Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Gul Aktan"'
Autor:
Seda Kanmaz, Dilara Ece Toprak, Cemile Busra Olculu, Ipek Dokurel, Erdem Simsek, Hepsen Mine Serin, Sanem Yılmaz, Gul Aktan, Sarenur Gokben, Hasan Tekgul
Publikováno v:
Epileptic Disorders. 25:218-228
Autor:
Maharram Imanli, Erdem Simsek, Afshin Dezhakam, Seda Kanmaz, Ipek Dokurel, Hepsen Mine Serin, Sanem Yilmaz, Gul Aktan, Hasan Tekgul
Objective. To evaluate the adaptability of trainees in pediatrics for the current seizure classification of the International League Against Epilepsy (ILAE-2017) with a modular education program (MEP) to provide a common language between neurologists
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d728fa93980015dc13a6586a3d27411
https://doi.org/10.21203/rs.3.rs-2655778/v1
https://doi.org/10.21203/rs.3.rs-2655778/v1
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:
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
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 4, Pp 356-358 (2019)
Congenital myasthenic syndromes (CMS) are neuromuscular hereditary diseases with the symptoms of fatigue, weakness, ptosis, ophthalmoparesis and respiratory problems. This disease group is classified as CMS originating from the presynaptic region, sy
Externí odkaz:
https://doaj.org/article/954ad7174129498daec961e084786056
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