Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Nurdan Çiftci"'
Autor:
Nurdan Çiftci, Ayşehan Akıncı, Ekrem Akbulut, Emine Çamtosun, İsmail Dündar, Mustafa Doğan, Leman Kayaş
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 160-171 (2023)
INTRODUCTION: Idiopathic hypogonadotropic hypogonadism (IHH) is classified into two groups-Kalman syndrome and normosmic IHH (nIHH). Half of all cases can be explained by mutations in >50 genes. Targeted gene panel testing with nexrt generation seque
Externí odkaz:
https://doaj.org/article/8a258e2999784d2c9e03036484c25077
Autor:
Şenay Güven Baysal, Nurdan Çiftci, İsmail Dündar, Mehmet Akif Büyükavcı, Fatma Hilal Yağın, Emine Çamtosun, Derya Doğan, Ayşehan Akıncı
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 172-181 (2023)
INTRODUCTION: With the diagnosis of chronic illness in children, a stressful period is likely to begin for both the affected child and their families. The aim of this study was to investigate the factors affecting chronic disease management by the pa
Externí odkaz:
https://doaj.org/article/249bbeb0793d4150b254bdae9fb11b1a
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 233-238 (2022)
The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone (T) from Δ4-androstenedione, and plays an important role in the final steps of androgen synthesis. 17β-HSD3 deficiency originates from mutat
Externí odkaz:
https://doaj.org/article/d1687b8456ca4afdbc979b0a4a9f70ce
Publikováno v:
Ege Tıp Dergisi. 62:61-67
Amaç: Tip 1 diabetes mellitus (T1DM) tanılı çocuklar diyabet öz bakımında gözetime ihtiyaç duymaktadırlar ve günün önemli bir kısmını geçirdikleri okuldaki koşullar hastalık yönetimini etkilemektedir. Bu çalışmanın amacı, T1D
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8967ef742ec9eafb206676912e8df3f5
https://doi.org/10.19161/etd.1262450
https://doi.org/10.19161/etd.1262450
Distal Renal Tubular Acidosis can be the Cause of Hypokalemia in Graves’ Disease: A Rare Association
Publikováno v:
Medical Records. 5:423-5
Distal renal tubular acidosis (dRTA) may rarely occur in the course of autoimmune diseases. We present a patient who was followed up with Graves' disease and vitiligo and who was diagnosed with dRTA upon detection of hypopotasemia. A 9.2-year-old gir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::27802bd13a0411ee3197b7e64e3794ec
https://doi.org/10.37990/medr.1180665
https://doi.org/10.37990/medr.1180665
Publikováno v:
Turkish Journal of Medical Sciences. 52:1863-1871
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b95d0e4cbb21b4f0c63c3eee05496b6e
https://doi.org/10.55730/1300-0144.5533
https://doi.org/10.55730/1300-0144.5533
Publikováno v:
Asthma Allergy Immunology. 19:136-141
Objective: There is no definitive consensus on asthma exacerbation scoring for preschool children with recurrent wheezing. The Clinical Asthma Score (CAS) and Asthma Severity Score (ASS) are two scoring systems that can be used in this population. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::944927925402bdf8286372b8d69b74d4
https://doi.org/10.21911/aai.607
https://doi.org/10.21911/aai.607
Publikováno v:
Journal of clinical research in pediatric endocrinology. 14(2)
The enzyme 17-β-hydroxysteroid dehydrogenase type 3 (17β-HSD3) catalyzes the biosynthesis of testosterone (T) from Δ4-androstenedione, and plays an important role in the final steps of androgen synthesis. 17β-HSD3 deficiency originates from mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::db93cda4e1c90b0c7c4a86b009e9f963
https://pubmed.ncbi.nlm.nih.gov/33389920
https://pubmed.ncbi.nlm.nih.gov/33389920
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