Publicaciones en colaboración con investigadores/as de Universidade Do Porto (8)

2023

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

    Antioxidants, Vol. 12, Núm. 11

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