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From:PLoS ONE (Vol. 17, Issue 3) Peer-ReviewedBackground Primary antibody deficiencies (PADs) without an identified monogenetic origin form the largest and most heterogeneous group of primary immunodeficiencies. These patients often remain undiagnosed for years...
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From:Journal of Immunology Research (Vol. 2014) Peer-ReviewedBackground and Aim. Portal hypertension has been reported in association with acquired and primary immune deficiencies without a comprehensive description of associated spleno-portal axis abnormalities. Pathological...
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From:Journal of Immunology Research (Vol. 2016) Peer-ReviewedWe assessed the prevalence of TNFRSF13B mutations and the clinical correlates in an Italian cohort of 189 CVID, 67 IgAD patients, and 330 healthy controls to substantiate the role of TACI genetic testing in diagnostic...
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From:PLoS ONE (Vol. 16, Issue 3) Peer-ReviewedSecondary antibody deficiencies (SAD) may require immunoglobulin replacement therapy (IgRT). While the intravenous route (IVIG) is broadly considered effective in SAD, the use of subcutaneous immunoglobulins (SCIG) is...