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World Neurosurgery|April 19, 2021
Awake Epilepsy Surgery in Patients with Focal Cortical DysplasiaKrasimir Minkin, Kaloyan Gabrovski, Petar Karazapryanov, et al.
Journal of Neurosurgery|January 22, 2026
Avascular stereoelectroencephalography planning: comparison between MRA and T1-weighted MRI with double contrastVelislav Pavlov, Petar Karazapryanov, Kaloyan Gabrovski, et al.
Clinical Neurology and Neurosurgery|July 25, 2016
Intraoperative fluorescein staining for benign brain tumorsKrasimir Minkin, Emanuil Naydenov, Kaloyan Gabrovski, et al.
Frontiers in Neurology|September 6, 2023
Development and results of the epilepsy surgery in Armenia: hope for a better futureBiayna Sukhudyan, Krasimir Minkin, Sevak Badalyan, et al.
Neuroscience Letters|March 15, 2011
One novel Dravet syndrome causing mutation and one recurrent MAE causing mutation in SCN1A geneIglika Yordanova, Tihomir Todorov, Petia Dimova, et al.
Epilepsy Research|January 29, 2013
15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in BulgariaAndrey Kirov, Petia Dimova, Albena Todorova, et al.
Mutation Research|April 25, 2012
Spontaneous recurrent mutations and a complex rearrangement in the MECP2 gene in the light of current models of mutagenesisTihomir Todorov, Albena Todorova, Cristina Motoescu, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 28, 2020
Low-grade epilepsy-associated tumour management with or without presurgical evaluation: a multicentre, retrospective, observational study of postsurgical epilepsy outcomeAleksandar J Ristić, Ioana Mindruta, Petia Dimova, et al.
The Turkish Journal of Pediatrics|October 27, 2020
SCN1A mutation spectrum in a cohort of Bulgarian patients with GEFS+ phenotypeValentina Peycheva, Nevyana Ivanova, Kunka Kamenarova, et al.
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