Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Safiye Gunes Sager"'
Publikováno v:
International Ophthalmology. 43:333-341
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5580a5f08c8f1f7ec472e5944ed03fe
https://doi.org/10.1007/s10792-022-02452-w
https://doi.org/10.1007/s10792-022-02452-w
Autor:
Safiye Gunes Sager, Ayberk Turkyilmaz, Hediye Pınar Gunbey, Elif Yuksel Karatoprak, Elif Sibel Aslan, Yasemin Akın
Background: Beck-Fahrner syndrome is caused by homozygous or heterozygous mutations in TET3 on chromosome 2p13. The general characteristics of this syndrome include behavioral abnormalities such as autistic features, attention-deficit hyperactivity d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c10af880260f6d3e4b56558921cc854
https://hdl.handle.net/20.500.12445/2841
https://hdl.handle.net/20.500.12445/2841
Autor:
Hediye Pinar Günbey, Ayberk Turkyilmaz, Yasemin Akin, Aysin Tuba Kaplan, Bahtisen Topcu, Safiye Gunes Sager
Publikováno v:
Clinical Dysmorphology. 31:45-49
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a0ae3f63ba4e749ee8b73ebe3b91f7a
https://doi.org/10.1097/mcd.0000000000000389
https://doi.org/10.1097/mcd.0000000000000389
Autor:
Ayberk Türkyılmaz, Safiye Gunes Sager
Publikováno v:
Molecular Syndromology. 13:56-63
Autosomal recessive primary microcephaly (MCPH) is a uncommon disorder due to congenital deficiency in the development of the cerebral cortex, characterized by a head circumference below 2 SD. MCPH is a group of diseases with genetic heterogeneity an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33a309150c37a4711e798584e9245372
https://doi.org/10.1159/000516201
https://doi.org/10.1159/000516201
Autor:
Andras, Fogarasi, Elisa, Fazzi, Ana R P, Smorenburg, Maria, Mazurkiewicz-Beldzinska, Argirios, Dinopoulos, Alena, Pobiecka, Dea, Schröder-van den Nieuwendijk, Josef, Kraus, Hasan, Tekgül, Maria, Koutsaki, Giovanni, Baranello, Simona, Bertoli, Elisa, Caramaschi, Duccio Maria, Cordelli, Ramona, De Amicis, Maria Luisa, Forchielli, Azzurra, Guerra, Althea, Lividini, Maddalena, Marchiò, Andrea, Rossi, Dea Schröder-van den, Nieuwendijk, Jędrzej, Fliciński, Barbara, Gurda, Anna, Lemska, Agnieszka, Matheisel, Zuzanna, Niwinska, Małgorzata, Pawłowicz, Agnieszka, Sawicka, Barbara, Steinborn, Marta, Szmuda, Anna, Winczewska-Wiktor, Marta, Zawadzka, Ebru, Arhan, Kursad, Aydin, Erhan, Bayram, Kursat Bora, Carman, Pinar, Edem, Deniz, Ertem, Özben Akıncı, Goktas, Serdal, Gungor, Goknur, Haliloglu, Aydan, Kansu, Mustafa, Kömür, Akmer, Mutlu, Ceyda Tuna, Kırsaçlıoğlu, Çetin, Okuyaz, Bilge, Özgör, Yesim, Ozturk, Safiye Gunes, Sager, Esra, Sarıgeçili, Mukadder Ayse, Selimoglu, Hepsen Mine Öztürk, Serin, Serap Tıraş, Teber, Gülten, Thomas, Dilsad, Turkdogan, Burcu, Volkan, Coşkun, Yarar, Sanem Keskin, Yilmaz
Purpose: To obtain information on characteristics, management, current objective nutritional status and perception of nutritional status of children with cerebral palsy (CP) from healthcare professionals (HCPs) and caregivers. Materials and methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9727200483ce29407dbc20f7e3e3d6a8
https://avesis.deu.edu.tr/publication/details/824a25c6-3f2f-4d7f-94fc-9d7cf13de9ea/oai
https://avesis.deu.edu.tr/publication/details/824a25c6-3f2f-4d7f-94fc-9d7cf13de9ea/oai
Autor:
Yakup Çağ, Safiye Güneş Sağer, Merve Akçay, İsmail Kaytan, Elif Söbü, Aydan Erdem, Yasemin Akın
Publikováno v:
Italian Journal of Pediatrics, Vol 50, Iss 1, Pp 1-6 (2024)
Abstract Background Childhood obesity has become a major global health problem. Obesity is associated with major health problems, such as diabetes, hypertension, dyslipidemia, cardiovascular disease. Obesity is also considered a risk factor for Pseud
Externí odkaz:
https://doaj.org/article/894d68171f7243389fa5dae9916d3f20
Purpose The present study aimed to identify the molecular etiology of non-syndromic congenital cataract (CC) using whole-exome sequencing (WES) analysis. Methods In the present study, ophthalmologic results and pedigree analysis of the families of 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9f7a43e2544fa5b18314616676f66f5d
https://doi.org/10.21203/rs.3.rs-1072160/v1
https://doi.org/10.21203/rs.3.rs-1072160/v1
Evaluation of optical coherence tomography findings in adolescents with genetic generalized epilepsy
Publikováno v:
European journal of ophthalmology. 32(6)
Objective To evaluate retinal nerve fiber layer (RNFL) thickness, central macular thickness (CMT), and subfoveal choroid thickness (CT) by using optical coherence tomography (OCT) in adolescents with newly diagnosed epilepsy and patients who had been
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19d6c73d6cc23c8bf5d7700aa6711ee1
https://pubmed.ncbi.nlm.nih.gov/34657446
https://pubmed.ncbi.nlm.nih.gov/34657446
Publikováno v:
Türk Oftalmoloji Dergisi, Vol 53, Iss 5, Pp 294-300 (2023)
Objectives:To compare the clinical findings and multimodal imaging of pediatric patients diagnosed with papilledema and pseudopapilledema with those of healthy individuals.Materials and Methods:Ninety children (0.05). The average, nasal, and temporal
Externí odkaz:
https://doaj.org/article/f87675343f324f37ac78b001151cba2b
Autor:
Mehmet Tolga Köle, Safiye Günes Sağer, Utku Batu, Nilüfer Çetiner Çine, Yakup Çağ, Yasemin Akin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract The purpose of the study is to explore the use of Calgary scoring (CS) and Modified Calgary scoring (MCS) in the differentiation of genetic generalized epilepsy and syncope in children. The study involved 117 patients aged − 1, sensitivity
Externí odkaz:
https://doaj.org/article/3ac938651c2c42b381044211985e734c