Browsing by Author Ramirez, Alfredo

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Showing results 1 to 5 of 5
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
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
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