Browsing by Author Kasten, Meike

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Showing results 1 to 6 of 6
Issue DateTitleAuthor(s)Citation
2012Depression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's diseaseKumar, Kishore; Bruggemann, Norbert; Buhmann, Carsten; Hagenah, Johann; Kasten, Meike; Kertelge, Lena; Klein, Christine; Lencer, Rebekka; Lohmann, Katja; Schmidt, Alexander; Siebner, Hartwig; Tadic, Vera; Van der Vegt, Joyce; Northern Clinical School: Kolling InstituteDepression and quality of life in monogenic compared to idiopathic, early-onset Parkinson's disease, Movement Disorders, vol.27, 6, 2012,pp 754-759
2012Frequency of the D620N mutation in VPS35 in Parkinson diseaseKumar, Kishore Raj; Sue, Carolyn; et al, Various; Heldmann, Marcus; Kasten, Meike; Kostic, Vladimir S; Ramirez, Alfredo; Segura-Aguilar, Juan; Simon, David K; Svetel, Marina; Tunc, Sinem; Vieregge, Peter; Weissbach, Anne; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFrequency of the D620N mutation in VPS35 in Parkinson disease, JAMA Neurology, vol.69, 10, 2012,pp 1360-1364
2012Frequency of the D620N mutation in VPS35 in Parkinson diseaseKumar, Kishore Raj; Sue, Carolyn; et al, Various; Heldmann, Marcus; Kasten, Meike; Kostic, Vladimir S; Ramirez, Alfredo; Segura-Aguilar, Juan; Simon, David K; Svetel, Marina; Tunc, Sinem; Vieregge, Peter; Weissbach, Anne; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineFrequency of the D620N mutation in VPS35 in Parkinson disease, JAMA Neurology, vol.69, 10, 2012,pp 1360-1364
2010Mutant Parkin Impairs Mitochondrial Function and Morphology in Human FibroblastsGrunewald, Anne; Sue, Carolyn; Vandebona, Himesha; Hemmelmann, Claudia; Kasten, Meike; Klein, Christine; Lohmann - Hedrich, K.; Orolicki, Slobodanka; Pramstaller, Peter P; Rakovic, Aleksandar; Ramirez, Alfredo; Schapira, Anthony H V; Voges, Lisa; Northern Clinical School: Kolling Institute; Northern Clinical School: Medicine; Northern Clinical School: Kolling InstituteMutant Parkin Impairs Mitochondrial Function and Morphology in Human Fibroblasts, PLoS One, vol.5, 9,pp e12962-1-e12962-6
2014Mutations in GNAL: A Novel Cause of Craniocervical DystoniaKumar, Kishore Raj; Sue, Carolyn; Bruggemann, Norbert; et al, Various; Ferbert, Andreas; Hagenah, Johann; Kasten, Meike; Lohmann, Katja; Lohnau, Thora; Masuho, Ikuo; Miyamoto, Ryosuke; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineMutations in GNAL: A Novel Cause of Craniocervical Dystonia, JAMA Neurology, vol.71, 4, 2014,pp 490-494
2013Whispering Dysphonia (DYT4 dystonia) Is Caused by a Mutation in the TUBB4 GeneKumar, Kishore; Park, Jin-Sung; Sue, Carolyn; Arns, Bjorn; Bruggemann, Norbert; Groen, Justus; Kasten, Meike; Lohmann, Katja; Lohnau, Thora; Rakovic, Aleksandar; Ramirez, Alfredo; Wilcox, Robert; Winkler, Susen; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineWhispering Dysphonia (DYT4 dystonia) Is Caused by a Mutation in the TUBB4 Gene, Annals of Neurology, vol.73, 4, 2013,pp 537-545