Lista de obras - Matthew S Buckland - Dominio Público Uruguay

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

artículo científico publicado en 2018

Absence of persistent Hepatitis E virus infection in antibody-deficient patients is associated with the transfer of antigen neutralising antibodies from immunoglobulin products

artículo científico publicado en 2019

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

scientific article published on 01 March 2014

Aspirin and the induction of tolerance by dendritic cells.

artículo científico publicado en 2009

Aspirin modified dendritic cells are potent inducers of allo-specific regulatory T-cells

artículo científico publicado en 2006

Aspirin-treated human DCs up-regulate ILT-3 and induce hyporesponsiveness and regulatory activity in responder T cells

artículo científico publicado en 2006

British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders. ⬇️

artículo científico publicado en 2017

Bronchiectasis and deteriorating lung function in agammaglobulinaemia despite immunoglobulin replacement therapy

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

scientific article published on 06 June 2019

Chronic fatigue syndrome and circulating cytokines: A systematic review

artículo científico

Clinical and laboratory features of seventy-eight UK patients with Good’s syndrome (thymoma and hypogammaglobulinaemia)

artículo científico publicado en 2018

Current clinical practice and challenges in the management of secondary immunodeficiency in hematological malignancies

artículo científico publicado en 2019

Cytokine responses to exercise and activity in patients with chronic fatigue syndrome: case-control study.

artículo científico publicado en 2017

Cytokine signature in chronic fatigue syndrome.

artículo científico publicado en 2017

Dark immunofluorescence: correlation with serum immunoglobulin abnormalities

artículo científico publicado en 2006

Differential role of naïve and memory CD4 T-cell subsets in primary alloresponses.

artículo científico publicado en 2010

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

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

artículo científico publicado en 2017

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

scientific article published on 20 December 2019

Fine matrix mapping of the macular region in normal subjects.

artículo científico publicado en 1995

Hereditary angioedema: an unusual cause of genital swelling presenting to a genitourinary medicine clinic.

artículo científico publicado en 2011

Hypogammaglobulinaemia after rituximab treatment-incidence and outcomes.

artículo científico publicado en 2014

Immune deficiency: changing spectrum of pathogens

artículo científico publicado en 2015

Immunodeficiency: updating the personalized medicine approach to diagnostics and therapeutics.

artículo científico publicado en 2012

Immunoglobulin use in immune deficiency in the UK: a report of the UKPID and National Immunoglobulin Databases

artículo científico publicado en 2018

In pursuit of excellence: an integrated care pathway for C1 inhibitor deficiency.

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Male X-chromosome Mosaicism leading to Carrier Phenotype and inheritance of Chronic Granulomatous Disease.

artículo científico publicado en 2018

Monogenic mimics of Behçet's disease in the young

artículo científico publicado en 2019

Non-histaminergic angioedema: focus on bradykinin-mediated angioedema.

artículo científico

Osteomyelitis complicating pyomyositis in HIV disease.

artículo científico publicado en 2004

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

artículo científico publicado en 2014

Pseudomonas infection in antibody deficient patients

artículo científico publicado en 2014

Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort

scientific article published on 17 July 2020

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

scholarly article by Hilary J Longhurst published in January 2018

Secondary antibody deficiency

scientific article published on 31 March 2014

Serological markers (anti-Saccharomyces cerevisiae mannan antibodies and antineutrophil cytoplasmic antibodies) in inflammatory bowel disease: diagnostic utility and phenotypic correlation.

artículo científico publicado en 2005

Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency.

artículo científico publicado en 2017

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

artículo científico publicado en 2019

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

artículo científico publicado en 2011

Syphilis masquerading as focal segmental glomerulosclerosis.

artículo científico publicado en 2014

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

artículo científico publicado en 2019

The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008-2012.

artículo científico publicado en 2014

The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017

artículo científico publicado en 2018

Therapeutic strategies in common variable immunodeficiency.

artículo científico publicado en 2003

Tolerogenic Donor-Derived Dendritic Cells Risk Sensitization In Vivo owing to Processing and Presentation by Recipient APCs.

artículo científico publicado en 2013

Treatment of COVID-19 with remdesivir in the absence of humoral immunity: a case report

artículo científico publicado en 2020

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 pati

scientific article published on 05 August 2019

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

scientific article published on 01 January 2014

Viral infection in primary antibody deficiency syndromes

artículo científico publicado en 2019

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

artículo científico publicado en 2020

Lista de obras de Matthew S Buckland

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

Absence of persistent Hepatitis E virus infection in antibody-deficient patients is associated with the transfer of antigen neutralising antibodies from immunoglobulin products

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

Aspirin and the induction of tolerance by dendritic cells.

Aspirin modified dendritic cells are potent inducers of allo-specific regulatory T-cells

Aspirin-treated human DCs up-regulate ILT-3 and induce hyporesponsiveness and regulatory activity in responder T cells

British Lung Foundation/United Kingdom Primary Immunodeficiency Network Consensus Statement on the Definition, Diagnosis, and Management of Granulomatous-Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency Disorders. ⬇️

Bronchiectasis and deteriorating lung function in agammaglobulinaemia despite immunoglobulin replacement therapy

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

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

Chronic fatigue syndrome and circulating cytokines: A systematic review

Clinical and laboratory features of seventy-eight UK patients with Good’s syndrome (thymoma and hypogammaglobulinaemia)

Current clinical practice and challenges in the management of secondary immunodeficiency in hematological malignancies

Cytokine responses to exercise and activity in patients with chronic fatigue syndrome: case-control study.

Cytokine signature in chronic fatigue syndrome.

Dark immunofluorescence: correlation with serum immunoglobulin abnormalities

Differential role of naïve and memory CD4 T-cell subsets in primary alloresponses.

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

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

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

Fine matrix mapping of the macular region in normal subjects.

Hereditary angioedema: an unusual cause of genital swelling presenting to a genitourinary medicine clinic.

Hypogammaglobulinaemia after rituximab treatment-incidence and outcomes.

Immune deficiency: changing spectrum of pathogens

Immunodeficiency: updating the personalized medicine approach to diagnostics and therapeutics.

Immunoglobulin use in immune deficiency in the UK: a report of the UKPID and National Immunoglobulin Databases

In pursuit of excellence: an integrated care pathway for C1 inhibitor deficiency.

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

Male X-chromosome Mosaicism leading to Carrier Phenotype and inheritance of Chronic Granulomatous Disease.

Monogenic mimics of Behçet's disease in the young

Non-histaminergic angioedema: focus on bradykinin-mediated angioedema.

Osteomyelitis complicating pyomyositis in HIV disease.

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

Pseudomonas infection in antibody deficient patients

Publisher Correction: Whole-genome sequencing of a sporadic primary immunodeficiency cohort

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

Secondary antibody deficiency

Serological markers (anti-Saccharomyces cerevisiae mannan antibodies and antineutrophil cytoplasmic antibodies) in inflammatory bowel disease: diagnostic utility and phenotypic correlation.

Successful outcome following allogeneic hematopoietic stem cell transplantation in adults with primary immunodeficiency.

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

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

Syphilis masquerading as focal segmental glomerulosclerosis.

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008-2012.

The United Kingdom Primary Immune Deficiency (UKPID) registry 2012 to 2017

Therapeutic strategies in common variable immunodeficiency.

Tolerogenic Donor-Derived Dendritic Cells Risk Sensitization In Vivo owing to Processing and Presentation by Recipient APCs.

Treatment of COVID-19 with remdesivir in the absence of humoral immunity: a case report

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 pati

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

Viral infection in primary antibody deficiency syndromes

Whole-genome sequencing of a sporadic primary immunodeficiency cohort