Lista de obras - Sinisa Savic - Dominio Público Uruguay

'Warning: allergic to penicillin': association between penicillin allergy status in 2.3 million NHS general practice electronic health records, antibiotic prescribing and health outcomes

scientific article published on 01 July 2019

A Case of Adult-Onset Still’s Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab. ⬇️

artículo científico publicado en 2018

A Case of SLC29A3 Spectrum Disorder-Unresponsive to Multiple Immunomodulatory Therapies ⬇️

artículo científico publicado en 2016

A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype

scientific article published on 04 April 2019

A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency ⬇️

artículo científico publicado en 2015

A new case of Fas-associated death domain protein deficiency and update on treatment outcomes ⬇️

artículo científico publicado en 2015

A novel RAG1 mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination ⬇️

artículo científico publicado en 2018

A novel RELA truncating mutation in familial Behçet's Disease-like mucocutaneous ulcerative condition

scientific article published on 23 September 2020

A novel TNFRSF1A splice mutation associated with increased nuclear factor kappaB (NF-kappaB) transcription factor activation in patients with tumour necrosis factor receptor associated periodic syndrome (TRAPS).

artículo científico publicado en 2007

A report of novel STIM1 deficiency and 6 year follow up of two previous cases associated with mild immunological phenotype

scholarly article published 18 October 2018

A role for human leucocyte antigens in the susceptibility to SARS-Cov-2 infection observed in transplant patients

artículo científico publicado en 2020

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7

artículo científico publicado en 2021

Anakinra as a diagnostic challenge and treatment option for systemic autoinflammatory disorders of undefined etiology

artículo científico publicado en 2016

Anakinra as a diagnostic challenge and treatment option for systemic autoinflammatory disorders of undefined genetic cause

artículo científico publicado en 2015

Anaphylaxis associated with general anaesthesia: Challenges and recent advances

Anaphylaxis to sugammadex

artículo científico publicado en 2014

Antihistamine-resistant chronic spontaneous urticaria remains undertreated: 2-year data from the AWARE study

artículo científico publicado en 2020

Arthritis in Two Patients With Partial Recombination Activating Gene Deficiency

artículo científico publicado en 2019

Autoimmune-autoinflammatory rheumatoid arthritis overlaps: a rare but potentially important subgroup of diseases ⬇️

artículo científico publicado en 2017

Autoinflammatory Disease in the Lung ⬇️

artículo científico publicado en 2018

Autoinflammatory diseases: update on classification diagnosis and management ⬇️

artículo científico publicado en 2016

Autoinflammatory syndromes and cellular responses to stress: pathophysiology, diagnosis and new treatment perspectives

artículo científico publicado en 2012

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

artículo científico publicado en 2017

Biallelic interferon regulatory factor 8 mutation: A complex immunodeficiency syndrome with dendritic cell deficiency, monocytopenia, and immune dysregulation ⬇️

artículo científico publicado en 2017

Biallelic mutations in IRF8 impair human NK cell maturation and function ⬇️

artículo científico publicado en 2016

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

British Society for Immunology/United Kingdom Primary Immunodeficiency Network consensus statement on managing non‐infectious complications of Common Variable Immunodeficiency Disorders

artículo científico publicado en 2019

COVID-19 meets Cystic Fibrosis: for better or worse?

artículo científico publicado en 2020

CVID patients with autoimmunity have elevated T cell expression of granzyme B and HLA-DR and reduced levels of Treg cells

artículo científico publicado en 2012

Canakinumab for the cryopyrin-associated periodic syndromes

artículo científico publicado en 2009

Characterising RAG1 and RAG2 with predictive genomics

Chlorhexidine allergy in the perioperative setting: a narrative review

artículo científico publicado en 2019

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study ⬇️

artículo científico publicado en 2016

Clinical genetics in 2014: New monogenic diseases span the immunological disease continuum

artículo científico publicado en 2014

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study ⬇️

artículo científico publicado en 2016

Combined Immunodeficiency With Late-Onset Progressive Hypogammaglobulinemia and Normal B Cell Count in a Patient With RAG2 Deficiency

scientific article published on 16 April 2019

Developing a behavioural intervention package to identify and amend incorrect penicillin allergy records in UK general practice and subsequently change antibiotic use

artículo científico publicado en 2020

Different CFTR modulator combinations downregulate inflammation differently in cystic fibrosis

artículo científico publicado en 2020

Differential effects of infliximab on absolute circulating blood leucocyte counts of innate immune cells in early and late rheumatoid arthritis patients

artículo científico publicado en 2012

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

Do defective B cells contribute to reduced Treg cells and autoimmunity in patients with Common Variable Immunodeficiency?

artículo científico publicado en 2012

Does this patient have periodic fever syndrome?

artículo científico

ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis

artículo científico publicado en 2019

Evidence of B Cell Clonality and Investigation Into Properties of the IgM in Patients With Schnitzler Syndrome

artículo científico publicado en 2020

Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment

artículo científico publicado en 2013

Excessive ENaC-mediated sodium influx drives NLRP3 inflammasome-dependent autoinflammation in Cystic Fibrosis

scholarly article published 31 October 2018

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

scientific article published on 20 December 2019

Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome

scientific article published on 14 October 2019

FRI0334 Safety of rituximab for remission maintenance in relapsing anca–associated vasculitis: repeat cycles on clinical relapse are associated with low rates of hypogammaglobulinaemia

Familial Mediterranean fever and related periodic fever syndromes/autoinflammatory diseases

artículo científico publicado en 2012

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. ⬇️

artículo científico publicado en 2016

Feasibility of abbreviated penicillin de-labelling in the elective surgical patients: the PADLES study – an early report

Fifth International Congress on Familial Mediterranean Fever and Systemic Autoinflammatory Diseases

artículo científico publicado en 2008

GRID - Genomics of Rare Immune Disorders: a highly sensitive and specific diagnostic gene panel for patients with primary immunodeficiencies

article

Germline TET2 Loss-Of-Function Causes Childhood Immunodeficiency And Lymphoma

artículo científico publicado en 2020

Glucose-6-Phosphatase Catalytic Subunit 3 (G6PC3) Deficiency Associated With Autoinflammatory Complications. ⬇️

artículo científico publicado en 2017

Hereditary systemic autoinflammatory diseases and Schnitzler's syndrome

artículo científico publicado en 2019

Histone deacetylases are dysregulated in rheumatoid arthritis and a novel histone deacetylase 3-selective inhibitor reduces interleukin-6 production by peripheral blood mononuclear cells from rheumatoid arthritis patients

artículo científico publicado en 2012

Home self-administration of omalizumab for chronic spontaneous urticaria ⬇️

artículo científico publicado en 2016

Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease

artículo científico publicado en 2018

Identification of Critical Transcriptomic Signaling Pathways in Patients with H Syndrome and Rosai-Dorfman Disease

artículo científico publicado en 2020

Incidence of suspected perioperative anaphylaxis: A multicenter snapshot study

artículo científico publicado en 2015

Inositol-Requiring Enzyme 1-Mediated Downregulation of MicroRNA (miR)-146a and miR-155 in Primary Dermal Fibroblasts across Three TNFRSF1A Mutations Results in Hyperresponsiveness to Lipopolysaccharide ⬇️

artículo científico publicado en 2018

Interleukin-1 Blockade: An Update on Emerging Indications

artículo científico publicado en 2017

International Retrospective Chart Review of Treatment Patterns in Severe Familial Mediterranean Fever, Tumor Necrosis Factor Receptor-Associated Periodic Syndrome, and Mevalonate Kinase Deficiency/Hyperimmunoglobulinemia D Syndrome ⬇️

artículo científico publicado en 2016

Involvement of X-box binding protein 1 and reactive oxygen species pathways in the pathogenesis of tumour necrosis factor receptor-associated periodic syndrome

artículo científico publicado en 2012

Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism-UK Single Center Experience ⬇️

artículo científico publicado en 2017

Ligelizumab for Chronic Spontaneous Urticaria

scientific article published on 01 October 2019

Long term management of patients with cryopyrin-associated periodic syndromes (CAPS): focus on rilonacept (IL-1 Trap).

artículo científico publicado en 2008

Mechanistic immunological based classification of rheumatoid arthritis

artículo científico publicado en 2018

Metabolic Reprograming of Cystic Fibrosis Macrophages via the IRE1α Arm of the Unfolded Protein Response Results in Exacerbated Inflammation

artículo científico publicado en 2019

Mixed results with baricitinib in biological-resistant adult-onset Still's disease and undifferentiated systemic autoinflammatory disease

artículo científico publicado en 2020

Mixed-methods evaluation of a behavioural intervention package to identify and amend incorrect penicillin allergy records in UK general practice

artículo científico publicado en 2022

Molecular genetic investigation, clinical features and response to treatment in 21 patients with Schnitzler's syndrome ⬇️

artículo científico publicado en 2017

Moving towards a systems-based classification of innate immune-mediated diseases

scientific article published on 27 February 2020

Multicentre experience of home omalizumab treatment for chronic spontaneous urticaria

artículo científico publicado en 2019

Natural killer cell receptor expression in patients with severe and recurrent Herpes simplex virus-1 (HSV-1) infections

artículo científico publicado en 2007

P01-026 – A case of FMF and hereditary coproporphyria

artículo científico publicado en 2013

PW02-013 - The role of IL6 and LPS in pathogenesis of TRAPS.

artículo científico publicado en 2013

PW02-031 - Genetic and clinical manifestations of CAPS.

artículo científico publicado en 2013

Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency

artículo científico publicado en 2019

Patient and Primary Care Physician Perceptions of Penicillin Allergy Testing and Subsequent Use of Penicillin-Containing Antibiotics: A Qualitative Study

scientific article published on 12 March 2019

Periodic fever syndrome and autoinflammatory diseases

artículo científico publicado en 2010

Potential Immune Biomarkers in Diagnosis and Clinical Management for Systemic Lupus Erythematosus ⬇️

artículo científico publicado en 2018

Predicting Severe Infection and Effects of Hypogammaglobulinemia During Therapy With Rituximab in Rheumatic and Musculoskeletal Diseases

artículo científico publicado en 2019

Predicting the Occurrence of Variants in RAG1 and RAG2

scientific article published on 06 August 2019

Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. ⬇️

artículo científico publicado en 2018

Proceedings of the 23rd Paediatric Rheumatology European Society Congress: part three: Genoa, Italy. 28 September – 01 October 2016.

artículo científico publicado en 2017

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

scientific article published on 17 July 2020

RNAseq Supports the Molecular Genetic Diagnosis of Late-Onset ADA Deficiency

scientific article published on 16 April 2019

Rationale for Evaluating PDE4 Inhibition for Mitigating against Severe Inflammation in COVID-19 Pneumonia and Beyond

scientific article published on 01 June 2020

Repeat cycles of rituximab on clinical relapse in ANCA-associated vasculitis: identifying B cell biomarkers for relapse to guide retreatment decisions ⬇️

artículo científico publicado en 2015

Resistant type II cryoglobulinaemic vasculitis successfully treated with bortezomib in a patient with SLE

Response to "Increased awareness of hypogammaglobulinemia after B-cell targeting therapies" by Karim MY

scientific article published on 05 March 2020

Retrospective case note review of chronic spontaneous urticaria outcomes and adverse effects in patients treated with omalizumab or ciclosporin in UK secondary care ⬇️

artículo científico publicado en 2015

SAT0482 Risk Factors for Severe Infection and Outcome of Secondary Hypogammaglobulinaemia in Patients with Autoimmune Rheumatic Diseases Treated with Rituximab: Preliminary Results from 400 Patients at A Single Centre: Table 1

article by M.Y. Md Yusof et al published June 2016 in Annals of the Rheumatic Diseases

Selective Response to Omalizumab in a Patient With Concomitant ncMCAS and POTS: What Does it Teach us About the Underlying Disease?

scholarly article by M Kacar et al published 1 August 2018 in Journal of Investigational Allergology and Clinical Immunology

Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease

artículo científico publicado en 2020

Sugammadex: the sting in the tail? ⬇️

scientific article published on 14 August 2018

TLR dependent XBP-1 activation induces an autocrine loop in rheumatoid arthritis synoviocytes ⬇️

artículo científico publicado en 2013

Teicoplanin allergy - an emerging problem in the anaesthetic allergy clinic ⬇️

artículo científico publicado en 2015

The Ca sensor STIM1 regulates the type I interferon response by retaining the signaling adaptor STING at the endoplasmic reticulum ⬇️

artículo científico publicado en 2019

The Efficacy, Safety and Tolerability of Canakinumab in the Treatment of Familial Mediterranean Fever: A Systematic Review of the Literature

scientific article published on 09 March 2020

The NLR network and the immunological disease continuum of adaptive and innate immune-mediated inflammation against self

artículo científico publicado en 2007

The NLRP3 inflammasome, a target for therapy in diverse disease states

artículo científico publicado en 2010

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

artículo científico publicado en 2018

The burgeoning field of innate immune-mediated disease and autoinflammation ⬇️

artículo científico publicado en 2016

Tocilizumab in Hospitalized Patients with Severe Covid-19 Pneumonia

artículo científico publicado en 2021

What is the utility of routine ANA testing in predicting development of biological DMARD-induced lupus and vasculitis in patients with rheumatoid arthritis? Data from a single-centre cohort

artículo científico publicado en 2014

Whole Genome Sequencing of Primary Immunodeficiency reveals a role for common and rare variants in coding and non-coding sequences

Whole-genome sequencing of a sporadic primary immunodeficiency cohort

artículo científico publicado en 2020

The role of dysregulated unfolded protein response and resistance to apoptosis in the pathogenesis of rheumatoid arthritis and non- response to anti-TNF therapies

tesis doctoral

Lista de obras de Sinisa Savic

'Warning: allergic to penicillin': association between penicillin allergy status in 2.3 million NHS general practice electronic health records, antibiotic prescribing and health outcomes

A Case of Adult-Onset Still’s Disease Caused by a Novel Splicing Mutation in TNFAIP3 Successfully Treated With Tocilizumab. ⬇️

A Case of SLC29A3 Spectrum Disorder-Unresponsive to Multiple Immunomodulatory Therapies ⬇️

A Report of Novel STIM1 Deficiency and 6-Year Follow-Up of Two Previous Cases Associated with Mild Immunological Phenotype

A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency ⬇️

A new case of Fas-associated death domain protein deficiency and update on treatment outcomes ⬇️

A novel RAG1 mutation reveals a critical in vivo role for HMGB1/2 during V(D)J recombination ⬇️

A novel RELA truncating mutation in familial Behçet's Disease-like mucocutaneous ulcerative condition

A novel TNFRSF1A splice mutation associated with increased nuclear factor kappaB (NF-kappaB) transcription factor activation in patients with tumour necrosis factor receptor associated periodic syndrome (TRAPS).

A report of novel STIM1 deficiency and 6 year follow up of two previous cases associated with mild immunological phenotype

A role for human leucocyte antigens in the susceptibility to SARS-Cov-2 infection observed in transplant patients

An Atypical Autoinflammatory Disease Due to an LRR Domain NLRP3 Mutation Enhancing Binding to NEK7

Anakinra as a diagnostic challenge and treatment option for systemic autoinflammatory disorders of undefined etiology

Anakinra as a diagnostic challenge and treatment option for systemic autoinflammatory disorders of undefined genetic cause

Anaphylaxis associated with general anaesthesia: Challenges and recent advances

Anaphylaxis to sugammadex

Antihistamine-resistant chronic spontaneous urticaria remains undertreated: 2-year data from the AWARE study

Arthritis in Two Patients With Partial Recombination Activating Gene Deficiency

Autoimmune-autoinflammatory rheumatoid arthritis overlaps: a rare but potentially important subgroup of diseases ⬇️

Autoinflammatory Disease in the Lung ⬇️

Autoinflammatory diseases: update on classification diagnosis and management ⬇️

Autoinflammatory syndromes and cellular responses to stress: pathophysiology, diagnosis and new treatment perspectives

Bialellic Mutations in Tetratricopeptide Repeat Domain 7A (TTC7A) Cause Common Variable Immunodeficiency-Like Phenotype with Enteropathy

Biallelic interferon regulatory factor 8 mutation: A complex immunodeficiency syndrome with dendritic cell deficiency, monocytopenia, and immune dysregulation ⬇️

Biallelic mutations in IRF8 impair human NK cell maturation and function ⬇️

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. ⬇️

British Society for Immunology/United Kingdom Primary Immunodeficiency Network consensus statement on managing non‐infectious complications of Common Variable Immunodeficiency Disorders

COVID-19 meets Cystic Fibrosis: for better or worse?

CVID patients with autoimmunity have elevated T cell expression of granzyme B and HLA-DR and reduced levels of Treg cells

Canakinumab for the cryopyrin-associated periodic syndromes

Characterising RAG1 and RAG2 with predictive genomics

Chlorhexidine allergy in the perioperative setting: a narrative review

Clinical and immunologic phenotype associated with activated phosphoinositide 3-kinase δ syndrome 2: A cohort study ⬇️

Clinical genetics in 2014: New monogenic diseases span the immunological disease continuum

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study ⬇️

Combined Immunodeficiency With Late-Onset Progressive Hypogammaglobulinemia and Normal B Cell Count in a Patient With RAG2 Deficiency

Developing a behavioural intervention package to identify and amend incorrect penicillin allergy records in UK general practice and subsequently change antibiotic use

Different CFTR modulator combinations downregulate inflammation differently in cystic fibrosis

Differential effects of infliximab on absolute circulating blood leucocyte counts of innate immune cells in early and late rheumatoid arthritis patients

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. ⬇️

Do defective B cells contribute to reduced Treg cells and autoimmunity in patients with Common Variable Immunodeficiency?

Does this patient have periodic fever syndrome?

ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis

Evidence of B Cell Clonality and Investigation Into Properties of the IgM in Patients With Schnitzler Syndrome

Evidence of NLRP3-inflammasome activation in rheumatoid arthritis (RA); genetic variants within the NLRP3-inflammasome complex in relation to susceptibility to RA and response to anti-TNF treatment

Excessive ENaC-mediated sodium influx drives NLRP3 inflammasome-dependent autoinflammation in Cystic Fibrosis

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

Exploratory Study of MYD88 L265P, Rare NLRP3 Variants, and Clonal Hematopoiesis Prevalence in Patients With Schnitzler Syndrome

FRI0334 Safety of rituximab for remission maintenance in relapsing anca–associated vasculitis: repeat cycles on clinical relapse are associated with low rates of hypogammaglobulinaemia

Familial Mediterranean fever and related periodic fever syndromes/autoinflammatory diseases

Familial autoinflammation with neutrophilic dermatosis reveals a regulatory mechanism of pyrin activation. ⬇️

Feasibility of abbreviated penicillin de-labelling in the elective surgical patients: the PADLES study – an early report

Fifth International Congress on Familial Mediterranean Fever and Systemic Autoinflammatory Diseases

GRID - Genomics of Rare Immune Disorders: a highly sensitive and specific diagnostic gene panel for patients with primary immunodeficiencies

Germline TET2 Loss-Of-Function Causes Childhood Immunodeficiency And Lymphoma

Glucose-6-Phosphatase Catalytic Subunit 3 (G6PC3) Deficiency Associated With Autoinflammatory Complications. ⬇️

Hereditary systemic autoinflammatory diseases and Schnitzler's syndrome

Histone deacetylases are dysregulated in rheumatoid arthritis and a novel histone deacetylase 3-selective inhibitor reduces interleukin-6 production by peripheral blood mononuclear cells from rheumatoid arthritis patients

Home self-administration of omalizumab for chronic spontaneous urticaria ⬇️

Hypomorphic caspase activation and recruitment domain 11 (CARD11) mutations associated with diverse immunologic phenotypes with or without atopic disease

Identification of Critical Transcriptomic Signaling Pathways in Patients with H Syndrome and Rosai-Dorfman Disease

Incidence of suspected perioperative anaphylaxis: A multicenter snapshot study

Inositol-Requiring Enzyme 1-Mediated Downregulation of MicroRNA (miR)-146a and miR-155 in Primary Dermal Fibroblasts across Three TNFRSF1A Mutations Results in Hyperresponsiveness to Lipopolysaccharide ⬇️

Interleukin-1 Blockade: An Update on Emerging Indications

International Retrospective Chart Review of Treatment Patterns in Severe Familial Mediterranean Fever, Tumor Necrosis Factor Receptor-Associated Periodic Syndrome, and Mevalonate Kinase Deficiency/Hyperimmunoglobulinemia D Syndrome ⬇️

Involvement of X-box binding protein 1 and reactive oxygen species pathways in the pathogenesis of tumour necrosis factor receptor-associated periodic syndrome

Late-Onset Cryopyrin-Associated Periodic Syndromes Caused by Somatic NLRP3 Mosaicism-UK Single Center Experience ⬇️

Ligelizumab for Chronic Spontaneous Urticaria

Long term management of patients with cryopyrin-associated periodic syndromes (CAPS): focus on rilonacept (IL-1 Trap).

Mechanistic immunological based classification of rheumatoid arthritis

Metabolic Reprograming of Cystic Fibrosis Macrophages via the IRE1α Arm of the Unfolded Protein Response Results in Exacerbated Inflammation

Mixed results with baricitinib in biological-resistant adult-onset Still's disease and undifferentiated systemic autoinflammatory disease

Mixed-methods evaluation of a behavioural intervention package to identify and amend incorrect penicillin allergy records in UK general practice

Molecular genetic investigation, clinical features and response to treatment in 21 patients with Schnitzler's syndrome ⬇️

Moving towards a systems-based classification of innate immune-mediated diseases

Multicentre experience of home omalizumab treatment for chronic spontaneous urticaria

Natural killer cell receptor expression in patients with severe and recurrent Herpes simplex virus-1 (HSV-1) infections

P01-026 – A case of FMF and hereditary coproporphyria

PW02-013 - The role of IL6 and LPS in pathogenesis of TRAPS.