Výsledky vyhledávání - "F M Schaffer"

Poststreptococcal reactive arthritis and silent carditis: a case report and review of the literature

Autor: F M, Schaffer, R, Agarwal, J, Helm, R L, Gingell, J M, Roland, K M, O'Neil

Publikováno v: Pediatrics. 93(5)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f38b957153b19c0d23d4b545db65e12a
https://pubmed.ncbi.nlm.nih.gov/8165093

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Intravenous gamma globulin administration to common variable immunodeficient women during pregnancy: case report and review of the literature

Autor: F M, Schaffer, J A, Newton

Publikováno v: Journal of perinatology : official journal of the California Perinatal Association. 14(2)

Women with common variable immunodeficiency have decreased serum concentrations of all immunoglobulin isotypes. Their offspring are at a high risk for the development of neonatal infection caused by the minimal quantity of maternal immunoglobulin G (

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f98ca0547c28ff607f3f9e60960deb7c
https://pubmed.ncbi.nlm.nih.gov/8014693

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Major histocompatibility complex class III genes and susceptibility to immunoglobulin A deficiency and common variable immunodeficiency

Autor: B O Barger, Harry W. Schroeder, John E. Volanakis, F M Schaffer, Rodney C.P. Go, Z B Zhu, K J Macon, R. D. Campbell, J Palermos, Max D. Cooper

We have proposed that significant subsets of individuals with IgA deficiency (IgA-D) and common variable immunodeficiency (CVID) may represent polar ends of a clinical spectrum reflecting a single underlying genetic defect. This proposal was supporte

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35856edad8439dd91b48d5e904e724e3
https://europepmc.org/articles/PMC295891/

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Lymphocyte abnormalities and complement activation in Kawasaki disease

Autor: R M, Laxer, F M, Schaffer, B L, Myones, W J, Yount, R D, Rowe, L, Rubin, L D, Stein, E W, Gelfand, E D, Silverman

Publikováno v: Progress in clinical and biological research. 250

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::12bfa576386fb34dfcdfb1c69fd58c3d
https://pubmed.ncbi.nlm.nih.gov/3423037

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Genotypic Studies of MHC Class III Genes in Individuals with IgA Deficiency and Common Variable Immunodeficiency

Autor: J Palermos, F M Schaffer, J. E. Volanakis, M. D. Cooper, Z B Zhu, B O Barger

Publikováno v: Progress in Immunology ISBN: 9783642837579

IgA deficiency (IgA-D) and common variable immunodeficiency (CVID) are heritable disorders both of which feature an arrest in B cell differentiation. IgA-D is characterized by a normal number of immature IgA-bearing B cells which fail to undergo diff

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3d88fe0043d836c7b9b42bb7336f0d07
https://doi.org/10.1007/978-3-642-83755-5_72

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Individuals with IgA deficiency and common variable immunodeficiency share polymorphisms of major histocompatibility complex class III genes

Autor: F M Schaffer, Max D. Cooper, J Palermos, John E. Volanakis, Z B Zhu, B O Barger

IgA deficiency and common variable immunodeficiency are heritable disorders that can occur within the same family. Both immunodeficiencies are characterized by arrests in B-cell differentiation that vary in the extent of the immunoglobulin isotypes i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfb0950dcd11f4b9991317b9398110ea
https://europepmc.org/articles/PMC298204/

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