Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Alev Özön"'
Autor:
Doğuş Vurallı, Yılmaz Yıldız, Alev Ozon, Ali Dursun, Nazlı Gönç, Ayşegül Tokatlı, H. Serap Sivri, Ayfer Alikaşifoğlu
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 275-286 (2022)
INTRODUCTION: Phosphomannomutase 2 deficiency (PMM2-CDG) is a disorder of protein N-glycosylation with a wide clinical spectrum. Hypoglycemia is rarely reported in PMM2-CDG. In this study, we evaluated cause, treatment options and outcomes in cases w
Externí odkaz:
https://doaj.org/article/350ef7fdfc1c4bbd8057957aeb6d01ea
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
Autor:
Doğuş Vurallı, Nazlı Gönç, Alev Özön, Saniye Ekinci, H. Serkan Doğan, Serdar Tekgül, Ayfer Alikaşifoğlu
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 17-28 (2022)
INTRODUCTION: Estrogen-secreting adrenocortical tumors (ACTs) are quite rare with feminizing adrenocortical tumors (FATs) accounting for 0.37-2% of all ACTs. The aim was to evaluate clinical and hormonal characteristics of FATS as well as treatment o
Externí odkaz:
https://doaj.org/article/bb59c52672de4ffba907c8c4fb618aa6
Publikováno v:
JCRPE, Vol 13, Iss 3, Pp 269-275 (2021)
Objective:Initial high-dose sodium levothyroxine (Na-LT4) (10-15 μg/kg/day) replacement for primary congenital hypothyroidism (CH) is recommended in guidelines. However, high-dose Na-LT4 risks iatrogenic hyperthyroidism. The aim of this study was to
Externí odkaz:
https://doaj.org/article/e82512dcf38d4cd19661f3d4c73f2eb0
Autor:
Nur Berna Çelik, Monique Losekoot, Emregül Işık, E. Nazlı Gönç, Ayfer Alikaşifoğlu, Nurgün Kandemir, Z. Alev Özön
Publikováno v:
JCRPE, Vol 16, Iss 4, Pp 481-488 (2024)
Insulin-like growth factor-1 (IGF-1) is the main driver of growth during prenatal life and acts through IGF-1 receptor (IGF1R). Patients with IGF1R defects exhibit variable phenotypic features. A 10.9-year-old boy presented with severe short stature,
Externí odkaz:
https://doaj.org/article/74d2e5b26f0a432fa8c3f5c851e65c15
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
Akademický článek
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Autor:
Nurgun Kandemir, Dogus Vuralli, Alev Ozon, Nazlı Gonc, Didem Ardicli, Lala Jalilova, Omer Nazim Gulcek, Ayfer Alikasifoglu
Publikováno v:
Journal of Diabetes, Vol 16, Iss 5, Pp n/a-n/a (2024)
Abstract Background Global variations in epidemiology of type 1 diabetes mellitus (T1DM) exist. This study is designed to examine demographic and clinical features of T1DM over the past 3 decades as well as evolving trends in epidemiology over last 5
Externí odkaz:
https://doaj.org/article/a8dfdacb5c674a91aa6756705a42d8df
Publikováno v:
Turkish Archives of Pediatrics/Türk Pediatri Arşivi
To determine the clinical, anthropometric, and laboratory parameters that could be used for differentiating central precocious puberty from premature thelarche in girls who had breast development between the ages of 3 and 8 years.The study included 3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6018c812fc8045ec9cf9411aebf8de09
https://pubmed.ncbi.nlm.nih.gov/32684758
https://pubmed.ncbi.nlm.nih.gov/32684758
Autor:
Emregül, Işık, Paolo, Beck Peccoz, Irene, Campi, Alev, Özön, Ayfer, Alikaşifoğlu, Nazlı, Gönç, Nurgün, Kandemir
Publikováno v:
The Turkish journal of pediatrics. 55(3)
Thyroid hormone resistance (THR) is a dominantly inherited syndrome characterized by reduced sensitivity to thyroid hormones. It is usually caused by mutations in the thyroid hormone receptor beta (THRB) gene. In the present report, we describe the c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccfabecb922669ffcc212aa2e2d4e998
https://pubmed.ncbi.nlm.nih.gov/24217081
https://pubmed.ncbi.nlm.nih.gov/24217081