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Action-semantic and syntactic deficits in subjects at risk for Huntington's disease
(British Psychological Soc, 2017-02)
Frontostriatal networks play critical roles in grounding action semantics and syntactic skills. Indeed, their atrophy distinctively disrupts both domains, as observed in patients with Huntington's disease (HD) and Parkinson's ...
Your misery is no longer my pleasure: Reduced schadenfreude in Huntington's disease families
(Elsevier Masson, 2016-10)
Schadenfreude – pleasure at others' misfortunes – has been systematically related to ventral striatum activity. This brain region is affected early in individuals with manifest and pre-manifest Huntington's disease (HD). ...
Is there a pathological alpha angle for hip impingement? A diagnostic test study
(Oxford University Press, 2016)
The normal value of alpha angle is controversial. The aim of this study was to compare the alpha angle in asymptomatic volunteers versus patients who had undergone surgery for symptomatic cam-type femoroacetabular impingement ...
Impairments in negative emotion recognition and empathy for pain in Huntington's disease families
(Pergamon-Elsevier Science Ltd, 2015)
DQ2, DQ7 and DQ8 Distribution and Clinical Manifestations in Celiac Cases and Their First-Degree Relatives
(MDPI AG, 2015)
HLA-linked genes are relevant to celiac disease (CD); the potential genetic differences present worldwide are not fully understood. Previous results suggest that the distribution of HLA-DQ2/DQ7/DQ8 in Chile may differ from ...
Language Deficits as a Preclinical Window into Parkinson's Disease: Evidence from Asymptomatic Parkin and Dardarin Mutation Carriers
(Cambridge University Press, 2017-02)
Objectives: The worldwide spread of Parkinson's disease (PD) calls for sensitive and specific measures enabling its early (or, ideally, preclinical) detection. Here, we use language measures revealing deficits in PD to ...
Fabry disease: clinical and genotypic aspects of three cases in first degree relatives
(Sociedade Brasileira de Dermatologia, 2014-01-01)
Fabry disease is an X-linked, lysosomal storage disease caused by the inherited deficiency of the enzyme α-galactosidase A. The diagnosis is usually late, with renal, cardiovascular and/or cerebral complications that reduce ...