Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Alev, Özön"'
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:
Doğuş Vurallı, Lala Jalilova, Ayfer Alikaşifoğlu, Z. Alev Özön, E. Nazlı Gönç, Nurgün Kandemir
Publikováno v:
JCRPE, Vol 16, Iss 1, Pp 11-20 (2024)
INTRODUCTION: Cardiovascular diseases (CVD) are the most important cause of morbidity and mortality in patients with type 1 diabetes (T1D). Children with T1D have a similar or higher prevalence of being overweight (OW) or obese (Ob) compared to healt
Externí odkaz:
https://doaj.org/article/5af2468fb2ac4eae8594ef96f28c44a5
Publikováno v:
JCRPE, Vol 14, Iss 4, Pp 463-468 (2022)
The purpose of this case series was to evaluate menstrual suppression in sex assigned at birth female adolescents identifying as male or gender non-conforming. A retrospective chart review of four gender minority youth (GMY), age 14-17, was performed
Externí odkaz:
https://doaj.org/article/e9e580f8c6b54f438415a268de4507c3
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, 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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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
Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency
Autor:
Nurgün, Kandemir, Doğuş, Vurallı, Ekim, Taşkıran, Nazlı, Gönç, Alev, Özön, Ayfer, Alikaşifoğlu, Engin, Yılmaz
Publikováno v:
The Turkish journal of pediatrics. 54(6)
Mutations in the prophet of Pit-1 (PROP-1) gene are responsible for most of the cases of combined pituitary hormone deficiencies (CPHD). We performed this study to determine the prevalence of PROP-1 mutations in a group of Turkish children with CPHD.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::761d67cd38dc19875dddfe566b57dae8
https://pubmed.ncbi.nlm.nih.gov/23692781
https://pubmed.ncbi.nlm.nih.gov/23692781