Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Gamze Ozgurhan"'
Autor:
Gamze Özgürhan, Serdar Cömert
Publikováno v:
Southern Clinics of Istanbul Eurasia, Vol 31, Iss 3, Pp 199-202 (2020)
INTRODUCTION[|]Low birth weight (LBW) is a worldwide public health problem, and in emerging countries in particular. In newborns, various maternal and socio-economical factors can lead to LBW. The purpose of this study is to evaluate the risk factors
Externí odkaz:
https://doaj.org/article/522b6e9f5dd443168c5701642d620301
Publikováno v:
European Journal of Breast Health, Vol 6, Iss 3, Pp 122-124 (2010)
Juvenile breast hypertrophy or juvenile gigantomastia is a rare disease characterized with rapid and excessive growth of the breast during adolescence. Although the deformity is benign, it affects patients physically and psychologically. Surgical app
Externí odkaz:
https://doaj.org/article/e04eafdfd08c4f6996fb34ec4d194b09
Autor:
Gamze Ozgurhan, Oznur Vermezoglu, Didem Ocal Topcu, Adem Karbuz, Aysel Vehapoglu, Bulent Hacihamdioglu
Publikováno v:
Case Reports in Infectious Diseases, Vol 2016 (2016)
Although rotavirus gastroenteritis is quite common in the pediatric population, secondary bacterial sepsis following rotavirus infection is a rare clinical entity. Gram-negative bacilli are the fifth most common cause of meningitis in infants but thi
Externí odkaz:
https://doaj.org/article/8c3319d2d26d468b99adbe87847ee2cc
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Infectious mononucleosis is an acute lymphoproliferative disorder caused by the Epstein-Barr virus (EBV) and seen most commonly in children and young adults. Clinical presentation of the disease is characterized by fever, tonsillopharyngitis, lymphad
Externí odkaz:
https://doaj.org/article/3329e7d93e0546678b3d732e28d7c917
Autor:
Aysel Vehapoglu, Gamze Ozgurhan, Ayşegul Dogan Demir, Selcuk Uzuner, Mustafa Atilla Nursoy, Serdar Turkmen, Arzu Kacan
Publikováno v:
Anemia, Vol 2014 (2014)
Background. The two most frequent types of microcytic anemia are beta thalassemia trait (β-TT) and iron deficiency anemia (IDA). We retrospectively evaluated the reliability of various indices for differential diagnosis of microcytosis and β-TT in
Externí odkaz:
https://doaj.org/article/6a2008ca41b14806a726d131e79a7f3e
Autor:
Serdar Cömert, Gamze Ozgurhan
Publikováno v:
İstanbul Medical Journal, Vol 21, Iss 5, Pp 370-374 (2020)
Introduction:When bilirubin attains high levels, it can lead to different degrees of brain damage. In this study, we aimed to evaluate the neurodevelopment status of term newborns treated for hyperbilirubinemia in the neonatal period.Methods:The stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7befdaa4fd69375b89c183339a0bdacd
https://doi.org/10.4274/imj.galenos.2020.48380
https://doi.org/10.4274/imj.galenos.2020.48380
Publikováno v:
Pediatric Hematology and Oncology. 37:676-686
Systemic iron homeostasis is regulated by the interaction of the peptide hormone, hepcidin and the iron exporter, ferroportin. The objective was to investigate the relationship between the consumption of cow-s milk and iron deficiency anemia in child
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::efbd934cdb39ecea23c7940e2984388b
https://doi.org/10.1080/08880018.2020.1782547
https://doi.org/10.1080/08880018.2020.1782547
Autor:
Gamze Ozgurhan, Serdar Cömert
Publikováno v:
İstanbul Medical Journal, Vol 21, Iss 4, Pp 301-306 (2020)
Introduction:Breast milk is not only the ideal nourishment for babies, but is also unique in terms of its health benefits for mothers and economic benefits for the society. The World Health Organization and United Nations Children’s Fund support ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b05b9225d1bea447aacc1281d429c931
https://doaj.org/article/cdd70803afdb411bb9926dd52e2f6e24
https://doaj.org/article/cdd70803afdb411bb9926dd52e2f6e24
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 11, Iss 1, Pp 34-40 (2019)
JCRPE, Vol 11, Iss 1, Pp 34-40 (2019)
KIRMIZIBEKMEZ, HEVES/0000-0002-8663-3452; Hacihamdioglu, Bulent/0000-0001-7070-6429 Objective: Vitamin D dependent rickets type 1A (VDDR1A) is an autosomal recessive disorder caused by mutations in the 1 alpha-hydroxylase gene (CYB27B1). As it may be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5a850a974986bc53ab6f3a0896beeb5
http://europepmc.org/articles/PMC6398191
http://europepmc.org/articles/PMC6398191
Autor:
Şükrü Aydemir, Fatih Varol, Tutku Özdoğan, Nedim Samancı, Serdar Cömert, Gamze Özgürhan, Müjde Tuba Çöğürlü
Publikováno v:
Sakarya Tıp Dergisi, Vol 13, Iss 4, Pp 557-566 (2023)
Giriş: Yenidoğan yoğun bakım ünitelerinde (YYBÜ) özellikle düşük doğum ağırlıklı bebeklerin klinik durumunu belirleme, mortalite riskini öngörme ve uygun yaklaşımı planlamanın yanı sıra üniteler arasında mortalite oranların
Externí odkaz:
https://doaj.org/article/f0513b92caab4e48b394fb16b9924143