Edibe Pempegül Yıldız

7PUBLICATIONS
20CO-AUTHORS
Disease surveillanceCondensed matter imagingInfant and child healthNeurology and neuromuscular diseasesOrganic geochemistry
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Publications (7)

|Jul 27, 2026
Electroclinical phenotypes-genetic characterization of developmental and epileptic encephalopathies in a cohort study.

|Apr 27, 2026
Vanishing White Matter with Cerebral Salt Wasting: A Case Report.

|Feb 18, 2026
The Impact of Trunk Control and Balance on Functional Skills in Ambulatory Children With Duchenne Muscular Dystrophy.

Gülsena Utku Umut, Zeynep Hoşbay, Edibe Pempegül Yıldız

|Jul 21, 2025
The long-term efficacy of nusinersen on respiratory functions in children with symptomatic spinal muscular atrophy type 1.

Mehmet Akif Kiliç, Fulya Kürekçi, Osman Kipoğlu

|Sep 12, 2022
Genetic and clinical evaluation of congenital myasthenic syndromes with long-term follow-up: experience of a tertiary center in Turkey.

Edibe Pembegul Yildiz, Mehmet Akif Kilic, Emek Uyur Yalcin

|Oct 04, 2021
Late onset Aicardi-Goutières syndrome case report: a rare white matter disease mimicking as pseudo-enzyme deficiency.

Melis Ulak Ozkan, Selahattin Katar, Edibe Pembegul Yildiz

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Frequent Collaborators

3 joint publications

Fulya Kürekçi

3 joint publications

Hülya Maraş Genç

2 joint publications

Mehmet Akif Kiliç

2 joint publications

Ayca Dilruba Aslanger