Compounds > arginine

arginine and Hypergammaglobulinemia

arginine has been researched along with Hypergammaglobulinemia in 3 studies

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's2 (66.67)29.6817
2010's1 (33.33)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aas-Hanssen, K; Bogen, B; Funderud, A; Munthe, LA; Thompson, KM1
Honjo, T; Mizutani, S; Morio, T; Muramatsu, M; Nonoyama, S; Zhu, Y1
Feneberg, W; Hoffmann, LA; Hohlfeld, R; Kümpfel, T; Lohse, P; Pöllmann, W; Rübsamen, H1

Other Studies

3 other study(ies) available for arginine and Hypergammaglobulinemia

ArticleYear
Idiotype-specific Th cells support oligoclonal expansion of anti-dsDNA B cells in mice with lupus.
    Journal of immunology (Baltimore, Md. : 1950), 2014, Sep-15, Volume: 193, Issue:6

    Topics: Animals; Antibodies, Antinuclear; Arginine; B-Lymphocytes; Base Sequence; Clonal Selection, Antigen-Mediated; DNA; Hypergammaglobulinemia; Immunoglobulin G; Immunoglobulin Heavy Chains; Immunoglobulin Idiotypes; Immunoglobulin Variable Region; Lupus Erythematosus, Systemic; Lymphocyte Activation; Mice; Mice, Inbred BALB C; Mice, Transgenic; Sequence Analysis, DNA; T-Lymphocytes, Helper-Inducer

2014
Type two hyper-IgM syndrome caused by mutation in activation-induced cytidine deaminase.
    Journal of medical and dental sciences, 2003, Volume: 50, Issue:1

    Topics: Adult; Arginine; B-Lymphocytes; CD40 Ligand; Child, Preschool; Consanguinity; Cytidine Deaminase; DNA Mutational Analysis; Female; Histidine; Humans; Hypergammaglobulinemia; Immunoglobulin Class Switching; Immunoglobulin M; Infant; Japan; Male; Middle Aged; Mutation; Siblings; Somatic Hypermutation, Immunoglobulin; Syndrome

2003
Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.
    Arthritis and rheumatism, 2007, Volume: 56, Issue:8

    Topics: Adult; Arginine; Diagnosis, Differential; Familial Mediterranean Fever; Female; Genetic Predisposition to Disease; Genetic Testing; Glutamine; Heterozygote; Humans; Hypergammaglobulinemia; Male; Middle Aged; Multiple Sclerosis; Mutation; Pedigree; Prospective Studies; Receptors, Tumor Necrosis Factor, Type I

2007