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Informationen zum Autor Kailash Bhatia is a Professor of Clinical Neurology in the Sobell Department of Motor Neuroscience and Movement Disorders at the Institute of Neurology, University College London and an Honorary Consultant Neurologist at the affiliated National Hospital for Neurology, London. Roberto Erro is Assistant Professor of Neurology in the Department of Neurology, Università degli Studi di Salerno, Italy and Honorary Research Associate in the Institute of Neurology, Sobell Department of Movement, University College London. Maria Stamelou is Assistant Professor of Neurology in the Department of Neurology, Philipps-Universität Marburg, Germany, Honorary Research Associatein the Sobell Department of Motor Neuroscience and Movement Disorders at the Institute of Neurology, University College London, and Head of Parkinson's Disease and Movement Disorders Department at HYGEIA Hospital, Athens. Klappentext A thorough collection of movement disorders cases, each discussed by international experts and accompanied by illustrative video content.Case based learning is very important for continued professional development, and the difficulty of diagnosing and managing movement disorders make these a particularly suitable subject. With an extensive video library, this book is invaluable for neurologists seeking to hone their diagnostic skills and general understanding of movement disorders. Inhaltsverzeichnis List of contributors; List of abbreviations; Section 1. Parkinsonism: 1. Parkinson disease; 2. Nonmotor Parkinson disease; 3. Isolated lower limb dystonia at onset of Parkin disease; 4. Parkinson's disease associated with SCNA mutations; 5. Steele-Richardson-Olszewski syndrome; 6. PSP-parkinsonism; 7. Corticobasal degeneration; 8. MSA - parkinsonian variant; 9. Prominent freezing of gait and speech disturbances due to Fahr disease; 10. A (familial) PSP look-alike; 11. Parkinsonian syndrome and sunflower cataracts: Wilson's disease; 12. Classic PD-like rest tremor in FTDP-17 due to a MAPT mutation; 13. Progressive parkinsonism with falls and supranuclear gaze palsy; 14. Very early onset parkinsonism; 15. Parkinsonism due to CSF1R mutation; Section 2. Dystonia: 16. Early-onset generalized dystonia: DYT1; 17. Early-onset jerky dystonia: an uncommon phenotype of DYT1; 18. Early-onset generalized dystonia with cranio-cervical involvement: DYT6; 19. Autosomal recessive isolated generalized dystonia: DYT2; 20. Dopa-responsive dystonia; 21. A complicated dopa-responsive dystonia: tyrosine hydroxylase deficiency; 22. Early onset generalized dystonia and macrocephaly: Glutaric Aciduria type 1; 23. PKAN misdiagnosed as 'progressive delayed-onset postanoxic dystonia'; 24. Oromandibular dystonia and freezing of gait: a novel presentation of neuroferritinopathy; 25. Generalized dystonia with oromandibular involvement and self-mutilations: Lesch-Nyhan syndrome; 26. Dystonia complicated by pyramidal signs, parkinsonism and cognitive impairment: HSP11; 27. H-ABC syndrome; 28. Dystonic opisthotonus; 29. Delayed-onset dystonia after lightning strike; Section 3. Tics: 30. Gilles de la Tourette syndrome; 31. Secondary tic disorders: Huntington disease; 32. Multiple hyperkinesias: tics and paroxysmal kinesigenic dyskinesia; 33. Functional tic disorders; Section 4. Chorea: 34. Huntington disease; 35. Generalized chorea with oromandibular involvement and tongue biting; 36. A Huntington disease look-alike: SCA17; 37. A newly recognized HD-phenocopy associated with C9orf72 expansion; 38. Persistent chorea due to anticholinergics in DYT6; 39. Dyskinesia without levodopa: long-term follow-up of mesencephalic transplant in PD; 40. Benign hereditary chorea; 41. Another cause of benign hereditary chorea; Section 5. Tremor: 42. Essential tremor; 43. Rest tremor and scans without evidence of dopaminergic deficit (SWEDD); 44. Neuropathic tremor; 45. A treatable disorder misdiagnosed as ET; 46. Thalamic tremor; 47. Shakin...
