Compounds > levodopa
Page last updated: 2024-08-17

levodopa and Amino Acid Metabolism Disorders, Inborn

levodopa has been researched along with Amino Acid Metabolism Disorders, Inborn in 12 studies

Research

Studies (12)

TimeframeStudies, this research(%)All Research%
pre-19902 (16.67)18.7374
1990's1 (8.33)18.2507
2000's4 (33.33)29.6817
2010's3 (25.00)24.3611
2020's2 (16.67)2.80

Authors

AuthorsStudies
Alrashidi, H; Barral, S; Barwick, K; Bertoldi, M; Bisello, G; Counsell, J; De La Fuente Barrigon, C; Heales, SJR; Krämer, K; Kurian, MA; Lignani, G; Lugarà, E; Ng, J; Pope, S; Rossignoli, G1
Blau, N; Burlina, A; Burlina, AP; Cazzorla, C; Giuliani, A; Gragnaniello, V; Gueraldi, D; Hoffmann, G; Opladen, T; Polo, G1
Elsea, SH; Hanchard, NA; Kennedy, AD; Magoulas, PL; Pappan, KL; Sun, Q1
Caine, C; Homma, S; Kim, JK; Monani, UR; Mosharov, EV; Nakanishi, K; Shohat, M1
Aeby, A; Blau, N; Burlina, A; de Klerk, JB; de Lonlay, P; de Rijk-van Andel, JF; Donati, MA; Geurtz, B; Grattan-Smith, PJ; Haeussler, M; Hoffmann, GF; Jung, H; Kamsteeg, EJ; Kok, F; Leuzzi, V; Megarbane, A; Monaghan, H; Renier, WO; Rondot, P; Ryan, MM; Seeger, J; Smeitink, JA; Steenbergen-Spanjers, GC; van der Knaap, MS; Verbeek, MM; Wassmer, E; Weschke, B; Wevers, RA; Wijburg, FA; Wilcken, B; Willemsen, MA; Zafeiriou, DI1
Assmann, B; Bräutigam, C; de Klerk, JB; Dionisi-Vici, C; Häussler, M; Hoffmann, GF; Naumann, M; Steenbergen-Spanjers, GC; Strassburg, HM; Wevers, RA1
Fahn, S; Furukawa, Y; Kish, SJ1
Hanley, WB; Kapatos, G; Kaufman, S; MacGregor, D; McInnes, RR; Milstien, S; Soldin, S; Van Loon, GR; Walsh, P; Warsh, JJ1
Kodama, H; Okabe, I; Shimoizumi, H; Yanagisawa, M1
Bräutigam, C; Hoffman, GF; Hyland, K; Knust, A; Sharma, RK; Wevers, RA1
Abeling, NG; Billatte de Villemeur, T; Cretz, M; DE Lonlay, P; Launay, JM; Nassogne, MC; Saudubray, JM; Steenberger-Spante, GC; Stoll, C; van Cruchten, AC; van den Heuvel, LP; van Gennip, AH; Wevers, RA1
berger, H; jarosch, E; Ludescher, E1

Other Studies

12 other study(ies) available for levodopa and Amino Acid Metabolism Disorders, Inborn

ArticleYear
Aromatic l-amino acid decarboxylase deficiency: a patient-derived neuronal model for precision therapies.
    Brain : a journal of neurology, 2021, 09-04, Volume: 144, Issue:8

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Dopamine Agents; Humans; Induced Pluripotent Stem Cells; Levodopa; Neurogenesis; Neurons

2021
Detection of 3-O-methyldopa in dried blood spots for neonatal diagnosis of aromatic L-amino-acid decarboxylase deficiency: The northeastern Italian experience.
    Molecular genetics and metabolism, 2021, Volume: 133, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Dopamine; Female; Humans; Infant, Newborn; Italy; Levodopa; Male; Neonatal Screening; Neurotransmitter Agents; Tandem Mass Spectrometry; Tyrosine

2021
Clinical Metabolomics to Segregate Aromatic Amino Acid Decarboxylase Deficiency From Drug-Induced Metabolite Elevations.
    Pediatric neurology, 2017, Volume: 75

    Topics: Amino Acid Metabolism, Inborn Errors; Aromatic-L-Amino-Acid Decarboxylases; Carbidopa; Child; Child, Preschool; Cohort Studies; Dopamine; Dopamine Agonists; Drug Combinations; Edetic Acid; Female; Humans; Infant; Levodopa; Male; Metabolic Networks and Pathways; Metabolomics; Vanilmandelic Acid

2017
A pathogenic S250F missense mutation results in a mouse model of mild aromatic l-amino acid decarboxylase (AADC) deficiency.
    Human molecular genetics, 2017, 11-15, Volume: 26, Issue:22

    Topics: Amino Acid Metabolism, Inborn Errors; Animals; Aromatic-L-Amino-Acid Decarboxylases; Corpus Striatum; Disease Models, Animal; Dopamine; Female; Genetic Therapy; Humans; Levodopa; Male; Mice; Mutation, Missense; Neostriatum; Parkinson Disease; Polymorphism, Single Nucleotide; Serotonin; Substantia Nigra

2017
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, Preschool; Disease Progression; Dopamine Agents; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Hypokinesia; Infant; Levodopa; Muscle Rigidity; Mutation, Missense; Phenotype; Promoter Regions, Genetic; Severity of Illness Index; Tyrosine 3-Monooxygenase

2010
Tyrosine hydroxylase deficiency causes progressive encephalopathy and dopa-nonresponsive dystonia.
    Annals of neurology, 2003, Volume: 54 Suppl 6

    Topics: Amino Acid Metabolism, Inborn Errors; Biogenic Monoamines; Brain Diseases, Metabolic; Child; Child, Preschool; Chromatography, High Pressure Liquid; Dopamine Agents; Dystonia; Female; Humans; Infant; Levodopa; Male; Mutation; Neurotransmitter Agents; Polymorphism, Genetic; Terminology as Topic; Tyrosine 3-Monooxygenase

2003
Dopa-responsive dystonia due to mild tyrosine hydroxylase deficiency.
    Annals of neurology, 2004, Volume: 55, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Diseases, Metabolic; Dystonia; GTP Cyclohydrolase; Humans; Levodopa; Male; Mutation; Phenotype; Tyrosine 3-Monooxygenase

2004
Biopterin synthesis defect. Treatment with L-dopa and 5-hydroxytryptophan compared with therapy with a tetrahydropterin.
    The Journal of clinical investigation, 1984, Volume: 73, Issue:2

    Topics: 5-Hydroxytryptophan; Amino Acid Metabolism, Inborn Errors; Biopterins; Carbidopa; Catecholamines; Dose-Response Relationship, Drug; Female; Humans; Infant; Levodopa; Neopterin; Neurotransmitter Agents; Pteridines; Pterins

1984
[Methylmalonic acidemia with bilateral MRI high intensities of the globus pallidus].
    No to hattatsu = Brain and development, 1993, Volume: 25, Issue:6

    Topics: Amino Acid Metabolism, Inborn Errors; Child; Dystonia; Female; Globus Pallidus; Humans; Levodopa; Magnetic Resonance Imaging; Methylmalonic Acid

1993
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 Acid; Humans; Hydroxyindoleacetic Acid; Hypokinesia; Levodopa; Methoxyhydroxyphenylglycol; Methylation; Muscle Hypotonia; Tetrahydrofolates; Tyrosine

2000
Tyrosine hydroxylase deficiency unresponsive to L-dopa treatment with unusual clinical and biochemical presentation.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:8

    Topics: Amino Acid Metabolism, Inborn Errors; Child, Preschool; Dopamine Agents; Epilepsy, Generalized; Humans; Levodopa; Male; Muscle Hypotonia; Treatment Failure; Tyrosine 3-Monooxygenase

2000
[Disturbance of the Histidine Reabsorption of the Renal Tubes in Patient with Cystine Lysinuria in Conjunction with Severe Cerebral Damage (author's transl)].
    Padiatrie und Padologie, 1975, Volume: 10, Issue:1

    Topics: Amino Acid Metabolism, Inborn Errors; Brain Damage, Chronic; Child; Cystinuria; Histidine; Humans; Intellectual Disability; Kidney Tubules; Levodopa; Lysine; Male; Parkinson Disease

1975