Autor/in Djarmati, Ana Hagenah, Johann 4 Brüggemann, Norbert 2 Kock, Norman 2 Reetz, Kathrin 2 Schmidt, Alexander 2 Steinlechner, Susanne 2 Boston, Heather 1 Buchmann, Inga 1 Bähre, Manfred 1 Büchel, Christian 1 Eckerle, Susanne 1 Fuchs, Tania 1 Gaser, Christian 1 Grünewald, Anne 1 Hedrich, Katja 1 Hilker, Rüdiger 1 Hiller, Anja 1 Kasten, Meike 1 Klein, Christine 1 Lasek, Kathrin 1 Lencer, Rebekka 1 Lohmann, Katja 1 Lohnau, Thora 1 Münchau, Alexander 1 Pawlack, Heike 1 Petersen, Dirk 1 Rakovi, Aleksandar 1 Schneider, Susanne A 1 Siebner, Hartwig R 1 Winkler, Susen 1 Zittel, Simone 1 van der Vegt, Joyce 1 alle zeigenListe einklappen
Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. Brüggemann, Norbert Hagenah, Johann Reetz, Kathrin Schmidt, Alexander Kasten, Meike Buchmann, Inga Eckerle, Susanne 2010 - Forschungsinformationssystem des UKE
Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study. Djarmati, Ana Schneider, Susanne A Lohmann, Katja Winkler, Susen Pawlack, Heike Hagenah, Johann Brüggemann, Norbert 2009 - Forschungsinformationssystem des UKE
Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers. Reetz, Kathrin Lencer, Rebekka Steinlechner, Susanne Gaser, Christian Hagenah, Johann Büchel, Christian Petersen, Dirk 2008 - Forschungsinformationssystem des UKE
Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit? Hedrich, Katja Hagenah, Johann Djarmati, Ana Hiller, Anja Lohnau, Thora Lasek, Kathrin Grünewald, Anne 2006 - Forschungsinformationssystem des UKE
