Showing results (1-10 of 22) with videos related to

Sort By:
Pageof 3
The Turkish Journal of Pediatrics|December 25, 2015
Turkish cases of early infantile epileptic encephalopathy: two novel mutations in the cyclin-dependent kinase-like 5 (CDKL5) geneSarenur Gökben, Gül Serdaroğlu, Sanem Yılmaz, et al.
Epilepsy & Behavior : E&B|May 7, 2011
Video/EEG recording of myoclonic absences in GLUT1 deficiency syndrome with a hot-spot R126C mutation in the SLC2A1 geneSarenur Gökben, Sanem Yılmaz, Joerg Klepper, et al.
The Turkish Journal of Pediatrics|April 8, 2020
Dropped head related lamin A/C associated congenital muscular dystrophy case; previously defined as emerydreifuss muscular dystrophyHande Tekin, Sanem Yılmaz, Hasan Tekgül, et al.
Case Reports in Medicine|May 1, 2014
A confusing coincidence: neonatal hypoglycemic seizures and hyperekplexiaNihat Demir, Murat Doğan, Sanem Yılmaz, et al.
Turk Pediatri Arsivi|October 18, 2019
A rare cause of brachial plexopathy: hereditary neuralgic amyotrophyHepsen Mine Serin, Sanem Yılmaz, Seda Kanmaz, et al.
Turkish Archives of Pediatrics|September 6, 2023
Adaptability of Pediatric Residents for the International League Against Epilepsy-2017 Seizure Classification with a Modular Education ProgramMuharrem İmanli, Erdem Şimşek, Afshin Dezhakam, et al.
The Turkish Journal of Pediatrics|July 3, 2023
Sleep problems in adolescents with epilepsy and their caregivers: associations with behavioural difficultiesİpek Dokurel Çetin, Birsen Şentürk, Sezen Köse, et al.
The Turkish Journal of Pediatrics|August 12, 2020
Neuropsychological outcome in cases with acute disseminated encephalomyelitisSeda Kanmaz, Sezen Köse, Cenk Eraslan, et al.
Pageof 3