Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Meliha, Demiral"'
Publikováno v:
Journal of Pediatric Research, Vol 11, Iss 3, Pp 185-188 (2024)
All-trans retinoic acid (ATRA), a derivative of vitamin A, has dramatically altered the treatment landscape for acute promyelocytic leukemia (APL). APL is characterized by the abnormal maturation of myeloid cells, which become arrested at the promyel
Externí odkaz:
https://doaj.org/article/906355b70e864180a4ea52df31bfa528
Autor:
Enver Şimşek, Oğuz Çilingir, Tülay Şimşek, Sinem Kocagil, Ebru Erzurumluoğlu Gökalp, Meliha Demiral, Çiğdem Binay
Publikováno v:
JCRPE, Vol 16, Iss 2, Pp 137-145 (2024)
INTRODUCTION: Maturity-onset diabetes of the young (MODY) is the most common type of monogenic diabetes. To date, mutations have been identified in 14 different genes of patients with a clinical diagnosis of MODY. This study screened mutations in 14
Externí odkaz:
https://doaj.org/article/dc998513a3bb459ca58f77550f1024b7
Autor:
Şervan Özalkak, Meliha Demiral, Edip Ünal, Funda Feryal Taş, Hüseyin Onay, Hüseyin Demirbilek, Mehmet Nuri Ozbek
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 329-333 (2023)
Congenital generalized lipodystrophy (CGL) is a rare, autosomal recessive disorder characterized by an almost complete absence of body fat. In CGL, patients may have hyperphagia due to leptin deficiency. Recombinant human leptin (metreleptin) has bee
Externí odkaz:
https://doaj.org/article/b651e69acbc8494fac0c0d6b3485c796
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 27, Iss 3, Pp 237-241 (2023)
Aim: In this study, it was aimed to examine the clinical and laboratory findings that can be used to predict central precocious puberty (CPP) in cases whose breast development started before the age of 8. Materials and Methods: The chronological age,
Externí odkaz:
https://doaj.org/article/7bfc89aa12bb4091a9d65dd340341496
Publikováno v:
Klinik Psikiyatri Dergisi, Vol 25, Iss 2, Pp 148-154 (2022)
INTRODUCTION: The presence of comorbid psychiatric conditions in chronic diseases makes the management of the disease difficult. Our study, we aimed to examine the relationship between psychiatric comorbid conditions and glycemic control in children
Externí odkaz:
https://doaj.org/article/035f914db99944e395eca7d2be54049e
Autor:
Şenay Savaş-Erdeve, Zehra Aycan, Semra Çetinkaya, Ayşe Pınar Öztürk, Firdevs Baş, Şükran Poyrazoğlu, Feyza Darendeliler, Elif Özsu, Zeynep Şıklar, Meliha Demiral, Edip Unal, Mehmet Nuri Özbek, Fatih Gürbüz, Bilgin Yüksel, Olcay Evliyaoğlu, Nesibe Akyürek, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 180-186 (2021)
Objective:To retrospectively evaluate the follow-up data in patients with 46,XX congenital adrenal hyperplasia (CAH) who were raised male.Methods:A national database was created. The data of patients were asked to be recorded in the data form.Results
Externí odkaz:
https://doaj.org/article/f9e01545ac464347a539fec859b71f5e
Autor:
Maha Sherif, Hüseyin Demirbilek, Atilla Çayır, Sophia Tahir, Büşra Çavdarlı, Meliha Demiral, Ayşe Nurcan Cebeci, Doğuş Vurallı, Sofia Asim Rahman, Edip Unal, Gönül Büyükyılmaz, Riza Taner Baran, Mehmet Nuri Özbek, Khalid Hussain
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 34-43 (2021)
Objective:Bi-allelic mutations in the wolframin gene (WFS1) cause Wolfram syndrome 1 (WS1 or DIDMOAD) characterized by non-autoimmune diabetes mellitus, optic atrophy, diabetes insipidus, sensorineural deafness, urinary tract abnormalities, and neuro
Externí odkaz:
https://doaj.org/article/98ad2c4ca25547f1b7b9db3e4bc101ad
Autor:
Edip Unal, Meliha Demiral, Birsen Baysal, Mehmet Ağın, Elif Gökçe Devecioğlu, Hüseyin Demirbilek, Mehmet Nuri Özbek
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 72-79 (2021)
Objective:The prevalence of celiac disease (CD) varies between 1% and 10% in patients with type 1 diabetes mellitus (T1DM). This study aimed to determine the frequency of spontaneous recovery of celiac serology and the biopsy-proven CD (BPCD) frequen
Externí odkaz:
https://doaj.org/article/2a3006ffcbb546aebcbf1460e144f5fa
Autor:
Meliha Demiral, Edip Unal, Birsen Baysal, Rıza Taner Baran, Hüseyin Demirbilek, Mehmet Nuri Özbek
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 295-302 (2020)
Objective:The aim was to determine the final adult height (FAH) achieved by recombinant human growth hormone (rhGH) treatment, the factors affecting FAH and the success of attaining the genetic potential.Methods:Data of 133 patients treated with rhGH
Externí odkaz:
https://doaj.org/article/3e87d44003e14d6b8391a76e802c7d50
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 275-280 (2020)
Objective:The tendency to reduce thyroid stimulating hormone (TSH) referral cut-off values in congenital hypothyroidism (CH) neonatal screening programs has resulted in an increase in the incidence of CH, but also the referral of infants with mild tr
Externí odkaz:
https://doaj.org/article/da9649e38402486aac50cf15236fa002