Person's Publications

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

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,

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

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

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,

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,