Zobrazeno 1 - 10
of 507
pro vyhledávání: '"Rita, Guerreiro"'
Autor:
Fernanda Rodrigues, Bernardete Pinheiro, Rita Guerreiro, Miguel Gouveia, João Eloi, Cristina Alves, Guilherme Castela, Alexandra Oliveira, Filipe Palavra, Iolanda Veiros, Margarida Borges
Publikováno v:
Revista Portuguesa de Farmacoterapia, Vol 14, Iss 3-4 (2023)
Introdução: A doença invasiva meningocócica (DIM) é uma infeção causada pela bactéria Neisseria meningitidis, manifestando-se habitualmente sob a forma de meningite (MM) e/ou septicémia (SM). O objetivo deste estudo é estimar os custos da D
Externí odkaz:
https://doaj.org/article/09754a830f494cc6aa6061251b9361d4
Publikováno v:
The Global Community Yearbook of International Law and Jurisprudence 2021, 2023.
Externí odkaz:
https://doi.org/10.1093/oso/9780197659083.003.0031
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-12 (2022)
Abstract In just over a decade, advances in genome-wide association studies (GWAS) have offered an approach to stratify individuals based on genetic risk for disease. Using recent Alzheimer's disease (AD) GWAS results as the base data, we determined
Externí odkaz:
https://doaj.org/article/76c9ae3280364d8fbaf0b2afda8e3792
Akademický článek
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Autor:
João André Sousa, Catarina Bernardes, Sara Bernardo-Castro, Miguel Lino, Inês Albino, Lino Ferreira, José Brás, Rita Guerreiro, Miguel Tábuas-Pereira, Inês Baldeiras, Isabel Santana, João Sargento-Freitas
Publikováno v:
Frontiers in Aging Neuroscience, Vol 15 (2023)
The existence of a selective blood-brain barrier (BBB) and neurovascular coupling are two unique central nervous system vasculature features that result in an intimate relationship between neurons, glia, and blood vessels. This leads to a significant
Externí odkaz:
https://doaj.org/article/ec0eea72fb9647388fc31765fe29ad4d
Publikováno v:
Molecular Neurodegeneration, Vol 17, Iss 1, Pp 1-15 (2022)
Abstract The search for rare variants in Alzheimer’s disease (AD) is usually deemed a high-risk - high-reward situation. The challenges associated with this endeavor are real. Still, the application of genome-wide technologies to large numbers of c
Externí odkaz:
https://doaj.org/article/22f29f201a354bb8893a661124ab6951
Autor:
Rita Guerreiro, Jose Bras
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-2 (2023)
Externí odkaz:
https://doaj.org/article/072774b5b75f4f87ab7a1641465c2382
Autor:
Nadia Dehghani, Gamze Guven, Celia Kun-Rodrigues, Catarina Gouveia, Kalina Foster, Hasmet Hanagasi, Ebba Lohmann, Bedia Samanci, Hakan Gurvit, Basar Bilgic, Jose Bras, Rita Guerreiro
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-12 (2021)
Abstract Background Copy number variants (CNVs) include deletions or multiplications spanning genomic regions. These regions vary in size and may span genes known to play a role in human diseases. As examples, duplications and triplications of SNCA h
Externí odkaz:
https://doaj.org/article/3333ee35e57a4fb0954bf1090899f4e8
Autor:
Miguel Tábuas-Pereira, Isabel Santana, Elizabeth Gibbons, Kimberly Paquette, Maria Rosário Almeida, Inês Baldeiras, Jose Bras, Rita Guerreiro
Publikováno v:
Frontiers in Neurology, Vol 13 (2022)
IntroductionFrontotemporal dementia (FTD) is considered to be part of a continuum with amyotrophic lateral sclerosis (ALS). Many genes are associated with both ALS and FTD. Yet, many genes associated with ALS have not been shown to cause FTD. We aime
Externí odkaz:
https://doaj.org/article/2d6edb0d93be4ea89c5da77b207c031a
Autor:
Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, Susanne Müller, Kajetan Bentele, Manuel Holtgrewe, Celia Kun-Rodrigues, Isabel Alonso, Maria do Carmo Macario, Ana Sofia Morgadinho, Ana Graça Velon, Gustavo Santo, Isabel Santana, Saana Mönkäre, Liina Kuuluvainen, Johanna Schleutker, Minna Pöyhönen, Liisa Myllykangas, Assunta Senatore, Daniel Berchtold, Katarzyna Winek, Andreas Meisel, Aleksandra Pavlovic, Vladimir Kostic, Valerija Dobricic, Ebba Lohmann, Hasmet Hanagasi, Gamze Guven, Basar Bilgic, Jose Bras, Rita Guerreiro, Dieter Beule, Ulrich Dirnagl, Celeste Sassi
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Recently, several genome-wide association studies identified PHACTR1 as key locus for five diverse vascular disorders: coronary artery disease, migraine, fibromuscular dysplasia, cervical artery dissection and hypertension. Although these re
Externí odkaz:
https://doaj.org/article/fd269f7adb7a4eddb42c68dbb59da734