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Inhaltsbereich

Medical NeuroScience Cluster Publications by
Bonelli-Nauer Silvia, Assoc.Prof.Priv.-Doz.Dr. :

2016 2014 2013 2012 2007 2006

2016 Original Articles

  • Hilger E, Zimprich F, Pataraia E, Aull-Watschinger S, Jung R, Baumgartner C, Bonelli S (2016) Psychoses in epilepsy: A comparison of postictal and interictal psychoses Epilepsy Behav, 60: 58-62

2014 Original Articles

  • Bonelli SB, Yogarajah M, Powell R, Thompson PJ, Samson R, Symms M, Koepp M, Duncan JS (2014) Verbal and Visual Memory Function in Temporal Lobe Epilepsy: Results of a Blocked Vs. Event-Related Analysis Epilepsia,

2013 Original Articles

  • Jung R, Aull-Watschinger S, Moser D, Czech T, Baumgartner C, Bonelli-Nauer S, Pataraia E (2013) Is reoperation an option for patients with temporal lobe epilepsy after failure of surgery? Seizure, 22 (7): 502-506
  • Bonelli S, Thompson P, Yogarajah M, Powell R, Samson R, McEvoy A, Symms M, Koepp M, Duncan J (2013) Memory reorganization following anterior temporal lobe resection: a longitudinal functional MRI study Brain, 136 (6): 1889-1900

2012 Original Articles

  • Bonelli S, Thompson P, Yogarajah M, Vollmar C, Powell R, Symms M, McEvoy A, Micallef C, Koepp M, Duncan J (2012) Imaging language networks before and after anterior temporal lobe resection: Results of a longitudinal fMRI study Epilepsia, 53 (4): 639-650

2007 Original Articles

  • Bonelli S, Lurger S, Zimprich F, Stogmann E, Assem-Hilger E, Baumgartner C (2007) Clinical Seizure Lateralization in Frontal Lobe Epilepsy Epilepsia, 48 (3): 517-523
  • Haubenberger D, Bonelli S, Hotzy C, Leitner P, Lichtner P, Samal D, Katzenschlager R, Djamshidian A, Brücke T, Steffelbauer M, Bancher C, Grossmann J, Ransmayr G, Strom TM, Meitinger T, Gasser T, Auff E, Zimprich A (2007) A novel LRRK2 mutation in an Austrian cohort of patients with Parkinson's disease Movement Disorders,

2006 Original Articles

  • Stogmann E, Lichtner P, Baumgartner C, Schmied M, Hotzy C, Asmus F, Leutmezer F, Bonelli S, Assem-Hilger E, Vass K, Hatala K, Strom TM, Meitinger T, Zimprich F, Zimprich A (2006) Mutations in the CLCN2 gene are a rare cause of idiopathic generalized epilepsy syndromes Neurogenetics,
  • Stogmann E, Lichtner P, Baumgartner C, Bonelli S, Assem-Hilger E, Leutmezer F, Schmied M, Hotzy C, Strom TM, Meitinger T, Zimprich F, Zimprich A (2006) Idiopathic generalized epilepsy phenotypes associated with different EFHC1 mutations Neurology,

 
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