Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Serap TURAN"'
Autor:
Büşra Gürpınar Tosun, Ahsen Karagözlü Akgül, Eda Almus, Sadık Abidoğlu, Serap Turan, Abdullah Bereket, Tülay Güran
Publikováno v:
JCRPE, Vol 15, Iss 3, Pp 324-328 (2023)
Clitoromegaly usually develops due to hyperandrogenism. There are a few cases of clitoromegaly described without clinical and biochemical hyperandrogenism. Clitoromegaly due to clitoral priapism and clitoral priapism after appendectomy have not been
Externí odkaz:
https://doaj.org/article/4336a957e9ec46a6a5383d1490e2287d
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
Autor:
Serap Turan, Steven Mumm, Ceren Alavanda, Betul Sare Kaygusuz, Busra Gurpinar Tosun, Ahmet Arman, Margaret Huskey, Tulay Guran, Shenghui Duan, Abdullah Bereket, Michael P. Whyte
Publikováno v:
JBMR Plus, Vol 6, Iss 8, Pp n/a-n/a (2022)
ABSTRACT Dysosteosclerosis (DSS), the term coined in 1968 for ultrarare dysplasia of the skeleton featuring platyspondyly with focal appendicular osteosclerosis, has become generic by encompassing the genetic heterogeneity recently reported for this
Externí odkaz:
https://doaj.org/article/8154fb917ffb49d3850c595ac9649403
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
Autor:
Erdal Eren, Ayça Törel Ergür, Şükriye Pınar İşgüven, Eda Çelebi Bitkin, Merih Berberoğlu, Zeynep Şıklar, Firdevs Baş, Servet Yel, Serpil Baş, Elif Söbü, Abdullah Bereket, Serap Turan, Halil Sağlam, Zeynep Atay, Oya Ercan, Tülay Güran, Mehmet Emre Atabek, Hüseyin Anıl Korkmaz, Aylin Kılınç Uğurlu, Ayşehan Akıncı, Esra Döğer, Enver Şimşek, Emine Demet Akbaş, Ayhan Abacı, Ülkü Gül, Sezer Acar, Eda Mengen Uçaktürk, Melek Yıldız, Edip Ünal, Ömer Tarım
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 149-156 (2019)
Objective:We aimed to report the characteristics at admission, diagnosis, treatment, and follow-up of cases of pediatric hyperprolactinemia in a large multicenter study.Methods:We reviewed the records of 233 hyperprolactinemic patients, under 18 year
Externí odkaz:
https://doaj.org/article/bfc431f9dff74272a2b6236d033334a3
Publikováno v:
Frontiers in Endocrinology, Vol 12 (2021)
Insulin degludec/insulin aspart (IDegAsp) is a fixed-ratio co-formulation of insulin degludec (IDeg), which provides long-lasting basal insulin coverage, and insulin aspart (IAsp), which targets post-prandial glucose. This expert panel aimed to provi
Externí odkaz:
https://doaj.org/article/d25011f81503401b84ee941684218469
Autor:
Gulin Sunter, Ece Oge Enver, Azad Akbarzade, Serap Turan, Pinar Vatansever, Dilek Ince Gunal, Goncagul Haklar, Abdullah Bereket, Kadriye Agan, Tulay Guran
Publikováno v:
BMC Neurology, Vol 18, Iss 1, Pp 1-6 (2018)
Abstract Background Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal insufficiency and steroid-resistant nephrotic syndrome. S1P lyase,
Externí odkaz:
https://doaj.org/article/bd219541ea214e42ad4d4ea3ea85a112
Publikováno v:
Journal of Istanbul University Faculty of Dentistry, Vol 49, Iss 1, Pp 51-55 (2015)
The aim of this article is to present intra- and extra-oral and cephalometric findings of three patients with a rare disease: the pycnodysostosis. Two cases had skeletal Class III malocclusion due to maxillary retrognathia and one had bimaxillary ret
Externí odkaz:
https://doaj.org/article/17a44bff3580424bb33846c8d9aafa0e
Autor:
Hulya Ozdemir, Ipek Akman, Senay Coskun, Utku Demirel, Serap Turan, Abdullah Bereket, Hulya Bilgen, Eren Ozek
Publikováno v:
International Journal of Endocrinology, Vol 2013 (2013)
Aim. To investigate obstetric features of pregnant women with thyroid disorders and thyroid function tests of their newborn infants. Methods. Women with hypothyroidism and having anti-thyroglobulin (ATG) and anti-thyroid peroxidase (anti-TPO) antibod
Externí odkaz:
https://doaj.org/article/192295c3e5ac451abb500a5834de5408
Autor:
Tarik Kirkgoz, Tulay Guran, Didem Helvacioglu, Tuba Seven Menevse, Mehmet Eltan, Serap Turan, Sare Betul Kaygusuz, Busra Gurpinar Tosun, Abdullah Bereket, Zehra Yavas Abali
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 14:10-16
To evaluate the efficacy of degludec/aspart (IDegAsp) insulin co-formulation in children and adolescents with poorly controlled type 1 diabetes (T1DM).Patients with poorly controlled T1DM on basal-bolus insulin regimes and having compliance problems
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf987c5b0d9045b52ce6fd63c3f678ac
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0113
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0113