Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- 1 Parkinson’s Disease
- 2 Nonmotor Parkinson’s Disease
- 3 Isolated Lower Limb Dystonia at Onset of Parkin Disease
- 4 Parkinson’s Disease Associated with SNCA Mutations
- 5 PSP: 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: Perry Syndrome
- 11 Parkinsonian Syndrome and Sunflower Cataracts: Wilson’s Disease
- 12 Classic PD-Like Rest Tremor in FTDP-17 Due to a MAPT Mutation
- 13 PSP Look-Alike due to CADASIL
- 14 Very Early Onset Parkinsonism: Juvenile HD
- 15 Parkinsonism Due to CSF1R Mutation
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
12 - Classic PD-Like Rest Tremor in FTDP-17 Due to a MAPT Mutation
from Section 1 - Parkinsonism
Published online by Cambridge University Press: 04 July 2017
Book contents
- Case Studies in Movement Disorders
- Case Studies in Movement Disorders
- Copyright page
- Contents
- Video Captions
- Contributors
- Preface
- Previously Published Cases
- Abbreviations
- Section 1 Parkinsonism
- 1 Parkinson’s Disease
- 2 Nonmotor Parkinson’s Disease
- 3 Isolated Lower Limb Dystonia at Onset of Parkin Disease
- 4 Parkinson’s Disease Associated with SNCA Mutations
- 5 PSP: 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: Perry Syndrome
- 11 Parkinsonian Syndrome and Sunflower Cataracts: Wilson’s Disease
- 12 Classic PD-Like Rest Tremor in FTDP-17 Due to a MAPT Mutation
- 13 PSP Look-Alike due to CADASIL
- 14 Very Early Onset Parkinsonism: Juvenile HD
- 15 Parkinsonism Due to CSF1R Mutation
- Section 2 Dystonia
- Section 3 Tics
- Section 4 Chorea
- Section 5 Tremor
- Section 6 Myoclonus
- Section 7 Ataxia
- Index
- Plate section
- References
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- Case Studies in Movement DisordersCommon and Uncommon Presentations, pp. 29 - 30Publisher: Cambridge University PressPrint publication year: 2017
References
Suggested Readings
Baizabal-Carvallo, JF, Jankovic, J. Parkinsonism, movement disorders and genetics in frontotemporal dementia. Nat. Rev. Neurol. 2016;12:175–85.CrossRefGoogle ScholarPubMed
Galimberti, D, Scarpini, E. Clinical phenotypes and genetic biomarkers of FTLD. J Neural Transm. 2012;119(7):851–60.Google Scholar
Siuda, J, Fujioka, S, Wszolek, ZK. Parkinsonian syndrome in familial frontotemporal dementia. Parkinsonism Relat. Disord. 2014;20(9):957–64.Google Scholar