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Publications

Defining B cell defects and correlation with complications in Common Variable Immune Deficiency patients.

Chapel H. and Patel S., (2019), J Allergy Clin Immunol

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

Schütz K. et al, (2019), J Clin Immunol

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), J Clin Immunol, 38

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

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, (2017), J Allergy Clin Immunol, 139, 1282 - 1292

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), Clin Exp Immunol, 184, 216 - 227

Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE.

Kienzler A-K. et al, (2016), Clin Immunol, 163, 17 - 21

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.

Anzilotti C. et al, (2015), J Allergy Clin Immunol, 136, 487 - 90.e2

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