C Cunningham-Rundles, C Bodian - Clinical Immunology, 1999 - Elsevier Common variable immunodeficiency (CVI) is a primary immunodeficiency disease
characterized by reduced serum immunoglobulins and heterogeneous clinical
features. In these studies we describe the clinical and immunological ... Cited by 508 - Related articles - BL Direct - All 6 versions
FA Bonilla, IL Bernstein, DA Khan, ZK Ballas …, 2005 - bragid.org.br * Department of Medicine, Children's Hospital Boston, and Department of
Pediatrics, Harvard Medical School, Boston, Massachusetts. † Department of
Medicine and Environmental Health, University of Cincin- nati College of ... Cited by 117 - Related articles - View as HTML - Library Search - All 23 versions
B Piqueras, C Lavenu-Bombled, L Galicier, … - Journal of clinical immunology, 2003 - Springer Common variable immunodeficiency (CVID) is a very heteroge- neous syndrome
defined by impaired immunoglobulin produc- tion. The functional classification
of CVID patients on the basis of in vitro immunoglobulin production is time ... Cited by 100 - Related articles - BL Direct - All 5 versions
- ►bloodjournal.org PD Arkwright, M Abinun, AJ Cant - Blood, 2002 - Am Soc Hematology Classification of autoimmune phenomena in primary immunodeficiency diseases is
problematic. One method of classification is based on the underlying genetic
defect. This results in a long list that does little to help clinicians ... Cited by 92 - Related articles - BL Direct - All 8 versions
MC Sneller - The American journal of the medical sciences, 2001 - journals.lww.com Common variable immunodeficiency (CVI) is a heterogeneous immunodeficiency
syndrome characterized by hypogammaglobulinemia, recurrent bacterial infections,
and a variety of immunological abnormalities. In addition to recurrent ... Cited by 77 - Related articles - BL Direct - All 4 versions
C Cunningham-Rundles - Current allergy and asthma reports, 2001 - Springer Serum Immunoglobulins and Diagnosis The diagnosis of CVID is made by determining
that the serum IgG, IgA and/or IgM is reduced by two or more stan- dard
deviations from the normal mean [1•,2••,3••,4••]. The IgG ... Cited by 67 - Related articles - All 3 versions
C Cunningham-Rundles - Blood reviews, 2002 - Elsevier Primary immune deficiencies have an estimated overall incidence of 1 in 10,000
individuals. These disorders are diverse, depending on the specific immune
functions involved, and lead to chronic or recurrent infections, ... Cited by 63 - Related articles - BL Direct - All 12 versions
M Michel, V Chanet, L Galicier, M Ruivard, Y … - Medicine, 2004 - journals.lww.com Abstract: To describe the main characteristics and outcome of autoimmune
thrombocytopenic purpura (AITP) in patients with common variable
immunodeficiency (CVID), we analyzed data from 21 patients and reviewed ... Cited by 61 - Related articles - BL Direct - All 3 versions
SD Gadola, HT Moins-Teisserenc, J … - Clinical and Experimental Immunology, 2000 - pubmedcentral.nih.gov Bare lymphocyte syndrome (BLS) is characterized by a severe down-regulation of
HLA class I and/or class II molecules. In type 1 BLS the defect is confined to
HLA class I molecules, while in type 2 BLS HLA class II molecules are down- ... Cited by 58 - Related articles - BL Direct - All 5 versions
GP Spickett - Clinical and experimental allergy: journal of the …, 2001 - ncbi.nlm.nih.gov 1: Clin Exp Allergy. 2001 Apr;31(4):536-42. Current perspectives on common
variable immunodeficiency (CVID). Spickett GP. Regional ... Cited by 58 - Related articles - BL Direct - All 4 versions
