Zobrazeno 1 - 10
of 18
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
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:
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
Autor:
Marialuisa Corbeddu, Emanuele Bellacchio, Alper Han Cebi, Ismail Saygin, Murat Cakir, Elif Sag, Aysenur Bahadir, Guldal Yilmaz, Guven Burcu, Francesco Callea
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 5139, p 5139 (2020)
International Journal of Molecular Sciences, Vol 21, Iss 5139, p 5139 (2020)
Particular fibrinogen gamma chain mutations occurring in the gamma-module induce changes that hamper gamma-gamma dimerization and provoke intracellular aggregation of the mutant fibrinogen, defective export and plasma deficiency. The hepatic storage
Autor:
Ümit Çobanoğlu, Aysenur Bahadir
Publikováno v:
International Journal of Hematology and Oncology. 26:179-181
Autor:
Melike Sezgin Evim, N. Ozbek, Gürcan Dikme, Baris Malbora, Sema Vural, Özlem Tüfekçi, O. Arman Bilir, Z. OnderSivis, Tiraje Celkan, Turan Bayhan, Serhat Karaman, Aysenur Bahadir
Publikováno v:
HemaSphere. 3:43-44
Publikováno v:
Journal of Paediatrics and Child Health. 50:721-725
Aim Despite being one of common preventable deficiency disorders, vitamin B12 (vit-B12) deficiency can lead to serious health problems both in children and adult. The familiar treatment through parenteral route for vit-B12 deficiency frequently leads
Publikováno v:
Turkish Journal of Hematology, Vol 31, Iss 1, Pp 68-74 (2014)
Turkish Journal of Hematology
Turkish Journal of Hematology
with respect to wild-type BCR-ABL in cellular assays [1]. The pharmacokinetic data showed that F317L is predicted to be moderately sensitive to dasatinib [2]. Jabbour et al. [3] published data on a cohort of 20 CML patients with F317L mutation and ev