Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Omer Guran"'
Introduction: The most prevalent method for evaluating lung expansion in high-frequency oscillatory ventilation (HFOV) is chest X-ray (CXR). The purpose of this study was to compare the accuracy of chest radiography with point-of-care ultrasound (POC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::659c15f4ed0891f1947ac67059da4c0e
https://doi.org/10.22541/au.168359956.68104766/v1
https://doi.org/10.22541/au.168359956.68104766/v1
Publikováno v:
Forbes Journal of Medicine. 2:154-157
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2e426e951cf15822cf31a96f994d21b
https://doi.org/10.4274/forbes.galenos.2021.36349
https://doi.org/10.4274/forbes.galenos.2021.36349
Autor:
Ece Oge Enver, Goncagül Haklar, Pinar Vatansever, Abdullah Bereket, Tulay Guran, Leyla Bilgin, Perran Boran, Omer Guran, Serap Turan
Publikováno v:
Pediatric research. 92(1)
BACKGROUND Interpretation of the results of steroid hormone measurements is challenging at early infancy. The liquid chromatography-tandem mass spectrometry (LC-MS/MS) method provides a powerful tool for diagnosing steroidogenesis disorders. We aimed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7583ec9774367884359ea3753bdfd19e
https://pubmed.ncbi.nlm.nih.gov/34556810
https://pubmed.ncbi.nlm.nih.gov/34556810
Publikováno v:
journal of Clinical Research in Pediatric Endocrinology. 3:98-100
Pseudohypoaldosteronism type 1 (PHA-1, MIM #264350) is caused by defective transepithelial sodium transport. Affected patients develop life-threatening neonatal-onset salt loss, hyperkalemia, acidosis, and elevated aldosterone levels due to end-organ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f47b126e61aed65bba1636bcfa7940d0
https://doi.org/10.4274/jcrpe.v3i2.20
https://doi.org/10.4274/jcrpe.v3i2.20
Autor:
Omer Guran, Gozde Yesil, Valeria Cormier Daire, Tulay Guran, Ilke Ipek Özahi, Sofia Dos Santos, Anne-Sophie Lebre
Publikováno v:
American journal of medical genetics. Part A. (9)
Stuve-Wiedemann Syndrome (SWS) (OMIM #601559) is an autosomal recessive disorder characterized by skeletal changes, bowing of the lower limb, severe osteoporosis and joint contractures, episodic hyperthermia, frequent respiratory infections, feeding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::961c8cb03db3d23ade8819e4a36cffc8
https://pubmed.ncbi.nlm.nih.gov/24988918
https://pubmed.ncbi.nlm.nih.gov/24988918
Publikováno v:
Forbes Tıp Dergisi, Vol 2, Iss 3, Pp 154-157 (2021)
Objective: To evaluate rotavirus epidemic in a neonatal intensive care unit (NICU) and to contribute to the literature on rotavirus outbreak in the newborn. Methods: An epidemic of rotavirus infection was seen in the NICU of our hospital in September
Externí odkaz:
https://doaj.org/article/cc5b8f77d3704dc48b4c8323bded3285
Autor:
Gülcan Seymen-Karabulut, Ayla Günlemez, Ayşe Sevim Gökalp, Şükrü Hatun, Fatma Kaya Narter, Mehmet Mutlu, Şebnem Kader, Demet Terek, Deniz Hanta, Emel Okulu, Leyla Karadeniz, H. Gözde Kanmaz Kutman, Ayşegül Zenciroğlu, Özmert M. A. Özdemir, Dilek Sarıcı, Muhittin Çelik, Nihat Demir, Özden Turan, Kıymet Çelik, Fatih Kılıçbay, Sinan Uslu, Sara Erol, Sabahattin Ertuğrul, Ilkay Er, Hasan Tolga Çelik, Merih Çetinkaya, Filiz Aktürk-Acar, Yakup Aslan, Gaffari Tunç, Ömer Güran, Ayşe Engin Arısoy
Publikováno v:
JCRPE, Vol 13, Iss 4, Pp 384-390 (2021)
Objective:Late neonatal hypocalcemia (LNH) is a common metabolic problem associated with hypoparathyroidism, high phosphate intake and vitamin D deficiency, often presenting with seizures. In this cross-sectional study, we aimed to evaluate the role
Externí odkaz:
https://doaj.org/article/646b7b0dc6e8458eb2d024d4ea2c5f3e
Autor:
Aysu Say, Uwe Kornak, Tulay Guran, Gulsun Karasu, Omer Guran, Ahu Turkoz Paketci, Serpil Değirmenci
Publikováno v:
Pediatric hematology and oncology. 29(4)
Malignant infantile osteopetrosis (MIOP) is a rare cause in the list of etiological factors of neonatal hypocalcemia in several textbooks. The most severe complication of MIOP is bone marrow suppression. The abnormal expansion of bone interferes with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::63b42b1a8fc39a5bd3f9e0c20ab848c3
https://pubmed.ncbi.nlm.nih.gov/22303931
https://pubmed.ncbi.nlm.nih.gov/22303931
Autor:
Gozde Yesil, Tulay Guran, Sevilay Topcuoglu, Suna Cesur, Abdullah Bereket, Oktav Bosnali, Ayşenur Cerrah Celayir, Omer Guran
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Congenital adrenal hyperplasia (CAH) is a group of disorders affecting the adrenal steroid synthesis. The most common form, 21-hydroxylase deficiency (21-OHD), leads to decreased production of cortisol and aldosterone with increased androgen secretio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4155c4447c723597ee756801fbedfeb
http://hdl.handle.net/20.500.12645/26752
http://hdl.handle.net/20.500.12645/26752
Publikováno v:
Acta paediatrica (Oslo, Norway : 1992). 96(8)
Aim: To determine the value of high-sensitivity C-reactive protein (hs-CRP) in predicting risk factors for coronary heart disease (CHD) in children. Methods: We measured hs-CRP levels in 51 children (11.79 ± 3.14 years) with risk factors for CHD (hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dcd41f9fbdaa34b1d7056571a64dfb0
https://pubmed.ncbi.nlm.nih.gov/17655623
https://pubmed.ncbi.nlm.nih.gov/17655623