carbidopa and Developmental Disabilities

carbidopa has been researched along with Developmental Disabilities in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	3 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bedell, JA; Bräutigam, C; Chang, YT; Hoffmann, GF; Hyland, K; Knust, A; Marsh, JL; McPherson, JD; Sharma, R	1
Blau, N; Connolly, MB; Demos, MK; Hyland, K; Lillquist, Y; Makhseed, N; Vallance, HD; Waters, PJ	1
Abeling, N; Bergmann, C; Blau, N; Häring, M; Häusler, M; Heimann, G; Ramaekers, VT; Senderek, J; Zerres, K	1

Trials

1 trial(s) available for carbidopa and Developmental Disabilities

Article	Year
A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa. Molecular genetics and metabolism, 2001, Volume: 73, Issue:2 Topics: 5-Hydroxytryptophan; Abnormalities, Multiple; Carbidopa; Child; Child, Preschool; Developmental Disabilities; DNA; DNA Mutational Analysis; Drug Therapy, Combination; Follow-Up Studies; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; Learning Disabilities; Male; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Syndrome; Tetrahydrofolates; Treatment Outcome; Tryptophan Hydroxylase	2001

Article

Year

A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopa.

Molecular genetics and metabolism, 2001, Volume: 73, Issue:2

Topics: 5-Hydroxytryptophan; Abnormalities, Multiple; Carbidopa; Child; Child, Preschool; Developmental Disabilities; DNA; DNA Mutational Analysis; Drug Therapy, Combination; Follow-Up Studies; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; Learning Disabilities; Male; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Oxidoreductases Acting on CH-NH Group Donors; Syndrome; Tetrahydrofolates; Treatment Outcome; Tryptophan Hydroxylase

2001

Other Studies

2 other study(ies) available for carbidopa and Developmental Disabilities

Article	Year
Levodopa-responsive aromatic L-amino acid decarboxylase deficiency. Annals of neurology, 2004, Volume: 55, Issue:3 Topics: Adolescent; Adult; Alanine; Antiparkinson Agents; Aromatic-L-Amino-Acid Decarboxylases; Binding Sites; Carbidopa; Chromatography, High Pressure Liquid; Developmental Disabilities; DNA Mutational Analysis; Drug Combinations; Electrochemistry; Family Health; Female; Glycine; Humans; Levodopa; Male; Models, Structural; Point Mutation; Protein Binding; Protein Conformation	2004
6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia. Annals of neurology, 2005, Volume: 58, Issue:1 Topics: 5-Hydroxytryptophan; Biopterins; Carbidopa; Cerebral Palsy; Child; Developmental Disabilities; Diagnostic Errors; Dopamine Agents; Female; Humans; Levodopa; Movement Disorders; Phenylalanine; Phenylketonurias; Phosphorus-Oxygen Lyases; Seizures	2005

Article

Year

Levodopa-responsive aromatic L-amino acid decarboxylase deficiency.

Annals of neurology, 2004, Volume: 55, Issue:3

Topics: Adolescent; Adult; Alanine; Antiparkinson Agents; Aromatic-L-Amino-Acid Decarboxylases; Binding Sites; Carbidopa; Chromatography, High Pressure Liquid; Developmental Disabilities; DNA Mutational Analysis; Drug Combinations; Electrochemistry; Family Health; Female; Glycine; Humans; Levodopa; Male; Models, Structural; Point Mutation; Protein Binding; Protein Conformation

2004

6-pyruvoyl-tetrahydropterin synthase deficiency with mild hyperphenylalaninemia.

Annals of neurology, 2005, Volume: 58, Issue:1

Topics: 5-Hydroxytryptophan; Biopterins; Carbidopa; Cerebral Palsy; Child; Developmental Disabilities; Diagnostic Errors; Dopamine Agents; Female; Humans; Levodopa; Movement Disorders; Phenylalanine; Phenylketonurias; Phosphorus-Oxygen Lyases; Seizures

2005