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Publications

Defining B-cell defects and correlation with complications in patients with common variable immune deficiency.

Chapel H. and Patel S., (2019), The Journal of allergy and clinical immunology, 144, 654 - 655

Correction to: Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.

Schütz K. et al, (2019), Journal of clinical immunology, 39, 225 - 227

Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.

Schütz K. et al, (2019), J Clin Immunol, 39, 45 - 54

Correction to: Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials.

Ballow M. et al, (2018), Journal of clinical immunology, 38, 539 - 539

Ralph Josiah Patrick Wedgwood (1924-2017).

Ochs HD. et al, (2018), J Clin Immunol, 38, 153 - 154

Assessment of Local Adverse Reactions to Subcutaneous Immunoglobulin (SCIG) in Clinical Trials.

Ballow M. et al, (2017), J Clin Immunol, 37, 517 - 518

Clinical challenges in the management of patients with B cell immunodeficiencies.

Hodkinson JP. and Chapel H., (2017), Clin Exp Immunol, 188, 323 - 325

Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann–Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease

Schwerd T. et al, (2017), Gut, 66, 1060 - 1073

When to initiate immunoglobulin replacement therapy (IGRT) in antibody deficiency: a practical approach.

Jolles S. et al, (2017), Clin Exp Immunol, 188, 333 - 341

Common Variable Immunodeficiency Disorders (CVID) – diagnoses of exclusion, especially combined immune defects

Chapel H., (2016), JACI in Practice

Long term outcomes of 176 patients with X-linked hyper IgM syndrome treated with or without hematopoietic cell transplantation.

de la Morena MT. et al, (2016), J Allergy Clin Immunol

Secondary immunodeficiency in lymphoproliferative malignancies.

Friman V. et al, (2016), Hematol Oncol, 34, 121 - 132

Chronic mucocutaneous candidiasis: characterization of a family with STAT-1 gain-of-function and development of an ex-vivo assay for Th17 deficiency of diagnostic utility.

Dhalla F. et al, (2016), Clinical and experimental immunology, 184, 216 - 227

Challenges in the Role of Gammaglobulin Replacement Therapy and Vaccination Strategies for Hematological Malignancy.

Sánchez-Ramón S. et al, (2016), Front Immunol, 7

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders.

Bonilla FA. et al, (2016), J Allergy Clin Immunol Pract, 4, 38 - 59

Genetic sharing and heritability of paediatric age of onset autoimmune diseases

Li YR. et al, (2015), Nature Communications, 6

The ratio of mean daily IgG increment/mean daily dose in immunoglobulin replacement therapy in primary antibody deficiencies.

Lucas M. et al, (2015), J Allergy Clin Immunol Pract, 3, 998 - 1000.e2

Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders.

van Schouwenburg PA. et al, (2015), Clin Immunol, 160, 301 - 314

Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases

Li YR. et al, (2015), Nature Medicine, 21, 1018 - 1027

Key stages of bone marrow B-cell maturation are defective in patients with common variable immunodeficiency disorders

(2015), Journal of Allergy and Clinical Immunology, 136, 487 - 490.e2

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