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Journal of Periodontology|March 10, 2018
Effects of colchicine on gingival inflammation, apoptosis, and alveolar bone loss in experimental periodontitisCüneyt Asım Aral, Kübra Aral, Arzu Yay, et al.Digestive Diseases and Sciences|April 11, 2008
Polymorphisms of the ICAM-1 gene are associated with biliary atresiaCigdem Arikan, Afig Berdeli, Murat Kilic, et al.Journal of Clinical Medicine Research|April 16, 2016
Recombinase Activating Gene 1 Deficiencies Without Omenn Syndrome May Also Present With Eosinophilia and Bone Marrow FibrosisEzgi Ulusoy, Neslihan Edeer Karaca, Elif Azarsiz, et al.Canadian Journal of Applied Physiology = Revue Canadienne De Physiologie Appliquee|April 28, 2005
Association between the ACE I/D gene polymorphism and physical performance in a homogeneous non-elite cohortF Sirri Cam, Muzaffer Colakoglu, Cevad Sekuri, et al.The Turkish Journal of Pediatrics|September 22, 2015
A newborn with pertussis accompanying nephrotic syndromeMünevver Kaynak-Türkmen, Fulya Cengiz-Erdem, Ferah Sönmez, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|April 16, 2013
A novel DAX-1 mutation presented with precocious puberty and hypogonadotropic hypogonadism in different members of a large pedigreeErdem Durmaz, Doga Turkkahraman, Afig Berdeli, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|January 18, 2008
FcgammaRIIIa-V/F 158 polymorphism in Turkish children with asthma bronchiale and allergic rhinitisDost Zeyrek, Remziye Tanac, Serdar Altinoz, et al.The Turkish Journal of Pediatrics|May 11, 2018
Hemolytic uremic syndrome with multiple organ involvement secondary to complement factor H p.Arg1215X mutationOsman Yeşilbaş, Esra Şevketoğlu, Mey Talip Petmezci, et al.The Turkish Journal of Pediatrics|April 11, 2019
Fever-induced Brugada syndrome in a 9-year-old boy presenting with acute chest painGülser Esen Besli, Sema Yıldırım, İbrahim Akalın, et al.Case Reports in Medicine|May 5, 2011
X-Linked Lymphoproliferative Syndrome and Common Variable Immunodeficiency May Not Be Differentiated by SH2D1A and XIAP/BIRC4 Genes Sequence AnalysisNesrin Gulez, Guzide Aksu, Afig Berdeli, et al.Pageof 14