Zobrazeno 1 - 10
of 45
pro vyhledávání: '"Hande Turan"'
Autor:
Erdal Eren, Semra Çetinkaya, Yasemin Denkboy Öngen, Ummahan Tercan, Şükran Darcan, Hande Turan, Murat Aydın, Fatma Yavuzyılmaz, Fatih Kilci, Beray Selver Eklioğlu, Nihal Hatipoğlu, Kübra Yüksek Acinikli, Zerrin Orbak, Emine Çamtosun, Şenay Savaş Erdeve, Emrullah Arslan, Oya Ercan, Feyza Darendeliler
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 256-263 (2024)
INTRODUCTION: Treatment adherence is crucial for the success of growth hormone (GH) therapy. Reported non-adherence rates in GH treatment have varied widely. Several factors may have an impact on adherence. Apart from these factors, the global impact
Externí odkaz:
https://doaj.org/article/46e75c7c45854b51a9360aaf41d86ff7
Autor:
Elif Özsu, Semra Çetinkaya, Semih Bolu, Nihal Hatipoğlu, Şenay Savaş Erdeve, Olcay Evliyaoğlu, Firdevs Baş, Atilla Çayır, İsmail Dündar, Emine Demet Akbaş, Seyid Ahmet Uçaktürk, Merih Berberoğlu, Zeynep Şıklar, Şervan Özalkak, Nursel Muratoğlu Şahin, Melikşah Keskin, Ülkü Gül Şiraz, Hande Turan, Ayşe Pınar Öztürk, Eda Mengen, Elif Sağsak, Fatma Dursun, Nesibe Akyürek, Sevinç Odabaşı Güneş, Zehra Aycan
Publikováno v:
JCRPE, Vol 16, Iss 3, Pp 297-305 (2024)
INTRODUCTION: Maturity onset diabetes of the young (MODY) occurs due to mutations in genes involved in pancreatic beta cell function and insulin secretion, has heterogeneous clinical and laboratory features, and account for 1-5% of all diabetes cases
Externí odkaz:
https://doaj.org/article/eb7e190aaeb24a0bb6a30c654ca0303b
Publikováno v:
BMC Endocrine Disorders, Vol 24, Iss 1, Pp 1-11 (2024)
Abstract Background A chronic autoimmune disease with an increasing incidence rate, type 1 diabetes mellitus (T1DM) is typified by the degeneration of the pancreatic beta cells. Diabetes management is significantly impacted by nutrition. Although it
Externí odkaz:
https://doaj.org/article/f2a8e978deff4b51bf3bda4109e14e52
Autor:
Yavuz Özer, Mehmet Yıldız, Hande Turan, Aydilek Dağdeviren Çakır, Gürkan Tarçın, Dilek Bingöl Aydın, Elvan Bayramoğlu, Fatih Haşlak, Sezgin Şahin, Amra Adrovic, Kenan Barut, Olcay Evliyaoğlu, Özgür Kasapçopur, Oya Ercan
Publikováno v:
Turkish Archives of Pediatrics, Vol 59, Iss 1, Pp 23-30 (2024)
Objective: Mercury poisoning is a condition with multiple-organ dysfunction that has effects on the central nervous system, gastrointestinal system, cardiovascular system, skin, lungs, and kidneys. It can be fatal or may result in sequelae such as ne
Externí odkaz:
https://doaj.org/article/624af3b4e8044c8ca6266b2a0dd87ebb
Publikováno v:
Archives of Endocrinology and Metabolism, Vol 68 (2024)
ABSTRACT Objective: This research aimed to evaluate retrospectively the effect of anastrozole on height gain and sex hormone levels in pubertal boys receiving growth hormone (GH). Materials and methods: Pubertal boys who received both GH and anastroz
Externí odkaz:
https://doaj.org/article/602697bacbbe459694a941c5f1a334c6
Autor:
Hande Turan, Gürkan Tarçın, Özgür Mete, Ada Bulut Sinoplu, Saadet Olcay Evliyaoğlu, Büge Öz, Oya Ercan
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 126-130 (2022)
Silent corticotroph tumors are composed of corticotroph cells, but do not manifest any biochemical or clinical evidence of hypercortisolism. A choristoma is a benign, congenital proliferation of histologically mature tissue elements normally not pres
Externí odkaz:
https://doaj.org/article/0f2dc468a88546eba3f2cdda78669d3a
Autor:
Hande Turan, Gönül Çatlı, Aslı Derya Kardelen, Ece Böber, Ayşehan Akıncı, Semra Çetinkaya, Özgecan Demirbaş, Eren Er, Saadet Olcay Evliyaoğlu, Bumin Dündar, Oya Ercan
Publikováno v:
JCRPE, Vol 14, Iss 1, Pp 29-36 (2022)
INTRODUCTION: Although the sensitivity and specificity of bilateral inferior petrosal sinus sampling (BIPSS) were shown to be quite high in adult patients, pediatric studies are limited in number and have conflicting results, since BIPSS is much less
Externí odkaz:
https://doaj.org/article/aebfb86ba88d4c4981432679b57689de
Autor:
Aslan Yilmaz, Yavuz Ozer, Nesrin Kaya, Hande Turan, Hazal Cansu Acar, Oya Ercan, Yildiz Perk, Olcay Evliyaoglu, Mehmet Vural
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-8 (2021)
Abstract Background Hypothyroxinemia is defined by low levels of thyroxine (T4) despite low or normal levels of thyroid-stimulating hormone (TSH). This study aimed to evaluate the factors associated with transient hypothyroxinemia of prematurity (THO
Externí odkaz:
https://doaj.org/article/20b6a3c643c5481bb633061d656eaa2b
Autor:
Hande Turan, Aydilek Dağdeviren Çakır, Yavuz Özer, Gürkan Tarçın, Bahar Özcabi, Serdar Ceylaner, Oya Ercan, Saadet Olcay Evliyaoğlu
Publikováno v:
JCRPE, Vol 13, Iss 2, Pp 232-238 (2021)
Corticosterone methyloxidase deficiency type 2 is an autosomal recessive disorder presenting with salt loss and failure to thrive in early childhood and is caused by inactivating mutations of the CYP11B2 gene. Herein, we describe four Turkish patient
Externí odkaz:
https://doaj.org/article/e3df53c6513f42b7977be99d23eae3b5
Autor:
Aydilek Dağdeviren Çakır, Hande Turan, Tiraje Celkan, Nil Çomunoğlu, Oya Ercan, Olcay Evliyaoğlu
Publikováno v:
JCRPE, Vol 12, Iss 1, Pp 117-121 (2020)
Carney complex (CNC) is a multiple neoplasia syndrome, characterized by pigmented lesions of the skin and mucosa, cardiac, cutaneous and other myxomas and multiple endocrine and non-endocrine tumors. Most of the cases have an inactivating mutation in
Externí odkaz:
https://doaj.org/article/95d43de1334f4a97a7e53495ba81d61b