Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Korcan Demir"'
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:
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
Autor:
Özge Besci, Reyhan Deveci Sevim, Kübra Yüksek Acinikli, Gözde Akın Kağızmanlı, Sezen Ersoy, Korcan Demir, Tolga Ünüvar, Ece Böber, Ahmet Anık, Ayhan Abacı
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 268-275 (2023)
INTRODUCTION: Both body weight (BW)- and body surface area (BSA)-based dosing regimens have been recommended for growth hormone (rhGH) replacement. The aim was to compare the two regimens to determine if either resulted in inadequate treatment depend
Externí odkaz:
https://doaj.org/article/ea5c25ee1f9740498a9298f7cec35805
Autor:
Tülay Güran, Didem Helvacıoğlu, Büşra Gürpınar Tosun, Zehra Yavaş Abalı, Fahriye Alır, Yusuf Taha Arslan, Giasim Molla, Berk Şahin, Mehmet Emir Sayar, Zeynep Atay, Belma Haliloğlu, Korcan Demir, Serap Turan, Seyhan Hıdıroğlu, Abdullah Bereket
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 154-159 (2023)
INTRODUCTION: Menarche is the endpoint of a sequence of maturational events of female puberty. The timing of menarche is a strongly heritable trait. However, secular trends suggest that lifestyle and environmental factors are important. To assess the
Externí odkaz:
https://doaj.org/article/d2736e83ecdc41d3b6598c629c5c4583
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:
Semra Gürsoy, Filiz Hazan, Ayça Aykut, Özlem Nalbantoğlu, Hüseyin Anıl Korkmaz, Korcan Demir, Behzat Özkan, Özgür Çoğulu
Publikováno v:
JCRPE, Vol 12, Iss 4, Pp 358-365 (2020)
Objective:SHOX gene mutations constitute one of the genetic causes of short stature. The clinical phenotype includes variable degrees of growth impairment, such as Langer mesomelic dysplasia (LMD), Léri-Weill dyschondrosteosis (LWD) or idiopathic sh
Externí odkaz:
https://doaj.org/article/02289d179bc0403abd95c92f1caed883
Autor:
Zeynep Şıklar, Serap Turan, Abdullah Bereket, Firdevs Baş, Tülay Güran, Azad Akberzade, Ayhan Abacı, Korcan Demir, Ece Böber, Mehmet Nuri Özbek, Cengiz Kara, Şükran Poyrazoğlu, Murat Aydın, Aslı Kardelen, Ömer Tarım, Erdal Eren, Nihal Hatipoğlu, Muammer Büyükinan, Nesibe Akyürek, Semra Çetinkaya, Elvan Bayramoğlu, Beray Selver Eklioğlu, Ahmet Uçaktürk, Saygın Abalı, Damla Gökşen, Yılmaz Kor, Edip Ünal, İhsan Esen, Ruken Yıldırım, Onur Akın, Atilla Çayır, Emine Dilek, Birgül Kırel, Ahmet Anık, Gönül Çatlı, Merih Berberoğlu
Publikováno v:
JCRPE, Vol 12, Iss 2, Pp 150-159 (2020)
Objective:Hypophosphatemic rickets (HR) is a rare renal phosphate-wasting disorder, which is usually X-linked and is commonly caused by PHEX mutations. The treatment and follow-up of HR is challenging due to imperfect treatment options.Methods:Here w
Externí odkaz:
https://doaj.org/article/57157ae9f20b435fb128022ec51d0c16