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World Journal of Pediatrics : WJP|August 30, 2011
Evaluation of adhesion molecules CD64, CD11b and CD62L in neutrophils and monocytes of peripheral blood for early diagnosis of neonatal infectionFerah Genel, Fusun Atlihan, Nesrin Gulez, 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.
Pediatric Allergy, Immunology, and Pulmonology|June 17, 2026
Clinical, Immunological Findings, and Outcomes of Children with Ataxia-Telangiectasia: A Single Center ExperienceSerenay Cetinoglu, Selime Ozen, Idil Akay Haci, et al.
Clinical and Experimental Medicine|May 22, 2009
Diverse phenotypic and genotypic presentation of RAG1 mutations in two cases with SCIDNeslihan Edeer Karaca, Guzide Aksu, Ferah Genel, et al.
Allergologia Et Immunopathologia|February 2, 2021
22q11.2 deletion syndrome: 20 years of experience from two pediatric immunology units and review of clues for diagnosis and disease managementSelime Ozen, Omer Akcal, Ilke Taskirdi, et al.
Scandinavian Journal of Immunology|March 18, 2022
Severe combined immunodeficiencies: Expanding the mutation spectrum in Turkey and identification of 12 novel variantsAyca Aykut, Asude Durmaz, Neslihan Karaca, et al.
Clinical Rheumatology|January 9, 2019
Correction to: Evaluation of the effects of miRNAs in familial Mediterranean feverHacer Orsdemir Hortu, Emin Karaca, Betul Sozeri, et al.
Clinical Rheumatology|February 15, 2018
Evaluation of the effects of miRNAs in familial Mediterranean feverHacer Orsdemir Hortu, Emin Karaca, Betul Sozeri, et al.
Case Reports in Immunology|October 5, 2016
Early Diagnosis and Hematopoietic Stem Cell Transplantation for IL10R Deficiency Leading to Very Early-Onset Inflammatory Bowel Disease Are Essential in Familial CasesNeslihan Edeer Karaca, Guzide Aksu, Ezgi Ulusoy, 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.
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