Zobrazeno 1 - 10
of 84
pro vyhledávání: '"Eda Mengen"'
Autor:
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 297-305 (2024)
INTRODUCTION: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases
Externí odkaz:
https://doaj.org/article/eb7e190aaeb24a0bb6a30c654ca0303b
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 233-240 (2020)
Objective:Adolescents with chronic disease are as likely to exhibit risk-taking behavior as their peers. The aim was to investigate the risk behaviors of adolescents with type 1 diabetes (T1D) and the effect of orthorexic eating behaviors (OEB) on gl
Externí odkaz:
https://doaj.org/article/1b9e5e28abbd4694a46582d4310c2741
Autor:
Fatma Derya Bulut, Semine Özdemir Dilek, Damla Kotan, Eda Mengen, Fatih Gürbüz, Bilgin Yüksel
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 261-268 (2020)
Objective:Mutations of the genes encoding transcription factors which play important roles in pituitary morphogenesis, differentiation and maturation may lead to combined pituitary hormone deficiency (CPHD). PROP1 gene mutations are reported as the m
Externí odkaz:
https://doaj.org/article/834c2557d203484c97842279ba83d755
Publikováno v:
JCRPE, Vol 12, Iss 3, Pp 308-314 (2020)
The 46,XX ovotesticular disorder of sex development (DSD) is rarely observed in humans. This disorder is generally described as ambiguous genitalia with the presence of ovarian and testicular tissues in different gonads or in the same gonad. Almost n
Externí odkaz:
https://doaj.org/article/a455cf3bc9a14e91819453abcf77f76b
Publikováno v:
JCRPE, Vol 12, Iss 2, Pp 206-211 (2020)
Adrenal hypoplasia is a rare congenital disorder. In spite of biochemical and molecular genetic evaluation, etiology in many patients with adrenal hypoplasia is not clear. MIRAGE syndrome is a recently recognized congenital disorder characterized by
Externí odkaz:
https://doaj.org/article/c369528b115848da87c28b64a9ab1049
Publikováno v:
JCRPE, Vol 12, Iss 2, Pp 202-205 (2020)
Pheochromocytomas and paragangliomas (PPGLs) are rare neuroendocrine tumors. The clinical presentation of pediatric PPGLs is highly variable. In cases with pheochromocytoma (PCC), excess catecholamine may stimulate myocytes and cause structural chang
Externí odkaz:
https://doaj.org/article/6e504cf9b63347e0a612f864090a4b6b
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 45-54 (2020)
Objective:There is an association between obesity and several inflammatory and oxidative markers in children. In this study, we analyzed thiol/disulfide homeostasis and serum ischemia-modified albumin (IMA) levels for the first time in order to clari
Externí odkaz:
https://doaj.org/article/50b01b4c0fb1442da2dc2d074c9e7c55
Autor:
Emine Azak, Seyit Ahmet Uçaktürk, İbrahim İlker Çetin, Hazım Alper Gürsu, Eda Mengen, Utku Pamuk
Publikováno v:
JCRPE, Vol 11, Iss 4, Pp 410-418 (2019)
Objective:Thyroid hormones have an important role in the regulation of the cardiovascular system. The aim of this study was to investigate the presence of subclinical myocardial dysfunction in children with euthyroid Hashimoto’s thyroiditis (eHT) w
Externí odkaz:
https://doaj.org/article/ba78ba27fdba4294a423bf3f9dc0cbfa
Publikováno v:
Journal of Behçet Uz Children's Hospital, Vol 10, Iss 3, Pp 306-308 (2020)
We present a newborn diagnosed with Beckwith-Wiedemann syndrome and hypoglycemia, and developed pulmonary hypertension due to initiated diazoxide treatment because of these indications. Beckwith-Wiedemann syndrome was considered due to abdominal wall
Externí odkaz:
https://doaj.org/article/f6596fd68e43417b994f7c0d7e379371
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