C. Slade

发表

Deficiency in complement factor B.

I. Winship, K. Bleasel, M. Nagel, 2013, The New England journal of medicine.

Comparison of Diagnostic Criteria for Common Variable Immunodeficiency Disorder

D. Gillis, R. Steele, R. Ameratunga, 2014, Front. Immunol..

Loss-of-Function in SMAD4 Might Not Be Critical for Human Natural Killer Cell Responsiveness to TGF-β

F. Souza-Fonseca-Guimaraes, N. Huntington, I. Winship, 2019, Front. Immunol..

Clinical Implications of Digenic Inheritance and Epistasis in Primary Immunodeficiency Disorders

E. Leung, K. Lehnert, V. Bryant, 2018, Front. Immunol..

A common human MLKL polymorphism confers resistance to negative regulation by phosphorylation

M. Kauppi, C. Vinuesa, J. Pearson, 2022, bioRxiv.

Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing

D. Gillis, K. Lehnert, Vanessa L. Bryant, 2018, Clinical Reviews in Allergy & Immunology.

Characterization of the clinical and immunological phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations.

William J. Astle, Sri V. V. Deevi, Kenneth G. C. Smith, 2020, The Journal of allergy and clinical immunology.

Biotinylation of ANCA target antigen improves assay performance for PR3-ELISA but not MPO-ELISA.

M. Hayman, M. Spellerberg, C. Slade, 2013, Pathology.

Case Report: Cytomegalovirus Disease Is an Under-Recognized Contributor to Morbidity and Mortality in Common Variable Immunodeficiency

J. Sasadeusz, J. Douglass, Lauren J. Howson, 2022, Frontiers in Immunology.

Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.

A. Schäffer, H. Cao, P. Browett, 2015, American journal of human genetics.

Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

P. Nilsson, J. Schwenk, Y. Mizuno, 2020, Frontiers in Immunology.

Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2

M. Bahlo, P. Hodgkin, T. Scerri, 2019, Journal of Clinical Immunology.

Cytomegalovirus in primary immunodeficiency

J. Sasadeusz, J. Douglass, Vanessa L. Bryant, 2021, Current opinion in infectious diseases.

The Rare Anaphylaxis-Associated FcγRIIa3 Exhibits Distinct Characteristics From the Canonical FcγRIIa1

Peter J. Hogarth, M. V. van Zelm, S. Kent, 2018, Front. Immunol..

Chemokines, their receptors and human disease: the good, the bad and the itchy

Vanessa L. Bryant, V. Bryant, C. Slade, 2015, Immunology and cell biology.

Pitfalls of immunotherapy: lessons from a patient with CTLA-4 haploinsufficiency

Z. Stark, S. Lunke, S. Ojaimi, 2018, Allergy, Asthma & Clinical Immunology.

Delayed Diagnosis and Complications of Predominantly Antibody Deficiencies in a Cohort of Australian Adults

M. V. van Zelm, P. Hodgkin, S. Holdsworth, 2018, Front. Immunol..

Epistatic interactions between mutations of TACI (TNFRSF13B) and TCF3 result in a severe primary immunodeficiency disorder and systemic lupus erythematosus

P. Hodgkin, A. Enders, P. Browett, 2017, Clinical & translational immunology.

Changing practice: no need to stop ACE inhibition for venom immunotherapy

C. Slade, J. Douglass, 2014, Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology.

Victorian Specialist Immunisation Services (VicSIS) – bolstering adult clinics for COVID-19 vaccines

E. Duckworth, H. Clothier, N. Crawford, 2022, Human vaccines & immunotherapeutics.

A common human MLKL polymorphism confers resistance to negative regulation by phosphorylation

Ashley P Ng, M. Kauppi, I. Wicks, 2023, bioRxiv.

A multicenter chart review of patient characteristics, treatment, and outcomes in hereditary angioedema: unmet need for more effective long-term prophylaxis

P. Keith, P. Busse, L. Diwakar, 2023, Allergy, Asthma & Clinical Immunology.

Proceed with Caution: STAT1 GOF Diagnosis Missed Due to Intronic SNP

S. Choo, S. Richards, A. Ferrante, 2020, Journal of Clinical Immunology.

Bronchiectasis is associated with delayed diagnosis and adverse outcomes in the New Zealand Common Variable Immunodeficiency Disorders cohort study

S. Ameratunga, A. Cavadino, B. McGettigan, 2021, Clinical and experimental immunology.

Fatal Enteroviral Encephalitis in a Patient with Common Variable Immunodeficiency Harbouring a Novel Mutation in NFKB2

M. Bahlo, P. Hodgkin, T. Scerri, 2019, Journal of Clinical Immunology.

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

J. Derisi, F. Rieux-Laucat, J. Fellay, 2023, Nature.