Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Yağmur Ünsal"'
Autor:
Yağmur Ünsal, Gamze Hayran
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 116-122 (2024)
Monocarboxylate transporter 8 (MCT8) deficiency is a rare genetic disorder characterized by peripheral thyrotoxicosis and severe cognitive and motor disability due to cerebral hypothyroidism. 3,3',5-triiodothyroacetic acid (Triac) was shown to improv
Externí odkaz:
https://doaj.org/article/fd71fab89a524055b58d8ca71b01f049
Autor:
Dicle Canoruc Emet, Hande Nur Karavar, Onur Gozmen, Arife Aslan Agyar, Yağmur Ünsal, Merve Canturk, Pınar Cengiz, Dogus Vuralli, Z. Alev Ozon, E. Nazlı Gonc
Publikováno v:
Journal of Diabetes, Vol 15, Iss 12, Pp 1011-1019 (2023)
Abstract Background Residual beta‐cell function and improvement in insulin sensitivity by reversal of glucose toxicity are two phenomena thought to be related to partial remission (PR). Body fat mass is the major determinant of insulin sensitivity.
Externí odkaz:
https://doaj.org/article/f326db3fcaf045ceb43025058221198d
Autor:
Nur Berna, Çelik, Yağmur, Ünsal, Dicle, Canoruç Emet, Ayşe, Mete Yeşil, Buse, Şencan, Elmas Nazlı, Gönç, Zeynep Alev, Özön, Elif Nursel, Özmert, Ayfer, Alikaşifoğlu
Publikováno v:
Turkish Archives of Pediatrics. 57:621-629
This study aimed to investigate the psychosocial impact of the pandemic in pediatric patients with congenital adrenal hyperplasia and their families and whether congenital adrenal hyperplasia imposes an additional burden compared to other endocrine d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::896e04c76eceaeb9d108a495d0047794
https://doi.org/10.5152/turkarchpediatr.2022.22096
https://doi.org/10.5152/turkarchpediatr.2022.22096
Autor:
Bora Gulhan, Yağmur Ünsal, Demet Baltu, Nur Berna Çelik Ertaş, Gülşah Özdemir, Eda Utine, H. Nursun Ozcan, Ali Duzova, Nazli Gönç
Publikováno v:
Blood Pressure Monitoring. 27:208-211
A genetic defect of 11 β-hydroxysteroid dehydrogenase causes apparent mineralocorticoid excess syndrome. Since 50 days of life, our patient was hospitalized several times for various reasons including hypokalemia. At the age of 3.3 years, she was di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0609c0b275d005dd941a02759b0ca26f
https://doi.org/10.1097/mbp.0000000000000583
https://doi.org/10.1097/mbp.0000000000000583
Autor:
Yagmur Unsal, Onur Gozmen, İdil Rana User, Hayriye Hızarcıoglu, Bora Gulhan, Saniye Ekinci, Tevfik Karagoz, Z. Alev Ozon, E. Nazlı Gonc
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundCafé-au-lait skin macules, Cushing syndrome (CS), hyperthyroidism, and liver and cardiac dysfunction are presenting features of neonatal McCune–Albright syndrome (MAS), CS being the rarest endocrine feature. Although spontaneous resoluti
Externí odkaz:
https://doaj.org/article/fddd74a8905c4363b73098cb61da4ebc