Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Muhittin Çelik"'
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
Publikováno v:
Van Tıp Dergisi, Vol 25, Iss 4, Pp 441-444 (2018)
INTRODUCTION: Acute gastroenteritis, is a major cause of mortality and morbidity especially in children who live at developing countries. In this study, it was aimed to determine the frequency of rotavirus, who were referred to our hospital with the
Externí odkaz:
https://doaj.org/article/967b1b762f1c41bea0374de4eefc2ceb
Publikováno v:
Artuklu International Journal of Health Sciences. 3:18-23
Introduction: In this study, the patients diagnosed with breath holding spell (BHS) or anoxic epileptic seizures and initiated at least one out of iron or piracetam or levetiracetam therapies were evaluated. Material and Methods: We retrospectively e
Publikováno v:
Journal of tropical pediatrics. 68(6)
Background Classic galactosemia (CG) is a rare hereditary disease that can cause serious morbidity and death if it is not diagnosed and treated in early periods of life. Clinical findings usually occur in the neonatal period after the neonate is fed
Autor:
Mustafa Yilmaz, Muhittin Çelik
Publikováno v:
Turk Dunyasi Dergisi. :47-76
Autor:
Ali Bulbul, Ömer Güran, Mesut Dursun, Vedat Baş, Umut Zubarioglu, Hulya Sirzai, Banu Kuran, Selda Arslan, Sinan Uslu, Muhittin Çelik, Evrim Kiray Bas
Publikováno v:
The Journal of Maternal-Fetal & Neonatal Medicine. 35:677-684
Objective: To evaluate the impact of preterm birth on bone health in preschool children. Methods: A total of 166 preschool children (aged 7-8 years) born preterm (n = 86, = 37 weeks of gestation) in our hospital were included in this prospective cros
WOS:000760266600001 PMID: 35166449 Introduction Herein, we aimed to discuss our experience in 16 newborn patients with Maple syrup urine disease (MSUD) who were treated with urgent renal replacement therapy (RRT). Methods The patients underwent conti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a30d69f31b1989d9fd9be0e77795fbbc
Wiley Online Library
Wiley Online Library
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric SocietyReferences. 64(1)
This study aimed to evaluate the indications, complications, and outcomes of peritoneal dialysis (PD) in term neonates from a state hospital.The demographic, clinical, and laboratory data of 67 newborn term infants who underwent PD within the first 4
Autor:
Muhittin Çelik, Osman Akdeniz
Publikováno v:
Iranian Journal of Pediatrics. 31
Background: Nonketotic hyperglycinemia (NKH) is a rare metabolism disorder with autosomal recessive transmission. Newborn infants characteristically present with hypotonia, lethargy, convulsions, and apnea and are generally lost within the first year
Introduction: Continuous Renal Replacement Therapy (CRRT) is a well-known treatment modality for patients with acute renal failure and has been increasingly used for the treatment of metabolic disorders such as Maple Syrup Urine Disease (MSUD) in rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64e28849f2f661750568570c56c557be
https://doi.org/10.21203/rs.3.rs-780920/v1
https://doi.org/10.21203/rs.3.rs-780920/v1