Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Aysenur Bahadir"'
Autor:
Elif Sag, Aysenur Bahadir, Mustafa Imamoglu, Sefa Sag, Gokce Pinar Reis, Erol Erduran, Murat Cakir
Publikováno v:
Clinical and Experimental Pediatrics, Vol 63, Iss 11, Pp 447-450 (2020)
Background Esophageal stricture (ES) is an uncommon clinic entity in pediatrics that may be congenital or acquired in childhood. Acquired noncaustic ES is very rare, and clinical features of affected patients are unknown. Purpose We aimed to evaluate
Externí odkaz:
https://doaj.org/article/d8c70dbfc9ff45abab53dc8214668234
Publikováno v:
İstanbul Kuzey Klinikleri, Vol 6, Iss 2, Pp 184-188 (2019)
Patients with leukemia can be presented with monoarthritis without any hematologic abnormalities. These patients may be misdiagnosed with juvenile idiopathic arthritis (JIA), and the main treatment can also be delayed. An 11-year-old girl was admitte
Externí odkaz:
https://doaj.org/article/9a4992a33008451daf485797274497b4
Publikováno v:
Medicine Science, Vol 6, Iss 3, Pp 576-8 (2017)
Oxymetholone, an androgen analogue, is widely used in the treatment of Fanconi aplastic anemia (FAA). Androgen is known to cause cerebral venous thrombosis (CVT). A 9-year-old girl under monitoring with a diagnosis of FAA presented to our hospital wi
Externí odkaz:
https://doaj.org/article/210c3ab3eaac458491f5f332c1a3690a
Autor:
Guven Burcu, Emanuele Bellacchio, Elif Sag, Alper Han Cebi, Ismail Saygin, Aysenur Bahadir, Guldal Yilmaz, Marialuisa Corbeddu, Murat Cakir, Francesco Callea
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 14, p 5139 (2020)
Particular fibrinogen γ chain mutations occurring in the γ-module induce changes that hamper γ-γ dimerization and provoke intracellular aggregation of the mutant fibrinogen, defective export and plasma deficiency. The hepatic storage predisposes
Externí odkaz:
https://doaj.org/article/09b5966f361e4129b031e7ac1eaeb771
Publikováno v:
Medicine Science, Vol 7, Iss 1, Pp 243-244 (2018)
No Abstract [Med-Science 2018; 7(1.000): 243-244]
Externí odkaz:
https://doaj.org/article/863bfc18d1684b30a32ac94f0c7251b0
Publikováno v:
Indian Journal of Hematology and Blood Transfusion. 39:340-343
Publikováno v:
Journal of Pediatric Hematology/Oncology. 44:e866-e868
Patients with primary hemophagocytic lymphohistiocytosis may present with different mutations and phenotypic findings. It is usually presented as case reports because of its rare occurrence. Here, we discuss a case diagnosed with familial hemophagocy
Publikováno v:
Irish Journal of Medical Science (1971 -). 191:739-744
The present study assesses the diagnostic significance of low ferritin levels in gastrointestinal diseases by evaluating the endoscopic findings of patients with low ferritin levels without anemia. The study included patients aged 0–18 years who un
Publikováno v:
Journal of Academic Research in Medicine. 10:232-236
Autor:
Erol Erduran, Elif Sag, Aysenur Bahadir, Sefa Sag, Mustafa İmamoğlu, Gokce Pinar Reis, Murat Cakir
Publikováno v:
Clinical and Experimental Pediatrics, Vol 63, Iss 11, Pp 447-450 (2020)
Clinical and Experimental Pediatrics
Clinical and Experimental Pediatrics
Background: Esophageal stricture (ES) is an uncommon clinic entity in pediatrics that may be congenital or acquired in childhood. Acquired noncaustic ES is very rare, and clinical features of affected patients are unknown.Purpose: We aimed to evaluat