Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Lia, Mano"'
1
Akademický článek
Influenza B-Associated Atypical Hemolytic Uremic Syndrome
Autor: Lia Mano, Telma Francisco, Joana Gaspar, Gabriela Pereira, Raquel Santos, Margarida Abranches
Publikováno v: Revista Portuguesa de Nefrologia e Hipertensão, Vol 36, Iss 2, Pp 80-83 (2022)
Hemolytic uremic syndrome (HUS) triggered by influenza virus (iHUS) is rare. Influenza A infections have been described to trigger atypical HUS (aHUS) in individuals with an underlying genetic complement dysregulation. To date there are only few rep
Externí odkaz: https://doaj.org/article/4088f1d584d349ae9d27009e82e6815a
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2
Akademický článek
X-linked hypophosphatemic rickets: a new mutation
Autor: Patrícia Maio, Lia Mano, Sara Rocha, Rute Baeta Baptista, Telma Francisco, Helena Sousa, João Parente Freixo, Margarida Abranches
Publikováno v: Brazilian Journal of Nephrology, Vol 43, Iss 2, Pp 279-282 (2020)
Abstract Phosphopenic rickets may be caused by mutations in the PHEX gene (phosphate regulating endopeptidase homolog X-linked). Presently, more than 500 mutations in the PHEX gene have been found to cause hypophosphatemic rickets. The authors report
Externí odkaz: https://doaj.org/article/3c0c29ebc1854ae7abc0ff4cb9e8832c
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3
Akademický článek
Responses of paediatric emergency departments to the first wave of the COVID-19 pandemic in Europe: a cross-sectional survey study
Autor: Antonio Chiaretti, Borja Gomez, Ian Maconochie, Silvia Bressan, Damian Roland, Luigi Titomanlio, Ana Sofia Simões, Liviana Da Dalt, Henriette A Moll, Vanessa Gorito, Michael Barrett, Lina Jankauskaite, Niccolo Parri, Rianne Oostenbrink, Dorine Borensztajn, Ruud Nijman, Michael Bennett, Mark Lyttle, Danilo Buonsenso, Romain Basmaci, Stuart Hartshorn, Roberto Velasco, Susanne Greber-Platzer, Shrouk Messahel, Sylvester Gomes, Clarissa Barber, Romain Guedj, Zanda Pucuka, Kate Honeyford, João Viana, Patricia Macao, Camille Aupiais, Samuel Rhedin, Jonas Thüminger, Sofia Reis, Katy Rose, Zsolt Bognar, Tisham De, Ruth Farrugia, Alexis Rybak, Asgeir Haraldsson, Caner Turan, Christoph Zurl, Corinne Vasilico, Daniel Weghuber, Daniela Kohlfuerst, Danielle Rose, Esra Akyüz Özkan, Fiona Leonard, Florian Hey, Florian Hoffman, Francisca Saraiva, Gábor Simon, Inês Mascarenhas, John Jensen, Julia Lischka, Katarina Vincek, Laszlo Fodor, Lia Mano, Malin Ryd Rinder, Matthias Schaffert, Merve Havan, Mojca Kolnik, Naomi Lin, Nuno Serrade Almeida, Orkun Aydın, Ozlem Teksam, Paddy Fitzpatrick, Petra Salamon, Rohan Mongru, Rosa Morello, Sandra Soares Cardoso, Sofia Rapti, Sonia Andrade Santos, Susana Castanhinha, Thibault de Groc, Urdur Jonsdottir, Valtýr Stefánsson Thors, Vanda Anacleto, Vytenis Masillonis
Publikováno v: BMJ Paediatrics Open, Vol 5, Iss 1 (2021)
Objective Understanding how paediatric emergency departments (PEDs) across Europe adapted their healthcare pathways in response to COVID-19 will help guide responses to ongoing waves of COVID-19 and potential future pandemics. This study aimed to eva
Externí odkaz: https://doaj.org/article/dff9fe2ef4644383ab3147acc2e48b31
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4
Akademický článek
Uso de Ecrãs em Crianças Pequenas: Os Riscos para o Neurodesenvolvimento e Qualidade do Sono
Autor: Catarina Ribeiro, Lia Mano, Sílvia Afonso
Publikováno v: Revista Portuguesa de Psiquiatria e Saúde Mental, Vol 7, Iss 2 (2021)
Externí odkaz: https://doaj.org/article/8e8143d2430f4331b08156261df57d9f
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5
Respective roles of non-pharmaceutical interventions in bronchiolitis outbreaks: an interrupted time-series analysis based on a multinational surveillance system
Autor: Lea, Lenglart, Naim, Ouldali, Kate, Honeyford, Zsolt, Bognar, Silvia, Bressan, Danilo, Buonsenso, Liviana, Da Dalt, Tisham, De, Ruth, Farrugia, Ian K, Maconochie, Henriette A, Moll, Rianne, Oostenbrink, Niccolo, Parri, Damian, Roland, Katy, Rose, Esra, Akyüz Özkan, François, Angoulvant, Camille, Aupiais, Clarissa, Barber, Michael, Barrett, Romain, Basmaci, Susana, Castanhinha, Antonio, Chiaretti, Sheena, Durnin, Patrick, Fitzpatrick, Laszlo, Fodor, Borja, Gomez, Susanne, Greber-Platzer, Romain, Guedj, Florian, Hey, Lina, Jankauskaite, Daniela, Kohlfuerst, Ines, Mascarenhas, Anna Maria, Musolino, Zanda, Pučuka, Sofia, Reis, Alexis, Rybak, Petra, Salamon, Matthias, Schaffert, Keren, Shahar-Nissan, Maria Chiara, Supino, Ozlem, Teksam, Caner, Turan, Roberto, Velasco, Ruud G, Nijman, Luigi, Titomanlio, Vanda, Anacleto, Orkun, Aydin, Elena, Bellelli, Ron, Berant, Thibault, De Groc, Sara, Geitoeira, Florian, Hoffmann, Franziska, Leeb, Fiona, Leonard, Mark, Lyttle, Lia, Mano, Vytenis, Masillonis, Rosa, Morello, Francisa, Saraiva, Gabor, Simon, Ines Silva, Costa, Joao Sous, Marques, Jonas, Thüminger, Corinne, Vasilico, Anna Chiara, Vittucci, Christoph, Zurl
Publikováno v: European Respiratory Journal, 61(2):2201172. European Respiratory Society
European Respiratory Journal
European Respiratory Journal, 2022, pp.2201172. ⟨10.1183/13993003.01172-2022⟩
BackgroundBronchiolitis is a major source of morbimortality among young children worldwide. Non-pharmaceutical interventions (NPIs) implemented to reduce the spread of severe acute respiratory syndrome coronavirus 2 may have had an important impact o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3873af3e2319416784b89e4876fb6c14
https://doi.org/10.1183/13993003.01172-2022
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6
Raquitismo hipofosfatêmico ligado ao X: uma nova mutação
Autor: João Parente Freixo, Telma Francisco, Helena Sousa, Margarida Abranches, Lia Mano, Sara Rocha, Patrícia Maio, Rute Baeta Baptista
Publikováno v: Brazilian Journal of Nephrology, Issue: ahead, Published: 04 SEP 2020
Brazilian Journal of Nephrology, Volume: 43, Issue: 2, Pages: 279-282, Published: 04 SEP 2020
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Agência para a Sociedade do Conhecimento (UMIC)-FCT-Sociedade da Informação
instacron:RCAAP
Jornal Brasileiro de Nefrologia
Brazilian Journal of Nephrology, Vol 43, Iss 2, Pp 279-282 (2020)
Brazilian Journal of Nephrology v.43 n.2 2021
Sociedade Brasileira de Nefrologia (SBN)
instacron:SBN
Phosphopenic rickets may be caused by mutations in the PHEX gene (phosphate regulating endopeptidase homolog X-linked). Presently, more than 500 mutations in the PHEX gene have been found to cause hypophosphatemic rickets. The authors report a clinic
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf8ccab7b9f1ddcc2784587f2cfa743a
http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0101-28002020005031201&lng=en&tlng=en
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