mevalonic acid has been researched along with Pyrexia in 11 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (9.09) | 18.2507 |
2000's | 7 (63.64) | 29.6817 |
2010's | 2 (18.18) | 24.3611 |
2020's | 1 (9.09) | 2.80 |
Authors | Studies |
---|---|
Brink, R; Deenick, EK; Fletcher, EK; Hissaria, P; Hodson, MP; Jurczyluk, J; Kaur, S; Kristianto, E; Masle-Farquhar, E; Mehr, S; Mulders-Manders, CM; Munoz, MA; O'Donoghue, SI; Perry, KA; Robertson, AA; Rogers, MJ; Simon, A; Skinner, OP; Xiao, Y; Zahra, DG | 1 |
Becken, B; Coppola, T; McDonald, MT; Panayotti, GM; Van Mater, H | 1 |
Baldovič, M; Dallos, T; Fehérvízyová, Z; Hlavatá, A; Kadasi, L; Kovacs, L; Paulovicova, E | 1 |
De Jong, JG; Drenth, JP; Kremer, HP; Scheffer, H; Simon, A; Van Der Meer, JW; Wevers, RA | 1 |
Haas, D; Hoffmann, GF | 1 |
Blanche, S; Cavazzana-Calvo, M; Cuisset, L; de Lonlay, P; Debré, M; Fischer, A; Neven, B; Prieur, AM; Quartier, P; Rabier, D; Rolland, MO; Valayannopoulos, V | 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 |
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 |
Caruso, U; Di Rocco, M; Loy, A; Picco, P; Wanders, RJ; Waterham, HR | 1 |
Chabrol, B; Divry, P; Kone-Paut, I; Philip, N; Tsimaratos, M | 1 |
11 other study(ies) available for mevalonic acid and Pyrexia
Article | Year |
---|---|
Increased core body temperature exacerbates defective protein prenylation in mouse models of mevalonate kinase deficiency.
Topics: Animals; Body Temperature; Fever; GTP Phosphohydrolases; Humans; Inflammasomes; Lipopolysaccharides; Mevalonate Kinase Deficiency; Mevalonic Acid; Mice; NLR Family, Pyrin Domain-Containing 3 Protein; Phosphotransferases (Alcohol Group Acceptor); Protein Prenylation | 2022 |
A case report of mevalonate kinase deficiency in a 14-month-old female with fevers and lower extremity weakness.
Topics: Antibodies, Monoclonal, Humanized; Brain; Exanthema; Female; Fever; Humans; Infant; Interleukin 1 Receptor Antagonist Protein; Magnetic Resonance Imaging; Mevalonate Kinase Deficiency; Mevalonic Acid; Muscle Weakness | 2019 |
Elevated immunoglobulin D levels in children with PFAPA syndrome.
Topics: Arthralgia; Child, Preschool; Cohort Studies; Diagnosis, Differential; Erythema; Exanthema; Female; Fever; Genotype; Humans; Immunoglobulin D; Infant; Lymphadenitis; Male; Mevalonate Kinase Deficiency; Mevalonic Acid; Pharyngitis; Stomatitis, Aphthous; Syndrome; Time Factors | 2010 |
Mevalonate kinase deficiency: Evidence for a phenotypic continuum.
Topics: Adolescent; Adult; Child; Child, Preschool; DNA Mutational Analysis; Enzyme Activation; Exanthema; Female; Fever; Humans; Immunoglobulin D; Infant; Lymphatic Diseases; Male; Mevalonic Acid; Middle Aged; Mutation; Periodicity; Phenotype; Phosphotransferases (Alcohol Group Acceptor); Recurrence; Registries; Syndrome | 2004 |
Mevalonate kinase deficiency and autoinflammatory disorders.
Topics: Bone Marrow Transplantation; Cholesterol; Fever; Humans; Inflammation; Metabolism, Inborn Errors; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Protein Prenylation; Transplantation, Homologous; Ubiquinone | 2007 |
Allogeneic bone marrow transplantation in mevalonic aciduria.
Topics: Biomarkers; Bone Marrow Transplantation; Child, Preschool; Cytokines; Failure to Thrive; Fever; Humans; Inflammation; Male; Metabolism, Inborn Errors; Mevalonic Acid; Mutation, Missense; Phosphotransferases (Alcohol Group Acceptor); Transplantation, Homologous | 2007 |
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 |
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 |
Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D.
Topics: Child, Preschool; DNA Mutational Analysis; Fever; Fibroblasts; Humans; Immunoglobulin A; Immunoglobulin D; Male; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor) | 2001 |
Mevalonic aciduria and hyper-IgD syndrome: two sides of the same coin?
Topics: C-Reactive Protein; Craniofacial Abnormalities; Female; Fever; Humans; Immunoglobulin A; Immunoglobulin D; Infant; Lymphatic Diseases; Male; Mevalonic Acid; Phosphotransferases (Alcohol Group Acceptor); Syndrome | 2001 |