Publications en collaboration avec des chercheurs de Universidade Do Porto (14)

2024

  1. 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

  1. Association of Torquetenovirus Viremia with Physical Frailty and Cognitive Impairment in Three Independent European Cohorts

    Gerontology, Vol. 69, Núm. 6, pp. 684-693

  2. Chronic Intermittent Hypoxia-Induced Dysmetabolism Is Associated with Hepatic Oxidative Stress, Mitochondrial Dysfunction and Inflammation

    Antioxidants, Vol. 12, Núm. 11

2022

  1. Suitability of salivary leucocytes to assess DNA repair ability in human biomonitoring studies by the challenge-comet assay

    Chemosphere, Vol. 307

2019

  1. Exploring Genetic Outcomes as Frailty Biomarkers

    Journals of Gerontology - Series A Biological Sciences and Medical Sciences, Vol. 74, Núm. 2, pp. 168-175

2018

  1. 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

  2. Frailty in older adults is associated with plasma concentrations of inflammatory mediators but not with lymphocyte subpopulations

    Frontiers in Immunology, Vol. 9, Núm. MAY

2009

  1. Familial clustering of migraine: Further evidence from a portuguese study

    Headache, Vol. 49, Núm. 3, pp. 404-411

  2. 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

  1. The C677T polymorphism in MTHFR is not associated with migraine in Portugal

    Disease Markers, Vol. 25, Núm. 2, pp. 107-113

  2. 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

  1. Recurrent ATP1A2 mutations in Portuguese families with familial hemiplegic migraine

    Journal of Human Genetics, Vol. 52, Núm. 12, pp. 990-998

2006

  1. Enxaqueca: Distribuição familiar numa população portuguesa

    Sinapse, Vol. 6, Núm. 1, pp. 48-53

  2. Nova mutação recorrente no gene ATP1A2 numa familia portuguesa com enxaqueca hemiplégica familiar tipo 2

    Sinapse, Vol. 6, Núm. 2, pp. 4-10