Results 51 to 60 of about 7,578 (214)
Novel NFKB2 Mutation in Early-Onset CVID [PDF]
, 2014 Common variable immunodeficiency (CVID) is heterogeneous, clinically, immunologically and genetically. The majority of genetic mechanisms leading to CVID remain elusive. We studied a Greek Cypriot family of non-consanguineous parents.
Jones, Alison +5 more
core +1 more source
Frontiers in Immunology, 2021 BackgroundAbout 20% of patients with common variable immunodeficiency (CVID) suffer from interstitial lung disease (ILD) as part of a systemic immune dysregulation.
David Friedmann +20 more
doaj +1 more source
Autoimmune Cytopenias In Common Variable Immunodeficiency (CVID) [PDF]
, 2012 Common variable immunodeficiency (CVID) is a humoral immunodeficiency whose primary diagnostic features include hypogammaglobulinemia involving two or more immunoglobulin isotypes and impaired functional antibody responses in the majority of patients ...
Jenna C. Podjasek +4 more
core +1 more source
Elevated levels of sCD14 in CVID. [PDF]
, 2013 Comparison of plasma levels of sCD14 in healthy controls and CVID patients before IVIg treatment. ** indicates p = 0.001.
Jorge Kalil (52916) +9 more
core +1 more source
CVID is a multifaceted disease [PDF]
, 2019 Common variable immunodeficiency disease (CVID) is the most common primary immunodeficiency in adults, and multiple organs may be involved. This is a case report of a 49-year-old female patient with granulomatous-lymphocytic interstitial lung disease ...
Dimitrova, Aneliya +3 more
core +2 more sources
JPGN Reports, EarlyView.Abstract Infantile‐onset inflammatory bowel disease (IOIBD) is a rare and severe subset of very‐early‐onset IBD, often associated with immune dysregulation and poor response to conventional therapies. Data regarding the use of Janus kinase inhibitors (JAKI) in this population is limited.
Smridhi Mahajan +2 more
wiley +1 more source
Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency
JEADV Clinical Practice, EarlyView.ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz +2 more
wiley +1 more source
Chronic activation profile in CVID patients. [PDF]
, 2016 Chronic activated T cells were determined in PBMC from 17 healthy controls and 42 CVID patients by surface markers CD4, CD8, CD38 and HLA-DR expression without stimulation and analyzed by flow cytometry.
Rafael Ribeiro Almeida (136344) +5 more
core +1 more source
British Journal of Haematology, EarlyView.Summary Childhood autoimmune neutropenia (AIN) encompasses heterogeneous entities; phenotype‐specific immunological profiles and their relationship to infection outcomes remain incompletely defined. To characterise clinical, immunological and long‐term outcomes across distinct phenotypes of childhood AIN.
Ioanna Saougou +5 more
wiley +1 more source
Inborn errors of immunity in children with neuroinflammation
Developmental Medicine &Child Neurology, EarlyView.Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu +5 more
wiley +1 more source