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The Turkish Journal of Pediatrics|January 14, 2025
Griscelli syndrome: Erdheim-Chester disease-like local presentation progressing to accelerated phaseTaha Solakoğlu, Gamze Sönmez, Ateş Kutay Tenekeci, et al.
Journal of Cosmetic Dermatology|August 20, 2021
TMC8 mutation in a Turkish family with epidermodysplasia verruciformis including laryngeal papilloma and recurrent skin carcinomaSaliha Esenboga, Deniz Cagdas, Nazli Eylem Alkanat, et al.
Journal of Clinical Immunology|June 3, 2025
Clinical and Immunological Features of a Large DiGeorge Syndrome CohortMerve Süleyman, Deniz Cagdas, Pelin Özlem Şimşek Kiper, et al.
Diagnostics (Basel, Switzerland)|August 14, 2025
Regulatory T Cell Sub-Populations in Patients with Distinct Autoimmune/Inflammatory Diseases With or Without Inborn Errors of ImmunitySevil Oskay Halacli, Dilan Inan, Saliha Esenboga, et al.
Immunologic Research|April 16, 2025
A patient with RFX5 variant causing an expression defect in both HLA ABC and HLA DRSerdar Goktas, Gamze Sonmez, Ali Şahin, et al.
Immunological Investigations|May 7, 2020
Frequency of HLA Class I and Class II Alleles in Patients with CVID from TurkeyBegum Ozbek, Cagman Tan, Ismail Yaz, et al.
Scandinavian Journal of Immunology|August 29, 2018
B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancyFehime K Eroglu, Fatima Aerts Kaya, Deniz Cagdas, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 20, 2024
Comparative analysis of protein expression profiles with genotypes in the diagnosis of Inborn Errors of ImmunitySevil Oskay Halacli, Deniz Cagdas, Saliha Esenboga, 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.
Immunological Investigations|March 11, 2021
Adenosine Deaminase Type II Deficiency: Severe Chronic Neutropenia, Lymphoid Infiltration in Bone Marrow, and Inflammatory FeaturesMerve Süleyman, Çağman Tan, Aysegul Uner, et al.
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