Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Sağlam, Halil"'
Autor:
Eren, Erdal, Yapıcı, Şenay, Çakır, Esra Deniz Papatya, Ceylan, Latife Aytekin, Sağlam, Halil, Tarım, Ömer
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Hyperprolactinemia may be due to various etiological factors and may present with different signs and symptoms. It is relatively less frequent in childhood than in adulthood. The aim of this study was to evaluate retrospectively the clinic
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Post-treatment endocrine disturbances are common in cancer patients who have received radiotherapy or chemotherapy. The objective of this study was to evaluate the thyroid functions of long-term survivors of pediatric Hodgkin’s lymphoma
Autor:
Sağlam, Halil, Tarım, Ömer
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Background and objectives: The prevalence of childhood obesity has been dramatically increasing worldwide. This study was performed to examine the prevalence and etiological factors of obesity in children aged 6−12 years and to investigate the rela
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
Objective: Hypophosphatasia (HPP) is a rare, commonly unrecognized hereditary mineralization defect with a dramatically poor prognosis in severe cases. This study is the first to examine the detailed clinical and laboratory characteristics of patient
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6f99d137c8e9a6e0731a63384329affa
http://hdl.handle.net/11452/30547
http://hdl.handle.net/11452/30547
Autor:
Şükran Darcan, Rüveyde Bundak, Cengiz Kara, Halil Saglam, Ahmet Uçaktürk, Filiz Tutunculer, Aysegul Yuksel, Tolga Ünüvar, Şükrü Hatun, Huseyin Demirbilek, Abdullah Bereket, Ergun Cetinkaya, Enver Simsek, Damla Gökşen Şimşek, Cigdem Binay, Yaşar Cesur
Hatun, Sukru/0000-0003-1633-9570; Mengen, Eda/0000-0003-1597-8418; binay, cigdem/0000-0002-7749-8818; UCAKTURK, Seyit Ahmet/0000-0001-8666-4454 WOS: 000381646900004 PubMed: 27423071 Aims: To evaluate the management strategies, glycemic control and co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0b3480578d3b5c10fb23403c872cb4a
https://hdl.handle.net/20.500.12645/4854
https://hdl.handle.net/20.500.12645/4854
Autor:
Erkan Sari, Tulay Guran, Aysşehan Akinci, Cengiz Kara, Selim Kurtoglu, Samim Özen, Gülay Karagüzel, Zehra Yavas Abali, Erdal Eren, Zeynep Atay, Filiz Tutunculer, Meltem Tayfun, Esra Döğer, Abdullah Bereket, Aysun Bideci, Semra Çetinkaya, Zehra Aycan, Gulcan Seymen Karabulut, Halil Saglam, Zeynep Şıklar, Serap Turan, Ediz Yeşilkaya, Leyla Akin, Şenay Savaş Erdeve
WOS: 000378819700011
PubMed ID: 26964727
Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of congenital adrenal hyperplasia (CAH), d
PubMed ID: 26964727
Aim: The causes of gonadotropin-independent precocious puberty are diverse, and often have overlapping clinical and biochemical features. With the exception of congenital adrenal hyperplasia (CAH), d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2dde1000097c3d4a93c51c7efc697346
https://hdl.handle.net/11424/241429
https://hdl.handle.net/11424/241429
Publikováno v:
Pediatrics International. 49:76-79
Background: The incidence of congenital hypothyroidism (CH) is expected to be elevated in iodine-deficient areas. In this study, the authors aimed to determine the incidence of transient and permanent CH in a large city which is known to be in the zo
Autor:
Uludağ Üniversitesi/Tıp Fakültesi/Pediatri Anabilim Dalı., Uludağ Üniversitesi/Tıp Fakültesi/Radyasyon Onkolojisi Anabilim Dalı., Demirkaya, Metin, Sevinir, Betül Berrin, Sağlam, Halil, Özkan, Lütfi, Akacı, Okan, AAH-1570-2021, C-7392-2019
Objective: Post-treatment endocrine disturbances are common in cancer patients who have received radiotherapy or chemotherapy. The objective of this study was to evaluate the thyroid functions of long-term survivors of pediatric Hodgkin's lymphoma tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9458::d1373d2a2b989b1a4a915e459f044549
http://hdl.handle.net/11452/23927
http://hdl.handle.net/11452/23927
Autor:
Morgan, Neil V., Forman, Julia R., Aycan, Zehra, Böber, Ece, Cesur, Yaşar, Kirby, Gail A., Pasha, Shanaz S., Çetinkaya, Semra Çağlar, Baş, Veysel Nihat, Demir, Korcan, Yuca, Sevil Arı, Meyer, Esther, Högler, Wolfgang, Timothy Barrett, Timothy, Mäher, Eamonn Richard
Objective Nonsyndromic autosomal recessively inherited non-goitrous congenital hypothyroidism (CHNG) can be caused by mutations in TSHR, PAX8, TSHB and NKX2-5. We aimed to investigate mutational frequencies of these genes and genotype/phenotype corre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______9458::f0f52c789e7ad5dacacddbf90ab20619
http://hdl.handle.net/11452/28370
http://hdl.handle.net/11452/28370
Publikováno v:
Pediatrics international : official journal of the Japan Pediatric Society. 47(1)