levodopa has been researched along with Developmental Disabilities in 11 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (27.27) | 18.2507 |
| 2000's | 4 (36.36) | 29.6817 |
| 2010's | 2 (18.18) | 24.3611 |
| 2020's | 2 (18.18) | 2.80 |
| Authors | Studies |
|---|---|
| Emrick, L; Hull, M; Parnes, M; Sadat, R | 1 |
| Janssen, E; Nicolai, J; Oosterloo, M; Rubio-Gozalbo, E; van Gassen, K | 1 |
| Blau, N; Dill, P; Somerville, A; Thöny, B; Wagner, M; Weber, P | 1 |
| Ohwada, M; Shintaku, H | 1 |
| 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 |
| Farrugia, R; Felice, A; Neville, BG; Parascandalo, R | 1 |
| Gök, F; Gökçay, E; Gül, D; Sayli, BS | 1 |
| Biaggioni, I; Butler, IJ; Hyland, K; Maller, A; Milstien, S | 1 |
| Dhondt, JL; Mikaeloff, Y; Pinton, F; Ponsot, G; Sevin, C | 1 |
| Earl, J; Fung, VS; Grattan-Smith, PJ; Steenbergen-Spanjers, GC; Wevers, RA; Wilcken, B | 1 |
11 other study(ies) available for levodopa and Developmental Disabilities
| Article | Year |
|---|---|
A case of treatable encephalopathy, developmental regression, and proximal tremor.
Topics: Brain Diseases; Developmental Disabilities; Dystonic Disorders; Humans; Infant; Levodopa; Male; Treatment Outcome; Tremor | 2021 |
Teaching Video NeuroImage: Improvement in Motor Development After Start of Levodopa in Tyrosine Hydroxylase Deficiency.
Topics: Developmental Disabilities; Dopamine Agents; Dystonic Disorders; Exome; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Infant; Levodopa; Male; Mutation; Treatment Outcome | 2021 |
Child neurology: paroxysmal stiffening, upward gaze, and hypotonia: hallmarks of sepiapterin reductase deficiency.
Topics: 5-Hydroxytryptophan; Alcohol Oxidoreductases; Behavior; Benserazide; Consanguinity; Developmental Disabilities; Dopamine Agents; Drug Combinations; Eye Movements; Female; Humans; Infant; Levodopa; Movement Disorders; Muscle Hypotonia; Nervous System Diseases; Neurotransmitter Agents; Phenylketonurias; Treatment Outcome | 2012 |
Long-term follow-up of tetrahydrobiopterin therapy in patients with tetrahydrobiopterin deficiency in Japan.
Topics: Adolescent; Adult; Biopterins; Child; Child, Preschool; Developmental Disabilities; Dopamine Agents; Drug Therapy, Combination; Female; Humans; Japan; Levodopa; Longitudinal Studies; Male; Phenylketonurias; Product Surveillance, Postmarketing; Retrospective Studies; Young Adult | 2013 |
Levodopa-responsive aromatic L-amino acid decarboxylase deficiency.
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.
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 |
Sepiapterin reductase deficiency: a congenital dopa-responsive motor and cognitive disorder.
Topics: Adolescent; Alcohol Oxidoreductases; Cerebral Palsy; Child; Child, Preschool; Circadian Rhythm; Cognition Disorders; Developmental Disabilities; Dopamine Agents; Dyskinesias; Female; Genotype; Humans; Levodopa; Male; Motor Activity; Movement Disorders | 2005 |
IgA deficiency associated with growth hormone deficiency in a boy with short arm deletion of chromosome 18 (46,XY,18p-).
Topics: Arginine; Child; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 18; Developmental Disabilities; Dwarfism, Pituitary; Growth Hormone; Humans; IgA Deficiency; Insulin; Intellectual Disability; Levodopa; Male; Pituitary Function Tests; Propranolol; Sequence Deletion | 1994 |
Aromatic L-amino acid decarboxylase deficiency: clinical features, diagnosis, and treatment of a second family.
Topics: 5-Hydroxytryptophan; Amino Acids, Cyclic; Aromatic-L-Amino-Acid Decarboxylases; Biogenic Monoamines; Child, Preschool; Consanguinity; Developmental Disabilities; Homovanillic Acid; Humans; Hydroxyindoleacetic Acid; Iran; Levodopa; Longitudinal Studies; Male; Methoxyhydroxyphenylglycol; Muscle Hypotonia; Pyridoxine | 1997 |
[Progressive convulsive encephalopathy: considering a abnormality of biopterin metabolism].
Topics: 5-Hydroxytryptophan; Algeria; Anticonvulsants; Biopterins; Brain; Child, Preschool; Consanguinity; Developmental Disabilities; Diet Therapy; Epilepsy; France; Humans; Levodopa; Magnetic Resonance Imaging; Male; Neopterin; Phenylalanine; Phenylketonurias | 1999 |
Tyrosine hydroxylase deficiency: clinical manifestations of catecholamine insufficiency in infancy.
Topics: Consanguinity; Developmental Disabilities; Dopamine; Female; Follow-Up Studies; Humans; Infant; Levodopa; Neurologic Examination; Norepinephrine; Parkinsonian Disorders; Tremor; Tyrosine 3-Monooxygenase | 2002 |