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Immunodeficiency-Like Phenotype, Recurrent Pulmonary Manifestations, and Persistent Polyarthritis: Mevalonate Kinase Deficiency Successfully Treated With Adalimumab

Archives of rheumatology, 2020-12, Vol.35 (4), p.627-628

2020

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Asymptomatic catheter related Rhizobium radiobacter infection in a haploidentical hemapoetic stem cell recipient

Journal of infection in developing countries, 2010-09, Vol.4 (8), p.530-532

2010

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Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

Nature genetics, 2016-09, Vol.48 (9), p.1071-1076

2016

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Very high immunoglobulin E levels in children: when from pediatrician to immunologist?

Minerva pediatrics, 2024-02, Vol.76 (1), p.13

2024

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The impact of Treosulfan-based conditioning for inborn errors of immunity: Is dose monitoring crucial?

Clinical transplantation, 2023-09, Vol.37 (9), p.e15083-e15083

2023

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Evaluation of the risk factors for BK virus‐associated hemorrhagic cystitis in pediatric bone marrow transplantation patients: Does post‐transplantation cyclophosphamide increase the frequency?

Pediatric transplantation, 2023-02, Vol.27 (1), p.e14364-n/a

2023

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Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Journal of clinical immunology, 2020-04, Vol.40 (3), p.539-542

2020

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Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature

Journal of clinical immunology, 2020-04, Vol.40 (3), p.466-474

2020

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A rare case of syndromic severe congenital neutropenia: JAGN1 mutation

Turkish journal of pediatrics, 2020-03, Vol.62 (2), p.326-331

2020

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Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia

Journal of clinical immunology, 2018-04, Vol.38 (3), p.273-277

2018

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Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with β-Thalassemia Major from Three Different Graft Types

Hemoglobin, 2021-01, Vol.45 (1), p.25-29

2021

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ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

Allergy (Copenhagen), 2020-04, Vol.75 (4), p.921-932

2020

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PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects

Journal of allergy and clinical immunology, 2019-01, Vol.143 (1), p.325-334.e2

2019

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COCUK SAGLIGININ DUZENLI IZLEMI VE PRIMER IMMUN YETMEZLIK HASTALARININ ERKEN TANINABILIRLIGI/REGULAR FOLLOW-UP IN CHILD HEALTH AND EARLY RECOGNITION OF PRIMARY IMMUNE DEFICIENCY DISORDERS

İstanbul Tıp Fakültesi dergisi = Journal of the Istanbul Faculty of Medicine, 2018-12, Vol.81 (4), p.145

2018

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COCUK SAGLIGININ DUZENLI IZLEMI VE PRIMER IMMUN YETMEZLIK HASTALARININ ERKEN TANINABILIRLIGI/REGULAR FOLLOW-UP IN CHILD HEALTH AND EARLY RECOGNITION OF PRIMARY IMMUNE DEFICIENCY DISORDERS

İstanbul Tıp Fakültesi dergisi = Journal of the Istanbul Faculty of Medicine, 2018-12, Vol.81 (4), p.145

2018

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Primary immunodeficiencies: HSCT experiences of a single center in Turkey

Pediatric transplantation, 2021-11, Vol.25 (7), p.e14063-n/a

2021

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Patients with Primary Immunodeficiencies in Pediatric Intensive Care Unit: Outcomes and Mortality-Related Risk Factors

Journal of clinical immunology, 2014-04, Vol.34 (3), p.309-315

2014

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Breastfeeding and Metabolic Programming

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Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency

Case reports in pediatrics, 2014-01, Vol.2014, p.614238-4

2014

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Diagnosis of Immediate Hypersensitivity to β-Lactam Antibiotics Can Be Made Safely with Current Approaches

International archives of allergy and immunology, 2012-01, Vol.157 (3), p.311-317

2012

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Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Journal of clinical immunology, 2021, Vol.41 (1), p.59-65

2021

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Evaluation of allergic sensitization and gastroesophageal reflux disease in children with recurrent croup

Pediatrics international, 2009-10, Vol.51 (5), p.661-665

2009

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Natural killer cell hyporesponsiveness and impaired development in a CD247-deficient patient

Journal of allergy and clinical immunology, 2016-03, Vol.137 (3), p.942-945.e4

2016

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Beslenme desteği tipi hematopoetik kök hücre nakil sonuçlarını etkiliyor mu? Bir pediatrik merkez deneyimi

Ege tłp bilimleri dergisi, 2019-12, Vol.2 (3), p.119-123

2019

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Immunodeficiency-Like Phenotype, Recurrent Pulmonary Manifestations, and Persistent Polyarthritis: Mevalonate Kinase Deficiency Successfully Treated With Adalimumab

Asymptomatic catheter related Rhizobium radiobacter infection in a haploidentical hemapoetic stem cell recipient

Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

Very high immunoglobulin E levels in children: when from pediatrician to immunologist?

The impact of Treosulfan-based conditioning for inborn errors of immunity: Is dose monitoring crucial?

Evaluation of the risk factors for BK virus‐associated hemorrhagic cystitis in pediatric bone marrow transplantation patients: Does post‐transplantation cyclophosphamide increase the frequency?

Biallelic Form of a Known CD3E Mutation in a Patient with Severe Combined Immunodeficiency

Invasive Saprochaete capitata Infection in a Patient with Autosomal Recessive CARD9 Deficiency and a Review of the Literature

A rare case of syndromic severe congenital neutropenia: JAGN1 mutation

Novel Mutation in CECR1 Leads to Deficiency of ADA2 with Associated Neutropenia

Primary T-cell immunodeficiency with functional revertant somatic mosaicism in CD247

Comparison of Hematopoietic Stem Cell Transplantation Results in Patients with β-Thalassemia Major from Three Different Graft Types

ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

PROMIDISα: A T-cell receptor α signature associated with immunodeficiencies caused by V(D)J recombination defects

COCUK SAGLIGININ DUZENLI IZLEMI VE PRIMER IMMUN YETMEZLIK HASTALARININ ERKEN TANINABILIRLIGI/REGULAR FOLLOW-UP IN CHILD HEALTH AND EARLY RECOGNITION OF PRIMARY IMMUNE DEFICIENCY DISORDERS

COCUK SAGLIGININ DUZENLI IZLEMI VE PRIMER IMMUN YETMEZLIK HASTALARININ ERKEN TANINABILIRLIGI/REGULAR FOLLOW-UP IN CHILD HEALTH AND EARLY RECOGNITION OF PRIMARY IMMUNE DEFICIENCY DISORDERS

Primary immunodeficiencies: HSCT experiences of a single center in Turkey

Patients with Primary Immunodeficiencies in Pediatric Intensive Care Unit: Outcomes and Mortality-Related Risk Factors

Breastfeeding and Metabolic Programming

Cernunnos/XLF Deficiency: A Syndromic Primary Immunodeficiency

Diagnosis of Immediate Hypersensitivity to β-Lactam Antibiotics Can Be Made Safely with Current Approaches

Novel Frameshift Autosomal Recessive Loss-of-Function Mutation in SMARCD2 Encoding a Chromatin Remodeling Factor Mediates Granulopoiesis

Evaluation of allergic sensitization and gastroesophageal reflux disease in children with recurrent croup

Natural killer cell hyporesponsiveness and impaired development in a CD247-deficient patient

Beslenme desteği tipi hematopoetik kök hücre nakil sonuçlarını etkiliyor mu? Bir pediatrik merkez deneyimi

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