List of bibliographic references
Number of relevant bibliographic references: 14.
List of associated KwdEn.i
Nombre de
documents | Descripteur |
|---|
| 12 | Humans |
| 10 | Nervous system diseases |
| 8 | Middle Aged |
| 7 | Female |
| 6 | Male |
| 6 | Parkinson disease |
| 6 | Rapid eye movement sleep |
| 6 | Sleep disorder |
| 5 | Aged |
| 4 | Adult |
| 4 | Behavior |
| 4 | Parkinson's disease |
| 4 | Restless legs syndrome |
| 4 | restless legs syndrome |
| 3 | Parkinson Disease (complications) |
| 3 | Parkinson Disease (physiopathology) |
| 3 | Polysomnography |
| 3 | Restless Legs Syndrome (genetics) |
| 3 | sleep |
| 2 | Case-Control Studies |
| 2 | Diagnosis |
| 2 | Electrodes, Implanted |
| 2 | Parkinson Disease (therapy) |
| 2 | Psychiatric Status Rating Scales |
| 2 | REM Sleep Behavior Disorder (complications) |
| 2 | REM Sleep Behavior Disorder (diagnosis) |
| 2 | REM Sleep Behavior Disorder (physiopathology) |
| 2 | REM sleep behavior disorder |
| 2 | Severity of Illness Index |
| 2 | Sleep |
| 2 | genetics |
| 1 | Adolescent |
| 1 | Aged, 80 and over |
| 1 | Antiparkinson Agents (administration & dosage) |
| 1 | Antiparkinson Agents (adverse effects) |
| 1 | Arm |
| 1 | Atonia |
| 1 | Behavioral disorder |
| 1 | Care |
| 1 | Chromosomes, Human, Pair 12 (genetics) |
| 1 | Chromosomes, Human, Pair 14 (genetics) |
| 1 | Chromosomes, Human, Pair 9 (genetics) |
| 1 | Cognition Disorders (complications) |
| 1 | Cognition Disorders (physiopathology) |
| 1 | Confidence Intervals |
| 1 | Dementia |
| 1 | Dementia (complications) |
| 1 | Dementia (epidemiology) |
| 1 | Dementia (physiopathology) |
| 1 | Diagnosis, Differential |
| 1 | Disorders of Excessive Somnolence (genetics) |
| 1 | Dorsal spine |
| 1 | Dyskinesia, Drug-Induced (physiopathology) |
| 1 | Dyskinesia, Drug-Induced (therapy) |
| 1 | Electric Stimulation (adverse effects) |
| 1 | Electric Stimulation Therapy |
| 1 | Electrical stimulus |
| 1 | Electroencephalography |
| 1 | Epidemiology |
| 1 | Essential |
| 1 | Europe (epidemiology) |
| 1 | Family study |
| 1 | France (epidemiology) |
| 1 | Frontal Lobe (physiopathology) |
| 1 | Functional Laterality |
| 1 | Gene Frequency (genetics) |
| 1 | Genetic Linkage |
| 1 | Genetic Markers |
| 1 | Genetic Predisposition to Disease |
| 1 | Genetic disease |
| 1 | Genotype |
| 1 | Globus Pallidus (anatomy & histology) |
| 1 | Globus Pallidus (physiopathology) |
| 1 | Haplotypes |
| 1 | Human |
| 1 | Hypersomnia |
| 1 | Inheritance Patterns |
| 1 | Instrumentation therapy |
| 1 | International Cooperation |
| 1 | Kyphosis |
| 1 | Levodopa (administration & dosage) |
| 1 | Levodopa (adverse effects) |
| 1 | Linkage Disequilibrium (genetics) |
| 1 | Logistic Models |
| 1 | Longitudinal Studies |
| 1 | Low frequency |
| 1 | Mass Screening |
| 1 | Medical screening |
| 1 | Mental Status Schedule |
| 1 | Motor system disorder |
| 1 | Movement Disorders (diagnosis) |
| 1 | Movement Disorders (etiology) |
| 1 | Multicenter study |
| 1 | Muscle, Skeletal (physiopathology) |
| 1 | Mutation |
| 1 | Mutation (genetics) |
| 1 | Myoclonus |
| 1 | Myoclonus (etiology) |
| 1 | Myoclonus (physiopathology) |
| 1 | Narcolepsy |
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