Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Antonieta Nieto"'
Publikováno v:
Psychiatry International, Vol 5, Iss 3, Pp 424-433 (2024)
This study investigates the relationship between semantic memory and social cognition in schizophrenia. The sample included 50 individuals with schizophrenia (mean age 42.54, SD 9.98; 14 women, 36 men) and 30 controls (mean age 42.06, SD 12.50; 6 wom
Externí odkaz:
https://doaj.org/article/ac3a90ada17f4087be4987fc9817a1f5
Autor:
Daniel Ferreira, Alejandra Machado, Yaiza Molina, Antonieta Nieto, Rut Correia, Eric Westman, José Barroso
Publikováno v:
Frontiers in Aging Neuroscience, Vol 9 (2017)
Objective: Increased variability in cognition with age has been argued as an indication of pathological processes. Focusing on early detection of neurodegenerative disorders, we investigated variability in cognition in healthy middle-aged adults. In
Externí odkaz:
https://doaj.org/article/ff81f005e262404f9471c07177971fe3
Publikováno v:
Journal of the International Neuropsychological Society : JINS.
Objective: Parkinson’s disease patients with subjective cognitive decline (PD-SCD) and mild cognitive impairment (PD-MCI) have an increased risk of dementia (PDD). Thus, the identification of early cognitive changes that can be useful predictors of
Autor:
Javier Pérez-Flores, Antonieta Nieto, Fernando Montón, Francisco Martínez-Burgallo, Marc Corral-Juan, Antoni Matilla-Dueñas
Publikováno v:
Neurocase
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
Autosomal recessive spinocerebellar ataxia type 10 (SCAR10) caused by a homozygous c.132dupA mutation in the anoctamin 10 gene is infrequent and little is known about its cognitive profile. Three siblings (1 male) with this mutation were assessed wit
Autor:
Erika de Nóbrega, Antonieta Nieto, Fernando Montón, Stephany Hess Medler, Atteneri Hernández-Torres
Publikováno v:
Journal of the International Neuropsychological Society : JINS. 27(4)
Objective:Friedreich’s ataxia (FRDA) is the most common hereditary ataxia. It is a neurodegenerative disorder, characterized by progressive ataxia. FRDA is also associated with cognitive impairments. To date, the evolution of cognitive functioning
Publikováno v:
Journal of Neurology. 266:745-754
Increasing evidence suggests that subjective cognitive decline is associated with Alzheimer’s disease pathology and with an increased risk for future dementia development. However, the clinical value of subjective cognitive decline in Parkinson’s
Publikováno v:
International Journal of Clinical and Health Psychology : IJCHP
Background/Objective: Almost no attention has been paid to depression in Friedreich ataxia (FRDA), a highly disabling cerebellar degenerative disease. Our aim was to study the presence and the profile of depressive symptoms in FRDA and their relation
Publikováno v:
Journal of the International Neuropsychological Society. 23:511-520
Objectives: Mild cognitive impairment is common in non-demented Parkinson disease patients (PD-MCI) and is considered as a risk factor for dementia. Executive dysfunction has been widely described in PD and the Verbal Fluency Tests (VFT) are often us
Publikováno v:
Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation. 29(2)
Friedreich ataxia (FRDA) is a chronic, progressive and highly disabling cerebellar degenerative disease. Despite this, little attention has been paid to the health-related quality of life (HRQOL) in this disease. The aim of the present study was to a
Publikováno v:
Archives of Clinical Neuropsychology. 31:811-818
Objective Addenbrooke's Cognitive Examination-Revised is a brief test battery for the detection and classification of mild cognitive impairment and dementia. The aims were to investigate the influence of age and education on the Spanish version of th