Browsing by Author Grunewald, A

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Issue DateTitleAuthor(s)Citation
2012ATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndromeSue, Carolyn; Arns, Bjorn; Grunewald, A; Klein, Christine; Munchau, Alexander; Rakovic, Aleksandar; Ramirez, Alfredo; Seibler, Philip; Northern Clinical School: MedicineATP13A2 mutations impair mitochondrial function in fibroblasts from patients with Kufor-Rakeb syndrome, Neurobiology of Aging, vol.33, 8, 2012,pp e1-e7
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
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