Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Teresa Lourenço"'
Publikováno v:
Saúde & Tecnologia, Iss 22 (2022)
Introdução – O acidente vascular cerebral (AVC) está intimamente relacionado com o aumento da ocorrência de quedas, assim como o medo de cair, também este um fator predisponente para quedas. As alterações ao nível do equilíbrio e da marcha
Externí odkaz:
https://doaj.org/article/57960c8fbbfc42098064766b487e06db
Autor:
Sílvia Freira, Teresa Lourenço, Rita Cerqueira, Purificação Tavares, Gabriela Pereira, Deolinda Barata, José Cabral
Publikováno v:
Acta Médica Portuguesa, Vol 22, Iss 3 (2009)
Hereditary pancreatitis is defined as a family history of two or more relatives with pancreatitis and clinical, biochemical, or radiologic evidence of pancreatitis. This is the fourth family described with hereditary pancreatitis related to mutation
Externí odkaz:
https://doaj.org/article/1a7b9467fbdc4f8f8fac7166e557b66d
Autor:
Rita Lourenço, Miguel Lança, Octávia Monteiro Gil, Joana Cardoso, Teresa Lourenço, José Pereira‑Leal, António Rodrigues, José Rueff, Susana Nunes Silva
Publikováno v:
Molecular Medicine Reports. 28
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::796a243fc005c107733419b4696feca3
https://doi.org/10.3892/mmr.2023.13023
https://doi.org/10.3892/mmr.2023.13023
Publikováno v:
2023 IEEE Underwater Technology (UT).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f4d429d4ea2442e80516d5202b1668e
https://doi.org/10.1109/ut49729.2023.10103429
https://doi.org/10.1109/ut49729.2023.10103429
Autor:
Ferdinando Bernardino Freitas, Maria Teresa Lourenço Marques Novo, Aida Simões Esteves, A. Paulo Gouveia Almeida
Publikováno v:
Frontiers in Physiology, Vol 2 (2012)
The aim of this study was to evaluate mosquito abundance, species diversity, larval and adult population dynamics in seven lagoons integrated in the wetland coastal system of the Algarve, Portugal, in the summer of 2007, as well as the screening of t
Externí odkaz:
https://doaj.org/article/fc38c96dd7494f869646445ee9a16435
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Made available in DSpace on 2020-01-16T16:40:13Z (GMT). No. of bitstreams: 1 6222_13254.pdf: 421837 bytes, checksum: 1984c155c30fd1ec0f8853e4c076acba (MD5) Previous issue date: 2018-06-25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::24d6613e64b946fc06caf09464e4bc9a
Autor:
Hildeberto Correia, Cristina Ferreira, Sónia Pedro, Filomena Brito, Bárbara Marques, Marta Amorim, Cristina Alves, Teresa Lourenço
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Molecular Cytogenetics
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Molecular Cytogenetics
Background: Analphoid supernumerary marker chromosomes (aSMC) constitute one of the smallest groups of SMC, and are characterized by a centromeric constriction but no detectable alpha-satellite DNA. These marker chromosomes cannot be properly identif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::186329a4d5a16716bac92d01852f1551
https://doi.org/10.1186/s13039-016-0295-z
https://doi.org/10.1186/s13039-016-0295-z
Autor:
Indira B. Taylor, Anne Goriely, Andrew O.M. Wilkie, Irene M.J. Mathijssen, A. Jeannette M. Hoogeboom, Jenny Morton, Richard B. Fisher, Louise C. Wilson, Elizabeth Sweeney, Alexa Kidd, John B. Mulliken, M. Teresa Lourenço, Steven A. Wall, Kazuya Matsumoto, Stephen R.F. Twigg, Han G. Brunner
Publikováno v:
American Journal of Human Genetics, 78, 999-1010
American Journal of Human Genetics, 78, 6, pp. 999-1010
American Journal of Human Genetics, 78(6), 999-1010. Cell Press
American Journal of Human Genetics, 78, 6, pp. 999-1010
American Journal of Human Genetics, 78(6), 999-1010. Cell Press
Contains fulltext : 51037.pdf (Publisher’s version ) (Closed access) Craniofrontonasal syndrome (CFNS) is an X-linked disorder that exhibits a paradoxical sex reversal in phenotypic severity: females characteristically have frontonasal dysplasia, c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c788208aa1ad47725322caa4cebe72f
https://doi.org/10.1086/504440
https://doi.org/10.1086/504440
Autor:
Santos, Ana Teresa Lourenço
Water is a limited resource for which demand is growing. Contaminated water from inadequate wastewater treatment provides one of the greatest health challenges as it restricts development and increases poverty in emerging and developing countries. Th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1437::b1a6cce93fe2730c6d07b4b3908bd64c
https://hdl.handle.net/10362/13797
https://hdl.handle.net/10362/13797
Publikováno v:
BMJ case reports. 2014
Marfan syndrome (MFS) is a genetic disorder of the connective tissue which rarely manifests in the neonatal period and has an ominous prognosis. A case of a first female offspring of healthy parents is described here. The pregnancy was uneventful and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74392654cddb5fadf580687d139f535d
https://pubmed.ncbi.nlm.nih.gov/24928929
https://pubmed.ncbi.nlm.nih.gov/24928929