Lehrstuhl für Neuropathologie

Same same but different: A Web-based deep learning application revealed classifying features for the histopathologic distinction of cortical malformations (2020) Kubach J, Muhlebner-Fahrngruber A, Soylemezoglu F, Miyata H, Niehusmann P, Honavar M, Rogerio F, et al. Journal article The coding and non-coding transcriptional landscape of subependymal giant cell astrocytomas (2020) Bongaarts A, Van Scheppingen J, Korotkov A, Mijnsbergen C, Anink JJ, Jansen FE, Spliet WG, et al. Journal article The MyoRobot technology discloses a premature biomechanical decay of skeletal muscle fiber bundles derived from R349P desminopathy mice (2019) Haug M, Meyer C, Reischl B, Prölß G, Vetter K, Iberl J, Nübler S, et al. Journal article Camptocormia as the presenting symptom in sporadic late onset nemaline myopathy: A case report (2019) Türk M, Nagel AM, Roemer F, Schlötzer-Schrehardt U, Thiel C, Winterholler M, Schröder R Journal article Predictive Value Of Preoperative Magnetoencephalography (MEG) For Seizure Outcome In Surgery Of Long Term Epilepsy Associated Tumors (2019) Roessler K, Heynold E, Kasper B, Coras R, Blumcke I, Hamer H, Buchfelder M, Rampp S Conference contribution 7 Tesla Hippocampal Subfield Analyses In Patients With Medically Refractory Epilepsy And Hippocampal Sclerosis (2019) Roessler K, Roesch J, Coras R, Blümcke I, Hamer H, Buchfelder M, Rampp S, Mennecke A Conference contribution Reoperation In Failed Epilepsy Surgery Using MEG, Neuronavigation And Intraoperative Mr Imaging (2019) Roessler K, Heynold E, Kasper B, Rampp S, Coras R, Blumcke I, Buchfelder M Conference contribution A Safe and Effective Magnetic Labeling Protocol for MRI-Based Tracking of Human Adult Neural Stem Cells (2019) Stroh A, Kressel J, Coras R, Dreyer AY, Fröhlich W, Förschler A, Lobsien D, et al. Journal article Disruptive recessive TTN missense mutations cause a wide range of clinico-pathological features (2019) Rees M, Fukuzawa A, Nikoopour R, Kho A, Qi J, Fernandez-Garcia M, Wraige E, et al. Conference contribution Sarcomeric pathology induced by homozygous expression of the myofibrillar myopathy - associated p.W2711X filamin C mutant (2019) Schuld J, Orfanos Z, Chevessier F, Unger A, Kirfel G, Van Der Ven P, Linke W, et al. Conference contribution