Publications & Works

Articles Published in Journals That Entered SCI, SSCI and AHCI Indexes

Elevated Interleukin-17A expression in amlodipine-induced gingival overgrowth

JOURNAL OF PERIODONTAL RESEARCH, vol.55, no.5, pp.613-621, 2020 (Journal Indexed in SCI) identifier identifier identifier

A rare form of congenital neutropenia: VPS45 deficiency

SCANDINAVIAN JOURNAL OF IMMUNOLOGY, vol.91, no.5, 2020 (Journal Indexed in SCI) identifier identifier identifier

ADA Deficiency: Evaluation of the Clinical and Laboratory Features and the Outcome

JOURNAL OF CLINICAL IMMUNOLOGY, vol.38, no.4, pp.484-493, 2018 (Journal Indexed in SCI) identifier identifier identifier

Effect of adipose tissue-derived inflammatory and proangiogenic cytokines on proliferative diabetic retinopathy

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI, vol.39, no.4, pp.495-502, 2014 (Journal Indexed in SCI) identifier identifier

H2AX gene does not have a modifier effect on ataxia-telangiectasia phenotype

INTERNATIONAL JOURNAL OF IMMUNOGENETICS, vol.38, no.3, pp.209-213, 2011 (Journal Indexed in SCI) identifier identifier identifier

Hereditary C1q deficiency: a new family with C1qA deficiency

TURKISH JOURNAL OF PEDIATRICS, vol.52, no.2, pp.184-186, 2010 (Journal Indexed in SCI) identifier identifier identifier

Articles Published in Other Journals

Refereed Congress / Symposium Publications in Proceedings

Outcome of Patients with Severe CombinedImmunodeficiency/ Combined Immunodeficiencydue to ADA Deficiency

The 44th Annual Meeting of the European Society for Blood andMarrow Transplantation: Physicians Poster Sessions, LİZBON, Portugal, 18 - 21 March 2018 identifier identifier identifier identifier

STK-4 DEFICIENCY AMONG PATIENTS WITH AUTOSOMAL RECESSIVE HIES PHENOTYPE

100th J Project Meeting, Antalya, Turkey, 12 - 14 March 2014, vol.34, pp.736 identifier identifier identifier

STK-4 DEFICIENCY AMONG PATIENTS WITH AUTOSOMAL RECESSIVE HIES PHENOTYPE

100th J Project Meeting, Antalya, Turkey, 12 - 14 March 2014, vol.34, pp.731 identifier

IL-10 RECEPTOR DEFECT IN A PATIENT WHO PRESENTED WITH EARLY-ONSET INFANTILE INFLAMATORY BOWEL DISEASE

15th Biennial Meeting European-Society-for-Immunodeficiency (ESID), Florence, Italy, 3 - 06 October 2012, vol.32, pp.69 identifier

A p22 deficient CGD patient associated with hypogammaglobulinemia

2nd European Congress of Immunology, (ECI 2009), Berlin, Germany, 13 - 16 September 2009

Sequence, methylation and expression analysis of H2AX gene in patients with Ataxia-telangiectasia

13th European-Soc-for-Immunodeficiencies/10th Int-Patient-Org-for-Primary-Immunodeficiencies/8th Int-Nursing-Group-for-Immunodeficiencies Meeting, Hertogenbosch, Netherlands, 16 - 19 October 2008, vol.154, pp.139 identifier

Chronic granulomatous disease CGD subgroup analysis of patients by FACScan with specific anti human NADPH oxidase components antibodies

1st Joint Meeting of European National Societies of Immunology -16th European Congress of Immunology, (EFİS), 6 - 09 September 2006

Books & Book Chapters