Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Tülay Öztürk"'
Autor:
Mehmet Coşkun, Elif Böncüoğlu, Şahika Şahinkaya, Elif Kıymet, Aybüke Akaslan Kara, Nuri Bayram, Ela Cem, İlker Devrim, Kamile Ötiken Arıkan, Tülay Öztürk Atasoy, Miray Yılmaz Çelebi, Mine Düzgöl
Publikováno v:
Pediatric Pulmonology
Background Studies investigating clinical and imaging findings of coronavirus disease 2019 (COVID‐19) pneumonia and predictors for lung injury mostly focus on adults. In this study, we aimed to evaluate the role of laboratory findings in predicting
Publikováno v:
Molecular Syndromology. 12:269-278
Craniofrontonasal syndrome (CFNS) is a rare X-linked genetic disorder which is characterized by coronal synostosis, widely spaced eyes, a central nasal groove, and various skeletal anomalies. Mutations in the EFNB1 gene in Xq13.1 are responsible for
Autor:
Heves Kırmızıbekmez, Serçin Güven, Betül Sözeri, Gulcan Seymen Karabulut, Tülay Öztürk, Fatma Dursun, Sevinç Kalın
Publikováno v:
Journal of Clinical Research in Pediatric Endocrinology
JCRPE, Vol 11, Iss 3, Pp 311-318 (2019)
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
Publikováno v:
Mol Syndromol
Craniofrontonasal syndrome (CFNS) is a rare X-linked genetic disorder which is characterized by coronal synostosis, widely spaced eyes, a central nasal groove, and various skeletal anomalies. Mutations in the EFNB1 gene in Xq13.1 are responsible for
Autor:
Bumin Dündar, Gönül Çatlı, Tülay Öztürk, Handan Güleryüz, Korcan Demir, Sezer Acar, Ece Böber, Ayhan Abaci, Tuğba Egeli, Hale Tuhan, Şule Can
Publikováno v:
Turkish Journal of Medical Sciences
Background/aim: We aimed to determine the presence of subclinical atherosclerosis using carotid intima-media thickness (CIMT) and biochemical parameters in children and adolescents with congenital adrenal hyperplasia (CAH). Materials and methods: Thi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a4ec7c133acb1d455024ae3b17866b6
https://avesis.deu.edu.tr/publication/details/4c943a8c-2e0c-4d39-a7fc-daaba11dcc3c/oai
https://avesis.deu.edu.tr/publication/details/4c943a8c-2e0c-4d39-a7fc-daaba11dcc3c/oai
Autor:
Elif Kıymet, İlker Devrim, Nuri Bayram, Miray Yılmaz Çelebi, Tülay Öztürk Atasoy, Şahika Şahinkaya, Ela Cem
Publikováno v:
Pediatric Infectious Disease Journal. 40:e283-e284
Autor:
Safiye Nazmiye ÖZTÜRK, Tülay ÖZTÜRK
Publikováno v:
Volume: 4, Issue: 3 71-78
OHS ACADEMY
OHS ACADEMY
İş Sağlığı ve Güvenliği (İSG), işyerinden kaynaklanan ve işçilerin refahını etkileyebilecek tehlikelerin öngörülmesi, tanınması, değerlendirilmesi ve kontrolü bilimi olarak tanımlanmaktadır. İstihdam veya iş ile uğraşan ki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087a46d86d7bb419cbc1b0a04bf23989
https://dergipark.org.tr/tr/pub/ohsacademy/issue/67588/787382
https://dergipark.org.tr/tr/pub/ohsacademy/issue/67588/787382
Publikováno v:
Mol Syndromol
WOS: 000508845700008
PubMed: 32021609
Myhre syndrome is a rare autosomal dominant multisystemic disorder. Typical features of this disorder include distinctive facial appearance, deafness, intellectual disability, cardiovascular abnormaliti
PubMed: 32021609
Myhre syndrome is a rare autosomal dominant multisystemic disorder. Typical features of this disorder include distinctive facial appearance, deafness, intellectual disability, cardiovascular abnormaliti
Autor:
Müge Tunçyürek, Ali Veral, Süha Süreyya Özbek, Gulgun Kavukcu, Yeşim Ertan, Tülay Öztürk, Mahir Akyildiz, Deniz Nart, Recep Gokhan Icoz, Özer Makay
Publikováno v:
Volume: 56, Issue: 3 115-123
Ege Tıp Dergisi
Ege Tıp Dergisi
Amaç: Bu çalışmanın amacı, kapsülsüz formları da dahil olmak üzere tiroid papiller karsinom folliküler varyantının (TPKFV) farklı formlarının sonografik özelliklerini sunmaktır. Başka bir amaç ise bu nadir tümörün önceki çal
Publikováno v:
Türk Pediatri Arşivi. 53:117-119
The diagnosis and management of pulmonary hydatid cyst disease represents an important clinical problem in countries of the world that are endemic to echinococcal infection. Atypical clinical and radiologic findings including multiple cavitary lesion