Compounds > mevalonic acid

mevalonic acid and Adiadochokinesis

mevalonic acid has been researched along with Adiadochokinesis in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's2 (33.33)29.6817
2010's1 (16.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Aróstegui, JI; Baña Souto, A; Couce, ML; Garcia-Villoria, J; Ribes, A; Ruiz Gomez, A; Torres, A; Vilaseca, MA; Yagüe, J1
Gibson, KM; Haas, D; Hoffmann, GF; Krastel, H; Mayatepek, E; Prietsch, V; Wanders, RJ; Waterham, HR; Zundel, D1
Bretón Martínez, JR; Cánovas Martínez, A; Casaña Pérez, S; Escribá Alepuz, J; Giménez Vázquez, F1
Charpentier, C; Divry, P; Gibson, KM; Hoffmann, GF; Hrebicek, M; Lehnert, W; Leichsenring, M; Mancini, J; Mayatepek, E; Sartor, K1
Berger, R; Gibson, KM; Hoffmann, G; le Coultre, R; Nyhan, WL; Smit, GP; Sweetman, L1
Berger, R; Bijsterveld, K; le Coultre, R; Schierbeek, H; Smit, GP1

Other Studies

6 other study(ies) available for mevalonic acid and Adiadochokinesis

ArticleYear
Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency.
    Pediatrics, 2012, Volume: 129, Issue:2

    Topics: Alleles; Brain; Cerebellar Ataxia; Cerebellum; Child; Diagnosis, Differential; DNA Mutational Analysis; Failure to Thrive; Fever of Unknown Origin; Genes, Recessive; Genetic Variation; Genotype; Humans; Infant; Interleukin 1 Receptor Antagonist Protein; Magnetic Resonance Imaging; Male; Mevalonate Kinase Deficiency; Mevalonic Acid; Myoclonic Cerebellar Dyssynergia; Phenotype; Psychomotor Disorders

2012
Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrum.
    Pediatrics, 2003, Volume: 111, Issue:2

    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
Mevalonic aciduria: report of two cases.
    Journal of inherited metabolic disease, 2007, Volume: 30, Issue:5

    Topics: Adolescent; Cerebellar Ataxia; Cholesterol; Gait; Humans; Intellectual Disability; Lipid Metabolism, Inborn Errors; Mevalonic Acid; Motor Skills; Muscle Hypotonia; Pedigree; Phosphotransferases (Alcohol Group Acceptor); Seizures; Verbal Behavior; Walking

2007
Clinical and biochemical phenotype in 11 patients with mevalonic aciduria.
    Pediatrics, 1993, Volume: 91, Issue:5

    Topics: Abnormalities, Multiple; Cerebellar Ataxia; Failure to Thrive; Female; Humans; Infant; Intellectual Disability; Lovastatin; Male; Mevalonic Acid; Phenotype; Phosphotransferases; Phosphotransferases (Alcohol Group Acceptor); Prednisone

1993
Mevalonate kinase deficiency in a child with cerebellar ataxia, hypotonia and mevalonic aciduria.
    European journal of pediatrics, 1988, Volume: 148, Issue:3

    Topics: Carboxy-Lyases; Cells, Cultured; Cerebellar Ataxia; Child; Fibroblasts; Humans; Male; Methylmalonyl-CoA Decarboxylase; Mevalonic Acid; Muscle Hypotonia; Phosphotransferases; Phosphotransferases (Alcohol Group Acceptor)

1988
Mevalonic aciduria: an inborn error of cholesterol biosynthesis?
    Clinica chimica acta; international journal of clinical chemistry, 1985, Oct-31, Volume: 152, Issue:1-2

    Topics: Cerebellar Ataxia; Child; Cholesterol; Gas Chromatography-Mass Spectrometry; Glucose Tolerance Test; Humans; Male; Metabolism, Inborn Errors; Mevalonic Acid

1985