Zobrazeno 1 - 10 of 18 pro vyhledávání: '"Erhan Ozbek"'
1
Neurodevelopmental evaluation of children with cyanotic congenital heart disease
Autor: Ferah Genel, Utku Karaarslan, Baris Erdur, İlksen Z Yilmaz, Erhan Ozbek, Timur Meşe
Background The aim of the study was to perform a neurodevelopmental evaluation of the children with cyanotic congenital heart disease and to determine the factors that affect the neurodevelopmental status. Methods The study was performed in the Pedia
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d9f64713fa3d4e4aa5bb74c063096599
https://avesis.deu.edu.tr/publication/details/9491219d-1f25-457d-9c04-8ccd687dd951/oai
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2
The relationship between hypernatremia and breast milk sodium levels in newborns with hypernatremic dehydration
Autor: Erhan Ozbek, İsmail Cengiz Öztürk, Leman Tekin Orgun, Özgür Olukman, Figen Isleten, Ferah Genel, Şebnem Çalkavur, Füsun Atlihan, Ali Orgun
Publikováno v: Volume: 5, Issue: 2 361-368
The European Research Journal
Objectives: Breast-feeding with high sodium content milk may cause hypernatremic dehydration in neonates (NHD). The number of cases with NHD tends to increase particularly in the higher temperature seasons. In this prospective case-control study, the
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6b9d81568cab365a480fb3d349af8931
https://dergipark.org.tr/tr/pub/eurj/issue/41339/373386
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3
Case report Asplenia in children with congenital heart disease as a cause of poor outcome
Autor: Erhan Ozbek, Baris Erdur, Semiha Bahceci Erdem, Nesrin Gulez, Ferah Genel, Timur Meşe
Publikováno v: Central European Journal of Immunology. 2:266-269
The absence of a spleen is a well-known risk factor for severe bacterial infections, especially due to encapsulated bacteria. Congenital asplenia can be part of multiple congenital abnormalities as in heterotaxy including Ivemark syndrome with congen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::cb493fb99e5f6e5cac3e0dea0d8c2f29
https://doi.org/10.5114/ceji.2015.52841
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4
Neurodevelopmental Outcome of Children with Congenital Hypothyroidism Diagnosed in a National Screening Program in Turkey
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
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7
Developmental problems in infants diagnosed as congenital cytomegalovirus infection
Autor: Zeynep Ilksen Yilmaz, Aycan Ünalp, Ferah Genel, İlker Devrim, Sukran Keskin Gozmen, Erhan Ozbek
Publikováno v: Journal of Dr. Behcet Uz Children's Hospital. 3:49-53
Objective: We aimed to assess developmental delays in older months of life in patients with congenital symptomatic cytomegalovirus infection in our study. Material and Methods: The developmental delays were determined by using Bayley Scales of Infant
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::482e3bb78e38f3b90a4cefdc9a7155d0
https://doi.org/10.5222/buchd.2013.049
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8
A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel
Autor: Behzat Özkan, Erhan Pariltay, Esra Ataman, Filiz Hazan, Korcan Demir, Erhan Ozbek, Ozdal Etlik
Publikováno v: Journal of Pediatric Endocrinology and Metabolism. 29
Aarskog-Scott syndrome (ASS) is a rare X-linked recessive genetic disorder caused by FGD1 mutations. FGD1 regulates the actin cytoskeleton and regulates cell growth and differentiation by activating the c-Jun N-terminal kinase signaling cascade. ASS
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86ee17b019cc6072e3da6540834627c4
https://doi.org/10.1515/jpem-2015-0482
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