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International Neurourology Journal|October 13, 2025
The Role of Urinary Secretory Immunoglobulin A in the Pathophysiology of Interstitial CystitisTuran Ozdemir, Bayram Aliyev, Kasim Emre Ergun, et al.
Asian Pacific Journal of Allergy and Immunology|February 27, 2021
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literatureElif Azarsiz, Neslihan Karaca, Emin Karaca, et al.
Indian Journal of Clinical Biochemistry : IJCB|February 8, 2019
Antı-β2 Glycoprotein I Antibodies in Children with Rheumatologic DisordersElif Azarsiz, Gamze Eman, Sanem Eren Akarcan, et al.
Orphanet Journal of Rare Diseases|February 26, 2026
Elevated serum zonulin is associated with high attack frequency in hereditary angioedema: providing insight into the gut-angioedema axisRagıp Fatih Kural, Kasım Okan, Onurcan Yildirim, et al.
Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology|August 1, 2022
Immunologic changes during desensitization with cow's milk: How it differs from natural tolerance or nonallergic state?Nursen Cigerci Gunaydin, Elif Azarsiz, Sunde Yilmaz Susluer, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 25, 2020
CSF levels of a set of neurotrophic factors (brain-derived neurotrophic factor, nerve growth factor) and neuropeptides (neuropeptide Y, galanin) in epileptic childrenHasan Tekgul, Hepsen Mine Serin, Erdem Simsek, et al.
Clinical Immunology (Orlando, Fla.)|May 22, 2014
A novel disease-causing CD40L mutation reduces expression of CD40 ligand, but preserves CD40 binding capacityNurşen C Günaydin, Janet Chou, Neslihan E Karaca, et al.
International Journal of Immunopathology and Pharmacology|July 7, 2018
Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patientsNeslihan Edeer Karaca, Ezgi Ulusoy Severcan, Burcu Guven Bilgin, et al.
Case Reports in Immunology|December 21, 2017
Gain-of-Function Mutations in STAT1: A Recently Defined Cause for Chronic Mucocutaneous Candidiasis Disease Mimicking Combined ImmunodeficienciesSanem Eren Akarcan, Ezgi Ulusoy Severcan, Neslihan Edeer Karaca, et al.
JMM Case Reports|November 28, 2018
Two male siblings with a novel LRBA mutation presenting with different findings of IPEX syndromeSanem Eren Akarcan, Neslihan Edeer Karaca, Guzide Aksu, et al.
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