Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Hasan, Tekgül"'
Autor:
Seda Kanmaz, Yavuz Ataş, Dilara Ece Toprak, Elif Hoşcoşkun, Cemile Büşra Ölçülü, Tuğçe İnce, Özlem Yılmaz, Gürsel Şen, Sanem Yılmaz, Hasan Tekgül
Publikováno v:
Journal of Pediatric Research, Vol 10, Iss 1, Pp 19-25 (2023)
Aim:To analyze trends in the prophylaxis of febrile convulsions (FC) in childhood by comparing two cohorts from the previous two decades (2007-2008 versus 2017-2018).Materials and Methods:The cohort consisted of 272 children with FC who were followed
Externí odkaz:
https://doaj.org/article/23a29ef76f9f430798018cf59c62fbd8
Autor:
Özlem Özdemir Balcı, Erdem Şimşek, Pınar Yazıcı Özkaya, Seda Kanmaz, İpek Dokurel, Hepsen Mine Serin, Sanem Yılmaz, Gül Aktan, Hasan Tekgül, Bülent Karapınar, Sarenur Gökben
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 3, Pp 228-235 (2022)
Aim:To evaluate the association of etiology, continuous electroencephalography (cEEG) findings and neuroimaging findings with short-term outcomes for patients admitted to a pediatric intensive care unit (PICU) for acute encephalopathy.Materials and M
Externí odkaz:
https://doaj.org/article/21d04f91056947eeb5d8fcc313a07a88
Autor:
Kürşad Aydın, Buket Dalgıç, Aydan Kansu, Hasan Özen, Mukadder Ayşe Selimoğlu, Hasan Tekgül, Bülent Ünay, Aysel Yüce
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
This review by a panel of pediatric gastroenterology-hepatology-nutrition and pediatric neurology experts aimed to address the significance of mid-upper arm circumference (MUAC) assessment in diagnosis of pediatric malnutrition. Specifically, the pot
Externí odkaz:
https://doaj.org/article/1898da980b2043c684f6706a754f34c8
Publikováno v:
Neurological Sciences and Neurophysiology, Vol 38, Iss 1, Pp 33-36 (2021)
Objectives: Tuberous sclerosis (TS) is a multisystemic disease with a genetic component. The central nervous system is most commonly involved. Renal involvement is also common. In this study, renal involvement was investigated descriptively and analy
Externí odkaz:
https://doaj.org/article/64cf098952e340ac90340b2d9a90873b
Autor:
Esra Işık, Hüseyin Onay, Tahir Atık, Aslı Ece Solmaz, Demet Terek, Sarenur Gökben, Hasan Tekgül, Ertürk Levent, Mehmet Kantar, Nilgün Kültürsay, Özgür Çoğulu, Ferda Özkınay
Publikováno v:
Erciyes Medical Journal, Vol 43, Iss 1, Pp 54-60 (2020)
Objective: Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous syndrome. TSC arises from mutations in either TSC1, at 9q34, or TSC2, at 16p13.3. Skin lesions, such as hypomelanotic macules, facial angiofibromas, shagreen patches,
Externí odkaz:
https://doaj.org/article/99fc6dca9da543fe868d978eb904ce12
Autor:
Gamze Sarıkaya Uzan, Atay Vural, Deniz Yüksel, Erhan Aksoy, Ülkühan Öztoprak, Mehmet Canpolat, Selcan Öztürk, Çelebi Yıldırım, Ayten Güleç, Hüseyin Per, Hakan Gümüş, Çetin Okuyaz, Meltem Çobanoğulları Direk, Mustafa Kömür, Aycan Ünalp, Ünsal Yılmaz, Ömer Bektaş, Serap Teber, Nargiz Aliyeva, Nihal Olgaç Dündar, Pınar Gençpınar, Esra Gürkaş, Sanem Keskin Yılmaz, Seda Kanmaz, Hasan Tekgül, Ayşe Aksoy, Gökçen Öz Tuncer, Elif Acar Arslan, Ayşe Tosun, Müge Ayanoğlu, Ali Burak Kızılırmak, Mohammadreza Yousefi, Muhittin Bodur, Bülent Ünay, Semra Hız Kurul, Uluç Yiş
Publikováno v:
Pediatric Neurology. 145:3-10
Autor:
Hepsen Mine Serin, Erdem Şimsek, Özge Altun Köroğlu, Seda Kanmaz, İpek Dökürel Çetin, Demet Terek, Sanem Yılmaz, Gül Aktan, Hasan Tekgül, Nilgün Kültürsay, Sarenur Gökben
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 4, Pp 336-341 (2019)
Aim:A brief resolved unexplained event (BRUE) is characterized by sudden alterations in an infant’s breathing, color, tone, or responsiveness. The aim of this study was to evaluate the necessity of electroencephalography (EEG) in high-risk BRUE cas
Externí odkaz:
https://doaj.org/article/8caa1e729446431c853c0b1cc3c208a7
Autor:
Hepsen Mine Serin, Erdem Şimşek, Seda Kanmaz, Sanem Yılmaz, Gül Aktan, Hasan Tekgül, Sarenur Gökben
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 9, Iss 2, Pp 93-100 (2019)
INTRODUCTION: Acquired demyelinating syndromes are immune-mediated demyelinating disorders of the central nervous system. Clinical spectrum includes acute disseminated encephalomyelitis, optic neuritis, transverse myelitis, clinically isolated syndro
Externí odkaz:
https://doaj.org/article/5e544539e51b4ffe900dc62a7b674c9a
Publikováno v:
Journal of Pediatric Research, Vol 5, Iss 2, Pp 76-81 (2018)
Aim: The aim of this study is to determine the risk factors of epilepsy development in children with cerebral palsy. Materials and Methods: Data of 234 cerebral palsy patients treated at Ege University Pediatrics Department, Child Neurology Divi
Externí odkaz:
https://doaj.org/article/4c59d9c42ae245968c09de3fb6aa9d44
Autor:
Seda Kanmaz, Erdem Şimşek, Hepsen Mine Serin, Murat Kadri Erdoğan, Sanem Yılmaz, Gül Aktan, Hasan Tekgül, Sarenur Gökben
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 2, Pp 163-165 (2019)
Hereditary neuropathy with a liability to pressure palsies (HNPP) represented by recurrent focal pressure neuropathies is rare in childhood. Here we present a 10-year-old girl admitted to our hospital with a recurrent weakness in her foot and diagnos
Externí odkaz:
https://doaj.org/article/0da798c745c9412e89c611f728dc5e9a