levodopa has been researched along with Spastic Paraplegia, Hereditary in 10 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 2 (20.00) | 18.2507 |
| 2000's | 3 (30.00) | 29.6817 |
| 2010's | 4 (40.00) | 24.3611 |
| 2020's | 1 (10.00) | 2.80 |
| Authors | Studies |
|---|---|
| Dupré, N; Estiar, MA; Gan-Or, Z; Leveille, E; Rouleau, GA; Trempe, JF; Varghaei, P; Veyron, S; Yoon, G | 1 |
| Bettencourt, C; Hardy, J; Houlden, H; Morris, HR; Singleton, AB | 1 |
| Berg, J; Crooks, K; Evans, J; Fan, Z; Felix, AC; Greenwood, R; Roche, M; Shiloh-Malawsky, Y; Tennison, M; Weck, K; Wilhelmsen, K | 1 |
| Bentivoglio, AR; Guidubaldi, A; Petracca, M; Piano, C; Santorelli, FM; Silvestri, G; Tessa, A | 1 |
| Everett, CM; Houlden, H; Kara, E; Maresh, KE | 1 |
| Jan, MM | 1 |
| Kang, SY; Lee, MH; Lee, SK; Sohn, YH | 1 |
| Cersósimo, MG; Micheli, F; Zúñiga Ramírez, C | 1 |
| Quinn, NP | 1 |
| Malyshev, IuI | 1 |
1 review(s) available for levodopa and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
Misdiagnoses in children with dopa-responsive dystonia.
Topics: Adolescent; Cerebral Palsy; Child; Child, Preschool; Diagnostic Errors; Dopamine Agents; Dystonia; Epilepsy; Female; Humans; Levodopa; Male; Spastic Paraplegia, Hereditary | 2004 |
9 other study(ies) available for levodopa and Spastic Paraplegia, Hereditary
| Article | Year |
|---|---|
GCH1 mutations in hereditary spastic paraplegia.
Topics: Adult; Canada; Child; Female; GTP Cyclohydrolase; Humans; Levodopa; Male; Middle Aged; Mutation; Parkinsonian Disorders; Pedigree; Phenotype; Spastic Paraplegia, Hereditary; Twins, Monozygotic | 2021 |
Exome sequencing expands the mutational spectrum of SPG8 in a family with spasticity responsive to L-DOPA treatment.
Topics: Adult; Age of Onset; Amino Acid Sequence; Base Sequence; Child; DNA Mutational Analysis; Dopamine Agents; Exome; Female; Humans; Levodopa; Male; Molecular Sequence Data; Muscle Spasticity; Mutation, Missense; Paraplegia; Pedigree; Proteins; Spastic Paraplegia, Hereditary | 2013 |
GCH1 heterozygous mutation identified by whole-exome sequencing as a treatable condition in a patient presenting with progressive spastic paraplegia.
Topics: Adult; Carbidopa; Codon, Nonsense; Dopamine Agonists; Drug Combinations; Dystonic Disorders; Exome; Female; GTP Cyclohydrolase; Heterozygote; Humans; Levodopa; Phenotype; Sequence Analysis, DNA; Spastic Paraplegia, Hereditary; Treatment Outcome | 2014 |
Novel mutations in SPG11 cause hereditary spastic paraplegia associated with early-onset levodopa-responsive Parkinsonism.
Topics: Adult; Antiparkinson Agents; Female; Genome-Wide Association Study; Humans; Levodopa; Magnetic Resonance Imaging; Mutation; Parkinson Disease; Proteins; Spastic Paraplegia, Hereditary | 2011 |
Clinical variability and L-Dopa responsive Parkinsonism in hereditary spastic paraplegia 11.
Topics: Adult; Humans; Levodopa; Male; Parkinsonian Disorders; Pedigree; Spastic Paraplegia, Hereditary | 2012 |
Levodopa-responsive parkinsonism in hereditary spastic paraplegia with thin corpus callosum.
Topics: Adolescent; Antiparkinson Agents; Benztropine; Cognition Disorders; Corpus Callosum; Electroencephalography; Female; Gait Disorders, Neurologic; Humans; Levodopa; Magnetic Resonance Imaging; Male; Muscle Weakness; Neuropsychological Tests; Parkinson Disease; Selegiline; Spastic Paraplegia, Hereditary; Tremor | 2004 |
Hereditary spastic paraplegia associated with dopa-responsive parkinsonism.
Topics: Antiparkinson Agents; Follow-Up Studies; Humans; Levodopa; Male; Middle Aged; Parkinson Disease; Spastic Paraplegia, Hereditary | 2006 |
Dopa-responsive dystonia.
Topics: Child; Dystonia; Genes, Dominant; Humans; Levodopa; Spastic Paraplegia, Hereditary | 1991 |
[Problems of diagnosis and treatment of deforming muscular dystrophy in children].
Topics: Child; Diagnosis, Differential; Drug Therapy, Combination; Haloperidol; Hand Deformities, Acquired; Humans; Hyperkinesis; Levodopa; Muscle Hypertonia; Muscular Dystrophies; Spastic Paraplegia, Hereditary | 1990 |