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Ancillary investigations to diagnose parkinsonism: a prospective clinical study.
Aerts MB, Esselink RA, Abdo WF, Meijer FJ, Drost G, Norgren N, Janssen MJ, Borm GF, Bloem BR, Verbeek MM. Aerts MB, et al. J Neurol. 2015 Feb;262(2):346-56. doi: 10.1007/s00415-014-7568-4. Epub 2014 Nov 9. J Neurol. 2015. PMID: 25381460
Stepwise logistic regression showed that the combination of tandem gait, axial UPDRS subscore, slow saccadic eye movements and dysphagia yielded an AUC of 0.93, adjusted for optimism. ...
Stepwise logistic regression showed that the combination of tandem gait, axial UPDRS subscore, slow saccadic eye mov
Video Representation of Dopamine-Responsive Multiple System Atrophy Cerebellar Type.
Doan J, Sheikh I, Elmer L, Rashid M. Doan J, et al. Am J Case Rep. 2021 Nov 15;22:e933995. doi: 10.12659/AJCR.933995. Am J Case Rep. 2021. PMID: 34776506 Free PMC article.
The initial neurological workup demonstrated bilateral cogwheel rigidity; difficulty with movement initiation. including standing up from a seated position; slow saccadic eye movements; masked facies (hypomimia); right ankle clonus; bilateral upper and …
The initial neurological workup demonstrated bilateral cogwheel rigidity; difficulty with movement initiation. including standing up from a …
RETINAL MANIFESTATIONS OF SPINOCEREBELLAR ATAXIA TYPE 7 IN TWO CONSECUTIVE GENERATIONS.
Yip G, Henao M, Huang LL. Yip G, et al. Retin Cases Brief Rep. 2017 Winter;11 Suppl 1:S86-S89. doi: 10.1097/ICB.0000000000000423. Retin Cases Brief Rep. 2017. PMID: 27632585
Patients display progressive cerebellar ataxia, dysarthria dysphagia, slow saccadic eye movements, and cone photoreceptor loss leading to progressive vision loss. ...
Patients display progressive cerebellar ataxia, dysarthria dysphagia, slow saccadic eye movements, and cone phot …
Spinocerebellar ataxia type 2 presenting with cognitive regression in childhood.
Ramocki MB, Chapieski L, McDonald RO, Fernandez F, Malphrus AD. Ramocki MB, et al. J Child Neurol. 2008 Sep;23(9):999-1001. doi: 10.1177/0883073808315622. Epub 2008 Mar 14. J Child Neurol. 2008. PMID: 18344458 Free PMC article.
Spinocerebellar ataxia type 2 typically presents in adulthood with progressive ataxia, dysarthria, tremor, and slow saccadic eye movements. Childhood-onset spinocerebellar ataxia type 2 is rare, and only the infantile-onset form has been well character …
Spinocerebellar ataxia type 2 typically presents in adulthood with progressive ataxia, dysarthria, tremor, and slow saccadic