Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Berna Eroğlu Filibeli"'
Autor:
Seyran Bulut, Gönül Çatlı, Berna Eroğlu Filibeli, Hayrullah Manyas, İlkay Ayrancı, Rabia Meral, Deniz Kızmazoğlu, Bumin Nuri Dündar
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 3, Pp 307-313 (2022)
Androgen-secreting adrenal tumors are aggressive cancers in childhood; however, they are rare in clinical practice. Children with adrenal carcinoma usually present with peripheral precocious puberty, premature pubarche, signs of virilization and clit
Externí odkaz:
https://doaj.org/article/e2bf000d396f438c8f4375d85b5a088c
Publikováno v:
Journal of Pediatric Research, Vol 9, Iss 2, Pp 192-196 (2022)
Childhood hypophosphatasia (HPP) presents with bowing of the limbs, poor mobility, chronic pain, short stature, fractures, and motor impairment. Enzyme replacement therapy (ERT) provides improved pulmonary and physical function in life-threatening pe
Externí odkaz:
https://doaj.org/article/faa57fa9ad994883aaf9de2443523dfc
Autor:
Berna Eroğlu Filibeli, Nesrin Havare, Huriye Erbak Yılmaz, Jülide Gülizar Yıldırım, Gönül Çatlı, Bumin N. Dündar
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 95-103 (2020)
Objective:Turner syndrome (TS) is one of the most common chromosomal abnormalities and an important cause of short stature and infertility due to ovarian failure in females. The aim was to evaluate the knowledge of TS among physicians and parents of
Externí odkaz:
https://doaj.org/article/fcf1b6c1ddfd4eabaa9c12c28e740085
Autor:
Melek Erdem, Özlem Tüfekçi, Sefa Kızıldağ, Sebnem Yılmaz, Deniz Kızmazoğlu, Berna Eroğlu Filibeli, Hale Ören
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 1, Pp 12-18 (2019)
Objective: In acute lymphoblastic leukemia (ALL), various clinical risk factors and genetic predispositions contribute to the development of bone complications during and after chemotherapy. In this study, we aimed to investigate whether vitamin D re
Externí odkaz:
https://doaj.org/article/a60aff8eedeb4ed4b90f1d47827885c6
Autor:
Berna Eroğlu Filibeli, İlkay Ayrancı, Hayrullah Manyas, Özgür Kırbıyık, Bumin N. Dündar, Gönül Çatlı
Publikováno v:
Güncel Pediatri. 20:97-102
Autor:
Elif Yiğit, Berk Ozyilmaz, İlkay Ayranci, Bumin Dündar, Gönül Çatlı, Hayrullah Manyas, Berna Eroğlu Filibeli
Publikováno v:
Volume: 19, Issue: 1 52-59
Güncel Pediatri
Güncel Pediatri
Giriş: Şiddetli ve erken başlangıçlı obezitenin genetik nedenlerinde monogenik obezite formları önemli bir yer tutmaktadır. Bu çalışmada, kliniğimizde monogenikobezite ön tanısı ile takip edilen olguların klinik ve moleküler genetik
Autor:
Huriye Erbak Yılmaz, Berna Eroğlu Filibeli, Bumin Dündar, Nesrin Havare, Jülide Gülizar Yildirim, Gönül Çatlı
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 12, Iss 1, Pp 95-103 (2020)
JCRPE, Vol 12, Iss 1, Pp 95-103 (2020)
Objective Turner syndrome (TS) is one of the most common chromosomal abnormalities and an important cause of short stature and infertility due to ovarian failure in females. The aim was to evaluate the knowledge of TS among physicians and parents of
Autor:
Hale Ören, Özlem Tüfekçi, Deniz Kızmazoğlu, Şebnem Yılmaz, Berna Eroğlu Filibeli, Sefa Kizildag, Melek Erdem
Publikováno v:
Turkish Journal of Hematology, Vol 36, Iss 1, Pp 12-18 (2019)
Turkish Journal of Hematology
Turkish Journal of Hematology
In acute lymphoblastic leukemia (ALL), various clinical risk factors and genetic predispositions contribute to the development of bone complications during and after chemotherapy. In this study, we aimed to investigate whether vitamin D receptor (Fif
Autor:
Hayrullah Manyas, İlkay Ayranci, Merve Saka Guvenc, Gönül Çatlı, Bumin Dündar, Berna Eroğlu Filibeli
Publikováno v:
Andrologia. 53
17 beta-hydroxysteroid dehydrogenase type 3 deficiency is a rare cause of 46 XY disorders of sexual development. Mutations in the HSD17B3 gene result in reduced activity of the 17 beta-HSD3 enzyme, decreasing the conversion of androstenedione to test
Autor:
Gönül Çatlı, Bumin Dündar, Hayrullah Manyas, İlkay Ayranci, Ozgur Kirbiyik, Berna Eroğlu Filibeli
Publikováno v:
Hormones (Athens, Greece). 21(1)
Purpose Heterozygous loss-of-function mutations in the glucokinase (GCK) gene cause MODY 2, which is characterized by asymptomatic fasting hyperglycemia and does not require insulin treatment. Conversely, homozygous loss-of-function mutations in the