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

Pediatric research, 2020-03, Vol.87 (4), p.745-752

2020

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Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience

Journal of clinical immunology, 2021-07, Vol.41 (5), p.992-1003

2021

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Nutritional status of children with primary immunodeficiency: A single center experience

Pediatric investigation, 2022-01, Vol.64 (1), p.e14996-n/a

2022

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Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency

Journal of pediatric hematology/oncology, 2020-08, Vol.42 (6), p.e434-e439

2020

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

Clinical rheumatology, 2022-09, Vol.41 (9), p.2883-2892

2022

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A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess

The Pediatric infectious disease journal, 2021-01, Vol.40 (1), p.66-69

2021

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Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency

Journal of Pediatric Endocrinology and Metabolism, 2020-07, Vol.33 (7), p.957-961

2020

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Neurologic Involvement in Primary Immunodeficiency Disorders

Journal of child neurology, 2018-04, Vol.33 (5), p.320-328

2018

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A single center experience on PI3K/AKT/MTOR signaling defects: Towards pathogenicity assessment for four novel defects

Pediatric allergy and immunology, 2024-09, Vol.35 (9), p.e14245

2024

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Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency

Neuropediatrics, 2020-06, Vol.51 (3), p.206-210

2020

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Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency

The Turkish journal of pediatrics, 2021-11, Vol.63 (6), p.1072-1077

2021

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A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly

Journal of pediatric hematology/oncology, 2018-04, Vol.40 (3), p.248-251

2018

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

Turkish journal of pediatrics, 2023-07, Vol.65 (4), p.698-703

2023

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

Turkish journal of pediatrics, 2023-05, Vol.65 (3), p.536-541

2023

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Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases

Pediatrics international, 2000-12, Vol.42 (6), p.647-650

2000

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Detection of parasites in children with chronic diarrhea

Pediatrics international, 2016-06, Vol.58 (6), p.531-533

2016

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Hematopoietic stem cell transplantation in children with Griscelli syndrome: A single‐center experience

Pediatric transplantation, 2017-11, Vol.21 (7), p.n/a

2017

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Frequencies of Human Leukocyte Antigen Alleles in Turkish Children with Kawasaki Disease

Journal of pediatric infectious diseases, 2024-09

2024

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

Turkish Archives of Pediatrics, 2023-07

2023

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Common variable immunodeficiency in a patient with neurofibromatosis

Pediatrics international, 2001-12, Vol.43 (6), p.691-693

2001

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Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency

European journal of pediatrics, 2009, Vol.168 (1), p.87-93

2009

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

Pediatric blood & cancer, 2014-05, Vol.61 (5), p.928-930

2014

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Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

The Journal of clinical investigation, 2003-08, Vol.112 (3), p.450-456

2003

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A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis

The Pediatric infectious disease journal, 2007-04, Vol.26 (4), p.366-368

2007

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Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss

Turkish journal of pediatrics, 2018, Vol.60 (3), p.270-276

2018

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

Clinical and Immunological Characteristics of 63 Patients with Chronic Granulomatous Disease: Hacettepe Experience

Nutritional status of children with primary immunodeficiency: A single center experience

Hemophagocytic Lymphohistiocytosis in Patients With Primary Immunodeficiency

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

A Patient With AIRE Mutation Who Presented With Severe Diarrhea and Lung Abscess

Three patients with glucose-6 phosphatase catalytic subunit 3 deficiency

Neurologic Involvement in Primary Immunodeficiency Disorders

A single center experience on PI3K/AKT/MTOR signaling defects: Towards pathogenicity assessment for four novel defects

Recurrent Demyelinating Episodes as Sole Manifestation of Inherited CD59 Deficiency

Hematopoietic stem cell transplantation complicated with EBV associated hemophagocytic lymphohistiocytosis in a patient with DOCK2 deficiency

A Rare Cause of Secondary Immunodeficiency: Generalized Lymphatic Anomaly

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

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

Transient hypogammaglobulinemia of infancy: Clinical and immunologic features of 40 new cases

Detection of parasites in children with chronic diarrhea

Hematopoietic stem cell transplantation in children with Griscelli syndrome: A single‐center experience

Frequencies of Human Leukocyte Antigen Alleles in Turkish Children with Kawasaki Disease

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

Common variable immunodeficiency in a patient with neurofibromatosis

Clinical heterogeneity can hamper the diagnosis of patients with ZAP70 deficiency

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

Griscelli syndrome restricted to hypopigmentation results from a melanophilin defect (GS3) or a MYO5A F-exon deletion (GS1)

A case of interleukin-12 receptor beta-1 deficiency with recurrent leishmaniasis

Advantage of the subcutaneous immunoglobulin replacement therapy in primary immunodeficient patients with or without secondary protein loss

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