levodopa has been researched along with Autosomal Chromosome Disorders in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 10 (76.92) | 18.2507 |
| 2000's | 3 (23.08) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Hattori, N; Miyazato, Y; Namihira, T; Shiroma, S | 1 |
| Brown, L; Dickson, D; Farrer, M; Skipper, L; Solida, A; Vingerhoets, FJ; Wider, C; Wszolek, ZK | 1 |
| Gök, F; Gökçay, E; Gül, D; Sayli, BS | 1 |
| Ishikawa, A; Miyatake, T | 1 |
| Nygaard, TG | 1 |
| Furukawa, Y; Mizuno, Y; Narabayashi, H; Nishi, K | 1 |
| Dasouki, M; Hiari, M; Mubaidin, A; Najim al-Din, AS; Wriekat, A | 1 |
| Chutorian, A | 1 |
| Heberlein, I; Müller, U; Nitschke, M; Otto, V; Steinberger, D; Vieregge, P | 1 |
| Perlmutter, JS; Racette, BA | 1 |
| Bergamaschi, R; Cacciari, E; Cicognani, A; Gualandi, S; Mazzanti, L; Nanni, S; Perri, A; Pirazzoli, P; Scarano, E; Zucchini, S | 1 |
| Calne, DB; Dobko, T; Mak, E; Markopoulou, K; Samii, A; Sossi, V; Stoessl, AJ; Wszolek, ZK | 1 |
| Ko, CH; Kong, CK; Lam, CW; Tong, SF | 1 |
2 review(s) available for levodopa and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Dopa-responsive dystonia.
Topics: Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Corpus Striatum; Diagnosis, Differential; DNA Mutational Analysis; Dystonia; Genes, Dominant; GTP Cyclohydrolase; Humans; Infant; Levodopa; Neural Pathways; Parkinson Disease, Secondary; Phenotype; Spinal Cord; Substantia Nigra | 1995 |
[Parkinsonian syndromes in children].
Topics: Adolescent; Adult; Child; Chromosome Aberrations; Chromosome Disorders; Humans; Levodopa; Parkinson Disease | 1997 |
11 other study(ies) available for levodopa and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Autosomal recessive juvenile Parkinson's disease with partial trisomy of chromosome 6q syndrome: a case report.
Topics: Adult; Antiparkinson Agents; Chromosome Disorders; Chromosomes, Human, Pair 6; Humans; Levodopa; Male; Parkinson Disease; Trisomy | 2004 |
Autosomal dominant dopa-responsive parkinsonism in a multigenerational Swiss family.
Topics: Adult; Aged; Antiparkinson Agents; Brain; Chromosome Disorders; Dihydroxyphenylalanine; DNA Mutational Analysis; Female; Genes, Dominant; Humans; Levodopa; Male; Middle Aged; Mutation; Parkinson Disease; Pedigree; Phenotype; Positron-Emission Tomography; Radiopharmaceuticals | 2008 |
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 |
A family with hereditary juvenile dystonia-parkinsonism.
Topics: Adult; Aged; Antiparkinson Agents; Chromosome Aberrations; Chromosome Disorders; Dystonia; Female; Follow-Up Studies; Genes, Dominant; Homovanillic Acid; Humans; Levodopa; Male; Middle Aged; Neurologic Examination; Parkinson Disease; Pedigree; Torticollis | 1995 |
A clue to the pathogenesis of dopa-responsive dystonia.
Topics: Biopterins; Chromosome Aberrations; Chromosome Disorders; Corpus Striatum; Dopamine; Dystonia; Humans; Levodopa; Neopterin; Tyrosine 3-Monooxygenase | 1995 |
Pallido-pyramidal degeneration, supranuclear upgaze paresis and dementia: Kufor-Rakeb syndrome.
Topics: Adolescent; Adult; Brain Diseases; Carbidopa; Child; Chromosome Aberrations; Chromosome Disorders; Consanguinity; Dementia; Electromyography; Extrapyramidal Tracts; Female; Globus Pallidus; Humans; Immobilization; Levodopa; Magnetic Resonance Imaging; Male; Pedigree; Syndrome | 1994 |
Dopa responsive dystonia with Turner's syndrome: clinical, genetic, and neuropsychological studies in a family with a new mutation in the GTP-cyclohydrolase I gene.
Topics: Adult; Antiparkinson Agents; Brain; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 14; Cognition Disorders; Dystonia; Exons; Female; GTP Cyclohydrolase; Humans; Levodopa; Magnetic Resonance Imaging; Middle Aged; Neuropsychological Tests; Pedigree; Point Mutation; Turner Syndrome | 1998 |
Levodopa responsive parkinsonism in an adult with Huntington's disease.
Topics: Adult; Antiparkinson Agents; Chromosome Aberrations; Chromosome Disorders; Chromosomes, Human, Pair 4; Humans; Huntington Disease; Levodopa; Male; Pedigree | 1998 |
Reduced spontaneous growth hormone secretion in patients with Turner's syndrome.
Topics: Adolescent; Age Determination by Skeleton; Child; Child, Preschool; Chromosome Aberrations; Chromosome Disorders; Dopamine Agents; Down Syndrome; Electronic Data Processing; Female; Growth Disorders; Human Growth Hormone; Humans; Karyotyping; Levodopa; Male; Radioimmunoassay; Turner Syndrome; X Chromosome | 1999 |
PET studies of parkinsonism associated with mutation in the alpha-synuclein gene.
Topics: Adult; alpha-Synuclein; Antiparkinson Agents; Brain Mapping; Caudate Nucleus; Chromosome Aberrations; Chromosome Disorders; Female; Gene Expression; Genes, Dominant; Greece; Humans; Levodopa; Male; Middle Aged; Mutation; Nerve Tissue Proteins; Parkinson Disease; Pedigree; Phosphoproteins; Putamen; Receptors, Dopamine; Synucleins; Tomography, Emission-Computed; United States | 1999 |
Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness.
Topics: Carbidopa; Child; Chromosome Aberrations; Chromosome Disorders; Circadian Rhythm; Drug Combinations; Dystonic Disorders; Gait; Genes, Dominant; GTP Cyclohydrolase; Humans; Levodopa; Male; Muscle Hypotonia; Muscle Weakness; Neurologic Examination; Point Mutation; Treatment Outcome | 2001 |