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Journal of Cosmetic Dermatology|April 21, 2018
Tumor necrosis factor α-308 G/A and interleukin 1 β-511 C/T gene polymorphisms in patients with scarring acneGulsen Akoglu, Cagman Tan, Deniz Cagdas Ayvaz, et al.Clinical Immunology (Orlando, Fla.)|February 6, 2017
A novel mutation in TAP1 gene leading to MHC class I deficiency: Report of two cases and review of the literatureDamla Hanalioglu, Deniz Cagdas Ayvaz, Tuba Turul Ozgur, et al.Journal of Child Neurology|February 10, 2018
Neurologic Involvement in Primary Immunodeficiency DisordersMirac Yildirim, Deniz Cagdas Ayvaz, Bahadir Konuskan, et al.Cognitive and Behavioral Neurology : Official Journal of the Society for Behavioral and Cognitive Neurology|September 20, 2014
Progressive neurodegenerative syndrome in a patient with X-linked agammaglobulinemia receiving intravenous immunoglobulin therapyAslihan Taskiran Sag, Esen Saka, Tuba Turul Ozgur, et al.Clinical Immunology (Orlando, Fla.)|January 9, 2018
A young girl with severe cerebral fungal infection due to card 9 deficiencyPinar Gur Cetinkaya, Deniz Cagdas Ayvaz, Betül Karaatmaca, et al.Clinical Immunology (Orlando, Fla.)|June 29, 2015
STK4 (MST1) deficiency in two siblings with autoimmune cytopenias: A novel mutationSevil Oskay Halacli, Deniz Cagdas Ayvaz, Cagman Sun-Tan, et al.Pediatric Allergy, Immunology, and Pulmonology|August 5, 2022
A Case of DOCK8 Deficient Hyper-IgE Syndrome Presenting Primarily With Eczema, Food Allergy, and AsthmaOzlem Cavkaytar, Deniz Cagdas Ayvaz, Ozlem Keskin, et al.Pediatric Research|October 24, 2019
A clinical score to guide in decision making for monogenic type I IFNopathiesHafize Emine Sönmez, Cagatay Karaaslan, Adriana A de Jesus, et al.Scientific Reports|May 24, 2026
Evaluation of bone mineral density in patients with severe congenital neutropenia: experience of six centers in TurkeyYasin Karali, Deniz Cagdas Ayvaz, Deniz Yilmaz Karapinar, et al.Pageof 1