Common Variable Immunodeficiency
What's New
Last Posted: Nov 01, 2018
- Common Variable Immunodeficiency with Genetic Defects Identified by Whole Exome Sequencing.
Li Ran et al. BioMed research international 2018 20183724630 - Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients.
Karaca Neslihan Edeer et al. International journal of immunopathology and pharmacology 322058738418779458 - Genetic screening of male patients with primary hypogammaglobulinemia can guide diagnosis and clinical management.
Vince Nicolas et al. Human immunology 2018 Apr - Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients.
Aghamohammadi Asghar et al. Expert Rev Clin Immunol 2014 Oct 10(10) 1405-17 - The Swiss National Registry for Primary Immunodeficiencies: Report on the first 6 years' activity 2008-2014.
Marschall Karin et al. Clin. Exp. Immunol. 2015 Jun 1.
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
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- Page last reviewed:Oct 1, 2020
- Page last updated:Jan 26, 2021
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