Istanbul University / İstanbul Üniversitesi

CLP1 founder mutation links tRNA splicing and maturation to cerebellar development and neurodegeneration (2014) Schaffer AE, Eggens VRC, Caglayan AO, Reuter M, Scott E, Coufal NG, Silhavy JL, et al. Journal article In response to commentary on cavernoma-related epilepsy: review and recommendations for management-report of the surgical task force of the ILAE commission on therapeutic strategies (2014) Rosenow F, Alonso-Vanegas MA, Baumgartner C, Blümcke I, Carreno M, Gizewski ER, Hamer H, et al. Journal article Building a network of ADPKD reference centres across Europe: the EuroCYST initiative (2014) Petzold K, Gansevoort RT, Ong ACM, Devuyst O, Rotar L, Eckardt KU, Koettgen A, et al. Journal article Human CLP1 mutations alter tRNA biogenesis, affecting both peripheral and central nervous system function (2014) Karaca E, Weitzer S, Pehlivan D, Shiraishi H, Gogakos T, Hanada T, Jhangiani SN, et al. Journal article Bone response to biomimetic implants delivering BMP-2 and VEGF: An immunohistochemical study (2013) Ramazanoglu M, Lutz R, Rusche P, Trabzon L, Kose GT, Prechtl C, Schlegel KA Journal article International consensus classification of hippocampal sclerosis in temporal lobe epilepsy: A Task Force report from the ILAE Commission on Diagnostic Methods (2013) Blümcke I, Thom M, Aronica E, Armstrong DD, Bartolomei F, Bernasconi A, Bernasconi N, et al. Journal article Cavernoma-related epilepsy: Review and recommendations for management - Report of the Surgical Task Force of the ILAE Commission on Therapeutic Strategies (2013) Rosenow F, Alonso-Vanegas MA, Baumgartner C, Blümcke I, Carreno M, Gizewski ER, Hamer H, et al. Journal article, Review article Good interobserver and intraobserver agreement in the evaluation of the new ILAE classification of focal cortical dysplasias (2012) Coras R, De Boer OJ, Armstrong D, Becker A, Jacques TS, Miyata H, Thom M, et al. Journal article, Review article Defining clinico-neuropathological subtypes of mesial temporal lobe epilepsy with hippocampal sclerosis (2012) Blümcke I, Coras R, Miyata H, Özkara C Journal article Four novel and two recurrent NHLRC1 (EPM2B) and EPM2A gene mutations leading to Lafora disease in six Turkish families (2012) Salar S, Yeni N, Gunduz A, Guler A, Gokcay A, Velioglu S, Gundogdu A, Caglayan SH Journal article