Page last updated: 2024-10-18

dihydroxyphenylalanine and Amino Acid Metabolism Disorders, Inborn

dihydroxyphenylalanine has been researched along with Amino Acid Metabolism Disorders, Inborn in 3 studies

Dihydroxyphenylalanine: A beta-hydroxylated derivative of phenylalanine. The D-form of dihydroxyphenylalanine has less physiologic activity than the L-form and is commonly used experimentally to determine whether the pharmacological effects of LEVODOPA are stereospecific.
dopa : A hydroxyphenylalanine carrying hydroxy substituents at positions 3 and 4 of the benzene ring.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19901 (33.33)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chen, PW1
Lee, NC2
Chien, YH2
Wu, JY1
Wang, PC1
Hwu, WL2
Muramatsu, S1
Tseng, SH1
Tzen, KY1
Snyder, RO1
Byrne, BJ1
Tai, CH1
Wu, RM1
Curtius, HC1
Baerlocher, K1
Völlmin, JA1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
SIngle-Stage, Open-Label, Safety and Efficacy Study of Adeno-Associated Virus Encoding Human Aromatic L-Amino Acid Decarboxylase by Magnetic Resonance MR-guided Infusion Into Midbrain in Pediatric Patients With AADC Deficiency[NCT02852213]Phase 131 participants (Anticipated)Interventional2016-07-31Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trials

1 trial available for dihydroxyphenylalanine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Gene therapy for aromatic L-amino acid decarboxylase deficiency.
    Science translational medicine, 2012, May-16, Volume: 4, Issue:134

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

2012

Other Studies

2 other studies available for dihydroxyphenylalanine and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Diagnosis of aromatic L-amino acid decarboxylase deficiency by measuring 3-O-methyldopa concentrations in dried blood spots.
    Clinica chimica acta; international journal of clinical chemistry, 2014, Apr-20, Volume: 431

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

2014
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