Table 2.
Overview of number of articles per movement disorder and diagnosis
| Movement disorder | Number of articles | Diagnosis (number of articles) |
|---|---|---|
| Tremor | 8 | Essential tremor (7) |
| Orthostatic tremor (1) | ||
| Tics | 6 | Tourette syndrome (6) |
| Dystonia | 20 | Essential blepharospasm (5) |
| DYT-TOR1A (5) | ||
| DYT-THAP1 (3) | ||
| Idiopathic cervical dystonia (3) | ||
| Dopa-responsive dystonia (2) | ||
| DYT-SGCE (1) | ||
| Neurodegeneration with brain iron accumulation (1) | ||
| Meige syndrome (1) | ||
| Focal, segmental, and/or generalized dystonia (4) | ||
| (Tardive dyskinesia in schizophrenic patients (1)) | ||
| Ataxia | 25 | Spinocerebellar ataxia (13) |
| Olivopontocerebellar atrophy (7) | ||
| Multi system atrophy of the cerebellar type (4) | ||
| Late cerebellar cortical atrophy (1) | ||
| Ataxia-telangietactasia (1) | ||
| Holmes type hereditary ataxia (1) | ||
| Not further specified cerebellar ataxia (1) | ||
| (Ataxia in patients with cryptogenic tonic–clonic seizures from infancy (1)) | ||
| Chorea | 27 | Huntington’s disease (27) |
| Chorea-acanthocytosis (1) | ||
| Myoclonus | 6 | Juvenile myoclonus epilepsy (3) |
| Lafora disease (1) | ||
| Myoclonus after a cardiac arrest (1) | ||
| Myoclonus epilepsy with ragged red fibres (1) | ||
| Functional disorder | 0 | |
| Metabolic disease | 7 | Wilson’s disease (3) |
| Niemann–Pick disease type C (1) | ||
| Salla disease (1) | ||
| Gluteric aciduria (1) | ||
| Galactosemia (1) | ||
| Autoimmune disorder | 5 | LGI1-antibody encephalitis (2) |
| Fisher’s syndrome (1) | ||
| NMDA-ab encephalitis (1) | ||
| Stiff person syndrome or cerebellar ataxia associated with anti-GAD65 antibodies (1) |