List of bibliographic references
Number of relevant bibliographic references: 27.
[20-40] [
0 - 20][
0 - 27]
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 18 | Humans |
| 11 | Female |
| 11 | Middle Aged |
| 11 | Nervous system diseases |
| 10 | Male |
| 9 | Adult |
| 8 | Aged |
| 7 | Human |
| 6 | DNA Mutational Analysis |
| 6 | Mutation |
| 5 | Genotype |
| 5 | Parkinson disease |
| 4 | Family Health |
| 4 | Parkinsonian Disorders (genetics) |
| 4 | Parkinsonism |
| 4 | Severity of Illness Index |
| 4 | Ubiquitin-Protein Ligases (genetics) |
| 4 | Young Adult |
| 3 | Adolescent |
| 3 | Follow-Up Studies |
| 3 | Gene |
| 3 | Gene Frequency |
| 3 | Genetics, Population |
| 3 | Mutation (genetics) |
| 3 | Parkin |
| 3 | Parkinson Disease (genetics) |
| 2 | Antiparkinson Agents (therapeutic use) |
| 2 | Brazil |
| 2 | Case-Control Studies |
| 2 | Chi-Square Distribution |
| 2 | Deep brain stimulation |
| 2 | Disability Evaluation |
| 2 | Family study |
| 2 | Genetic Linkage |
| 2 | Genetic Predisposition to Disease (genetics) |
| 2 | Genetic determinism |
| 2 | Haplotypes |
| 2 | Levodopa (therapeutic use) |
| 2 | Lod Score |
| 2 | Magnetic Resonance Imaging |
| 2 | Parkinson Disease (epidemiology) |
| 2 | Parkinson's disease |
| 2 | Parkinsonian Disorders (therapy) |
| 2 | Pedigree |
| 2 | Phenotype |
| 2 | Polymorphism, Single Nucleotide (genetics) |
| 2 | Protein-Serine-Threonine Kinases (genetics) |
| 2 | Retrospective Studies |
| 2 | Spinocerebellar Ataxias (diagnosis) |
| 2 | deep brain stimulation |
| 1 | 14q22–q24 |
| 1 | Age of Onset |
| 1 | Aged, 80 and over |
| 1 | Alleles |
| 1 | Analysis of Variance |
| 1 | Anticipation, Genetic |
| 1 | Antiparkinson Agents (adverse effects) |
| 1 | Aspartic Acid (genetics) |
| 1 | Ataxia |
| 1 | Autosomal character |
| 1 | Basal Ganglia (pathology) |
| 1 | Basal Ganglia (physiopathology) |
| 1 | Brain Mapping (methods) |
| 1 | CYP2D6 polymorphism |
| 1 | Carbonyl Cyanide m-Chlorophenyl Hydrazone (pharmacology) |
| 1 | Cerebellar ataxia |
| 1 | Cerebellum (pathology) |
| 1 | Cerebellum (physiopathology) |
| 1 | Cerebral Cortex (pathology) |
| 1 | Cerebral Cortex (physiopathology) |
| 1 | Child |
| 1 | Child, Preschool |
| 1 | Chromosome Aberrations |
| 1 | Chromosome Mapping |
| 1 | Chromosomes, Human, Pair 14 (genetics) |
| 1 | Chromosomes, Human, Pair 16 |
| 1 | Chromosomes, Human, Pair 3 (genetics) |
| 1 | Corpus callosum |
| 1 | Cytochrome P-450 CYP2D6 (genetics) |
| 1 | Cytochrome P450 |
| 1 | DYT1 |
| 1 | Deep Brain Stimulation |
| 1 | Deep Brain Stimulation (methods) |
| 1 | Disease Progression |
| 1 | Dyskinesia, Drug-Induced |
| 1 | Dystonia |
| 1 | Dystonic Disorders (genetics) |
| 1 | Epidemiology |
| 1 | Essential |
| 1 | Essential Tremor (genetics) |
| 1 | Europe |
| 1 | European Continental Ancestry Group |
| 1 | European Continental Ancestry Group (genetics) |
| 1 | Evaluation scale |
| 1 | Evolution |
| 1 | Exons (genetics) |
| 1 | Exploration |
| 1 | France |
| 1 | France (epidemiology) |
| 1 | France (ethnology) |
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