Showing results (71-80 of 98) with videos related to
Sort By:
Pageof 10
Clinical and Experimental Immunology|July 26, 2021
Clinical and laboratory findings in patients with leukocyte adhesion deficiency type I: A multicenter study in TurkeyIsmail Yaz, Begum Ozbek, Hacer Neslihan Bildik, 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.Respiratory Medicine|July 2, 2022
Antimycobacterial prophylaxis regarding Bacillus Calmette-Guérin -associated complications in children with primary immunodeficiencyBeste Ozsezen, Ebru Yalçın, Dilber Ademhan Tural, et al.Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|September 23, 2024
A single center experience on PI3K/AKT/MTOR signaling defects: Towards pathogenicity assessment for four novel defectsHacer Neslihan Bildik, Saliha Esenboga, Sevil Oskay Halaclı, et al.American Journal of Medical Genetics. Part A|October 5, 2019
ADA2 deficiency in a patient with Noonan syndrome-like disorder with loose anagen hair: The co-occurrence of two rare syndromesOzlem Akgun-Dogan, Pelin O Simsek-Kiper, Ekim Taskiran, et al.Journal of Periodontology|November 3, 2021
Cytokine profile in serum and gingival crevicular fluid of children with inflammatory bowel disease: A case-control studyBuket Acar, Ersin Gümüş, Selcen Özcan-Bulut, et al.Journal of Clinical Immunology|October 21, 2025
Beyond the Classical Triad: Atypical Presentations and Regulatory T Cell Phenotyping in a Cohort of IPEX PatientsIsmail Yaz, Sevil Oskay Halacli, Canberk Ipsir, et al.Pediatric Pulmonology|April 18, 2026
Primary Ciliary Dyskinesia: Do We Need to Test for Primary Immune Deficiency Routinely?Halime Nayir Buyuksahin, Nagehan Emiralioglu, Canan Caka, et al.Journal of Clinical Immunology|May 11, 2018
ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the OutcomeDeniz Cagdas, Pınar Gur Cetinkaya, Betül Karaatmaca, et al.Haematologica|October 13, 2018
Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and functionTala Shahin, Dominik Aschenbrenner, Deniz Cagdas, et al.Pageof 10