Browsing by Author Kumar, Kishore

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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
2013Targeted next generation sequencing in SPAST-negative hereditary spastic paraplegiaBlair, Nicholas; Kumar, Kishore; Liang, Christina; Ng, Karl; Sue, Carolyn; Vandebona, Himesha; Gölnitz, Uta; Grünewald, A.; Klein, Christine; Rolfs, Arndt; Saviouk, Viatcheslav; Sharpe, David; School of Public Health: Public Health; Northern Clinical School: Kolling Institute; Northern Clinical School: Kolling Institute; Central Clinical School: Medicine; Northern Clinical School: Medicine; Northern Clinical School: Kolling InstituteTargeted next generation sequencing in SPAST-negative hereditary spastic paraplegia, Journal of Neurology, vol.260, 10, 2013,pp 2516-2522
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