Chest Complications in Patients with Primary Antibody Deficiency Syndromes (PADS)

[1]  H. Chapel,et al.  Interstitial lung disease in patients with common variable immunodeficiency disorders: several different pathologies? , 2019, Clinical and experimental immunology.

[2]  K. Hiroshima,et al.  Intravenous Immunoglobulin Monotherapy for Granulomatous Lymphocytic Interstitial Lung Disease in Common Variable Immunodeficiency , 2017, Internal medicine.

[3]  M. Putti,et al.  Efficacy of mycophenolate on lung disease and autoimmunity in children with immunodeficiency , 2017, Pediatric pulmonology.

[4]  Smita Y. Patel,et al.  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. , 2017, The journal of allergy and clinical immunology. In practice.

[5]  C. Zuiani,et al.  Humoral primary immunodeficiency diseases: clinical overview and chest high-resolution computed tomography (HRCT) features in the adult population. , 2017, Clinical radiology.

[6]  A. Gamian,et al.  A case report of lymphoid intestitial pneumonia in common variable immunodeficiency , 2017, Medicine.

[7]  T. Harville Can we effectively use radiographic imaging and clinical parameters for making an earlier diagnosis of granulomatous interstitial lung disease in patients with common variable immunodeficiency? , 2017, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[8]  V. Iyer,et al.  Predictors of granulomatous lymphocytic interstitial lung disease in common variable immunodeficiency. , 2017, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

[9]  V. Rodriguez,et al.  O014 Splenomegaly and IgA deficiency predicts granulomatous lymphocytic interstitial lung disease (GLILD) in common variable immunodeficiency (CVID) , 2016 .

[10]  M. Beasley,et al.  Lung Disease in Primary Antibody Deficiencies. , 2016, The journal of allergy and clinical immunology. In practice.

[11]  Jonathan H. Chung,et al.  Clinical Predictors of a Diagnosis of Common Variable Immunodeficiency-related Granulomatous-Lymphocytic Interstitial Lung Disease. , 2016, Annals of the American Thoracic Society.

[12]  A. Nicholson,et al.  Rare idiopathic interstitial pneumonias: LIP and PPFE and rare histologic patterns of interstitial pneumonias: AFOP and BPIP , 2016, Respirology.

[13]  Smita Y. Patel,et al.  Hypomorphic function and somatic reversion of DOCK8 cause combined immunodeficiency without hyper-IgE , 2016, Clinical immunology.

[14]  A. Mackinnon,et al.  Granulomatous and lymphocytic interstitial lung disease: a spectrum of pulmonary histopathologic lesions in common variable immunodeficiency--histologic and immunohistochemical analyses of 16 cases. , 2015, Human pathology.

[15]  G. Shi,et al.  Clinical characteristics of patients with chronic obstructive pulmonary disease with comorbid bronchiectasis: a systemic review and meta-analysis , 2015, International journal of chronic obstructive pulmonary disease.

[16]  C. Catalano,et al.  Lung Magnetic Resonance Imaging with Diffusion Weighted Imaging Provides Regional Structural as well as Functional Information Without Radiation Exposure in Primary Antibody Deficiencies , 2015, Journal of Clinical Immunology.

[17]  F. Bonilla,et al.  Primary Immune Deficiencies – Principles of Care , 2014, Front. Immunol..

[18]  P. Klenerman,et al.  A mutation in X‐linked inhibitor of apoptosis (G466X) leads to memory inflation of Epstein–Barr virus‐specific T cells , 2014, Clinical and experimental immunology.

[19]  I. Quinti,et al.  Adequate Patient’s Outcome Achieved with Short Immunoglobulin Replacement Intervals in Severe Antibody Deficiencies , 2014, Journal of Clinical Immunology.

[20]  C. Cunningham-Rundles,et al.  Tertiary lymphoid neogenesis is a component of pulmonary lymphoid hyperplasia in patients with common variable immunodeficiency. , 2014, The Journal of allergy and clinical immunology.

[21]  S. Holland,et al.  B-cell activating factor (BAFF) is elevated in chronic granulomatous disease. , 2013, Clinical immunology.

[22]  Smita Y. Patel,et al.  Confirmation and improvement of criteria for clinical phenotyping in common variable immunodeficiency disorders in replicate cohorts. , 2012, The Journal of allergy and clinical immunology.

[23]  J. Orange,et al.  Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy , 2012, Clinical and experimental immunology.

[24]  A. Exley,et al.  Respiratory disease in common variable immunodeficiency and other primary immunodeficiency disorders. , 2012, Clinical radiology.

[25]  C. Cunningham-Rundles,et al.  Morbidity and mortality in common variable immune deficiency over 4 decades. , 2012, Blood.

[26]  A. Fischer,et al.  Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency , 2011, Front. Immun..

[27]  S. Travis,et al.  Review of gastric cancer risk factors in patients with common variable immunodeficiency disorders, resulting in a proposal for a surveillance programme , 2011, Clinical and experimental immunology.

[28]  Mirjam van der Burg,et al.  Educational paper , 2011, European Journal of Pediatrics.

[29]  D. Solé,et al.  Pulmonary complications in patients with antibody deficiency. , 2011, Allergologia et immunopathologia.

[30]  A. Plebani,et al.  Effectiveness of Immunoglobulin Replacement Therapy on Clinical Outcome in Patients with Primary Antibody Deficiencies: Results from a Multicenter Prospective Cohort Study , 2011, Journal of Clinical Immunology.

[31]  J. Orange,et al.  Impact of trough IgG on pneumonia incidence in primary immunodeficiency: A meta-analysis of clinical studies. , 2010, Clinical immunology.

[32]  J. Litzman,et al.  Association of FcRn expression with lung abnormalities and IVIG catabolism in patients with common variable immunodeficiency. , 2010, Clinical immunology.

[33]  E. López-Granados,et al.  Infection outcomes in patients with common variable immunodeficiency disorders: relationship to immunoglobulin therapy over 22 years. , 2010, The Journal of allergy and clinical immunology.

[34]  D. Guinee Update on nonneoplastic pulmonary lymphoproliferative disorders and related entities. , 2010, Archives of pathology & laboratory medicine.

[35]  Steven M. Holland,et al.  Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015 , 2009, Front. Immun..

[36]  P. D. de Jong,et al.  Detection of pulmonary complications in common variable immunodeficiency , 2009, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

[37]  J. Litzman,et al.  Mannose‐binding lectin gene polymorphic variants predispose to the development of bronchopulmonary complications but have no influence on other clinical and laboratory symptoms or signs of common variable immunodeficiency , 2008, Clinical and experimental immunology.

[38]  Lennart Hammarstrom,et al.  Common variable immunodeficiency disorders: division into distinct clinical phenotypes. , 2008, Blood.

[39]  A. Plebani,et al.  Long-Term Follow-Up and Outcome of a Large Cohort of Patients with Common Variable Immunodeficiency , 2007, Journal of Clinical Immunology.

[40]  C. Cunningham-Rundles,et al.  X-Linked Agammaglobulinemia: Report on a United States Registry of 201 Patients , 2006, Medicine.

[41]  P. Lipsky,et al.  Patients with Chronic Granulomatous Disease Have a Reduced Peripheral Blood Memory B Cell Compartment1 , 2006, The Journal of Immunology.

[42]  H. White,et al.  Lymphoproliferative disease in antibody deficiency: a multi‐centre study , 2003, Clinical and experimental immunology.

[43]  T. Colby,et al.  Pulmonary interstitial disease in Ig deficiency. , 2002, Chest.

[44]  A Stead,et al.  Humoral immunity and bronchiectasis , 2002, Clinical and experimental immunology.

[45]  L. Notarangelo,et al.  Clinical, immunological, and molecular analysis in a large cohort of patients with X-linked agammaglobulinemia: an Italian multicenter study. , 2002, Clinical immunology.

[46]  Ş. Arslan,et al.  Magnetic Resonance Imaging May Be a Valuable Radiation-Free Technique for Lung Pathologies in Patients with Primary Immunodeficiency , 2015, Journal of Clinical Immunology.

[47]  L. Goodman,et al.  Use of Combination Chemotherapy for Treatment of Granulomatous and Lymphocytic Interstitial Lung Disease (GLILD) in Patients with Common Variable Immunodeficiency (CVID) , 2012, Journal of Clinical Immunology.

[48]  G. Driessen,et al.  Primary antibody deficiencies , 2011 .