neuron loss in familial PD with PINK1 mutations von Hilker, Rüediger, Pilatus, Ulrich, Eggers, Carsten, Hagenah, Johann, Roggendorf, Julia, Baudrexel, Simon, Klein, Johannes C, Neumaier, Bernd, Fink, Gereon R, Steinmetz, Helmuth, Klein, Christine, Hattingen, Elke

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Clinical neuroimaging and electrophysiological assessment of three DYT6 dystonia families von Zittel, Simone, Moll, Christian K.E., Brüggemann, Norbert, Tadic, Vera, Hamel, Wolfgang, Kasten, Meike, Lohmann, Katja, Lohnau, Thora, Winkler, Susen, Gerloff, Christian, Schönweiler, Rainer, Hagenah, Johann, Klein, Christine, Münchau, Alexander, Schneider, Susanne A.

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Phosphatase and Tensin Homolog (PTEN)-induced Putative Kinase 1 (PINK1)-dependent Ubiquitination of Endogenous Parkin Attenuates Mitophagy von Rakovic, Aleksandar, Shurkewitsch, Katharina, Seibler, Philip, Grünewald, Anne, Zanon, Alessandra, Hagenah, Johann, Krainc, Dimitri, Klein, Christine

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Phosphatase and tensin homolog (PTEN)-induced putative kinase 1 (PINK1)-dependent ubiquitination of endogenous Parkin attenuates mitophagy: study in human primary fibroblasts and i... von Rakovic, Aleksandar, Shurkewitsch, Katharina, Seibler, Philip, Grünewald, Anne, Zanon, Alessandra, Hagenah, Johann, Krainc, Dimitri, Klein, Christine

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Phenotypic spectrum of musician's dystonia: A task-specific disorder? von Schmidt, Alexander, Jabusch, Hans-Christian, Altenmüller, Eckart, Enders, Leonie, Saunders-Pullman, Rachel, Bressman, Susan B., Münchau, Alexander, Klein, Christine, Hagenah, Johann

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Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers von Brüggemann, Norbert, Mitterer, Manfred, Lanthaler, Andrea J, Djarmati, Ana, Hagenah, Johann, Wiegers, Karin, Winkler, Susen, Pawlack, Heike, Lohnau, Thora, Pramstaller, Peter P, Klein, Christine, Lohmann, Katja

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Age‐ and sex‐related heterogeneity in prodromal Parkinson's disease von 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

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Repeat length in spinocerebellar ataxia type 4 (SCA4) predicts age at onset and disease severity von Dalski, Andreas, Pauly, Martje G., Hanssen, Henrike, Hagenah, Johann, Hellenbroich, Yorck, Schmidt, Christian, Strohschehn, Jassemien, Spielmann, Malte, Zühlke, Christine, Brüggemann, Norbert

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