Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Bahar Toklu Baysal"'
Autor:
Semra Gursoy, Esra Ataman, Bahar Toklu Baysal, Berk Özyılmaz, Pınar Gençpınar, Ayşe Semra Hız, Uluç Yiş, Aycan Ünalp, Nihal Olgaç Dündar, Ayfer Ülgenalp, Derya Erçal
Publikováno v:
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 206-210 (2020)
Background and Aims:PCDH19 gene, which encodes protocadherin 19, is associated with epilepsy and intellectual disability, mainly in affected females. The clinical manifestations are heterogeneous and the main features include early onset seizure, gen
Externí odkaz:
https://doaj.org/article/c09e579b34b3452381f5265ddeb77d7b
Autor:
Ünsal Yılmaz, Selvinaz Edizer, Zeynep Akışin, Melis Köse, Yiğithan Güzin, Gürkan Gürbüz, Bahar Toklu Baysal, Serdar Sarıtaş, Serdar Pekuz, Hatice Hilal Kırkgöz, Merve Yavuz, Aycan Ünalp
Publikováno v:
The Turkish journal of pediatrics. 64(2)
2nd International Behcet Uz Children's Congress -- MAR 04-07, 2020 -- Izmir, TURKEY Background. We aimed to investigate the effectiveness of ketogenic diet (KD) in children with various types of refractory epilepsy. Methods. A total of 91 children (4
Autor:
Ayfer Ülgenalp, Uluç Yiş, Nihal Olgaç Dündar, Aycan Ünalp, Esra Ataman, Bahar Toklu Baysal, Pinar Gencpinar, Ayşe Semra Hız, Berk Ozyilmaz, Derya Erçal, Semra Gürsoy
Publikováno v:
Annals of Indian Academy of Neurology
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 206-210 (2020)
Annals of Indian Academy of Neurology, Vol 23, Iss 2, Pp 206-210 (2020)
Background and Aims:PCDH19 gene, which encodes protocadherin 19, is associated with epilepsy and intellectual disability, mainly in affected females. The clinical manifestations are heterogeneous and the main features include early onset seizure, gen
Autor:
Bahar Toklu Baysal, Kübra Gündüz, Selvinaz Edizer, Serdar Pekuz, Aycan Ünalp, Ceyda Hayretdağ, Ender Coçkunpınar, Elif Güdeloğlu
Aims The term "epileptic encephalopathy" is used to describe a possible relationship between epilepsy and developmental delay. The pathogenesis of developmental encephalopathies, independent of epilepsy, can be defined by genetic control mechanisms.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19ee76f2c6005b33e5f9312be73ffde0
https://doi.org/10.21203/rs.3.rs-1111620/v1
https://doi.org/10.21203/rs.3.rs-1111620/v1
Autor:
Selvinaz Edizer, Serdar Sarıtaş, Yiğithan Güzin, Zeynep Akışın, Ünsal Yılmaz, Aycan Ünalp, Bahar Toklu Baysal
Publikováno v:
Epilepsybehavior : EB. 124
Background Sleep disorders are common in drug-resistant children with epilepsy and their mothers. Ketogenic diet therapy (KDT) may have positive effects on sleep quality. The aim of this study was to evaluate the sleep quality of children with epilep
Publikováno v:
Journal of Pediatric Infectious Diseases. 13:224-228
Objectives Fever is an abnormal elevation of body temperature that occurs as part of a specific biologic response that is mediated and controlled by the central nervous system. In neonates, it may indicate a serious underlying disease. With this stud
Autor:
Gürkan Gürbüz, Ünsal Yılmaz, Bahar Toklu Baysal, Tansel Çalık, Zeynep Akışın, Selvinaz Edizer, Melis Köse, Aycan Ünalp
Publikováno v:
The journal of Dr. Behcet Uz Children s Hospital.
Autor:
Erhan Ozbek, Korcan Demir, Baris Erdur, Behzat Özkan, Ferah Genel, Bahar Toklu Baysal, Bora Baysal
Objective: To study the factors affecting a neurodevelopmental status of children with congenital hypothyroidism, diagnosed on national screening program. Methods: The study was performed in the Pediatric Endocrinology Department of Dr. Behcet Uz Chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::669f228d4e2dd23a3ccf7cd603751fde
https://avesis.deu.edu.tr/publication/details/a373f311-b2b6-46f2-935e-faac6251d4e5/oai
https://avesis.deu.edu.tr/publication/details/a373f311-b2b6-46f2-935e-faac6251d4e5/oai
Publikováno v:
American Journal of Internal Medicine. 6:86
Many chromosomal anomalies manifest with epilepsy. Only few typical EEG and seizure type have been identified in genetic syndromes. Identification of typical seizure and EEG findings of certain genetic syndromes may serve as a guide for genetic analy
Autor:
Baysal BT; Departments of Pediatrics and Pediatric Endocrinology, Dr. Behcet Uz Children's Hospital; and Departments of Neonatology and Pediatric Endocrinology, Dokuz Eylul University, School of Medicine Izmir, Turkey. Correspondence to: Dr Bahar Toklu Baysal, Department of Pediatrics, Dr. Behcet Uz Children's Hospital, Izmir, Turkey. bahartoklu@hotmail.com., Baysal B, Genel F, Erdur B, Ozbek E, Demir K, Ozkan B
Publikováno v:
Indian pediatrics [Indian Pediatr] 2017 May 15; Vol. 54 (5), pp. 381-384. Date of Electronic Publication: 2017 Mar 29.