Yazar "Öztürk, Gülten" için listeleme
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Acute flaccid myelitis outbreak through 2016-2018: A multicenter experience from Turkey
Ünver, Olcay; Türkdoğan, Dilşad; Güler, Serhat; Kipoğlu, Osman; Güngör, Mesut; Paketçi, Cem; Carman, Kürşat Bora; Öztürk, Gülten; Maraş Genç, Hülya; Özkan, Mehpare; Olgaç Dündar, Nihal; Işık, Uğur; Karatoprak, Elif; Kılıç, Betül; Özkale, Murat; Bayram, Erhan; Yarar, Coşkun; Sözen, Hatice Gülhan; Sager, Güneş; Sakarya Güneş, Ayfer; Kahraman Koytak, Pınar; Karadağ Saygı, Evrim; Ekinci, Gazanfer; Saltık, Sema; Çalışkan, Mine; Kara, Bülent; Yiş, Uluç; Aydınlı, Nur (Elsevier Science Ltd., 2021)Aim: We aim to describe the demographic characteristics, etiology, neurophysiology, imaging findings, treatment, prognosis, and prognostic factors of acute flaccid myelitis. Methods: The clinical data, laboratory test and, ... -
The genetic profile of childhood neuromuscular disorders: A single center experience
Tezel, Oğuzhan; Öztürk, Gülten; Ünver, Olcay; Polat, H.; Ayaz, Akif; Özcan, S. Aksoy; Türkdoğan, Dilşad (Pergamon-Elsevier Science Ltd., 2023)Neuromuscular Diseases are a heterogeneous group of childhood disorders, and differential diagnosis can be challenging. Although there is no definitive treatment for the most of this group of diseases, early diagnosis is ... -
Shared biological pathways and processes in patients with intellectual disability: A multicenter study
Günay, Çaǧatay; Aykol, Duygu; Özsoy, Özlem; Sönmezler, Ece; Hancı, Yaren Sena; Kara, Bülent; Akkoyunlu Sünnetçi, Deniz; Çine, Naci; Deniz, Adnan; Öztürk, Gülten (Georg Thieme Verlag, 2023)Background Although the underlying genetic causes of intellectual disability (ID) continue to be rapidly identified, the biological pathways and processes that could be targets for a potential molecular therapy are not ... -
Stress-induced Childhood Onset Neurodegeneration with Ataxia and Seizures (CONDSIAS) presenting with torticollis attacks: Phenotypic variability of the same mutation in two Turkish patients
Öztürk, Gülten; Ayaz, Akif; Topçu, Yasemin; Akyüz, Gülcan; Ünver, Olcay; Akbeyaz, İsmail; Ekinci, Gazanfer; Türkdoğan, Dilşad (Wolters Kluwer Medknow Publications, 2022)Two patients with the same genetic mutation in ADPRHL2 gene, which takes a role in DNA repair, transcription, telomer function, and apoptosis are presented.[1] Developmental delay, intellectual disability, epilepsy, ...