Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Heves Kırmızıbekmez"'
Publikováno v:
JCRPE, Vol 14, Iss 3, Pp 324-333 (2022)
INTRODUCTION: Resilience in diabetes refers to the capacity overcome diabetes-related challenges to achieve favorable psychosocial and health outcomes. Despite the known benefits of resilience in adolescents with type 1 diabetes mellitus (T1DM), ther
Externí odkaz:
https://doaj.org/article/ca1e595a7dfc4e3dad3aab111fabd670
Autor:
Fatma Dursun, Tülay Atasoy Öztürk, Serçin Güven, Heves Kırmızıbekmez, Gülcan Seymen Karabulut, Sevinç Kalın, Betül Sözeri
Publikováno v:
JCRPE, Vol 11, Iss 3, Pp 311-318 (2019)
Generalized arterial calcification of infancy (GACI) is a rare autosomal-recessive disorder, characterized by calcification of the internal elastic lamina, fibrotic myointimal proliferation of muscular arteries and resultant arterial stenosis. Treatm
Externí odkaz:
https://doaj.org/article/bf2de6bfe7c344f6a7ccac7ab57ff98f
Publikováno v:
JCRPE, Vol 11, Iss 1, Pp 34-40 (2019)
Objective:Vitamin D dependent rickets type 1A (VDDR1A) is an autosomal recessive disorder caused by mutations in the 1α-hydroxylase gene (CYB27B1). As it may be confused with nutritional rickets and hypophosphatemic rickets, genetic analysis is impo
Externí odkaz:
https://doaj.org/article/c3db3d0f84df4f24923dc6ac82d8494c
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 4, Iss 2, Pp 188-191 (2017)
Clinical presentation of hypopituitarism may be variable in the neonate. Symptoms are generally non-specific, ranging from absent to severe, and even life-threatening due to adrenocorticotrophic hormone deficiency. We report a neonate who presented w
Externí odkaz:
https://doaj.org/article/c2cb16d0ff684387a96300db9a50db25
Autor:
Fatma Dursun, Heves Kırmızıbekmez
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 4, Iss 1, Pp 97-99 (2017)
Cushing's syndrome (CS) is common after oral steroid use and has also been reported following topical or inhaled use, but it is extremely uncommon after intranasal administration. This is the case of a 6-year-old child who developed Cushing's syndrom
Externí odkaz:
https://doaj.org/article/77fce4360a8547d3b5ed287781445567
Autor:
Heves Kırmızıbekmez, Rahime Gül Yesiltepe Mutlu, Serdar Moralıoğlu, Ahmet Tellioğlu, Ayşenur Cerrah Celayir
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Congenital adrenal hyperplasia (CAH) is a group of inherited defects of cortisol biosynthesis. A case of classical CAH due to 21-hydroxylase deficiency (21-OHD) with early onset of salt waste and concurrence of meningomyelocele (MMC) was presented he
Externí odkaz:
https://doaj.org/article/fe8fddac671b4b9abe315cce4b68421f
Autor:
Fatma Dursun, Şeyma Meliha Su Dur, Ceyhan Şahin, Heves Kırmızıbekmez, Murat Hakan Karabulut, Asım Yörük
Publikováno v:
Case Reports in Pediatrics, Vol 2015 (2015)
Prepubertal gynecomastia due to testis tumors is a very rare condition. Nearly 5% of the patients with testicular mass present with gynecomastia. Sertoli cell tumors are sporadic in 60% of the reported cases, while the remaining is a component of mul
Externí odkaz:
https://doaj.org/article/375266abc8da4ee2800b0a0b5d5102ec
Autor:
Fatma Dursun, Zekeriya İlçe, İlkay Tosun, Pınar Atla, Sevinç Kalın, Fatma Tuğba Güvenç, Ülkü Miray Yıldırım, Heves Kırmızıbekmez
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism. 36:96-100
Adrenocortical tumor (ACT) is a rare malignant tumor which usually present with Cushing syndrome and virilization. Paraneoplastic syndromes (PNS) due to neoplasms can occur with peptides or cytokines secreted by the tumor. Here, we report a 13-month-
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology.
Autor:
Heves Kırmızıbekmez
Publikováno v:
Ümraniye Pediatri Dergisi - Journal of Umraniye Pediatrics.