S. Keleş

发表

Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

Mark S. Anderson, Chun Jimmie Ye, Gabriela K. Fragiadakis, 2022, Science immunology.

Sublingual immunotherapy in children with allergic rhinoconjunctivitis mono-sensitized to house-dust-mites: a double-blind-placebo-controlled randomised trial.

A. Eifan, M. Nursoy, I. Barlan, 2013, Respiratory medicine.

A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

D. Chaussabel, J. Casanova, P. Li, 2018, Science Immunology.

Patients with CD3G mutations reveal a role for human CD3γ in Treg diversity and suppressive function.

L. Notarangelo, İ. Reisli, L. Henderson, 2018, Blood.

Dedicator of cytokinesis 8-deficient patients have a breakdown in peripheral B-cell tolerance and defective regulatory T cells.

R. Geha, W. Al-Herz, T. Chatila, 2014, The Journal of allergy and clinical immunology.

Hematopoietic Stem Cell Transplantation Outcomes for 11 Patients with Dedicator of Cytokinesis 8 (DOCK8) Deficiency

L. Notarangelo, J. Chou, W. Al-Herz, 2017 .

Hematopoietic stem cell transplantation outcomes for 11 patients with dedicator of cytokinesis 8 deficiency.

Douglas R. McDonald, L. Notarangelo, R. Geha, 2016, The Journal of allergy and clinical immunology.

Transient hypogammaglobulinemia and unclassified hypogammaglobulinemia: ‘Similarities and differences’

İ. Reisli, H. Artaç, A. Ozen, 2010, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Exaggerated follicular helper T‐cell responses in patients with LRBA deficiency caused by failure of CTLA4‐mediated regulation

R. Geha, J. Chou, T. Chatila, 2017, The Journal of allergy and clinical immunology.

Clinical efficacy and immunological mechanisms of sublingual and subcutaneous immunotherapy in asthmatic/rhinitis children sensitized to house dust mite: an open randomized controlled trial

A. Eifan, I. Barlan, T. Akkoç, 2010, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Anaphylaxis to multiple pollen allergen sublingual immunotherapy

A. Eifan, I. Barlan, S. Keleş, 2007, Allergy.

Clinical features and risk factors in children with acute asthma attack

İ. Reisli, H. Artaç, Cüneyt Karagöl, 2012 .

Recessive inborn errors of type I IFN immunity in children with COVID-19 pneumonia

J. Casanova, R. Lifton, M. Zatz, 2022, The Journal of experimental medicine.

The risk of COVID-19 death is much greater and age dependent with type I IFN autoantibodies

P. Gregersen, J. Casanova, L. Rowen, 2022, Proceedings of the National Academy of Sciences of the United States of America.

The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

Mark S. Anderson, J. Casanova, L. Rowen, 2022, Research square.

A Stk4-Foxp3–NF-κB p65 transcriptional complex promotes Treg cell activation and homeostasis

T. Chatila, C. Angelini, Mehdi Benamar, 2022, Science Immunology.

DOCK8 Regulates STAT3 Activation and Promotes Th17 Cell Differentiation

R. Geha, İ. Reisli, W. Al-Herz, 2016 .

Defects Along the Th17 Differentiation Pathway Underlie Genetically Distinct Forms of the Hyper IgE Syndrome

İ. Reisli, T. Chatila, A. Somer, 2010 .

PRACTITIONER ’ S CORNER Inhaled 1-Antitrypsin Administered to Treat Pneumatocele in Autosomal Dominant Hyperimmunoglobulin E Syndrome

T. Chatila, I. Barlan, S. Barış, 2013 .

Serum Vitamins A, D, and Zinc Levels in Children with Coronavirus Disease 2019 and Multisystem Inflammatory Syndrome in Children

A. Yılmaz, Ö. M. Akcan, S. Pekcan, 2022, Journal of Pediatric Infectious Diseases.

DOCK8 deficiency: Insights into pathophysiology, clinical features and management.

T. Chatila, C. Biggs, S. Keleş, 2017, Clinical immunology.

Comparing the levels of CTLA‐4‐dependent biological defects in patients with LRBA deficiency and CTLA‐4 insufficiency

İ. Reisli, A. Yildiran, S. Barış, 2022, Allergy.

İ. Reisli, S. Ozen, I. Gursel, 2017, The Journal of allergy and clinical immunology.

Regulatory B cells in patients suffering from inborn errors of immunity with severe immune dysregulation.

C. Königs, P. Bader, M. Seidel, 2022, Journal of autoimmunity.

Characteristics and Prevalence of Intrapulmonary Shunt Detected by Contrast Echocardiography With Harmonic Imaging in Liver Transplant Candidates

Spiegelhalter Dj, O. Miller, A. Gürler, 2004 .

Long Term Follow-up of Hyperimmunoglobulin M Syndrome Cases

G. Deniz, I. Barlan, S. Barış, 2010 .

Clinical and laboratory evaluation of Turkish children with IgG subclass deﬁciency

İ. Reisli, S. Aytekin, M. Keskin, 2022 .

CD3G Gene Defects in Familial Autoimmune Thyroiditis

İ. Reisli, N. Morgan, H. Artaç, 2014, Scandinavian journal of immunology.

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

J. Casanova, J. Uitto, L. Abel, 2022, The Journal of experimental medicine.

Inhaled alpha1-antitrypsin administered to treat pneumatocele in autosomal dominant hyperimmunoglobulin E syndrome.

T. Chatila, I. Barlan, S. Barış, 2013, Journal of investigational allergology & clinical immunology.

A novel approach in allergen-specific immunotherapy: combination of sublingual and subcutaneous routes.

I. Barlan, T. Akkoç, E. Karakoc‐Aydiner, 2011, The Journal of allergy and clinical immunology.

Variable presentation of primary immune deficiency: Two cases with CD3 gamma deficiency presenting with only autoimmunity

İ. Reisli, N. Morgan, Isabel Sánchez Guiú, 2013, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Mark S. Anderson, J. Casanova, J. Fellay, 2021, The Journal of experimental medicine.

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

J. Casanova, T. Maniatis, R. Silverman, 2022, Science.

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.

Chronic Granulomatous Disease Presenting with Invasive Aspergillosis and Hypogammaglobulinemia

A. Eifan, I. Barlan, C. Ozdemir, 2016 .

Immunological mechanism of postherpetic neuralgia and effect of pregabalin treatment on the mechanism: a prospective single-arm observational study

Resul Yılmaz, Sema Tuncer Uzun, A. Mercan, 2021, The Korean journal of pain.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Edward R B McCabe, Bodo Grimbacher, Christoph Klein, 2009, The Journal of allergy and clinical immunology.

Defects along the T(H)17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome.

T. Chatila, M. Yılmaz, A. Somer, 2009, The Journal of allergy and clinical immunology.

Inherited DOCK2 Deficiency in Patients with Early-Onset Invasive Infections.

Toshiro K. Ohsumi, D. Goldstein, M. Knip, 2015, The New England journal of medicine.

Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency

M. Afarideh, A. Ghajar, R. Geha, 2017, The Journal of allergy and clinical immunology.

Identification of a novel mutation in ZAP70 and prenatal diagnosis in a Turkish family with severe combined immunodeficiency disorder.

T. Chatila, E. Karaca, M. Ozen, 2013, Gene.

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Jacques Fellay, Agatha Schlüter, Aurora Pujol, 2020, Science.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

T. Chatila, S. Holland, C. Klein, 2009, The Journal of allergy and clinical immunology.

Single-cell analysis of FOXP3 deficiencies in humans and mice unmasks intrinsic and extrinsic CD4+ T cell perturbations

F. Rieux-Laucat, C. Benoist, T. Chatila, 2020, Nature Immunology.

Dedicator of cytokinesis 8 regulates signal transducer and activator of transcription 3 activation and promotes TH17 cell differentiation.

Hao Wu, R. Geha, W. Al-Herz, 2016, The Journal of allergy and clinical immunology.

Dominant-negative mutations in human IL6ST underlie hyper-IgE syndrome

David R. Murdock, J. Rosenfeld, B. Lambrecht, 2020, The Journal of experimental medicine.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

STK4 deficiency and EBV-associated lymphoproliferative disorders, emphasis on histomorphology, and review of literature

A. Sağlam, D. Çağdaş, A. Uner, 2021, Virchows Archiv.

Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening.

T. Chatila, J. Puck, M. Dasouki, 2011, Clinical immunology.

Memory B cells and serum immunoglobulins are associated with disease severity and mortality in patients with COVID-19

İ. Reisli, Fatih Çölkesen, Eray Yıldız, 2022, Postgraduate Medical Journal.

Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

Mark S. Anderson, P. Gregersen, R. Nussbaum, 2021, Science Immunology.

An Unexpected Infection in Loss-of-Function Mutations in STAT3: Malignant Alveolar Echinococcosis in Liver.

D. Altun, A. Ikinciogullari, E. Çiftçi, 2020, Iranian journal of allergy, asthma, and immunology.

Human genetic and immunological determinants of critical COVID-19 pneumonia

Mark S. Anderson, P. Gregersen, J. Casanova, 2022, Nature.

DCLRE1C (ARTEMIS) mutations causing phenotypes ranging from atypical severe combined immunodeficiency to mere antibody deficiency.

A. Schäffer, U. Pannicke, K. Schwarz, 2015, Human molecular genetics.

Late-presenting congenital diaphragmatic hernia associated with ectopic thoracic kidney

H. Artaç, S. Keleş, Midhat Elmaci, 2006, European Journal of Pediatrics.

Evaluation of Clinical and Immunological Characteristics of Children with Common Variable Immunodeficiency

G. Alkan, S. Keleş, I. Reisli, 2018, International journal of pediatrics.

Dock8 Functions as an Adaptor That Links Toll-like Receptor– Myd88 Signaling to B Cell Activation Hhs Public Access

Alessandro Plebani, Rima Wakim, Kate Fitzgerald, 2022 .

DOCK8 Functions as an Adaptor that Links TLR–MyD88 Signaling to B Cell Activation

Schneider, Douglas R. McDonald, Ghassan, 2012 .

Hematopoietic stem cell transplantation in serine/threonine kinase 4 (STK4) deficiency: Report of two cases and literature review

K. Yalçın, V. Uygun, G. Karasu, 2022, Pediatric transplantation.

B cell-intrinsic requirement for STK4 in humoral immunity in mice and human subjects.

L. Notarangelo, S. Tangye, T. Phan, 2019, The Journal of allergy and clinical immunology.

The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency.

A. Schäffer, V. Lougaris, R. Geha, 2015, The Journal of allergy and clinical immunology.

Combined Immunodeficiency due to DOCK8 Deficiency: A Tribute to Prof. Isil

T. Chatila, S. Keleş, 2015 .

Immune deficiencies , infection , and systemic immune disorders Defects along the TH 17 differentiation pathway underlie genetically distinct forms of the hyper IgE syndrome

T. Chatila, M. Yılmaz, A. Somer, 2009 .

Hematopoietic stem cell transplantation from unrelated donors in children with DOCK8 deficiency

M. Yılmaz, Ahmet Özen, V. Uygun, 2017, Pediatric 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.

Would mean platelet volume/platelet count ratio be used as a novel formula to predict 22q11.2 deletion syndrome?

A. Zamani, H. Artaç, M. Yıldırım, 2016, Asian Pacific journal of allergy and immunology.

F-BAR domain only protein 1 (FCHO1) deficiency is a novel cause of combined immune deficiency in human subjects.

L. Notarangelo, R. Geha, J. Chou, 2019, The Journal of allergy and clinical immunology.

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

R. Nussbaum, J. Casanova, M. Gut, 2021, Science immunology.

Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021

J. Casanova, A. Šedivá, Y. Rodina, 2022, Frontiers in Immunology.

Intrauterine detection of DCLRE1C (Artemis) mutation by restriction fragment length polymorphism

E. Kurar, Hasan Kapaklı, Ş. Güner, 2019, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Evaluation of the 10 Warning Signs in Primary and Secondary Immunodeficient Patients

Alaaddin Yorulmaz, Yahya Gul, S. Guner, 2022, Frontiers in Immunology.

Evaluation of The 10 Warning Signs In Immunodeficient Patients: Additional Suggestions

Ş. Güner, S. Keleş, I. Reisli, 2021 .

Plasmacytoid dendritic cell depletion in DOCK8 deficiency: rescue of severe herpetic infections with IFN-α 2b therapy.

Douglas R. McDonald, R. Geha, W. Al-Herz, 2014, The Journal of allergy and clinical immunology.

Congenital aneurysm of the muscular interventricular septum in a child.

B. Oran, S. Karaaslan, O. Başpınar, 2005, The Turkish journal of pediatrics.

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score.

A. Gennery, A. Worth, L. Hammarström, 2019, The Journal of allergy and clinical immunology.

Abatacept as a Long-Term Targeted Therapy for LRBA Deficiency.

İ. Reisli, T. Chatila, A. Al-Shaibi, 2019, The journal of allergy and clinical immunology. In practice.

Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA.

Toshiro K. Ohsumi, R. Geha, J. Chou, 2015, The Journal of allergy and clinical immunology.

Clinical Spectrum of LIG4 Deficiency Is Broadened with Severe Dysmaturity, Primordial Dwarfism, and Neurological Abnormalities

İ. Reisli, D. Gent, S. Keles, 2013, Human mutation.

Cysteine and hydrophobic residues in CDR3 serve as distinct T-cell self-reactivity indices.

L. Notarangelo, S. Holland, K. Dobbs, 2019, The Journal of allergy and clinical immunology.

Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency.

R. Geha, T. Chatila, M. Massaad, 2014, Clinical immunology.

Plasmacytoid Dendritic Cell Depletion in DOCK8 Deficiency: Rescue of Severe Herpetic Infections with Interferon Alpha-2b Therapy

Douglas R. McDonald, R. Geha, W. Al-Herz, 2014 .

Spatio-temporal gradient of cortical neuron death contributes to microcephaly in knock-in mouse model of ligase 4 syndrome.

Maria K. Lehtinen, L. Notarangelo, Melody P. Lun, 2019, The American journal of pathology.

DOCK 8 functions as an adaptor that links Toll-like receptor – MyD 88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012 .

Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder

T. Chatila, C. Woda, S. Rosen, 2015, Pediatric Nephrology.

Could immune cells be associated with nephropathy in Fabry disease patients?

H. Esen, K. Turkmen, I. Baloglu, 2023, International Urology and Nephrology.

Clinical, immunological features and follow up of 20 patients with dedicator of cytokinesis 8 (DOCK8) deficiency

A. Ikinciogullari, C. Aytekin, F. Doğu, 2020, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

ILC3 deficiency and generalized ILC abnormalities in DOCK8‐deficient patients

İ. Reisli, T. Chatila, M. Oukka, 2020, Allergy.

Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome

T. Chatila, N. Rezaei, M. Shabani, 2019, Pediatric blood & cancer.

DOCK8 Deficiency Presenting as an IPEX-Like Disorder

R. Geha, J. Chou, T. Chatila, 2017, Journal of Clinical Immunology.

DOCK8 and STAT3 dependent inhibition of IgE isotype switching by TLR9 ligation in human B cells.

R. Geha, W. Al-Herz, T. Chatila, 2017, Clinical immunology.

Can Atopic Diseases be Differentiated from Hyper IgE Syndrome by Serum IgE and Blood Eosinophil Levels

S. Barış, E. Nain, A. Kıykım, 2017 .

Flow cytometry diagnosis of dedicator of cytokinesis 8 (DOCK8) deficiency.

Douglas R. McDonald, R. Geha, W. Al-Herz, 2014, The Journal of allergy and clinical immunology.

Successful engraftment of donor marrow after allogeneic hematopoietic cell transplantation in autosomal-recessive hyper-IgE syndrome caused by dedicator of cytokinesis 8 deficiency.

Douglas R. McDonald, R. Geha, T. Chatila, 2010, The Journal of allergy and clinical immunology.

Combined Immunodeficiency due to a loss of function mutation in DNA Polymerase Delta 1.

Hao Wu, T. Chatila, L. Henderson, 2020, The Journal of allergy and clinical immunology.

Combined immunodeficiency caused by a loss-of-function mutation in DNA polymerase delta 1

Hao Wu, L. Henderson, Wenjun Xie, 2019 .

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Andrew J. Oler, Eglantine Ferrand Devouge, P. Gregersen, 2023, Genome Medicine.

Chilaiditi syndrome as a cause of respiratory distress

H. Artaç, O. Koc, H. Alp, 2006, European Journal of Pediatrics.

Long-Term Experience of Subcutaneous Immunoglobulin Therapy in Pediatric Primary Immunodeficient Patients with Low and Normal Body Weight

Yahya Gul, Hasan Kapaklı, S. Guner, 2021, Journal of Clinical Immunology.

Long-Term Experience of Subcutaneous Immunoglobulin Therapy in Pediatric Primary Immunodeficient Patients with Low and Normal Body Weight

Yahya Gul, Hasan Kapaklı, S. Guner, 2021, Journal of Clinical Immunology.

Reactivation of Tuberculosis and COVID-19 in Pediatric Patients

N. Poyraz, A. Yılmaz, Ö. Metin Akcan, 2022, Journal of Pediatric Infectious Diseases.

Relationship Between T Regulatory Cell Levels (CD4+, CD25+, CD127- T cells) and the Presence of Autoantibodies in Adult Patients with Selective IgA Deficiency

Fatih Çölkesen, Eray Yıldız, G. Aytekin, 2020 .

An Adolescent with Hyperimmunoglobulinemia D and Periodic Fever Syndrome Responding to Simvastatin Treatment

I. Barlan, S. Barış, C. Ozdemir, 2011 .

Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency

J. Casanova, A. Bousfiha, S. Ehl, 2022, The Journal of experimental medicine.

Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

Andrew J. Oler, Eglantine Ferrand Devouge, P. Gregersen, 2023, Genome Medicine.

Neonatal BCG vaccination induces IL‐10 production by CD4+ CD25+ T cells

A. Eifan, I. Barlan, M. Akın, 2010, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Atopy and allergic diseases in immunoglobulin A deficiency

H. Artaç, Cüneyt Karagöl, Bahar Göktürk, 2012 .

DOCK8 Deficiency Presenting as an IPEX-Like Disorder

R. Geha, J. Chou, T. Chatila, 2017, Journal of Clinical Immunology.

An association between immune status and chest CT scores in COVID‐19 patients

İ. Reisli, Fatih Çölkesen, Eray Yıldız, 2021, International journal of clinical practice.

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X‐Linked Syndrome Associated with Neonatal Epidermolysis Bullosa Acquisita

L. Notarangelo, T. Chatila, L. Schneider, 2015, Pediatric dermatology.

Efficacy of intravenous immunoglobulin treatment in immunocompromised children with H1N1 influenza: a clinical observation

H. Artaç, S. Pekcan, S. Guner, 2016, The clinical respiratory journal.

Defective Treg generation and increased type 3 immune response in leukocyte adhesion deficiency 1.

H. Canatan, A. Eken, S. Barış, 2023, Clinical immunology.

The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity.

R. Geha, A. Bousfiha, W. Al-Herz, 2022, The journal of allergy and clinical immunology. In practice.

REACTIVATION OF TUBERCULOSIS AND COVID-19

N. Poyraz, S. Pekcan, O. Akcan, 2021 .

A Rose Amongst the Thorns: the Mission of the J Project in a Conflictual World

A. Šedivá, J. Litzman, I. Tuzankina, 2022, Journal of Clinical Immunology.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Retrospective analysis of patients with severe combined immunodeficiency and alternative diagnostic criteria: A 20‐year single centre experience

S. Aytekin, S. Guner, H. Tokgoz, 2023, International journal of immunogenetics.

Iatrogenic vitamin D intoxiciation in infancy: Three cases

H. Artaç, Y. Koksal, E. Unal, 2007 .

Combined Immunodeficiency due to DOCK8 Deficiency: A Tribute to Prof. Işıl Berat Barlan, M.D.

S. Keleş, 2015 .

Regulatory T Cell Deficiency and Immune dysregulation, Polyendocrinopathy, Enteropathy, X-Linked-Like Disorder Due to Loss of Function Mutations in LRBA

R. Geha, J. Chou, M. Massaad, 2015 .

Successful interferon-alpha 2b therapy for unremitting warts in a patient with DOCK8 deficiency.

R. Geha, T. Chatila, M. Massaad, 2014, Clinical immunology.

DOCK8 functions as an adaptor that links Toll-like receptor–MyD88 signaling to B cell activation

Douglas R. McDonald, L. Notarangelo, A. Plebani, 2012, Nature Immunology.

Efficacy of intravenous immunoglobulin treatment in immunocompromised children with H1N1 influenza: a clinical observation

H. Artaç, S. Pekcan, S. Guner, 2016, The clinical respiratory journal.

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

J. Derisi, F. Rieux-Laucat, J. Fellay, 2023, Nature.

Immune Dysregulation, Polyendocrinopathy, Enteropathy, X‐Linked Syndrome Associated with Neonatal Epidermolysis Bullosa Acquisita

L. Notarangelo, T. Chatila, L. Schneider, 2015, Pediatric dermatology.

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome (vol 124, pg 1289, 2009)

T. Chatila, J. Puck, S. Ehl, 2010 .

Higher COVID-19 pneumonia risk associated with anti-IFN-α than with anti-IFN-ω auto-Abs in children

V. Tillmann, P. Soler-Palacín, T. Ozcelik, 2024, The Journal of experimental medicine.

Vaccine breakthrough hypoxemic COVID-19 pneumonia in patients with auto-Abs neutralizing type I IFNs

Mark S. Anderson, Chun Jimmie Ye, P. Gregersen, 2022, Science Immunology.

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.

Deficient T Cell Receptor Excision Circles (TRECs) in autosomal recessive hyper IgE syndrome caused by DOCK8 mutation: implications for pathogenesis and potential detection by newborn screening.

T. Chatila, J. Puck, M. Dasouki, 2011, Clinical immunology.

Clinical and laboratory evaluation of Turkish children with IgG subclass deficiency.

M. Kocaoğlu, Ş. Güner, S. Keleş, 2022, Pediatrics and neonatology.

Association of NK cell subsets and cytotoxicity with FCGR3A gene polymorphism in functional NK cell deficiency

E. Kurar, Ş. Güner, S. Keleş, 2024, Revista da Associacao Medica Brasileira.

CD3G Gene Defects in Familial Autoimmune Thyroiditis

H. Artaç, J. Dongen, H. Tokgoz, 2014, Scandinavian journal of immunology.

Intraoral and maxillofacial abnormalities in patients with autosomal dominant hyper-IgE syndrome

E. Bernatowska, L. Izakovicova-Holla, I. Tar, 2023, Central-European journal of immunology.

Variable presentation of primary immune deficiency: Two cases with CD3 gamma deficiency presenting with only autoimmunity

N. Morgan, H. Tokgoz, U. Çalişkan, 2013, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.