4 documents found, page 1 of 1
The impact of trait anxiety and autism traits on olfactory abilities of the gen...
Barros, F.; Figueiredo, C.; Costa, A.; Morais, S.; Madeira, N.; Soares, S.Introduction: Autism Spectrum Disorders (ASD) are characterized by atypical sensory processing, including in olfactory domain. However, since ASD is a complex condition characterized by marked heterogeneity in severity and symptoms, variables with significant manifestation in this condition, such as trait anxiety, may have been adding confounds to results. Importantly, perceptual abnormalities found in ASD seem...
Report on territorial impact projections. FLAGSHIP Project Report D7.2
Lüer, C.; Böhme, K.; Jæger, S.; Hans, S.; Madeira, N.; Holstein, F.; Toptsidou, M.; Tulumello, Simone; Bina, Olivia; Ferrão, JoãoThe FLAGSHIP project addresses forward-looking methodologies in relation to Grand Societal Challenges and aims to develop tools and model frameworks beyond the state of the art. For a discussion of Grand Societal Challenges and their impacts on Europe’s future development, Europe’s territorial diversity needs to be taken into consideration because different regions and cities are affected by different challenge...
Profile of depressive symptoms in women in the perinatal and outside the perina...
Pereira, A. T.; Marques, Mariana; Soares, M. J.; Maia, B. R.; Bos, S.; Valente, J.; Nogueira, V.; Roque, C.; Madeira, N.; Macedo, A.Purposes To analyze which Beck Depression Inventory-II (BDI-II) and Postpartum Depression Screening Scores (PDSS) total and dimensional scores, as well as symptomatic answers proportions significantly differ between women in the perinatal period (pregnant/postpartum) without major depression, with major depression and women outside the perinatal period. Methods 572 pregnant women in the third trimester complete...
Doença de Pompe Juvenil: Estudo Retrospetivo de Casuística Clínica
Loureiro-Neves, F.; Garcia, P.; Madeira, N.; Araújo, H.; Rodrigues, F.; Estevão, M.; Lacerda, L.; Diogo-Matos, L.ntrodução: A doença de Pompe ou glicogenose tipo II é uma doença autossómica recessiva por deficiência de maltase ácida. É uma entidade rara, com prevalência de 1/40.000 nas populações holandesa e afro-americana e 1/46000 na população australiana. Embora se distingam três formas de apresentação (infantil, juvenil e do adulto), observa-se um amplo espectro clínico. Em Portugal está disponível terapêutica enzimát...