FAC ENFERMERIA
Centro
Universidade Do Porto
Oporto, PortugalPublicaciones en colaboración con investigadores/as de Universidade Do Porto (19)
2024
-
Toxoplasma gondii IgG Serointensity Is Positively Associated With Frailty
The journals of gerontology. Series A, Biological sciences and medical sciences, Vol. 79, Núm. 3
2023
-
Association of Torquetenovirus Viremia with Physical Frailty and Cognitive Impairment in Three Independent European Cohorts
Gerontology, Vol. 69, Núm. 6, pp. 684-693
-
Chronic Intermittent Hypoxia-Induced Dysmetabolism Is Associated with Hepatic Oxidative Stress, Mitochondrial Dysfunction and Inflammation
Antioxidants, Vol. 12, Núm. 11
2022
2019
-
Exploring Genetic Outcomes as Frailty Biomarkers
Journals of Gerontology - Series A Biological Sciences and Medical Sciences, Vol. 74, Núm. 2, pp. 168-175
2018
-
Frailty Syndrome and Genomic Instability in Older Adults: Suitability of the Cytome Micronucleus Assay As a Diagnostic Tool
Journals of Gerontology - Series A Biological Sciences and Medical Sciences, Vol. 73, Núm. 7, pp. 864-872
-
Frailty in older adults is associated with plasma concentrations of inflammatory mediators but not with lymphocyte subpopulations
Frontiers in Immunology, Vol. 9, Núm. MAY
2015
-
BAX and BCL-2 polymorphisms, as predictors of proliferative vitreoretinopathy development in patients suffering retinal detachment: The Retina 4 project
Acta Ophthalmologica, Vol. 93, Núm. 7, pp. e541-e549
-
Predicting proliferative vitreoretinopathy: Temporal and external validation of models based on genetic and clinical variables
British Journal of Ophthalmology, Vol. 99, Núm. 1, pp. 41-48
2013
-
A genetic case-control study confirms the implication of SMAD7 and TNF locus in the development of proliferative vitreoretinopathy
Investigative Ophthalmology and Visual Science, Vol. 54, Núm. 3, pp. 1665-1678
-
The T309G MDM2 gene polymorphism is a novel risk factor for proliferative vitreoretinopathy
PLoS ONE, Vol. 8, Núm. 12
-
The p53 codon 72 polymorphism (rs1042522) is associated with proliferative vitreoretinopathy: The retina 4 project
Ophthalmology, Vol. 120, Núm. 3, pp. 623-628
2009
-
Familial clustering of migraine: Further evidence from a portuguese study
Headache, Vol. 49, Núm. 3, pp. 404-411
-
First mutation in the voltage-gated NaV1.1 subunit gene SCN1A with co-occurring familial hemiplegic migraine and epilepsy
Cephalalgia, Vol. 29, Núm. 3, pp. 308-313
2008
-
The C677T polymorphism in MTHFR is not associated with migraine in Portugal
Disease Markers, Vol. 25, Núm. 2, pp. 107-113
-
Two novel functional mutations in the Na+, K+ -ATPase α2-subunit ATP1A2 gene in patients with familial hemiplegic migraine and associated neurological phenotypes
Clinical Genetics, Vol. 73, Núm. 1, pp. 37-43
2007
-
Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine
Journal of Human Genetics, Vol. 52, Núm. 12, pp. 990-998
2006
-
Enxaqueca: Distribuição familiar numa população portuguesa
Sinapse, Vol. 6, Núm. 1, pp. 48-53
-
Nova mutação recorrente no gene ATP1A2 numa familia portuguesa com enxaqueca hemiplégica familiar tipo 2
Sinapse, Vol. 6, Núm. 2, pp. 4-10