The DOI matches its Crossref record; 29 of the 29 references it cites were found in a registry or an index.
Comparative analysis of the gait disorder of normal pressure hydrocephalus and Parkinson's disease
Open accessAbstract
OBJECTIVES: Comparative gait analyses in neurological diseases interfering with locomotion are of particular interest, as many hypokinetic gait disorders have the same main features. The aim of the present study was (1) to compare the gait disturbance in normal pressure hydrocephalus and Parkinson's disease; (2) to evaluate which variables of the disturbed gait pattern respond to specific treatment in both diseases; and (3) to assess the responsiveness to visual and acoustic cues for gait improvement. METHODS: In study 1 gait analysis was carried out on 11 patients with normal pressure hydrocephalus, 10 patients with Parkinson's disease, and 12 age matched healthy control subjects, on a walkway and on a treadmill. In study 2, patients with normal pressure hydrocephalus were reinvestigated after removal of 30 ml CSF, and patients with Parkinson's disease after administration of 150 mg levodopa. In part 3 visual cues were provided as stripes fixed on the walkway and acoustic cues as beats of a metronome. RESULTS: The gait disorder in both diseases shared the feature of a reduced gait velocity, due to a diminished and highly variable stride length. Specific features of the gait disturbance in normal pressure hydrocephalus were a broad based gait pattern with outward rotated feet and a diminished height of the steps. After treatment in both diseases, the speed increased, due to an enlarged stride length, now presenting a lower variability. All other gait variables remained unaffected. External cues only mildly improved gait in normal pressure hydrocephalus, whereas they were highly effective in raising the stride length and cadence in Parkinson's disease. CONCLUSION: The gait pattern in normal pressure hydrocephalus is clearly distinguishable from the gait of Parkinson's disease. As well as the basal ganglia output connections, other pathways and structures most likely in the frontal lobes are responsible for the gait pattern and especially the disturbed dynamic equilibrium in normal pressure hydrocephalus. Hypokinesia and its responsiveness to external cues in both diseases are assumed to be an expression of a disturbed motor planning.
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Cites
Hughes, A. J., Daniel, S. E., Kilford, L., & Lees, A. J. (1992) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.55.3.181 · Cited by 10,378
Symptomatic Occult Hydrocephalus with Normal Cerebrospinal-Fluid Pressure: A Treatable Syndrome
Adams, R. D., Fisher, C. M., Hakim, S., Ojemann, R. G., & Sweet, W. H. (1965) · New England Journal of Medicine · doi:10.1056/nejm196507152730301 · Cited by 1,370
The special clinical problem of symptomatic hydrocephalus with normal cerebrospinal fluid pressure
Hakim, S., & Adams, R. D. (1965) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(65)90016-x · Cited by 1,259
Symptomatic occult hydrocephalus with "normal cerebrospinal fluid pressure".
Bh, M. (1970) · PubMed · Cited by 1,035
Stride length regulation in Parkinson's disease: Normalization strategies and underlying mechanisms
Morris, M. E., Iansek, R., Matyas, T. A., & Summers, J. J. (1996) · Brain · doi:10.1093/brain/119.2.551 · Cited by 873
The pathogenesis of gait hypokinesia in Parkinson's disease
Morris, M. E., Iansek, R., Matyas, T. A., & Summers, J. J. (1994) · Brain · doi:10.1093/brain/117.5.1169 · Cited by 709
Human walking and higher‐level gait disorders, particularly in the elderly
Nutt, J. G., Marsden, C. D., & Thompson, P. D. (1993) · Neurology · doi:10.1212/wnl.43.2.268 · Cited by 674
Normal-pressure hydrocephalus: Predicting the results of cerebrospinal fluid shunting
Stein, S. C., & Langfitt, T. W. (1974) · Journal of Neurosurgery · doi:10.3171/jns.1974.41.4.0463 · Cited by 385
Quantitative analysis of gait in Parkinson patients: increased variability of stride length
Blin, O., Ferrandez, A. M., & Serratrice, G. (1990) · Journal of the Neurological Sciences · doi:10.1016/0022-510x(90)90184-o · Cited by 381
Talking while walking: The effect of a dual task in aging and Alzheimer's disease
Camicioli, R., Howieson, D., Lehman, S., & Kaye, J. (1997) · Neurology · doi:10.1212/wnl.48.4.955 · Cited by 332
Cited by
NAKAJIMA, M., YAMADA, S., MIYAJIMA, M., ISHII, K., KURIYAMA, N., KAZUI, H., KANEMOTO, H., SUEHIRO, T., YOSHIYAMA, K., KAMEDA, M., et al. (2021) · Neurologia medico-chirurgica · doi:10.2176/nmc.st.2020-0292 · Cited by 594
Loss of white matter integrity is associated with gait disorders in cerebral small vessel disease
de Laat, K. F., Tuladhar, A. M., van Norden, A. G. W., Norris, D. G., Zwiers, M. P., & de Leeuw, F.-E. (2011) · Brain · doi:10.1093/brain/awq343 · Cited by 296
Frenkel-Toledo, S., Giladi, N., Peretz, C., Herman, T., Gruendlinger, L., & Hausdorff, J. M. (2005) · Journal of NeuroEngineering and Rehabilitation · doi:10.1186/1743-0003-2-23 · Cited by 285
Fasudil attenuates aggregation of α-synuclein in models of Parkinson’s disease
Tatenhorst, L., Eckermann, K., Dambeck, V., Fonseca-Ornelas, L., Walle, H., Lopes da Fonseca, T., Koch, J. C., Becker, S., Tönges, L., Bähr, M., et al. (2016) · Acta Neuropathologica Communications · doi:10.1186/s40478-016-0310-y · Cited by 158
Cancela, J., Pastorino, M., Arredondo, M., Nikita, K., Villagra, F., & Pastor, M. (2014) · Sensors · doi:10.3390/s140304618 · Cited by 63
“The gait disturbances in PD may be divided into two types [3]: (1) continuous, mainly characterised by a reduction of gait speed [13] and (2) episodic [14,15].”
Background
Metadata
- Authors
- Stolze, H.
- Venue
- Journal of Neurology, Neurosurgery & Psychiatry
- Publisher
- BMJ
- Published
- 2001-03-01
- Volume
- 70
- Issue
- 3
- Pages
- 289-297
- ISSN
- 0022-3050 (ISSN-L)
- OpenAlex
- W2170585559
- Cited by
- 369
- References
- 29
- FWCI
- 23.22
- Type
- journal article
- Language
- en
- Open access
- bronze
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