The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.
Pure akinesia with gait freezing: A third clinical phenotype of progressive supranuclear palsy
Abstract
The clinical syndrome of pure akinesia has most often been associated with progressive supranuclear palsy (PSP) and is characterized by difficulty initiating gait and “freezing” during walking, writing and speaking. Similar syndromes have been described under the rubrics of primary progressive freezing gait and primary gait ignition failure. We investigated the specificity of the clinical syndrome of pure akinesia with gait freezing (PAGF) for PSP‐tau pathology. Among 749 patients archived at the QSBB, only 7 fulfilled proposed diagnostic criteria of: gradual onset of freezing of gait or speech; absent limb rigidity and tremor; no sustained response to levodopa; and no dementia or ophthalmoplegia in the first 5 years of disease. In these cases detailed pathological examination was performed. PSP was the pathological diagnosis in six patients, and Parkinson's disease (PD) in the seventh. As defined, this syndrome had a positive predictive value of 86% for PSP‐tau pathology. In the cases with PSP there were no additional features of coexistent vascular or PD and the median PSP‐tau score was 3, reflecting relative mild tau load. The clinical syndrome of PAGF appears to have a high specificity for PSP‐tau pathology. This relatively uncommon presentation of PSP‐tau pathology has less severe tau accumulation than in the more common, “classic” PSP clinical phenotype: Richardson's disease. © 2007 Movement Disorder Society
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Neurotransmitters and neuromodulators in the basal ganglia
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Cited by
Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria
Höglinger, G. U., Respondek, G., Stamelou, M., Kurz, C., Josephs, K. A., Lang, A. E., Mollenhauer, B., Müller, U., Nilsson, C., Whitwell, J. L., et al. (2017) · Movement Disorders · doi:10.1002/mds.26987 · Cited by 2,359
Parkinson's Disease and Parkinsonism
Hayes, M. T. (2019) · The American Journal of Medicine · doi:10.1016/j.amjmed.2019.03.001 · Cited by 823
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Williams, D. R., & Lees, A. J. (2009) · The Lancet Neurology · doi:10.1016/s1474-4422(09)70042-0 · Cited by 650
Self-citationInvited review: Neuropathology of tauopathies: principles and practice
Kovacs, G. G. (2015) · Neuropathology and Applied Neurobiology · doi:10.1111/nan.12208 · Cited by 492
Neuropathology of variants of progressive supranuclear palsy
Dickson, D. W., Ahmed, Z., Algom, A. A., Tsuboi, Y., & Josephs, K. A. (2010) · Current Opinion in Neurology · doi:10.1097/wco.0b013e32833be924 · Cited by 386
Metadata
- Authors
- Williams, D. R., Holton, J. L., Strand, K., Revesz, T., & Lees, A. J.
- Venue
- Movement Disorders
- Publisher
- Wiley
- Published
- 2007-08-21
- Volume
- 22
- Issue
- 15
- Pages
- 2235-2241
- ISSN
- 0885-3185 (ISSN-L)
- 1531-8257
- OpenAlex
- W2073413677
- Cited by
- 241
- References
- 5
- FWCI
- 4.91
- Type
- journal article
- Language
- en
- Open access
- closed
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