Movement Disorders: A Video Atlas

<p>Foreward:  Stanley Fahn</p><p>Introduction</p><p>Section I.  Parkinsonism and related disorders</p><p>1.  Examination of a patient with Parkinson’s disease<br>2.  Parkinson’s disease: Hoehn &amp; Yahr Staging <br>3.  Young Onset Parkinson’s Disease<br>4.  Tremor Dominant Parkinson’s disease<br>5.  Parkinson’s disease: Levodopa-induced dyskinesia<br>6.  Parkinson’s disease: Diphasic dyskinesia<br>7.  Parkinson’s disease: The On-Off phenomeneon<br>8.  Parkinson’s disease: Freezing of gait<br>9.  Parkinsonism with Pisa syndrome<br>10.  Parkinson’s disease with camptocormia<br>11.  Apathy in Parkinson’s disease<br>12.  Punding in Parkinson’s disease<br>13.  Parkinson’s disease due to PARK2<br>14.  Parkinson’s disease treated with deep brain stimulation <br>15.  Multiple System Atrophy<br>16.  Progressive Supranuclear Palsy<br>17.  Progressive Supranuclear Palsy with apraxia of eyelid opening<br>18.  Vascular parkinsonism<br>19.  Corticobasal degeneration<br>20.  Drug-induced parkinsonism<br>21.  Toxin-induced parkinsonism<br>22.  HIV-induced parkinsonism</p><p>Section II. Tremor</p><p>1. Examination of patients with essential tremor<br>2. Parkinsonian rest, postural, and re-emergent tremor<br>3. Essential tremor: Voice and head tremor<br>4. Cerebellar tremor<br>5. Holmes midbrain tremor<br>6. Wilson’s Disease with wingbeating tremor<br>7. Primary writing tremor<br>8. Orthostatic tremor<br>9. Hyperthyroid tremor<br>10. Drug-induced tremor<br>11. Dystonic tremor<br>12. Neuropathic tremor<br>13. Psychogenic tremor</p><p>Section III. Dystonia</p><p>1. Examination of a patient with non-DYT1 generalized dystonia <br>2. DYT1 generalized dystonia<br>3. Segmental dystonia treated with deep brain stimulation<br>4. Cervical dystonia: Rotational torticollis<br/>5. Cervical dystonia: Torticollis with dystonic head tremor6. Cervical dystonia: Anterocollis<br>7. Cervical dystonia: Retrocollis<br>8. Cervical dystonia: Sensory tricks<br>9. Secondary cervical dystonia following brainstem hemorrhage<br>10. Secondary hemidystonia following head trauma<br>11. Essential blepharospasm<br>12. Orofacial dystonia and dyskinesia<br>13. Orofacial dystonia with lower facial and platysma dystonia<br>14. Meige syndrome<br>15. Tongue protrusion dystonia<br>16. Spasmodic (laryngeal) dystonia<br>17. Writer’s cramp<br>18. Writer’s cramp with mirror movements<br>19. Musician’s dystonia in a guitarist<br>20. Musician’s dystonia in a violinist<br>21. Rower’s dystonia<br>22. Neurodegeneration with brain iron accumulation<br>23. Spinocerebellar ataxia-type 2 with dystonia<br>24. Tardive dystonia<br>25.       Tardive dystonia treated with deep brain stimulation<br>26. Wilson’s disease with dystonia<br>27.       Rapid-onset dystonia-parkinsonism<br>28. Anterocollis in parkinsonism<br>29. Sandifer’s syndrome<br>30. Adrenoleukodystrophy</p><p>Section IV. Choreiform disorders</p><p>1. Huntington’s disease<br>2. Late onset Huntington’s disease<br>3. Juvenile Huntington’s disease<br>4. Huntington’s disease-Like 2<br>5. Sydenham’s chorea<br>6. Benign hereditary chorea<br>7. Chorea-acanthocytosis<br>8. Chorea-acanthocytosis with feeding dystonia<br>9. Chorea-acanthocytosis with head drops and trunk flexions<br>10. Hemichorea-hemiballismus<br>11. Chorea in Creutzfeld-Jakob disease<br>12. Tardive dyskinesia<br>13. Drug-induced akathisia<br>14. Edentulous dyskinesia<br>15. Painful legs and moving toes <br>16. “Postpump” chorea<br>17. Belly dancer’s dyskinesia<br>18. Pseudoathetosis</p><p>Section V. Myoclonus</p><p>1. Brainstem myoclonus<br>2. Palatal myoclonus<br>3. Posthypoxic myoclonus<br>4. Essential myoclonus<br/>5. Negative myoclonus 6. Propriospinal myoclonus<br>7. Myoclonus-dystonia syndrome<br>8. Opsoclonus-myoclonus-ataxia syndrome<br>9. Progressive myoclonic epilepsy<br>10. Hemifacial spasm<br>11. Epilepsia partialis continua<br>12. Anti-NMDA-receptor encephalitis<br>13. Psychogenic myoclonus</p><p>Section VI. Cerebellar ataxia</p><p>1. Examination of a patient with cerebellar ataxia <br>2. Spinocerebellar ataxia-type 2<br>3. Spinocerebellar ataxia-type 3<br>4. Spinocerebellar ataxia-type 6<br>5. Spinocerebellar ataxia-type 7<br>6. Spinocerebellar ataxia-type 17<br>7. Ataxia with oculomotor apraxia-type1<br>8. Ataxia with oculomotor apraxia-type 2<br>9. Friedreich’s ataxia<br>10.       Multiple System Atrophy with cerebellar ataxia</p><p>Section VII. Tic disorders</p><p>1. Motor tic disorder<br>2. Adult onset tic disorder <br>3. Tourette syndrome: Complex tics<br>4. Tourette syndrome: Malignant dystonic tics<br>5. Tourette syndrome: Self-injurious behavior<br></p>