Browsing by Author Lohmann, Katja

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Showing results 1 to 7 of 7
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
2012Genetics of Parkinson disease and other movement disordersKumar, Kishore; Klein, Christine; Lohmann, Katja; Northern Clinical School: Kolling InstituteGenetics of Parkinson disease and other movement disorders, Current Opinion In Neurology, vol.25, 4, 2012,pp 466-474
2013Glucocerebrosidase mutations in a Serbian Parkinson's disease populationKumar, Kishore Raj; Sue, Carolyn; Alcalay, Roy N; Gobel, Anna; Grunewald, A; Klein, Christine; Kostic, Vladimir S; Krainc, Dimitri; Kresojevic, Nikola D; Lohmann, Katja; Mazzulli, Joseph R; Ramirez, Alfredo R; Rolfs, Arndt; Svetel, Marina; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineGlucocerebrosidase mutations in a Serbian Parkinson's disease population, European Journal of Neurology, vol.20, 2, 2013,pp 402-405
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
2017Screening study of TUBB4A in isolated dystoniaKumar, Kishore Raj; Bruggemann, Norbert; Chung, Sun Ju; Defazio, Giovanni; Domingo, Aloysius; Klein, Christine; Lohmann, Katja; Mir, Pablo; Ozelius, Laurie J.; Rakovic, Aleksandar; Schaake, Susen; Simonyan, Kristina; Vulinovic, Franca; Northern Clinical School: Kolling InstituteScreening study of TUBB4A in isolated dystonia, Parkinsonism and Related Disorders, vol.41, N/A, 2017,pp 118-120
2012Two Faces of the Same Coin: Benign Familial Infantile Seizures and Paroxysmal Kinesigenic Dyskinesia Caused by PRRT2 MutationsKumar, Kishore; Sue, Carolyn; Christen, Hans-Jurgen; Grunewald, A; Hagenah, Johann; Hartmann, Hans; Klein, Christine; Leben, Matthias; Lohmann, Katja; Munchau, Alexander; Redyk, Katharina; Schmidt, Alexander; Northern Clinical School: Kolling Institute; Northern Clinical School: MedicineTwo Faces of the Same Coin: Benign Familial Infantile Seizures and Paroxysmal Kinesigenic Dyskinesia Caused by PRRT2 Mutations, JAMA Neurology (formerly Archives of Neurology), vol.69, 5, 2012,pp 668-670
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