Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Kürşad, Aydın"'
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 39, Iss 1, Pp 21-27 (2022)
Purpose: Electrical status epilepticus during slow sleep (ESES) is an electroclinical syndrome with a specific electroencephalogram (EEG) pattern characterized by epileptic seizures, cognitive decline, and behavioral problems. The EEG pattern is defi
Externí odkaz:
https://doaj.org/article/7064c291fa3a441487e5e3c75fbf6b5a
Publikováno v:
Pediatric Neurology. 133:40-47
Background: Hemophagocytic lymphohistiocytosis (HLH) is a rare and fatal disease and may also present with central nervous system findings at the beginning without specific diagnostic criteria. Brain magnetic resonance imaging (MRI) findings are dive
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14a878bf0b7a8a88d043e6fe6062d4d0
https://doi.org/10.1016/j.pediatrneurol.2022.05.010
https://doi.org/10.1016/j.pediatrneurol.2022.05.010
Publikováno v:
Brain and Development. 42:756-761
Background Genetic defects in the NFU1, an iron-sulfur cluster scaffold protein coding gene, which is vital in the final stage of assembly for iron sulfur proteins, have been defined as multiple mitochondrial dysfunctions syndrome I. This disorder is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f93a71d7768a70bd542af35c5b5ef3ea
https://doi.org/10.1016/j.braindev.2020.07.009
https://doi.org/10.1016/j.braindev.2020.07.009
Autor:
Merve Hilal Dolu, Yasemin Topçu, Haydar Ali Taşdemir, Şiar Dursun, Ilknur Erol, Betül Kılıç, Kürşad Aydın
Publikováno v:
Brain and Development. 42:572-580
Aim To present seven new genetically confirmed cases of biotin–thiamin-responsive basal ganglia disease (BTBGD) with different clinical and brain magnetic resonance imaging (MRI) characteristics. Material and methods Genetic variants, clinical pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89a8adb3af6bd5fa7f9b180cb6e3517c
https://doi.org/10.1016/j.braindev.2020.05.008
https://doi.org/10.1016/j.braindev.2020.05.008
Publikováno v:
European Journal of Paediatric Neurology. 28:228-236
Neuronal ceroid lipofuscinosis type 2 (CLN2) disease is a rare, paediatric-onset, neurodegenerative disorder characterised in its early stages by language delay, seizures and loss of motor function. It is rapidly progressive and ultimately results in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fa9bbf4ba1f2cf39f30e29cebca4979
https://doi.org/10.1016/j.ejpn.2020.07.009
https://doi.org/10.1016/j.ejpn.2020.07.009
Autor:
Tülay Kamaşak, Esra Serdaroğlu, Özlem Yılmaz, Betül Aydın Kılıç, Burçin G. Polat, Irmak Erdoğan, A.Derda Yücel Şen, Nalan Özen, Betül Diler Durgut, Nihal Yıldız, Pınar Özkan Kart, Beril Dilber, Elif Acar Arslan, Sevim Şahin, Yasemin Topçu, Pınar Gencpinar, H. Mine Serin, Semra A. Hız, Kürşat Bora Çarman, Nihal Olgaç Dündar, Çetin Okuyaz, Kürşad Aydın, Ayşe Serdaroğlu, Hasan Tekgül, Ali Cansu
Publikováno v:
Epilepsy research. 184
Objective: To evaluate the effectiveness and tolerability of clobazam therapy in the pediatric population in terms of seizure semiology, epileptic syndromes, and etiological subgroups. Methods: A retrospective cohort study was conducted consisting of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cc2ab158cd7c0d2df04a436a841a20fd
https://pubmed.ncbi.nlm.nih.gov/35749975
https://pubmed.ncbi.nlm.nih.gov/35749975
Autor:
Bülent Ünay, Esra Gürkaş, Meral Karadag, Ozgen Hur, Cefa Nil Karademir, Nihal Olgaç Dündar, Yakup Peduk, Mine Serin, Ali Cansu, Gonca Kılıç Yıldırım, Çetin Okuyaz, Coskun Yarar, Hasan Tekgul, Kürşad Aydın, Kursat Bora Carman, Betul Kilic Aydin, Pınar Özkan Kart, Serdal Güngör, Pinar Gencpinar, Selver Durmus, Nefise Arıbas Oz, Hüseyin Per, Meltem Çobanoğulları Direk
Background Many studies evaluating the nutritional status of children with cerebral palsy (CP) have focused on energy requirements and protein intake. The present work aimed to assess nutritional status and micronutrient levels of children with (CP).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::309cc4bbeb2da9058ebfaaf1ef2075f8
https://hdl.handle.net/11454/77591
https://hdl.handle.net/11454/77591
Autor:
Betül Kılıç, Esra Serdaroğlu, Burçin Gönüllü Polat, Tuğçe İnce, Gülnur Esenülkü, Yasemin Topçu, Ayşe Serdaroğlu, Şenay Haspolat, Hasan Tekgül, Çetin Okuyaz, Ali Cansu, Kürşad Aydın
Purpose:Valproic acid (VPA) is frequently used and effective in juvenile myoclonic epilepsy (JME). Recently, levetiracetam (LEV) has been suggested as a monotherapy in JME. This study aimed to evaluate antiseizure medication (ASM) use in patients wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f9088d29b56823ea936ad2364c8c195
https://hdl.handle.net/20.500.12511/9490
https://hdl.handle.net/20.500.12511/9490
Autor:
Dilşad Yıldız Miniksar, Betül Kılıç, Mahmut Kılıç, Ökkeş Hakan Miniksar, Yasemin Topçu, Kürşad Aydın
Background We aimed to examine suicide probability, factors affecting suicide, and personality traits of children and adolescents diagnosed with epilepsy, and to compare their results with those of children without epilepsy. Methods Fifty-six childre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0715d364d3c5d8c5f3d6496b5884274e
https://hdl.handle.net/20.500.12511/9450
https://hdl.handle.net/20.500.12511/9450