Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Özlem Hergüner"'
Autor:
Serap Bilge, Gülen Gül Mert, Özlem Hergüner, Duygu Özcanyüz, Sevcan Tuğ Bozdoğan, Ömer Kaya, Cengiz Havalı
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-8 (2022)
Abstract Pontocerebellar hypoplasia (PCH) constitutes a heterogeneous neurodegenerative/neurodevelopmental disorder of the pons and cerebellum with onset in the prenatal period. Our study aimed to present different clinical and radiological manifesta
Externí odkaz:
https://doaj.org/article/c5f6643437e849afb48ed31bb7ed9bbd
Autor:
Gülen GÜL MERT, Neslihan ÖZCAN, Şeyda BEŞEN, Kemal YAR, Özlem HERGÜNER, Faruk İNCECİK, Şakir ALTUNBAŞAK
Publikováno v:
Cukurova Medical Journal, Vol 44, Iss 2, Pp 447-452 (2019)
Amaç: Psödotümör serebri tanısı alan hastaların klinik ve nörogörüntüleme bulguları, etiyolojileri, tedavi şekilleri ve süreleri, tedaviye yanıtları ve nörolojik sekel varlıkları gözden geçirildiGereç ve Yöntem: Çalışmaya da
Externí odkaz:
https://doaj.org/article/5baf55d859d54a6f8303906f0a7ae4c0
Autor:
Ali Topaloglu, Bilgin Yüksel, Güler Özer, Neslihan Mungan, Özlem Hergüner, Süreyya Soyupak, Zeliha Haytoğlu
Publikováno v:
Cukurova Medical Journal, Vol 41, Iss 1, Pp 21-27 (2016)
Purpose: We investigated the neurological outcome of 38 late-diagnosed phenylketonuria patients with magnetic resonance imaging (MRI), electroencephalography (EEG), visual evoked potentials (VEP), intelligence quotients (IQ) and examined the correlat
Externí odkaz:
https://doaj.org/article/b7341f464d4a469f9f194e923466cca2
Autor:
Faruk İNCECİK, Özlem HERGÜNER, Şeyda BESEN, Zeliha HAYTOĞLU, Şakir ALTUNBAŞAK, Mustafa YILMAZ
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 0, Pp 75-78 (2015)
Ailevi Akdeniz Ateşi (FMF) nükseden ve kendini sınırlayan ateş, peritonit, plörit ve artrit atakları ile karakterize otozomal resesif geçişli polisistemik bir hastalıktır. Nörofibromatozis tip 1 (NF1) hastalığının karakteristik özell
Externí odkaz:
https://doaj.org/article/333070eb6e5a46ea918cb66e2bc6a431
Autor:
Faruk İNCECİK, Özlem HERGÜNER, Gülen MERT, Şeyda BESEN, Deniz KOR, Berna YILMAZ, Neslihan MUNGAN, Şakir ALTUNBAŞAK
Publikováno v:
Cukurova Medical Journal, Vol 40, Iss 0, Pp 5-7 (2015)
McArdle hastalığı, çizgili kasta glikojen fosforilaz enziminin eksikliği sonucu gelişen, otozomal resesif kalitim gösteren bir hastalık olarak tanımlanmaktadır. Hastalar genellikle çabuk yorulma ve egzersiz sonrası güçsüzlük ile birli
Externí odkaz:
https://doaj.org/article/3e9df1059a714799a7fbca7cc5f65bff
Autor:
Nilgün TANRIVERDİ, Ayfer PAZARBAŞI, Dilara Süleymanova KARAHAN, İlker GÜNEY, Deniz TAŞTEMİR, Erdal TUNÇ, Osman DEMİRHAN, Özlem HERGÜNER
Publikováno v:
Cukurova Medical Journal, Vol 38, Iss 3, Pp 540-545 (2013)
Giriş: Zeka geriliği, genel populasyonda %2-3 gibi oldukça yüksek bir oranda bulunan ve vakaların %50"sinden fazlasında sebebi bulunamayan bir sağlık problemidir. En önemli nedenlerinden birisi kromozom düzensizlikleri olup hasta seçimi ve
Externí odkaz:
https://doaj.org/article/e82f085f51e243bc8969ec56328fc47b
Autor:
Tamer Çelik, Özlem Hergüner
Publikováno v:
JEURMEDS. 3:23-28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69b986c173752d48b6e4376bfd76e1ee
https://doi.org/10.5578/jeurmeds.20220105
https://doi.org/10.5578/jeurmeds.20220105
Status epilepticus according to International League Against Epilepsy (ILAE) 2015’ classification is a seizure that lasts longer than 5 minutes or has more than 1 seizure within 5 minutes, without returning to a normal level of consciousness betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::420ce8d705612984a87fa06050d15db5
https://doi.org/10.21203/rs.3.rs-2496564/v1
https://doi.org/10.21203/rs.3.rs-2496564/v1
Publikováno v:
Journal of Pediatric Genetics.
Global developmental delay (GDD)/intellectual disability (ID) is common in children and its etiology is unknown in many cases. Chromosomal abnormalities are predominant genetic causes of GDD/ID. The aim of this study is to determine the genetic risk
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d1f909f9fcd8cd84dadc5e6ece8f5cbb
https://doi.org/10.1055/s-0042-1758872
https://doi.org/10.1055/s-0042-1758872
Autor:
Serap Bilge, Gülen Gül Mert, M Özlem Hergüner, Faruk İncecik, Özgür Sürmelioğlu, Sevcan Bilen, Levent Yılmaz
Background:Sudden onset of unilateral weakness of upper and lower muscles of one side of the face is defined as peripheral facial nerve palsy. Peripheral facial nerve palsy is often idiopathic and sometimes it could be due to infectious, traumatic, n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7e5f461094e94e3851760ff131fb4a7
https://doi.org/10.21203/rs.3.rs-2065969/v1
https://doi.org/10.21203/rs.3.rs-2065969/v1