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Treatment of chronic or relapsing COVID-19 in immunodeficiency

Journal of allergy and clinical immunology, 2022-02, Vol.149 (2), p.557-561.e1

2022

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Is ipsilateral administration of COVID-19 vaccine boosters the optimal approach?

EBioMedicine, 2023-12, Vol.98, p.104852-104852, Article 104852

2023

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Primary vs. secondary antibody deficiency: clinical features and infection outcomes of immunoglobulin replacement

PloS one, 2014-06, Vol.9 (6), p.e100324

2014

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Viral infection in primary antibody deficiency syndromes

Reviews in medical virology, 2019-07, Vol.29 (4), p.e2049-n/a

2019

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The influence of time on the sensitivity of SARS-CoV-2 serological testing

Scientific reports, 2022-06, Vol.12 (1), p.10517-10517, Article 10517

2022

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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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Absence of Persistent Hepatitis E Virus Infection in Antibody-Deficient Patients Is Associated With Transfer of Antigen-Neutralizing Antibodies From Immunoglobulin Products

The Journal of infectious diseases, 2019-01, Vol.219 (2), p.245-253

2019

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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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Low IgA and IgM Is Associated with a Higher Prevalence of Bronchiectasis in Primary Antibody Deficiency

Journal of clinical immunology, 2017-05, Vol.37 (4), p.329-331

2017

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Successful rapid push subcutaneous desensitization in a patient with delayed local hypersensitivity reactions to immunoglobulins

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2019-11, Vol.7 (8), p.2906-2908

2019

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Dendritic cells as a tool to induce transplantation tolerance: obstacles and opportunities

Transplantation, 2011-01, Vol.91 (1), p.2-7

2011

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Secondary antibody deficiency

Expert review of clinical immunology, 2014-05, Vol.10 (5), p.583-591

2014

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A type III complement factor D deficiency: Structural insights for inhibition of the alternative pathway

Journal of allergy and clinical immunology, 2018-07, Vol.142 (1), p.311-314.e6

2018

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Chronic Granulomatous Disorder–Associated Colitis Can Be Accurately Evaluated with MRI Scans and Fecal Calprotectin Level

Journal of clinical immunology, 2019-07, Vol.39 (5), p.494-504

2019

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Stability of gut microbiome after COVID-19 vaccination in healthy and immuno-compromised individuals

Life science alliance, 2024-04, Vol.7 (4), p.e202302529

2024

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Preventing kidney transplant failure by screening for antibodies against human leucocyte antigens followed by optimised immunosuppression: OuTSMART RCT

Efficacy and mechanism evaluation, 2023-09, p.1-68

2023

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Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease

The journal of allergy and clinical immunology in practice (Cambridge, MA), 2018-09, Vol.6 (5), p.1775-1777.e1

2018

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Erratum to: Low IgA and IgM is Associated with a Higher Prevalence of Bronchiectasis in Primary Antibody Deficiency

Journal of clinical immunology, 2017-05, Vol.37 (4), p.332-332

2017

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Acquired C1 inhibitor deficiency: should we monitor for associated antibody deficiency?

Annals of allergy, asthma, & immunology, 2014-03, Vol.112 (3), p.265-267

2014

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Successful treatment of acute hepatitis C virus in HIV positive patients using the European AIDS Treatment Network guidelines for treatment duration

Journal of clinical virology, 2011-12, Vol.52 (4), p.367-369

2011

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Real-world outcomes in hereditary angioedema: first experience from the Icatibant Outcome Survey in the United Kingdom

Allergy, asthma, and clinical immunology, 2018-08, Vol.14 (1), p.28-28, Article 28

2018

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Use of recombinant C1 inhibitor in patients with resistant or frequent attacks of hereditary or acquired angioedema

EJD. European journal of dermatology, 2014, Vol.24 (1), p.28-34

2014

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An Artemis polymorphic variant reduces Artemis activity and confers cellular radiosensitivity

DNA repair, 2010-09, Vol.9 (9), p.1003-1010

2010

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1385 Berotralstat prophylaxis for Hereditary Angioedema – an audit of use in a cohort of patients at a tertiary centre

Archives of disease in childhood, 2022-08, Vol.107 (Suppl 2), p.A214-A215

2022

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Treatment of chronic or relapsing COVID-19 in immunodeficiency

Is ipsilateral administration of COVID-19 vaccine boosters the optimal approach?

Primary vs. secondary antibody deficiency: clinical features and infection outcomes of immunoglobulin replacement

Viral infection in primary antibody deficiency syndromes

The influence of time on the sensitivity of SARS-CoV-2 serological testing

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

Absence of Persistent Hepatitis E Virus Infection in Antibody-Deficient Patients Is Associated With Transfer of Antigen-Neutralizing Antibodies From Immunoglobulin Products

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

Low IgA and IgM Is Associated with a Higher Prevalence of Bronchiectasis in Primary Antibody Deficiency

Successful rapid push subcutaneous desensitization in a patient with delayed local hypersensitivity reactions to immunoglobulins

Dendritic cells as a tool to induce transplantation tolerance: obstacles and opportunities

Secondary antibody deficiency

A type III complement factor D deficiency: Structural insights for inhibition of the alternative pathway

Chronic Granulomatous Disorder–Associated Colitis Can Be Accurately Evaluated with MRI Scans and Fecal Calprotectin Level

Stability of gut microbiome after COVID-19 vaccination in healthy and immuno-compromised individuals

Preventing kidney transplant failure by screening for antibodies against human leucocyte antigens followed by optimised immunosuppression: OuTSMART RCT

Male X-chromosome mosaicism leading to carrier phenotype and inheritance of chronic granulomatous disease

Erratum to: Low IgA and IgM is Associated with a Higher Prevalence of Bronchiectasis in Primary Antibody Deficiency

Acquired C1 inhibitor deficiency: should we monitor for associated antibody deficiency?

Successful treatment of acute hepatitis C virus in HIV positive patients using the European AIDS Treatment Network guidelines for treatment duration

Real-world outcomes in hereditary angioedema: first experience from the Icatibant Outcome Survey in the United Kingdom

Use of recombinant C1 inhibitor in patients with resistant or frequent attacks of hereditary or acquired angioedema

Update to the study protocol, including statistical analysis plan, for the multicentre, randomised controlled OuTSMART trial: a combined screening/treatment programme to prevent premature failure of renal transplants due to chronic rejection in patients with HLA antibodies

An Artemis polymorphic variant reduces Artemis activity and confers cellular radiosensitivity

1385 Berotralstat prophylaxis for Hereditary Angioedema – an audit of use in a cohort of patients at a tertiary centre

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