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Clinical and Immunological Features of 78 Adult Patients with Primary Selective IgG Subclass Deficiencies.
Arch Immunol Ther Exp (Warsz). 2019 Oct;67(5):325-334. doi: 10.1007/s00005-019-00556-3. Epub 2019 Jul 30.
Arch Immunol Ther Exp (Warsz). 2019.
PMID: 31363786
Free article.
The purpose of this study is to describe both clinical and immunological features in large cohort of adult patients with IgG subclass deficiency, and response to immunoglobulin therapy. This is a retrospective study of data obtained from electronic medical records and pape …
The purpose of this study is to describe both clinical and immunological features in large cohort of adult patients with IgG subclass …
Serum IgG subclass concentrations before and after administration of intravenous immunoglobulin in common variable immunodeficiency.
Ozawa T, Motoyoshi F, Kato Y, Kondo N, Orii T.
Ozawa T, et al.
J Clin Lab Immunol. 1992;38(1):29-39.
J Clin Lab Immunol. 1992.
PMID: 1343346
In light of the above results of replacement therapy with IVIGs, we should consider the IgG subclass levels for patients such as CVI or selective IgG subclass deficiency....
In light of the above results of replacement therapy with IVIGs, we should consider the IgG subclass levels for patients such as CVI or s …
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Immunoglobulin subclass concentration in preterm infants treated prophylactically with different intravenous immunoglobins.
Amato M, Hüppi P, Imbach P, Llauto A, Bürgi W.
Amato M, et al.
Am J Perinatol. 1995 Sep;12(5):306-9. doi: 10.1055/s-2007-994481.
Am J Perinatol. 1995.
PMID: 8540928
Clinical Trial.
The most immature infants have critically low concentrations of all immunoglobulin G (IgG) subclasses, associated with a higher risk for pyogenic, respiratory, and meningeal infection. Selective IgG subclass deficiency is an established indication for …
The most immature infants have critically low concentrations of all immunoglobulin G (IgG) subclasses, associated with a higher risk for pyo …
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H syndrome: 5 new cases from the United States with novel features and responses to therapy.
Bloom JL, Lin C, Imundo L, Guthery S, Stepenaskie S, Galambos C, Lowichik A, Bohnsack JF.
Bloom JL, et al.
Pediatr Rheumatol Online J. 2017 Oct 17;15(1):76. doi: 10.1186/s12969-017-0204-y.
Pediatr Rheumatol Online J. 2017.
PMID: 29041934
Free PMC article.
The patients share many of the characteristics previously reported with H syndrome, including hyperpigmentation, hypertrichosis, short stature, insulin-dependent diabetes, arthritis and systemic inflammation, as well as some novel features, including selective IgG …
The patients share many of the characteristics previously reported with H syndrome, including hyperpigmentation, hypertrichosis, short statu …
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