Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy and PEHO-like syndrome: Report of two cases

Por Yiş, Uluç, Hız, Semra, Anal, Özden, Dirik, Eray
Publicado em 2011

A novel mutation in the glycine decarboxylase gene in patient with non-ketotic hyperglycinemia

Por Kose, Engin, Yis, Uluc, Hiz, Semra, Arslan, Nur
Publicado no Neurosciences (Riyadh) (2017)

Parieto-occipital encephalomalacia in children; clinical and electrophysiological features of twenty-seven cases

Por Karaoğlu, Pakize, Polat, Ayşe İpek, Yiş, Uluç, Hız, Semra
Publicado no J Pediatr Neurosci (2015)