mevalonic acid has been researched along with Hypergammaglobulinemia in 15 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (6.67) | 18.2507 |
2000's | 14 (93.33) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Buurman, SW; Frenkel, J; Houten, SM; Kuis, W; Mandey, SH; Rijkers, GT; Wanders, RJ; Waterham, HR | 1 |
Frenkel, J; Houten, SM; Kuis, W; Rijkers, GT; Wanders, RJ; Waterham, HR | 1 |
Gibson, KM; Haas, D; Hoffmann, GF; Krastel, H; Mayatepek, E; Prietsch, V; Wanders, RJ; Waterham, HR; Zundel, D | 1 |
Drenth, JP; Drewe, E; Kelley, RI; Powell, RJ; Simon, A; Stalenhoef, AF; van der Meer, JW | 1 |
Haas, D; Hoffmann, GF | 1 |
de Barse, MM; de Koning, TJ; Dorland, L; Duran, M; Frenkel, J; Houten, SM; Huijbers, WA; Kuis, W; Poll-The, BT; Rijkers, GT; Romeijn, GJ; van Royen-Kerkhof, A; Wanders, RJ; Waterham, HR | 1 |
Drenth, JP; Frenkel, J; Houten, SM; Kuis, W; Poll-The, BT; van der Meer, JW; Wanders, RJ; Waterham, HR | 1 |
de Barse, MM; de Koning, TJ; Dorland, L; Duran, M; Frenkel, J; Houten, SM; Kuis, W; Poll-The, BT; Romeijn, GJ; Wanders, RJ; Waterham, HR | 1 |
Frenkel, J; Houten, SM; Kuis, W; Poll-The, BT; Wanders, RJ; Waterham, HR | 1 |
Houten, SM; Wanders, RJ; Waterham, HR | 1 |
Duran, M; Frenkel, J; Houten, SM; Kuijpers, TW; Kuis, W; Poll-The, BT; Rijkers, GT; van Luijk, W; Wanders, RJ; Waterham, HR | 1 |
Alvarez-Blanco, MJ; de Dios García-Díaz, J | 1 |
Dorland, L; Frenkel, J; Mayatepek, E; Weemaes, CM; Willemsen, MA | 1 |
Haas, D; Hoffmann, GF; Kelley, RI | 1 |
Kelley, RI; Takada, I | 1 |
4 review(s) available for mevalonic acid and Hypergammaglobulinemia
Article | Year |
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Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome.
Topics: Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypergammaglobulinemia; Immunoglobulin D; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Simvastatin; Syndrome | 2006 |
[Identification of the gene for hyper-IgD syndrome: a model of modern genetics].
Topics: Biomarkers; DNA Mutational Analysis; Familial Mediterranean Fever; Humans; Hypergammaglobulinemia; Immunoglobulin D; Lipid Metabolism, Inborn Errors; Mevalonic Acid; Mutation, Missense; Phosphotransferases (Alcohol Group Acceptor); Syndrome | 2000 |
Biochemical and genetic aspects of mevalonate kinase and its deficiency.
Topics: Amino Acid Sequence; Animals; Cloning, Molecular; Conserved Sequence; Enzyme Activation; Enzyme Inhibitors; Familial Mediterranean Fever; Humans; Hypergammaglobulinemia; Immunoglobulin D; Liver; Mevalonic Acid; Molecular Sequence Data; Phosphotransferases (Alcohol Group Acceptor); Sequence Alignment; Subcellular Fractions | 2000 |
Inherited disorders of cholesterol biosynthesis.
Topics: Abnormalities, Multiple; Alleles; Child; Cholesterol; Chondrodysplasia Punctata; Humans; Hypergammaglobulinemia; Immunoglobulin D; Lipid Metabolism, Inborn Errors; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Smith-Lemli-Opitz Syndrome | 2001 |
1 trial(s) available for mevalonic acid and Hypergammaglobulinemia
Article | Year |
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Simvastatin treatment for inflammatory attacks of the hyperimmunoglobulinemia D and periodic fever syndrome.
Topics: Adolescent; Adult; Double-Blind Method; Familial Mediterranean Fever; Female; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypergammaglobulinemia; Male; Mevalonic Acid; Middle Aged; Simvastatin; Syndrome; Treatment Outcome | 2004 |
10 other study(ies) available for mevalonic acid and Hypergammaglobulinemia
Article | Year |
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Lack of isoprenoid products raises ex vivo interleukin-1beta secretion in hyperimmunoglobulinemia D and periodic fever syndrome.
Topics: Antibodies; CD2 Antigens; CD28 Antigens; Cell Division; Cells, Cultured; Child; Diterpenes; Familial Mediterranean Fever; Farnesol; Female; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Hypergammaglobulinemia; Immunoglobulin D; Interleukin-1; Lovastatin; Male; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Polyisoprenyl Phosphates; T-Lymphocytes | 2002 |
Temperature dependence of mutant mevalonate kinase activity as a pathogenic factor in hyper-IgD and periodic fever syndrome.
Topics: Alleles; Amino Acid Substitution; Body Temperature; Cells, Cultured; Familial Mediterranean Fever; Fibroblasts; Genes, Recessive; Humans; Hydroxymethylglutaryl CoA Reductases; Hypergammaglobulinemia; Immunoglobulin D; Isoleucine; Leukocytes, Mononuclear; Mevalonic Acid; Mutation; Phosphotransferases (Alcohol Group Acceptor); Skin; Valine | 2002 |
Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrum.
Topics: Adolescent; Cerebellar Ataxia; Child; Female; Growth Disorders; Humans; Hypergammaglobulinemia; Immunoglobulin D; Intellectual Disability; Male; Metabolism, Inborn Errors; Mevalonic Acid; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Psychomotor Disorders; Sweet Syndrome | 2003 |
Mutations in MVK, encoding mevalonate kinase, cause hyperimmunoglobulinaemia D and periodic fever syndrome.
Topics: Amino Acid Substitution; Cloning, Molecular; Escherichia coli; Female; Fever; Genes, Recessive; Humans; Hypergammaglobulinemia; Immunoglobulin D; Indonesia; Lymphocytes; Male; Mevalonic Acid; Netherlands; Periodicity; Phosphotransferases (Alcohol Group Acceptor); Point Mutation; Recombinant Proteins; Recurrence; Syndrome | 1999 |
Mevalonic aciduria in 12 unrelated patients with hyperimmunoglobulinaemia D and periodic fever syndrome.
Topics: Acidosis; Familial Mediterranean Fever; Humans; Hypergammaglobulinemia; Immunoglobulin D; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor) | 2000 |
Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: high frequency of 3 mutations in the mevalonate kinase gene.
Topics: Acidosis; Alleles; Familial Mediterranean Fever; Gene Frequency; Humans; Hypergammaglobulinemia; Immunoglobulin D; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Point Mutation | 2000 |
Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D.
Topics: Child; Child, Preschool; DNA, Complementary; Familial Mediterranean Fever; Female; Fever; Genes, Recessive; Humans; Hypergammaglobulinemia; Immunoglobulin D; Male; Mevalonic Acid; Mutation; Periodicity; Phosphotransferases (Alcohol Group Acceptor); Polymerase Chain Reaction; Sequence Analysis, DNA; Syndrome | 2001 |
High IgD could be a nonpathogenetic diagnostic marker of the hyper-IgD and periodic fever syndrome.
Topics: Adult; Biomarkers; Female; Fever; Genes, Recessive; Humans; Hypergammaglobulinemia; Immunoglobulin D; Male; Mevalonic Acid; Pedigree; Syndrome | 2001 |
Increased urinary leukotriene E(4) during febrile attacks in the hyperimmunoglobulinaemia D and periodic fever syndrome.
Topics: Adolescent; Child; Chromatography, Gas; Chromatography, High Pressure Liquid; Familial Mediterranean Fever; Humans; Hypergammaglobulinemia; Immunoglobulin D; Leukotriene E4; Mass Spectrometry; Mevalonic Acid; Radioisotope Dilution Technique | 2001 |
Hereditary periodic fever.
Topics: Familial Mediterranean Fever; Gas Chromatography-Mass Spectrometry; Humans; Hypergammaglobulinemia; Immunoglobulin D; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Sensitivity and Specificity | 2002 |