𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cognitive function in multiple system atrophy of the cerebellar type

✍ Scribed by Katrin Bürk; Irene Daum; Udo Rüb


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
61 KB
Volume
21
Category
Article
ISSN
0885-3185

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Dementia represents an exclusion criterion for the diagnosis of multiple system atrophy (MSA), but there have been reports of fronto‐executive dysfunction in patients with MSA of the striatonigral type (MSA‐P). To study the cognitive profile of MSA, 20 patients with MSA of the cerebellar type (MSA‐C) were subjected to an extensive neuropsychological test battery comprising tests for IQ, attention, verbal and visuospatial memory, as well as executive function. There was evidence for impaired verbal memory and verbal fluency. Test performance was not related to the severity of motor disability. Regarding the similar cognitive syndrome of MSA‐P, the otherwise subclinical problems in MSA‐C result from subcortical rather than from cerebellar dysfunction. © 2006 Movement Disorder Society


📜 SIMILAR VOLUMES


Pathological laughter and crying in pati
✍ Josef Parvizi; Jeffrey Joseph; Daniel Z. Press; Jeremy D. Schmahmann 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 146 KB

## Abstract In the cerebellar type of multiple system atrophy (MSA‐C), the burden of pathological changes involves the cerebellum and its associated brainstem structures in the basis pontis and the inferior olivary nucleus, and as a result, the clinical phenotype is dominated early on by the cerebe

Cortical atrophy in the cerebellar varia
✍ Christian Brenneis; Sylvia M. Boesch; Karl E. Egger; Klaus Seppi; Christoph Sche 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 376 KB

## Abstract This study aimed to determine in vivo the atrophy patterns in clinically established cerebellar variant of multiple‐system atrophy (MSA‐C) using voxel‐based morphometry (VBM). Thirteen patients with MSA‐C (12 probable, 1 possible) and 13 healthy controls matched for age and sex were inc

Brainstem metabolites in multiple system
✍ Yuhei Takado; Hironaka Igarashi; Kenshi Terajima; Takayoshi Shimohata; Tetsutaro 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 430 KB

## Abstract **Background:** The aim of this study was to find biomarkers of disease severity in multiple system atrophy of cerebellar type by imaging disease specific regions using proton magnetic resonance spectroscopy on a 3.0 T system. **Methods:** We performed proton magnetic resonance spectro

Very late-onset Friedreich's ataxia with
✍ José Berciano; Jon Infante; Antonio García; José Miguel Polo; Victor Volpini; On 📂 Article 📅 2005 🏛 John Wiley and Sons 🌐 English ⚖ 95 KB

## Abstract Very late‐onset Friedreich's ataxia (VLOFA) is characterized by symptomatic onset after 40 years of age and, usually, a benign phenotype. We describe a sporadic case with onset at 53 years of age and a novel VLOFA phenotype mimicking multiple system atrophy (MSA) of cerebellar type asso

Presentation, diagnosis, and management
✍ Martin Köllensperger; Felix Geser; Jean-Pierre Ndayisaba; Sylvia Boesch; Klaus S 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 132 KB

## Abstract Multiple system atrophy (MSA) is a Parkinson's Disease (PD)‐like α‐synucleinopathy clinically characterized by dysautonomia, parkinsonism, cerebellar ataxia, and pyramidal signs in any combination. We aimed to determine whether the clinical presentation of MSA as well as diagnostic and