I. Tezcan

I. Tezcan, M. Yılmaz, Ö. Sanal, 2014, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Griscelli syndrome types 1 and 3: analysis of four new cases and long-term evaluation of previously diagnosed patients

I. Tezcan, Ö. Sanal, A. Metin, 2012, European Journal of Pediatrics.

Two genes are responsible for Griscelli syndrome at the same 15q21 locus.

A. Fischer, I. Tezcan, F. Ersoy, 2000, Genomics.

Defective anti-polysaccharide antibody response in patients with ataxia-telangiectasia.

O. Sanal, I. Tezcan, F. Ersoy, 2004, The Turkish journal of pediatrics.

Thirty years of primary immunodeficiencies in Turkey

O. Sanal, I. Tezcan, 2011, Annals of the New York Academy of Sciences.

Clinical Variants of Ataxia-Telangiectasia

O. Sanal, I. Tezcan, F. Ersoy, 1993 .

Investigation of Genetic Defects in Severe Combined Immunodeficiency Patients from Turkey by Targeted Sequencing

O. Sanal, I. Tezcan, I. Bilic, 2017, Scandinavian journal of immunology.

Flow Cytometry is a Reliable Tool in the Diagnosis of STK4 Deficiency

I. Tezcan, D. Çağdaş, Sevil OSKAY HALACLI, 2020 .

Severe graft versus host disease in a patient with globoid cell leukodystrophy following umbilical cord blood transplantation: resemblance to the twitcher mouse model.

I. Tezcan, B. Anlar, D. Uçkan, 2007, The Turkish journal of pediatrics.

Successful hematopoietic stem cell transplantation after myeloablative conditioning in three patients with dedicator of cytokinesis 8 deficiency (DOCK8) related Hyper IgE syndrome

I. Tezcan, D. Çetinkaya, A. Yüce, 2018, Bone Marrow Transplantation.

DOCK8 Deficiency: Clinical and Immunological Phenotype and Treatment Options - a Review of 136 Patients

J. Orange, A. Schulz, R. Geha, 2015, Journal of Clinical Immunology.

Long-term survival in severe combined immune deficiency: the role of persistent maternal engraftment.

O. Sanal, I. Tezcan, F. Ersoy, 2005, The Journal of pediatrics.

Respiratory system findings in pediatric patients with primary immunodeficiency

I. Tezcan, U. Ozcelik, N. Kiper, 2021, Pediatric pulmonology.

A clinical score to guide in decision making for monogenic type I IFNopathies

I. Tezcan, B. Anlar, S. Ozen, 2019, Pediatric Research.

Diagnosis of Interstitial Lung Disease Caused by Possible Hypersensitivity Pneumonitis in a Child: Think CGD

I. Tezcan, N. Kiper, M. de Boer, 2017, Journal of Clinical Immunology.

A Monogenic Disease with a Variety of Phenotypes: Deficiency of Adenosine Deaminase 2

S. Özen, I. Tezcan, A. Erden, 2019, The Journal of Rheumatology.

Allogeneic bone marrow transplantation in Fanconi anemia from Turkey: a report of four cases.

I. Tezcan, D. Uçkan, M. Alikaşifoğlu, 1998, Pediatric transplantation.

Successful treatment of severe myasthenia gravis developed after allogeneic hematopoietic stem cell transplantation with plasma exchange and rituximab

D. Yalnızoǧlu, I. Tezcan, S. Unal, 2014, Pediatric blood & cancer.

Polymorphisms in FAS and CASP8 genes may contribute to the development of ALPS phenotype: a study in 25 patients with probable ALPS.

I. Tezcan, Ö. Sanal, Çağman Tan, 2015, The Turkish journal of pediatrics.

AB0574 A MONOGENIC DISEASE WITH WIDE RANGE OF SYMPTOMS: DEFICIENCY OF ADENOSINE DEAMINASE 2

S. Özen, I. Tezcan, A. Erden, 2019, Abstracts Accepted for Publication.

Low T Cell Numbers Resembling T−B+ SCID in a Patient with Wiskott–Aldrich Syndrome and the Outcome of Two Hematopoietic Stem Cell Transplantations

I. Tezcan, T. Ariga, D. Çetinkaya, 2016, Journal of Clinical Immunology.

G‐CSF‐mobilized haploidentical peripheral blood stem cell transplantation in children with poor prognostic nonmalignant disorders

I. Tezcan, D. Uçkan, A. Ikinciogullari, 2008, American journal of hematology.

Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency

I. Tezcan, B. Anlar, D. Çağdaş, 2019, Neuropediatrics.

The HLA groups and their relationship with clinical features in Turkish children and adolescents with celiac disease.

I. Tezcan, N. Balamtekin, G. Baysoy, 2021, The Turkish journal of pediatrics.

Clinical and genetic features of the patients with X‐Linked agammaglobulinemia from Turkey: Single‐centre experience

O. Sanal, I. Tezcan, D. Çağdaş, 2018, Scandinavian journal of immunology.

Evaluation of periodontal status and cytokine/chemokine profile of GCF in patients with severe congenital neutropenia

E. Karabulut, I. Tezcan, D. Ayvaz, 2020, Odontology.

Bone marrow transplantation with Favorable outcome in three patients with LPS-responsive beige-like anchor (LRBA) deficiency.

I. Tezcan, B. Kuşkonmaz, D. Çağdaş, 2019, Clinical immunology.

Agranulocytosis: A Rare Complication of Infectious Mononucleosis and Recovery After IVIG Therapy.

I. Tezcan, M. Ceyhan, A. Ölmez, 2003, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Molecular and clinical heterogeneity in CLCN7‐dependent osteopetrosis: report of 20 novel mutations

E. Lanino, I. Tezcan, S. Phadke, 2010, Human mutation.

ISG15 deficiency and increased viral resistance in humans but not mice

O. Sanal, I. Tezcan, A. García-Sastre, 2016, Nature Communications.

The Effect of IVIG on Superoxide Generation in Primary Humoral Immunodeficiencies

O. Sanal, I. Tezcan, F. Ersoy, 2016, The Annals of Clinical and Analytical Medicine.

High levels of delayed radiation-induced apoptosis observed in lymphoblastoid cell lines from ataxia-telangiectasia patients.

H. Blattmann, O. Sanal, I. Tezcan, 2001, International journal of radiation oncology, biology, physics.

Ultrastructural findings of bone marrow in a case with malignant osteopetrosis following successful allogeneic bone marrow transplantation.

I. Tezcan, P. Korkusuz, M. Tuncer, 1999, The Turkish journal of pediatrics.

The effect of mannose-binding protein gene polymorphisms in recurrent respiratory system infections in children and lung tuberculosis.

O. Sanal, I. Tezcan, F. Ersoy, 2003, The Turkish journal of pediatrics.

The efficacy of immunoglobulin replacement therapy in the long-term follow-up of the B-cell deficiencies (XLA, HIM, CVID).

O. Sanal, I. Tezcan, F. Ersoy, 2005, The Turkish journal of pediatrics.

Transcriptional silencing of RFXAP in MHC class II-deficiency.

I. Tezcan, P. J. van den Elsen, M. van Eggermond, 2008, Molecular immunology.

IDDM in an Adolescent Patient With Common Variable Immunodeficiency

I. Tezcan, A. Metin, H. Özyürek, 1997, Diabetes Care.

Selective IgA deficiency with unusual features: Development of common variable immunodeficiency, Sjögren's syndrome, autoimmune hemolytic anemia and immune thrombocytopenic purpura

I. Tezcan, F. Ersoy, Ö. Sanal, 1995, Acta paediatrica Japonica : Overseas edition.

Evaluation of periodontal status and cytokine response in children with familial Mediterranean fever or systemic juvenile idiopathic arthritis

E. Karabulut, S. Özen, I. Tezcan, 2022, Clinical Oral Investigations.

Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function

I. Tezcan, S. Twigg, A. Wilkie, 2018, Haematologica.

Acute myeloid leukemia in a child with dedicator of cytokinesis 8 (DOCK8) deficiency

I. Tezcan, D. Uçkan, S. Barış, 2017, Pediatric blood & cancer.

Additional Diverse Findings Expand the Clinical Presentation of DOCK8 Deficiency

O. Sanal, I. Tezcan, Dara M Strauss-Albee, 2012, Journal of Clinical Immunology.

Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency

I. Tezcan, F. Gumruk, T. Arıkoğlu, 2020, Journal of pediatric endocrinology & metabolism : JPEM.

Two SCID cases with Cernunnos‐XLF deficiency successfully treated by hematopoietic stem cell transplantation

M. van der Burg, P. Revy, I. Tezcan, 2012, Pediatric transplantation.

Successful outcome with second hematopoietic stem cell transplantation in a patient with IL-10R deficiency

I. Tezcan, D. Çetinkaya, D. Ayvaz, 2016, Bone Marrow Transplantation.

Changes in hepatitis B virus serology in bone marrow transplanted children

I. Tezcan, D. Uçkan, M. Tuncer, 2002, Pediatric transplantation.

Economic Burden of Primary Immunodeficiency (PIDD) In Turkey

I. Tezcan, N. Kutukculer, A. Ikinciogullari, 2016 .

A novel mutation leading to a deletion in the SH3 domain of Bruton's tyrosine kinase.

O. Sanal, I. Tezcan, F. Ersoy, 2006, The Turkish journal of pediatrics.

Tumor necrosis factor α‐308 G/A and interleukin 1 β‐511 C/T gene polymorphisms in patients with scarring acne

I. Tezcan, D. Ayvaz, G. Akoglu, 2019, Journal of cosmetic dermatology.

A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly.

I. Tezcan, C. Akyuz, D. Çağdaş, 2018, Journal of pediatric hematology/oncology.

Corrigendum to “Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency” [Clin. Immunol. 110 (2004) 22–29]

A. Plebani, J. Litzman, O. Sanal, 2004 .

Homozygous C2 deficiency: association with defective alternative pathway function and immunoglobulin deficiency.

O. Sanal, I. Tezcan, L. Yel, 1996, International Archives of Allergy and Immunology.

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

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

Tuberculin skin test positivity in pediatric allogeneic BMT recipients and donors in Turkey

I. Tezcan, U. Ozcelik, D. Uçkan, 2007, Pediatric transplantation.

Evaluation of the peripheral blood T and B cell subsets and IRF‐7 variants in adult patients with severe influenza virus infection

I. Tezcan, D. Ayvaz, Ş. Alp, 2022, Health science reports.

Hypophosphatemia and hypouricemia in pediatric allogeneic bone marrow transplant recipients

I. Tezcan, D. Uçkan, M. Tuncer, 2003, Pediatric transplantation.

Selective IgM deficiency: Follow‐up and outcome

I. Tezcan, D. Çağdaş, O. Cimen, 2021, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Childhood-onset Takayasu arteritis and immunodeficiency: case-based review

I. Tezcan, S. Ozen, A. Duzova, 2022, Clinical Rheumatology.

Clinical features of chronic granulomatous disease: a series of 26 patients from a single center.

O. Sanal, I. Tezcan, F. Ersoy, 2010, The Turkish journal of pediatrics.

Bruton tyrosine kinase gene mutations in Turkish patients with presumed X‐linked agammaglobulinemia

H. Kanegane, I. Tezcan, F. Ersoy, 2001, Human mutation.

Clinical Features and HSCT Outcome for SCID in Turkey

Gulsum H. Karasu, A. Elhan, I. Tezcan, 2019, Journal of Clinical Immunology.

Erratum: Human intracellular ISG15 prevents interferon-α±/β 2 over-amplification and auto-inflammation (Nature 517 (2015) (89-93) 10.1038/nature13801))

J. Casanova, L. Notarangelo, Y. Crow, 2015 .

Atypical combined immunodeficiency due to Artemis defect: a case presenting as hyperimmunoglobulin M syndrome and with LGLL.

I. Tezcan, J. de Villartay, D. Ayvaz, 2013, Molecular immunology.

A single‐center study points to diverse features and outcome in patients with Hyperimmunoglobulin M Syndrome and Class‐ Switch Recombination defects

I. Tezcan, Ö. Sanal, D. Çağdaş, 2022, Scandinavian journal of immunology.

Cernunnos deficiency: a case report.

O. Sanal, I. Tezcan, T. Turul, 2011, Journal of investigational allergology & clinical immunology.

Clinical and immunological aspects of hyper-IgM syndrome.

O. Sanal, I. Tezcan, F. Ersoy, 1990, The Turkish journal of pediatrics.

Periodical gingival bleeding as a presenting symptom of periodontitis due to underlying cyclic neutropenia. Case report.

O. Sanal, I. Tezcan, F. Ersoy, 1993, Australian dental journal.

Defective pneumococcal antibody response in patients with recurrent respiratory tract infections.

I. Tezcan, Ö. Sanal, B. Erman, 2017, The Turkish journal of pediatrics.

In case of recurrent wheezing and bronchiolitis: Think again, it may be a primary immunodeficiency.

I. Tezcan, D. Ayvaz, S. Esenboğa, 2019, Asian Pacific journal of allergy and immunology.

B lymphocyte subsets and outcomes in patients with an initial diagnosis of transient hypogammaglobulinemia of infancy

I. Tezcan, Ö. Sanal, F. K. Eroğlu, 2018, Scandinavian journal of immunology.

Hematopoietic stem cell transplantation from a donor with Klinefelter syndrome for Wiskott–Aldrich syndrome

I. Tezcan, D. Çetinkaya, Y. Balcı, 2008, Pediatric Transplantation.

DOCK8 deficiency with hypereosinophilia and the syndrome of inappropriate antidiuretic hormone secretion during herpes infection.

I. Tezcan, D. Çağdaş, M. Gürsel, 2023, The Turkish journal of pediatrics.

Impaired IgG Antibody Production to Pneumococcal Polysaccharides in Patients with Ataxia–Telangiectasia

O. Sanal, I. Tezcan, F. Ersoy, 1999, Journal of Clinical Immunology.

Serum IgD Concentrations in Patients with Ataxia Telangiectasia and with Selective IgA Deficiency

O. Sanal, I. Tezcan, F. Ozaltin, 1998, International Archives of Allergy and Immunology.

Levels of pro- and anti-inflammatory cytokines in cystic fibrosis patients with or without gingivitis.

E. Karabulut, I. Tezcan, N. Kiper, 2020, Cytokine.

Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

I. Tezcan, C. Koşukcu, D. Çağdaş, 2020, Journal of Clinical Immunology.

Diversity in STK4 Deficiency and Review of the Literature.

S. Özen, O. Sanal, I. Tezcan, 2021, The journal of allergy and clinical immunology. In practice.

Hypomorphic RAG1 defect in a child presented with pulmonary hemorrhage and digital necrosis.

S. Özen, I. Tezcan, R. Topaloğlu, 2017, Clinical immunology.

Clinical and Osteopetrosis-Like Radiological Findings in Patients with Leukocyte Adhesion Deficiency Type III

I. Tezcan, S. Kilic, A. Metin, 2023, Journal of Clinical Immunology.

Statins and IL-1β, IL-10, and MPO Levels in Gingival Crevicular Fluid: Preliminary Results

E. Karabulut, I. Tezcan, S. G. Oz, 2016, Inflammation.

A rare form of congenital neutropenia: VPS45 deficiency

I. Tezcan, A. Üner, D. Çağdaş, 2020, Scandinavian journal of immunology.

A Novel Interleukin 17 Receptor A Mutation in a Child with Chronic Mucocutaneous Candidiasis and Staphylococcal Skin Infections

I. Tezcan, B. Cavdarli, D. Çağdaş, 2023, Turkish archives of pediatrics.

Frequency of HLA Class I and Class II Alleles in Patients with CVID from Turkey

I. Tezcan, C. Koşukcu, D. Çağdaş, 2020, Immunological investigations.

An infant with ZAP-70 deficiency with disseminated mycobacterial disease

I. Tezcan, D. Ayvaz, M. Burg, 2016, Journal of Clinical Immunology.

Expression of HLA class I and class II genes in patients with multiple skin warts

I. Tezcan, D. Çağdaş, Çağman Tan, 2021, Experimental Dermatology.

Increased availability of family donors for hematopoietic stem cell transplantation in a population with increased incidence of consanguinity

I. Tezcan, D. Uçkan, Y. Balcı, 2011, Clinical transplantation.

Isolated testicular and bone relapse in children with acute myeloblastic leukemia and chronic graft versus host disease after allogeneic BMT.

I. Tezcan, D. Uçkan, M. Tuncer, 2007, Turkish Journal of Pediatrics.

Clinical Features and HSCT Outcome for SCID in Turkey

Gulsum H. Karasu, A. Elhan, I. Tezcan, 2019, Journal of Clinical Immunology.

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

O. Sanal, I. Tezcan, M. Hershfield, 2018, Journal of Clinical Immunology.

Functional analysis of naturally occurring DCLRE1C mutations and correlation with the clinical phenotype of ARTEMIS deficiency.

M. van der Burg, E. Mejstrikova, L. Notarangelo, 2015, The Journal of allergy and clinical immunology.

Association of interleukin-1 beta (+3954) gene polymorphism and gingival crevicular fluid levels in patients with aggressive and chronic periodontitis.

I. Tezcan, O. O. Yücel, E. Berker, 2013, Genetic counseling.

Primary immunodeficiency disorders in children with Non-Cystic Fibrosis Bronchiectasis.

I. Tezcan, U. Ozcelik, N. Kiper, 2020, European annals of allergy and clinical immunology.

Lymphocyte Subgroups and KREC Numbers in Common Variable Immunodeficiency: A Single Center Study

I. Tezcan, C. Koşukcu, D. Çağdaş, 2020, Journal of Clinical Immunology.

IgG subclass deficiency in children with recurrent infections.

O. Sanal, I. Tezcan, A. Göçmen, 1991, The Turkish journal of pediatrics.

Necessity of keratinized tissues for dental implants: a clinical, immunological, and radiographic study.

E. Karabulut, I. Tezcan, S. Uysal, 2015, Clinical implant dentistry and related research.

TMC8 mutation in a Turkish family with epidermodysplasia verruciformis including laryngeal papilloma and recurrent skin carcinoma

I. Tezcan, K. Boztug, D. Çağdaş, 2021, Journal of cosmetic dermatology.

GIMAP5 deficiency reveals a mammalian ceramide-driven longevity assurance pathway

R. Lifton, I. Tezcan, D. Schwefel, 2024, Nature immunology.

Allogeneic bone marrow transplantation for children with myelodysplastic syndrome.

I. Tezcan, D. Uçkan, M. Çetin, 2000, The Turkish journal of pediatrics.

Recurrent Oral Aphtha, Diarrhea, Pneumonia, And Respiratory Distress Since Infancy: STAT1 GOF defect

I. Tezcan, N. Kiper, D. Ayvaz, 2020 .

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

I. Tezcan, S. Barış, A. Ikinciogullari, 2024, Journal of clinical immunology.

Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre

M. van der Burg, O. Sanal, I. Tezcan, 2023, Clinical and experimental immunology.

Antioxidant enzymes in red blood cells and lymphocytes of ataxia-telangiectasia patients.

Y. Aksoy, O. Sanal, I. Tezcan, 2004, The Turkish journal of pediatrics.

ORAI1 defect in a patient with disseminated CMV infection and severe hypotonia.

I. Tezcan, K. Oguz, D. Çağdaş, 2023, The Turkish journal of pediatrics.