Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Tülay Güran"'
Autor:
Didem Helvacıoğlu, Tülay Güran
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 4-10 (2024)
3'-Phosphoadenosine 5'-phosphosulfate synthase 2 (PAPSS2) deficiency is a rare disorder due to biallelic pathogenic variants in the PAPSS2 gene. This disorder was first described in 1998 by Ahmad et al. and Faiyaz ul Haque et al. To date, 79 patients
Externí odkaz:
https://doaj.org/article/4ad4f01e7aa044138f97f7d9f79ac8a5
Autor:
Hazal Arıkan Gacemer, Büşra Gürpınar Tosun, Didem Helvacıoğlu, Zehra Yavaş Abalı, Belma Haliloğlu, Serap Demircioğlu Turan, Abdullah Bereket, Tülay Güran
Publikováno v:
Global Pediatrics, Vol 8, Iss , Pp 100155- (2024)
Although hypothalamic-pituitary-gonadal axis activation and hormone levels in mini-puberty are similar to the pubertal period1, its role in human development and reproduction has not been fully elucidated2. We aimed to evaluate the effects of somatic
Externí odkaz:
https://doaj.org/article/63492e38e2ee4167bb170ead73ef30ac
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:
Avinaash Maharaj, Ruth Kwong, Jack Williams, Christopher Smith, Helen Storr, Ruth Krone, Debora Braslavsky, Maria Clemente, Nanik Ram, Indraneel Banerjee, Semra Çetinkaya, Federica Buonocore, Tülay Güran, John C Achermann, Louise Metherell, Rathi Prasad
Publikováno v:
Endocrine Connections, Vol 11, Iss 8, Pp 1-13 (2022)
Sphingosine-1-phosphate lyase (SGPL1) insufficiency syndrome (SPLIS) is an autosomal recessive multi-system disorder, which mainly incorporates steroid-resistant nephrotic syndrome and primary adrenal insufficiency. Other variable endocrine manifesta
Externí odkaz:
https://doaj.org/article/998cb49010bf449f9664169eafe1b31b
Autor:
Tarık Kırkgöz, Mehmet Eltan, Sare Betül Kaygusuz, Zehra Yavaş Abalı, Didem Helvacıoğlu, Tuba Seven Menevşe, Büşra Gürpınar Tosun, Tülay Güran, Abdullah Bereket, Serap Demircioğlu
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 10-16 (2022)
INTRODUCTION: To evaluate the efficacy of degludec/aspart (IDegAsp) insulin co-formulation in children and adolescents with poorly controlled type 1 diabetes (T1DM). METHODS: Patients with poorly controlled T1DM on basal-bolus insulin regimes and hav
Externí odkaz:
https://doaj.org/article/9b4e9ffa674640829bd915ce8ce01ac7
Autor:
Tülay Güran, Başak Tezel, Meltem Çakır, Ayşehan Akıncı, Zerrin Orbak, Mehmet Keskin, Beray Selver Eklioğlu, Alev Ozon, Mehmet Nuri Özbek, Gülay Karagüzel, Nihal Hatipoğlu, Fatih Gürbüz, Filiz Mine Çizmecioğlu, Cengiz Kara, Enver Şimşek, Firdevs Baş, Murat Aydın, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 287-294 (2020)
Objective:Turkish Directorate of Public Health introduced the first pilot screening program for congenital adrenal hyperplasia (CAH) in four Turkish cities in 2017, and in 2018 extended the program, with a slight change in screening strategy, to four
Externí odkaz:
https://doaj.org/article/7f7e63806add4ccfa5a30c6a2471ecb8
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
Autor:
Tülay Güran, Başak Tezel, Fatih Gürbüz, Beray Selver Eklioğlu, Nihal Hatipoğlu, Cengiz Kara, Enver Şimşek, Filiz Mine Çizmecioğlu, Alev Ozon, Firdevs Baş, Murat Aydın, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 13-23 (2019)
Objective:Congenital adrenal hyperplasia (CAH) is the most common form of primary adrenal insufficiency in children. Neonatal screening for CAH is effective in detecting the salt-wasting (SW) form and in reducing mortality. In this study, our aim was
Externí odkaz:
https://doaj.org/article/d5a9e17ac4384c83bc5cd06841996b64