Common Variable Immunodeficiency Clinical Manifestations Are Shaped by Presence and Type of Heterozygous NFKB1 Variants. [PDF]
Yin J +8 more
europepmc +1 more source
Movement Disorders Associated with 22q11.2 Microdeletion: A Scoping Review
Abstract Background Movement disorders have recently emerged as important neurologic manifestations of the 22q11.2 microdeletion that affects nearly one in every 2000 live births. Objective We aimed to map the existing evidence regarding the spectrum, diagnosis and treatment, and etiopathogenesis of movement disorders associated with 22q11.2 ...
Nikolai Gil D. Reyes +6 more
wiley +1 more source
Common variable immunodeficiency and autoimmune diseases: A 10-year single-center experience. [PDF]
Sadi Aykan F +5 more
europepmc +1 more source
Gut microbial dysbiosis, IgA, and Enterococcus in common variable immunodeficiency with immune dysregulation. [PDF]
Berbers RM +18 more
europepmc +1 more source
Common Variable Immunodeficiency-Like Enteropathy Associated with Rituximab B-Cell Depletion Therapy. [PDF]
Hakimian D +4 more
europepmc +1 more source
Granulomatous Brain Involvement in Common Variable Immunodeficiency: A Case Report. [PDF]
Rocha M +4 more
europepmc +1 more source
Diverse phenotypic manifestations of small intestinal mucosa in non-infectious common variable immunodeficiency bowel disease: A case report. [PDF]
He T +8 more
europepmc +1 more source
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Common variable immunodeficiency
Current Allergy and Asthma Reports, 2001Common variable immunodeficiency (CVID) is a common primary immnodeficiency disease, the hallmark of which is hypogammaglobulinemia. Due to the lack of antibodies, patients usually have recurrent bacterial infections, but there are a number of other puzzling manifestations, including inflammatory conditions, autoimmune disease, and the development of ...
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Common Variable Immunodeficiency
The Indian Journal of Pediatrics, 2016Common variable immunodeficiency (CVID) is the most common primary immunodeficiency of young adolescents and adults which also affects the children. The disease remains largely under-diagnosed in India and Southeast Asian countries. Although in majority of cases it is sporadic, disease may be inherited in a autosomal recessive pattern and rarely, in ...
Biman, Saikia, Sudhir, Gupta
openaire +3 more sources

