A classical phenotype of Duchenne muscular dystrophy in a girl with X; autosome translocation

por Uzunhan, Tuğce Aksu, Altunoğlu, Umut, Yıldız, Edibe Pembegul, Aydınlı, Nur
Publicado 2014

Triosephosphate Isomerase Deficiency: E105D Mutation in Unrelated Patients and Review of the Literature

por Selamioğlu, Arzu, Karaca, Meryem, Balcı, Mehmet Cihan, Körbeyli, Hüseyin Kutay, Durmuş, Aslı, Yıldız, Edibe Pembegül, Karaman, Serap, Gökçay, Gülden Fatma
Publicado 2023

Pediatric LGI1 and CASPR2 autoimmunity associated with COVID 19: Morvan syndrome

por Kilic, Mehmet Akif, Yoruk Yildirim, Zeynep Nagihan, Oner, Adil, Yesil, Elif, Aksu, Bagdagül, Yildiz, Edibe Pembegul, Yilmaz, Alev, Caliskan, Meliha Mine
Publicado 2021