Zobrazeno 1 - 10
of 110
pro vyhledávání: '"Yılmaz Ağladıoğlu"'
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 334-335 (2023)
Externí odkaz:
https://doaj.org/article/6d79443ee6fd42299e6fa5a030861841
Autor:
Erdem Gönüllü, Ahmet Soysal, Serkan Atıcı, Mesut Engin, Osman Yeşilbaş, Tuba Kasap, Atiye Fedakar, Emre Bilgiç, Emine Betül Tavil, Ercan Tutak, İsmail Yıldız, Teoman Akçay, Sebahat Yılmaz Ağladıoğlu, Turan Tunç, İlkay Can, Metin Karaböcüoğlu, Nalan Karabayır
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 17, Iss 8, Pp 2389-2396 (2021)
Developing an effective and safe vaccine against Covid-19 will facilitate return to normal. Due to hesitation toward the vaccine, it is crucial to explore the acceptability of the COVID-19 vaccine to the public and healthcare workers. In this cross-s
Externí odkaz:
https://doaj.org/article/f88661adc6ee43e4a9d0d71d31f23111
Autor:
Eviz E; Koç University Faculty of Medicine; Koç University Hospital, Division of Pediatric Endocrinology and Diabetes, İstanbul, Turkey, Yeşiltepe Mutlu G; Koç University Faculty of Medicine; Koç University Hospital, Division of Pediatric Endocrinology and Diabetes, İstanbul, Turkey, Yılmaz Ağladıoğlu S; Memorial Ataşehir Hospital, Clinic of Pediatric Endocrinology and Diabetes, İstanbul, Turkey, Hatun Ş; Koç University Faculty of Medicine; Koç University Hospital, Division of Pediatric Endocrinology and Diabetes, İstanbul, Turkey
Publikováno v:
Journal of clinical research in pediatric endocrinology [J Clin Res Pediatr Endocrinol] 2023 Aug 23; Vol. 15 (3), pp. 334-335. Date of Electronic Publication: 2023 Jun 20.
Autor:
H. Nur Peltek Kendirci, Sebahat Yılmaz Ağladıoğlu, Veysel N. Baş, Aşan Önder, Semra Çetinkaya, Zehra Aycan
Publikováno v:
International Journal of Endocrinology, Vol 2015 (2015)
Objective. GnRH analogues (GnRHa) are used in the treatment of central precocious puberty (CPP). The purpose of this study was to evaluate the efficacy of treatment with a GnRHa (leuprolide acetate) in patients with CPP. Subjects and Methods. A total
Externí odkaz:
https://doaj.org/article/9685c17368154a5e926acaaa949f6958
Autor:
Esra niz P. De Cakir, Eda Mengen, Olcay Evliyaoğlu, Paolo Giacobini, A. Kemal Topaloglu, Ihsan Turan, Gaspard Delpouve, Gamze Akkus, Feyza Darendeliler, Aysegul Yuksel, Asli rya De Kardelen, Fatih Gurbuz, Aydilek Dagdeviren Cakir, Sebahat Yılmaz Ağladıoğlu, Semine Özdemir Dilek, Bilgin Yüksel, Gaetan Ternier, Bahar Ozcabi, Hamdi Cihan Emeksiz, Emregul Isik, Leman Damla Kotan
Publikováno v:
Genet Med
Genetics in Medicine
Genetics in Medicine
Purpose Idiopathic hypogonadotropic hypogonadism (IHH) is characterized by absent puberty and subsequent infertility due to gonadotropin-releasing hormone (GnRH) deficiency. IHH can be accompanied by normal or compromised olfaction (Kallmann syndrome
Autor:
Özmert M.A. Özdemir, Havva Evrengül, Hacer Ergin, Sebahat Yılmaz Ağladıoğlu, Emre Tepeli, Ceren Çirali
Publikováno v:
Pediatrics International. 58:912-915
Neonatal Bartter syndrome (NBS) is a rare autosomal recessive renal tubular disorder. This disease is characterized by hypokalemia, hypochloremia, and metabolic alkalosis that is often associated with failure to thrive and recurrent episodes of dehyd
Publikováno v:
Hormone Research in Paediatrics. 84:54-61
Background: The urinary C-peptide/creatinine ratio (UCPCR) and fasting C-peptide level can assess beta-cell function in clinical practice. In the present study, the use of the UCPCR and fasting C-peptide levels was investigated in the differential di
Publikováno v:
Issue: 2 132-135
Pamukkale Tıp Dergisi
Pamukkale Tıp Dergisi
Hipotalamik hamartom, hipotalamusun neoplastik olmayan nadir görülen heterotopik lezyonudur. Tipik olarak erken puberteye neden olduğundan, erken pubertenin ayırıcı tanısında akılda bulunması önemlidir. Biz burada hipotalamik hamartomu bul
Autor:
Semra Çetinkaya, Merve Ergin, Veysel Nijat Baş, Aşan Önder, Zehra Aycan, Cemile Koca, Sebahat Yılmaz Ağladıoğlu, Havva Nur Peltek Kendirci
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: To investigate serum asymmetric dimethylarginine (ADMA) levels in children with isolated growth hormone deficiency (GHD) and to determine the effect of GH replacement therapy on these levels. Methods: 31 patients diagnosed with isola
Autor:
Havva Nur Peltek Kendirci, Sebahat Yılmaz Ağladıoğlu, Aşan Önder, Veysel Nijat Baş, Semra Çetinkaya, Şenay Savaş Erdeve, Zehra Aycan
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Hyperinsulinemic hypoglycemia (HIH) is a genetically heterogeneous disorder with both familial and sporadic variants. Patients with HIH may present during the neonatal period, infancy, or childhood and may show transient, prolonged, and pe