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Indian Journal of Pediatrics|May 22, 2002
Reflex sympathetic dystrophy in childhoodHasan Tekgül, Guil Serdaroglu, Meltem Uyar, et al.Journal of Child Neurology|March 27, 2002
Coagulation abnormalities and acquired von Willebrand's disease type 1 in children receiving valproic acidGül Serdaroglu, Sarenur Tütüncüoglu, Kaan Kavakli, et al.Seizure|February 15, 2016
The efficacy, tolerability and safety of levetiracetam therapy in a pediatric populationHasan Tekgül, Pinar Gencpinar, Dilek Çavuşoğlu, et al.The Turkish Journal of Pediatrics|May 23, 2013
Changing views of cerebral palsy over 35 years: the experience of a centerAyşe Tosun, Sarenur Gökben, Gül Serdaroğlu, 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|January 3, 2014
Electrophysiologic assessment of spasticity in children using H-reflexHasan Tekgül, Muzaffer Polat, Ayşe Tosun, 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.The Turkish Journal of Pediatrics|January 29, 2020
The case of pyridoxine dependent epilepsy misdiagnosed as non-ketotic hyperglycinemiaHande Gazeteci-Tekin, Melis Demir, Gül Aktan, et al.Seizure|October 5, 2013
The effect of antiepileptic drugs on thyroid function in childrenUnsal Yılmaz, Tuba Sevim Yılmaz, Gülçin Akıncı, et al.The Turkish Journal of Pediatrics|May 8, 2007
Miller Fisher syndrome: a case with pattern of pure sensory polyneuropathy concomitant with anti-GQ1B antibodyGülçin Akinci, Muzaffer Polat, Ayşe Tosun, et al.Pageof 5