mevalonic acid and Pyrexia

mevalonic acid has been researched along with Pyrexia in 11 studies

Research

Studies (11)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (9.09)18.2507
2000's7 (63.64)29.6817
2010's2 (18.18)24.3611
2020's1 (9.09)2.80

Authors

AuthorsStudies
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, DG1
Becken, B; Coppola, T; McDonald, MT; Panayotti, GM; Van Mater, H1
Baldovič, M; Dallos, T; Fehérvízyová, Z; Hlavatá, A; Kadasi, L; Kovacs, L; Paulovicova, E1
De Jong, JG; Drenth, JP; Kremer, HP; Scheffer, H; Simon, A; Van Der Meer, JW; Wevers, RA1
Haas, D; Hoffmann, GF1
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, V1
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, HR1
Duran, M; Frenkel, J; Houten, SM; Kuijpers, TW; Kuis, W; Poll-The, BT; Rijkers, GT; van Luijk, W; Wanders, RJ; Waterham, HR1
Alvarez-Blanco, MJ; de Dios García-Díaz, J1
Caruso, U; Di Rocco, M; Loy, A; Picco, P; Wanders, RJ; Waterham, HR1
Chabrol, B; Divry, P; Kone-Paut, I; Philip, N; Tsimaratos, M1

Other Studies

11 other study(ies) available for mevalonic acid and Pyrexia

ArticleYear
Increased core body temperature exacerbates defective protein prenylation in mouse models of mevalonate kinase deficiency.
    The Journal of clinical investigation, 2022, 10-03, Volume: 132, Issue:19

    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.
    BMC pediatrics, 2019, 07-20, Volume: 19, Issue:1

    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.
    Neuro endocrinology letters, 2010, Volume: 31, Issue:6

    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.
    Neurology, 2004, Mar-23, Volume: 62, Issue:6

    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.
    The New England journal of medicine, 2007, Jun-28, Volume: 356, Issue:26

    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.
    The New England journal of medicine, 2007, Jun-28, Volume: 356, Issue:26

    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.
    Nature genetics, 1999, Volume: 22, Issue:2

    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.
    Rheumatology (Oxford, England), 2001, Volume: 40, Issue:5

    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.
    Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology, 2001, Volume: 86, Issue:5

    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.
    Journal of inherited metabolic disease, 2001, Volume: 24, Issue:3

    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?
    Journal of inherited metabolic disease, 2001, Volume: 24, Issue:3

    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