Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Nurdan Çiftçi"'
Autor:
Sevgi Demiröz Taşolar, Ahmet Sığırcı, Nurdan Çiftçi, Aslınur Cengiz, Güleç Mert Doğan, Ayşehan Akıncı
Publikováno v:
İstanbul Medical Journal, Vol 24, Iss 3, Pp 346-350 (2023)
Introduction:Although more common in adults, autoimmune thyroiditis (AT) is one of the most common thyroid diseases in children and adolescents. Salivary gland involvement has been described in many studies of patients with AT. Several inflammatory s
Externí odkaz:
https://doaj.org/article/b517de393fea4980ba0c7c8384132214
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 225-229 (2023)
Variants of the melanocortin-4 receptor (MC4R) gene are the most common cause of monogenic obesity. It has been shown that, while obesity cannot be controlled with diet and exercise, glucagon-like-peptide-1 receptor agonists (GLP-1 RA) provide weight
Externí odkaz:
https://doaj.org/article/1eec7118741341a587aace35a21468b8
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 88-99 (2021)
Objective:Primary adrenal insufficiency (PAI) is a rare but potentially life-threatening condition. In childhood, PAI is usually caused by monogenic diseases. Although congenital adrenal hyperplasia (CAH) is the most common cause of childhood PAI, nu
Externí odkaz:
https://doaj.org/article/4e0e3d24c0a841f09d3a185e4526084f
Publikováno v:
Journal of Pediatric Research, Vol 6, Iss 1, Pp 24-28 (2019)
Aim:Coagulation and fibrinolytic systems play an important role in the pathogenesis of complicated pneumonia. This study aims to evaluate and compare coagulation and fibrinolytic system markers and natural anticoagulant proteins with acute phase reac
Externí odkaz:
https://doaj.org/article/6f1a50b9922742108f23beed6f0e2b96
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:225-229
Variants of the melanocortin-4 receptor (MC4R) gene are the most common cause of monogenic obesity. In this situation; while obesity cannot be controlled with diet and exercise, it was shown that Glucagon-like-peptide-1 receptor agonists (GLP-1 RA) p
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:233-238
The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone from Δ4-androstenedione, and plays an important role in the final steps of androgen synthesis. 17β-HSD3 deficiency originates from mutations
Publikováno v:
Ankara Üniversitesi Tıp Fakültesi Mecmuas, Vol 74, Iss 1, Pp 68-75 (2021)
Objectives:In children, the frequency of malignancy in thyroid nodules is higher than in adults. The aim of our study was to determine the effective factors in assigning malignant nodules in children with thyroid nodule.Materials and Methods:This is
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 13, Iss 1, Pp 88-99 (2021)
JCRPE, Vol 13, Iss 1, Pp 88-99 (2021)
Objective: Primary adrenal insufficiency (PAI) is a rare but potentially life-threatening condition. In childhood, PAI is usually caused by monogenic diseases. Although congenital adrenal hyperplasia (CAH) is the most common cause of childhood PAI, n
Publikováno v:
The Turkish journal of pediatrics. 64(1)
The study aim was to examine changes in trends of presenting features during the diagnosis of patients followed up with newly diagnosed Type 1 diabetes mellitus (T1DM) over the past 24 years.The study was retrospective. Patients with a diagnosis of T
Publikováno v:
Journal of clinical research in pediatric endocrinology.
Variants of the melanocortin-4 receptor (