Page last updated: 2024-10-21

homovanillic acid and Decreased Muscle Tone

homovanillic acid has been researched along with Decreased Muscle Tone in 5 studies

Homovanillic Acid: A 3-O-methyl ETHER of (3,4-dihydroxyphenyl)acetic acid.
homovanillate : A hydroxy monocarboxylic acid anion which is obtained by deprotonation of the carboxy group of homovanillic acid.
homovanillic acid : A monocarboxylic acid that is the 3-O-methyl ether of (3,4-dihydroxyphenyl)acetic acid. It is a catecholamine metabolite.

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's2 (40.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Horvath, GA1
Demos, M1
Shyr, C1
Matthews, A1
Zhang, L1
Race, S1
Stockler-Ipsiroglu, S1
Van Allen, MI1
Mancarci, O1
Toker, L1
Pavlidis, P1
Ross, CJ1
Wasserman, WW1
Trump, N1
Heales, S1
Pope, S1
Cross, JH1
van Karnebeek, CD1
Doummar, D1
Clot, F1
Vidailhet, M1
Afenjar, A1
Durr, A1
Brice, A1
Mignot, C1
Guet, A1
de Villemeur, TB1
Rodriguez, D1
Mak, CM1
Lam, CW1
Siu, TS1
Chan, KY1
Siu, WK1
Yeung, WL1
Hui, J1
Wong, VC1
Low, LC1
Ko, CH1
Fung, CW1
Chen, SP1
Yuen, YP1
Lee, HC1
Yau, E1
Chan, B1
Tong, SF1
Tam, S1
Chan, YW1
Maller, A1
Hyland, K2
Milstien, S1
Biaggioni, I1
Butler, IJ1
Bräutigam, C1
Wevers, RA1
Sharma, RK1
Knust, A1
Hoffman, GF1

Other Studies

5 other studies available for homovanillic acid and Decreased Muscle Tone

ArticleYear
Secondary neurotransmitter deficiencies in epilepsy caused by voltage-gated sodium channelopathies: A potential treatment target?
    Molecular genetics and metabolism, 2016, Volume: 117, Issue:1

    Topics: Autistic Disorder; Channelopathies; Child; Drug Resistant Epilepsy; Epilepsy; Exome; Female; Homovan

2016
Infantile hypokinetic-hypotonic syndrome due to two novel mutations of the tyrosine hydroxylase gene.
    Movement disorders : official journal of the Movement Disorder Society, 2009, Apr-30, Volume: 24, Issue:6

    Topics: DNA Mutational Analysis; Female; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; Muscle

2009
Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.
    Molecular genetics and metabolism, 2010, Volume: 99, Issue:4

    Topics: Age of Onset; Asian People; Child; Child, Preschool; Dystonia; Female; Galactorrhea; Homovanillic Ac

2010
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family.
    Journal of child neurology, 1997, Volume: 12, Issue:6

    Topics: 5-Hydroxytryptophan; Amino Acids, Cyclic; Aromatic-L-Amino-Acid Decarboxylases; Biogenic Monoamines;

1997
The influence of L-dopa on methylation capacity in aromatic L-amino acid decarboxylase deficiency: biochemical findings in two patients.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:4

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Dopamine; Homovanillic A

2000