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homovanillic acid and Amino Acid Metabolism Disorders, Inborn

homovanillic acid has been researched along with Amino Acid Metabolism Disorders, Inborn in 13 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 Excerpts

ExcerptRelevanceReference
" Consequently, this reaction has long been used to measure tyrosine in tyrosinosis and tyrosinemia, homovanillic acid in neuroblastoma, and 5-hydroxy-3-indoleacetic acid in the carcinoid tumor."3.66The chemical basis and specificity of the nitrosonaphthol reaction. ( Knight, JA; Robertson, G; Wu, JT, 1983)

Research

Studies (13)

TimeframeStudies, this research(%)All Research%
pre-19908 (61.54)18.7374
1990's1 (7.69)18.2507
2000's3 (23.08)29.6817
2010's1 (7.69)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Willemsen, MA1
Verbeek, MM1
Kamsteeg, EJ1
de Rijk-van Andel, JF1
Aeby, A1
Blau, N1
Burlina, A1
Donati, MA1
Geurtz, B1
Grattan-Smith, PJ1
Haeussler, M1
Hoffmann, GF1
Jung, H1
de Klerk, JB1
van der Knaap, MS1
Kok, F1
Leuzzi, V1
de Lonlay, P1
Megarbane, A1
Monaghan, H1
Renier, WO1
Rondot, P1
Ryan, MM1
Seeger, J1
Smeitink, JA1
Steenbergen-Spanjers, GC1
Wassmer, E1
Weschke, B1
Wijburg, FA1
Wilcken, B1
Zafeiriou, DI1
Wevers, RA2
Pons, R1
Ford, B1
Chiriboga, CA1
Clayton, PT1
Hinton, V1
Hyland, K2
Sharma, R1
De Vivo, DC1
Coppus, AW1
Fekkes, D1
Verhoeven, WM1
Tuinier, S1
Egger, JI1
van Duijn, CM1
Knight, JA1
Robertson, G1
Wu, JT1
Bräutigam, C1
Sharma, RK1
Knust, A1
Hoffman, GF1
Karoum, F1
Ruthven, CR1
Sandler, M1
Inoue, F1
Matsuo, S1
Yoshioka, H1
Takeuchi, Y1
Yamanaka, H1
Kodo, N1
Kinugasa, A1
Sawada, T1
Tanaka, K1
Yoneda, M1
Nakajima, T1
Miyatake, T1
Owada, M1
Hyman, SL1
Porter, CA1
Page, TJ1
Iwata, BA1
Kissel, R1
Batshaw, ML1
Niederwieser, A1
Curtius, HC3
Baerlocher, K1
Völlmin, JA2
Rampini, S1
Bosshard, HR1
Müller, M1
Melançon, SB1
Grignon, B1
Dallaire, L1
Potier, M1

Reviews

2 reviews available for homovanillic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment, and prognosis.
    Neurology, 2004, Apr-13, Volume: 62, Issue:7

    Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Child; Child

2004
[Detection, differential diagnosis, and prenatal diagnosis of tetrahydrobiopterin deficiency].
    Archives francaises de pediatrie, 1987, Volume: 44 Suppl 1

    Topics: Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Biopterins; Diagnosis, Differential;

1987

Other Studies

11 other studies available for homovanillic acid and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
    Brain : a journal of neurology, 2010, Volume: 133, Issue:Pt 6

    Topics: Age of Onset; Amino Acid Metabolism, Inborn Errors; Brain; Brain Diseases; Catecholamines; Child, Pr

2010
Plasma amino acids and neopterin in healthy persons with Down's syndrome.
    Journal of neural transmission (Vienna, Austria : 1996), 2007, Volume: 114, Issue:8

    Topics: Aged; Amino Acid Metabolism, Inborn Errors; Amino Acids; Biomarkers; Comorbidity; Dopamine; Down Syn

2007
The chemical basis and specificity of the nitrosonaphthol reaction.
    Clinical chemistry, 1983, Volume: 29, Issue:11

    Topics: Amino Acid Metabolism, Inborn Errors; Carcinoid Tumor; Chemical Phenomena; Chemistry; Guaiacol; Homo

1983
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
Urinary phenolic acid and alcohol excretion in the newborn.
    Archives of disease in childhood, 1975, Volume: 50, Issue:8

    Topics: Alcohols; Amino Acid Metabolism, Inborn Errors; Bilirubin; Birth Weight; Catecholamines; Creatinine;

1975
Tryptophan therapy for non-ketotic hyperglycinaemia.
    Journal of inherited metabolic disease, 1992, Volume: 15, Issue:3

    Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Female; Glycine; Homovanillic Acid; Humans;

1992
Dihydrobiopterin synthesis defect: an adult with diurnal fluctuation of symptoms.
    Neurology, 1987, Volume: 37, Issue:3

    Topics: Adult; Alcohol Oxidoreductases; Amino Acid Metabolism, Inborn Errors; Biopterins; Circadian Rhythm;

1987
Behavior management of feeding disturbances in urea cycle and organic acid disorders.
    The Journal of pediatrics, 1987, Volume: 111, Issue:4

    Topics: Adult; Amino Acid Metabolism, Inborn Errors; Anorexia; Argininosuccinic Acid; Behavior Therapy; Chil

1987
Pathogenesis of phenylketonuria: inhibition of DOPA and catecholamine synthesis in patients with phenylketonuria.
    Clinica chimica acta; international journal of clinical chemistry, 1972, Volume: 42, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Catecholamines; Catechols; Child; Child, Preschool; Deuterium;

1972
Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load.
    Pediatric research, 1974, Volume: 8, Issue:7

    Topics: Administration, Oral; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Chromatography,

1974
[Comparative study of urine and serum organic acids in newborn infants using gas chromatography].
    L'union medicale du Canada, 1974, Volume: 103, Issue:4

    Topics: Acids; Amino Acid Metabolism, Inborn Errors; Benzoates; Blood Chemical Analysis; Caprylates; Chromat

1974