ATROFIA ESPINOCEREBELOSA PDF

do PEATE, com ocorrência de 71% na ataxia de Friedreich’s, em que apenas a onda I foi identificada e 71% na atrofia oli- vopontocerebelar. Nueve casos poseían antecedentes familiares de ataxia cerebelosa: 2 casos de atrofia espinocerebelosa tipo 2 (SCA2), 1 caso del tipo 1 (SCA1), 3 casos de. E. Huntington esclerosis multiple demencia cuerpos de Lewy. E. Parkinson atrofia espinocerebelosa encefalopatia vascular degeneracion lobar fronto- temporal.

Author: Yokree Tojazilkree
Country: Brunei Darussalam
Language: English (Spanish)
Genre: Personal Growth
Published (Last): 12 December 2018
Pages: 278
PDF File Size: 3.79 Mb
ePub File Size: 13.57 Mb
ISBN: 158-9-77350-161-2
Downloads: 88213
Price: Free* [*Free Regsitration Required]
Uploader: Balabar

Timing functions of the cerebellum.

Am Wtrofia Hum Genet, 89pp. La ataxia espinocerebelosa 36 SCA First SAC36 patients in Europe: Spanish version of the Boston naming test in Buenos Aires. After subjects signed informed consent forms, we drew samples for genetic testing and created a detailed pedigree.

To a certain extent, clinical heterogeneity of SCA reflects the wide range of genetic alterations causing them. J Neurol,pp. The problems of assessing executive functions. Durante el WCST ambos grupos mostraron: Mov Disord, 27pp.

TOP Related  CHANGEMAN TOOL IN MAINFRAME PDF

British Magazine Publishes Cuban Studies on Ataxia

Map of Costa da Morte, in the Atlantic coast of Galicia. Int J Psychol ; Subscribe to our Newsletter. Neurol Clin, 31pp. The most relevant findings from complementary tests in patients with SCA36 15,16 are the following: Neurol Res, 33pp.

There was a problem providing the content you requested

Neurology, 58pp. American Psychiatric Association, Procedural learning and neostriatal dysfunction in man. Dynamic dopamine modulation in the basal ganglia: Since many people are at risk for this disease, we will continue our investigations aimed at elucidating the underlying atrofiia molecular mechanisms and discovering effective treatment.

InKobayashi et al.

Sporadic ataxia with adult onset: Symptoms progress slowly; appendicular ataxia, dysmetria, dysdiadochokinesia, and cerebellar or mixed dysarthria cerebellar and bulbar appear at later stages. Hooper visual organization test VOT Manual. Psychological Assessment Resources, None of our patients displayed dysautonomia or extrapyramidal symptoms, although Miyashiro et al.

Recent developments in Parkinson’s disease, Vol. Algunos factores potencialmente limitantes de nuestro estudio deben tenerse en cuenta.

TOP Related  AMBROXOL MECANISMO DE ACCION PDF

Lancet Neurol, 3pp. Based on the data provided by the patients themselves, the syndrome followed an autosomal dominant inheritance pattern. The exact size of the allele containing a large expansion can be determined with Southern blot, although this is not usually necessary.

Normative data for the Trail making esponocerebelosa. Eur J Neurol, 19pp.

Since many people are at risk for this disease, we will continue espioncerebelosa investigations aimed at elucidating the underlying pathogenic molecular mechanisms and discovering effective treatment.