Zobrazeno 1 - 10
of 33
pro vyhledávání: '"İbrahim Mert Erbaş"'
Autor:
Fulya Mete Kalaycı, Özlem Gürsoy Doruk, İbrahim Mert Erbaş, Osman Tolga İnce, Makbule Neslişah Tan, Adem Aydın, Ayhan Abacı, Ece Böber, Korcan Demir
Publikováno v:
JCRPE, Vol 16, Iss 2, Pp 185-191 (2024)
INTRODUCTION: The hypothalamic-pituitary-gonadal axis is active during minipuberty, the timing of which coincides with infantile colic. To the best of our knowledge, the relationship between these entities has not been previously investigated. METHO
Externí odkaz:
https://doaj.org/article/4cde639c97ef496c9c071a92d680685b
Autor:
Hüseyin Anıl Korkmaz, Ali Devebacak, İbrahim Mert Erbaş, Cumali Değirmenci, Nilüfer Uyar, Filiz Afrashi, Behzat Özkan
Publikováno v:
JCRPE, Vol 15, Iss 4, Pp 390-396 (2023)
INTRODUCTION: The aim of this study was to compare the development of early diabetic retinopathy (DR) findings, a microvascular complication, between patients with isolated type 1 diabetes mellitus (T1DM) (Group 1), concurrent T1DM and autoimmune thy
Externí odkaz:
https://doaj.org/article/166fe5c95b8d422bb33e3e2e2624f852
Autor:
İbrahim Mert Erbaş, İrem Ceren Erbaş, Gözde Akın Kağızmanlı, Kübra Yüksek Acinikli, Özge Besci, Korcan Demir, Ece Böber, Nurşen Belet, Ayhan Abacı
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 248-256 (2023)
INTRODUCTION: The aim was to evaluate the adverse events seen after Coronavirus disease-2019 (COVID-19) vaccination in pediatric patients with diagnosed endocrinological problems and to compare them with healthy controls. METHODS: In this cross-sect
Externí odkaz:
https://doaj.org/article/545d471e1fe14a4da4db3a820c4b90cc
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 302-307 (2022)
INTRODUCTION: Early puberty is development of secondary sex characteristics earlier than the expected normal age range. We subjectively observed an increased frequency of early puberty during the Coronavirus disease-2019 (COVID-19) lockdown and aimed
Externí odkaz:
https://doaj.org/article/1c5643cc237c43a49dc875b050ed02df
Autor:
Özge Besci, İbrahim Mert Erbaş, Tuncay Küme, Kübra Yüksek Acinikli, Ayhan Abacı, Ece Böber, Korcan Demir
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 145-152 (2022)
INTRODUCTION: Objective: Since there is no gold standard laboratory variable for adjustment of treatment in congenital adrenal hyperplasia (CAH), the aim was to assess the use of a 4-hour profile of serum 17-hydroxyprogesterone (17-OHP) to determine
Externí odkaz:
https://doaj.org/article/56008d0aa1484a5f9ef7943e86e7c801
Autor:
İbrahim Mert Erbaş, Ahu Paketçi, Serkan Turan, Ali Rıza Şişman, Korcan Demir, Ece Böber, Ayhan Abacı
Publikováno v:
JCRPE, Vol 14, Iss 2, Pp 179-187 (2022)
INTRODUCTION: Objective: C1q/tumor necrosis factor-related proteins (CTRPs) are recently described members of the adipokine family. CTRP-13, a new member of this family, has been shown to increase insulin sensitivity and had an anorexigenic effect on
Externí odkaz:
https://doaj.org/article/eccf9caf74464693be38c061b2fd8f7b
Autor:
İbrahim Mert Erbaş, Korcan Demir
Publikováno v:
JCRPE, Vol 13, Iss 1, Pp 1-14 (2021)
Resistance to thyroid hormone alpha occurs due to pathogenic, heterozygous variants in THRA. The entity was first described in 2012 and to date only a small number of patients with varying severity have been reported. In this review, we summarize and
Externí odkaz:
https://doaj.org/article/763ebb62c97a4c3e9415f5f36c81ce02
Autor:
İbrahim Mert Erbaş, İrem Ceren Erbaş, Gözde Akın Kağızmanlı, Kübra Yüksek Acinikli, Özge Besci, Korcan Demir, Ece Böber, Nurşen Belet, Ayhan Abacı
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef56af0052c7f8b20455c1a8e9e043ac
https://avesis.deu.edu.tr/publication/details/ca8a9281-6b6b-48b0-8fc4-74de8c83da92/oai
https://avesis.deu.edu.tr/publication/details/ca8a9281-6b6b-48b0-8fc4-74de8c83da92/oai
Autor:
Özge Besci, Kashyap Amratlal Patel, Gizem Yıldız, Özlem Tüfekçi, Kübra Yüksek Acinikli, İbrahim Mert Erbaş, Ayhan Abacı, Ece Böber, Meral Torun Bayram, Şebnem Yılmaz, Korcan Demir
Publikováno v:
Hormones. 21:501-506
Introduction SLC29A3 spectrum disorder is an autosomal, recessively inherited, autoinflammatory, multisystem disorder characterized by distinctive cutaneous features, including hyperpigmentation or hypertrichosis, hepatosplenomegaly, hearing loss, ca
Publikováno v:
Cutaneous and Ocular Toxicology. 40:359-364
Background and aim Retinopathy of prematurity (ROP) is the major ocular problem of preterm infants that occurs with abnormal proliferation of immature retinal vessels. Although pentoxifylline (PTX) was reported to inhibit vasculogenesis and neovascul