Zobrazeno 1 - 10
of 122
pro vyhledávání: '"Cengiz, Kara"'
Publikováno v:
JCRPE, Vol 15, Iss 2, Pp 214-219 (2023)
Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is an X-linked disease caused by activating mutations in the arginine vasopressin (AVP) receptor-2 (AVPR2) gene. Affected patients excrete concentrated urine despite very low levels of AVP, a
Externí odkaz:
https://doaj.org/article/b74f29ebb75f4189ad8a7bc39af2aebf
Autor:
Cengiz Kara, Jamala Mammadova, Ümmet Abur, Cagri Gumuskaptan, Elif İzci Güllü, Ayhan Dağdemir, Murat Aydın
Publikováno v:
European Thyroid Journal, Vol 12, Iss 3, Pp 1-11 (2023)
Objective: Guidelines on congenital hypothyroidism (CH) recommend that genetic testing should aim to improve diagnosis, treatment or prognosis, but it is unclear which patients would benefit most from the genetic investigation. We aimed to i nvestiga
Externí odkaz:
https://doaj.org/article/1d0774e9acdc4b0398ebd44eeec6ddd7
Autor:
İbrahim Kartal, Abdurrahman Alaçam, Ayhan Dağdemir, Cengiz Kara, Oğuz Salih Dinçer, Canan Albayrak, Murat Elli
Publikováno v:
Diabetology & Metabolic Syndrome, Vol 14, Iss 1, Pp 1-10 (2022)
Abstract Objectives In this study, it was aimed to determine the prevalence and clinical features of obesity and metabolic syndrome, which are long-term effects of survivors after treatment in children with leukemia and lymphoma. Patients and Methods
Externí odkaz:
https://doaj.org/article/d8d96eea0c604a07bf835f3e76ec3e78
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
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 55-62 (2020)
Objective:To determine the prevalence of obesity and metabolic syndrome (MetS) in children and adolescents with type 1 diabetes (T1D) and to compare the widely accepted and used diagnostic criteria for MetS established by the International Diabetes F
Externí odkaz:
https://doaj.org/article/9a730d2dbed84e64a0f7dae46b4699c1
Autor:
Korcan Demir, Hakan Döneray, Cengiz Kara, Zeynep Atay, Semra Çetinkaya, Atilla Çayır, Ahmet Anık, Erdal Eren, Ahmet Uçaktürk, Gülay Can Yılmaz, Ayça Törel Ergür, Mustafa Kendirci, Zehra Aycan, Abdullah Bereket, Murat Aydın, Zerrin Orbak, Behzat Özkan
Publikováno v:
JCRPE, Vol 11, Iss 2, Pp 140-148 (2019)
Objective:No large study has been conducted to date to compare the effectiveness of prednisolone, alendronate and pamidronate as first-line treatment in children with hypercalcemia due to vitamin D intoxication. The aim was to perform a multicenter,
Externí odkaz:
https://doaj.org/article/86d046d1aa254ddeb16fd5ef57b5393f
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
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology. 15:214-219
Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is an X-linked disease caused by activating mutations in the arginine vasopressin (AVP) receptor-2 (AVPR2) gene. Affected patients excrete concentrated urine despite very low levels of AVP, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ecfe53c55308026a1ce198a2cbbc81a
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0191
https://doi.org/10.4274/jcrpe.galenos.2021.2021.0191
Autor:
Mehmet Giray Sönmez, Cengiz Kara
Publikováno v:
Journal of Urological Surgery, Vol 4, Iss 4, Pp 189-194 (2017)
Objective: The aim of this study was to evaluate the efficacy of low-intensity linear shockwave treatment (LI-ESWT) in patients with severe arteriogenic erectile dysfunction (ED) by comparing LI-ESWT combined with daily use of phosphodiesterase type
Externí odkaz:
https://doaj.org/article/9a77a0b04fee4493a075390321a3e1c0