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Editorial: Updates on the pathogenesis of common variable immunodeficiency (CVID)

Frontiers in immunology, 2023-01, Vol.13, p.1130418-1130418

2023

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Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee

Journal of clinical immunology, 2022-10, Vol.42 (7), p.1473-1507

2022

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Inflammation and Neutrophil Oxidative Burst in a Family with NFKB1 p.R157X LOF and Sterile Necrotizing Fasciitis

Journal of clinical immunology, 2023-07, Vol.43 (5), p.1007-1018

2023

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Inborn Errors of Immunity on the Island of Ireland — a Cross-Jurisdictional UKPID/ESID Registry Report

Journal of clinical immunology, 2022-08, Vol.42 (6), p.1293-1299

2022

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Rubella virus-associated granulomas controlled with allogeneic hematopoietic stem cell transplantation

Journal of clinical immunology, 2024-10, Vol.44 (7), p.159, Article 159

2024

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The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

Journal of clinical immunology, 2022-10, Vol.42 (7), p.1508-1520

2022

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IRF2BP2 Mutation Is Associated with Increased STAT1 and STAT5 Activation in Two Family Members with Inflammatory Conditions and Lymphopenia

Pharmaceuticals (Basel, Switzerland), 2021-08, Vol.14 (8), p.797

2021

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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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Novel cytoskeletal mutations with immunodeficiency: Why is the raven like a writing desk?

Journal of allergy and clinical immunology, 2018-11, Vol.142 (5), p.1444-1446

Seppänen, Mikko R.J.

2018

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Supplementation of the ESID registry working definitions for the clinical diagnosis of inborn errors of immunity with encoded human phenotype ontology (HPO) terms

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2020-05, Vol.8 (5), p.1778-1778

2020

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The GAIN Registry — a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation

Journal of clinical immunology, 2023-08, Vol.43 (6), p.1289-1301

2023

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Clinical efficacy of SARS‐CoV‐2 Omicron‐neutralizing antibodies in immunoglobulin preparations for the treatment of agammaglobulinemia in patients with primary antibody deficiency

Journal of medical virology, 2024-06, Vol.96 (6), p.e29738-n/a

2024

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Behçet disease (BD) and BD‐like clinical phenotypes: NF‐κB pathway in mucosal ulcerating diseases

Scandinavian journal of immunology, 2020-11, Vol.92 (5), p.e12973-n/a

2020

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Correction to: Inborn Errors of Immunity on the Island of Ireland — a Cross‑Jurisdictional UKPID/ESID Registry Report

Journal of clinical immunology, 2022-08, Vol.42 (6), p.1300-1300

2022

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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Frontiers in immunology, 2019-12, Vol.10, p.2770-2770

2019

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Immunoglobulin E—an Innocent Bystander in Host Defense?

Journal of clinical immunology, 2018-04, Vol.38 (3), p.223-224

2018

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Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling

Journal of clinical immunology, 2023-02, Vol.43 (2), p.358-370

2023

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Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency

Journal of clinical immunology, 2020-04, Vol.40 (3), p.503-514

2020

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L1CAM, INP10, P-cadherin, tPA and ITGB4 over-expression in malignant pleural mesotheliomas revealed by combined use of cDNA and tissue microarray

Carcinogenesis (New York), 2005-01, Vol.26 (1), p.17-25

2005

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Glimpses into treating GLILD

Journal of allergy and clinical immunology, 2023-08, Vol.152 (2), p.365-367

2023

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What drives cross-segment diversity in returns and risks? Evidence from Japanese and U.S. firms

The International journal of accounting, 2010-03, Vol.45 (1), p.44-76

2010

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Functional Definition of Progenitors Versus Mature Endothelial Cells Reveals Key SoxF-Dependent Differentiation Process

Circulation (New York, N.Y.), 2017-02, Vol.135 (8), p.786-805

2017

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A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency

The American journal of gastroenterology, 2019-04, Vol.114 (4), p.648-655

2019

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Tonsillar granuloma associated with hypogammaglobulinemia

Allergy, asthma, and clinical immunology, 2020-05, Vol.16 (1), p.43-6, Article 43

2020

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A statistical model for comparing future wind power scenarios with varying geographical distribution of installed generation capacity

Wind energy (Chichester, England), 2016-04, Vol.19 (4), p.665-679

2016

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Editorial: Updates on the pathogenesis of common variable immunodeficiency (CVID)

Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee

Inflammation and Neutrophil Oxidative Burst in a Family with NFKB1 p.R157X LOF and Sterile Necrotizing Fasciitis

Inborn Errors of Immunity on the Island of Ireland — a Cross-Jurisdictional UKPID/ESID Registry Report

Rubella virus-associated granulomas controlled with allogeneic hematopoietic stem cell transplantation

The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

IRF2BP2 Mutation Is Associated with Increased STAT1 and STAT5 Activation in Two Family Members with Inflammatory Conditions and Lymphopenia

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

Novel cytoskeletal mutations with immunodeficiency: Why is the raven like a writing desk?

Supplementation of the ESID registry working definitions for the clinical diagnosis of inborn errors of immunity with encoded human phenotype ontology (HPO) terms

The GAIN Registry — a New Prospective Study for Patients with Multi-organ Autoimmunity and Autoinflammation

Clinical efficacy of SARS‐CoV‐2 Omicron‐neutralizing antibodies in immunoglobulin preparations for the treatment of agammaglobulinemia in patients with primary antibody deficiency

Behçet disease (BD) and BD‐like clinical phenotypes: NF‐κB pathway in mucosal ulcerating diseases

Correction to: Inborn Errors of Immunity on the Island of Ireland — a Cross‑Jurisdictional UKPID/ESID Registry Report

Novel TMEM173 Mutation and the Role of Disease Modifying Alleles

Immunoglobulin E—an Innocent Bystander in Host Defense?

Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling

Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency

L1CAM, INP10, P-cadherin, tPA and ITGB4 over-expression in malignant pleural mesotheliomas revealed by combined use of cDNA and tissue microarray

Glimpses into treating GLILD

What drives cross-segment diversity in returns and risks? Evidence from Japanese and U.S. firms

Functional Definition of Progenitors Versus Mature Endothelial Cells Reveals Key SoxF-Dependent Differentiation Process

A High Prevalence of Gastrointestinal Manifestations in Common Variable Immunodeficiency

Tonsillar granuloma associated with hypogammaglobulinemia

A statistical model for comparing future wind power scenarios with varying geographical distribution of installed generation capacity

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