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A Case of Anti-SAE1 Dermatomyositis

Case reports in immunology, 2022, Vol.2022, p.9000608-4

2022

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IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

Case reports in immunology, 2020-09, Vol.2020, p.1-5

2020

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Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation

Case Reports in Immunology, 2019, Vol.2019, p.1724083-4

2019

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European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

Journal of clinical immunology, 2020-05, Vol.40 (4), p.576-591

2020

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In Vitro Fertilization Using Luteinizing Hormone-Releasing Hormone Injections Resulted in Healthy Triplets without Increased Attack Rates in a Hereditary Angioedema Case

Case Reports in Immunology, 2018-01, Vol.2018, p.2706751-4

2018

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Medical algorithm: Diagnosis and management of antibody immunodeficiencies

Allergy (Copenhagen), 2021-12, Vol.76 (12), p.3841-3844

2021

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Subcutaneous immunoglobulin 16.5% for the treatment of pediatric patients with primary antibody immunodeficiency

Expert review of clinical immunology, 2023-01, Vol.19 (1), p.7-17

2023

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CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

Frontiers in immunology, 2019-01, Vol.9, p.3135-3135

2019

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Registry‐based analysis of Icatibant and C1‐inhibitor use in treatment of laryngeal attacks of hereditary angioedema

Clinical and experimental allergy, 2022-08, Vol.52 (8), p.994-997

2022

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Prognosis of Good syndrome mortality and morbidity of thymoma associated immunodeficiency in perspective

Clinical immunology (Orlando, Fla.), 2016-10, Vol.171, p.12-17

2016

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Long-term efficacy, safety, and tolerability of a subcutaneous immunoglobulin 16.5% (cutaquig®) in the treatment of patients with primary immunodeficiencies

Clinical and experimental immunology, 2022-12, Vol.210 (2), p.91-103

2022

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Common variable immunodeficiency patients display elevated plasma levels of granulocyte activation markers elastase and myeloperoxidase

International journal of immunopathology and pharmacology, 2019, Vol.33, p.2058738419843381-2058738419843381

2019

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PLAUR splicing pattern in hereditary angioedema patients’ monocytes and macrophages

Molecular biology reports, 2023-06, Vol.50 (6), p.4975-4982

2023

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Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy

Journal of clinical immunology, 2018-10, Vol.38 (7), p.810-815

2018

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Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

Frontiers in immunology, 2022-11, Vol.13, p.1011646-1011646

2022

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Corrigendum: Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

Frontiers in immunology, 2023-06, Vol.14, p.1226814-1226814

2023

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CEBPE -Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

Frontiers in immunology, 2018-03, Vol.9 (MAR), p.588-588

2018

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Antibody forming cells and plasmablasts in peripheral blood in CVID patients after vaccination

Vaccine, 2011-05, Vol.29 (24), p.4142-4150

2011

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Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period

Mediators of inflammation, 2019-01, Vol.2019, p.9515628-12

2019

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Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience

Journal of clinical immunology, 2016-08, Vol.36 (6), p.610-618

2016

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Terminally differentiated memory T cells are increased in patients with common variable immunodeficiency and selective IgA deficiency

Central-European journal of immunology, 2017-01, Vol.42 (3), p.244-251

2017

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Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression

The Journal of immunology (1950), 2010-12, Vol.185 (11), p.6431-6438

2010

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

Central-European journal of immunology, 2023-01, Vol.48 (3), p.228-236

2023

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Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation

Journal of clinical immunology, 2020-04, Vol.40 (3), p.435-446

2020

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A Case of Anti-SAE1 Dermatomyositis

IPEX Syndrome with Normal FOXP3 Protein Expression in Treg Cells in an Infant Presenting with Intractable Diarrhea as a Single Symptom

Sirolimus for the Treatment of Airway Obstruction due to Indolent T-Lymphoblastic Proliferation

European Society for Immunodeficiencies (ESID) and European Reference Network on Rare Primary Immunodeficiency, Autoinflammatory and Autoimmune Diseases (ERN RITA) Complement Guideline: Deficiencies, Diagnosis, and Management

In Vitro Fertilization Using Luteinizing Hormone-Releasing Hormone Injections Resulted in Healthy Triplets without Increased Attack Rates in a Hereditary Angioedema Case

Medical algorithm: Diagnosis and management of antibody immunodeficiencies

Subcutaneous immunoglobulin 16.5% for the treatment of pediatric patients with primary antibody immunodeficiency

CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID

Registry‐based analysis of Icatibant and C1‐inhibitor use in treatment of laryngeal attacks of hereditary angioedema

Prognosis of Good syndrome mortality and morbidity of thymoma associated immunodeficiency in perspective

Long-term efficacy, safety, and tolerability of a subcutaneous immunoglobulin 16.5% (cutaquig®) in the treatment of patients with primary immunodeficiencies

Common variable immunodeficiency patients display elevated plasma levels of granulocyte activation markers elastase and myeloperoxidase

PLAUR splicing pattern in hereditary angioedema patients’ monocytes and macrophages

Treatment of Hereditary Angioedema Attacks with Icatibant and Recombinant C1 Inhibitor During Pregnancy

Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

Corrigendum: Do common infections trigger disease-onset or -severity in CTLA-4 insufficiency?

CEBPE -Mutant Specific Granule Deficiency Correlates With Aberrant Granule Organization and Substantial Proteome Alterations in Neutrophils

Novel SAMD9 Mutation in a Patient With Immunodeficiency, Neutropenia, Impaired Anti-CMV Response, and Severe Gastrointestinal Involvement

Antibody forming cells and plasmablasts in peripheral blood in CVID patients after vaccination

Neutrophils Are Dysregulated in Patients with Hereditary Angioedema Types I and II in a Symptom-Free Period

Role of Flow Cytometry in the Diagnosis of Chronic Granulomatous Disease: the Egyptian Experience

Terminally differentiated memory T cells are increased in patients with common variable immunodeficiency and selective IgA deficiency

Characterization of lymphocyte subsets in patients with common variable immunodeficiency reveals subsets of naive human B cells marked by CD24 expression

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

Deep Intronic Mutation in SERPING1 Caused Hereditary Angioedema Through Pseudoexon Activation

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