Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Estela Nogueira"'
Autor:
Sofia Jorge, Kendrah Kidd, Petr Vylet’al, Estela Nogueira, Lauren Martin, Katrice Howard, Veronika Barešová, Kateřina Hodaňová, Aleš Hnízda, Oana Moldovan, Catarina Silveira, Ana Margarida Coutinho, José António Lopes, Anthony J. Bleyer, Stanislav Kmoch, Martina Živná
Publikováno v:
Kidney International Reports, Vol 8, Iss 5, Pp 1112-1116 (2023)
Externí odkaz:
https://doaj.org/article/578e96a7a178440d98d7e8bb2fdeb468
Autor:
João Bernardo, João Oliveira, Filipe Marques, Joana Gameiro, Cristina Outerelo, Estela Nogueira, Sofia Jorge, José António Lopes
Publikováno v:
Revista Portuguesa de Nefrologia e Hipertensão, Vol 36, Iss 2, Pp 106-114 (2022)
Introduction: Dysproteinemia is associated with kidney damage and treatment of underlying conditions is crucial to minimize kidney damage. The aim of this study was to describe and analyze the characteristics and outcome of the patients diagnosed wit
Externí odkaz:
https://doaj.org/article/972d7549e3984bca8b1b8c6ac29aa0d8
Autor:
Marta Casal Moura, Carolina Branco, Joana Martins-Martinho, José Luís Ferraro, Alvise Berti, Estela Nogueira, Cristina Ponte
Publikováno v:
Therapeutic Advances in Musculoskeletal Disease, Vol 14 (2022)
In the past decade, unprecedented progress has been made in understanding the pathogenesis, diagnosis, assessment, and treatment of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAVs). International collaborations and input fro
Externí odkaz:
https://doaj.org/article/105ab7310d2e49108f3e3e3af25fc023
Autor:
André Weigert, Marie-Louise Bergman, Lígia A. Gonçalves, Iolanda Godinho, Nádia Duarte, Rita Abrantes, Patrícia Borges, Ana Brennand, Vanessa Malheiro, Paula Matoso, Onome Akpogheneta, Lindsay Kosack, Pedro Cruz, Estela Nogueira, Magda Pereira, Ana Ferreira, Marco Marques, Telmo Nunes, João Faro-Viana, Jocelyne Demengeot, Carlos Penha-Gonçalves
Publikováno v:
Frontiers in Medicine, Vol 8 (2021)
Background: Patients on hemodialysis (HD) are at higher risk for COVID-19, overall are poor responders to vaccines, and were prioritized in the Portuguese vaccination campaign.Objective: This work aimed at evaluating in HD patients the immunogenicity
Externí odkaz:
https://doaj.org/article/086c515bdc274611af01fcc9b62024a1
Autor:
Marta Pereira, Noélia Lopez, Iolanda Godinho, Sofia Jorge, Estela Nogueira, Fernando Neves, Alice Fortes, António G. Costa
Publikováno v:
Brazilian Journal of Nephrology, Vol 39, Iss 1, Pp 36-41
Abstract Introduction: Intra-atrial catheter (IAC) placement through an open surgical approach has emerged as a life-saving technique in hemodialysis (HD) patients with vascular access exhaustion. Objective: To assess the complications of IAC placeme
Externí odkaz:
https://doaj.org/article/39e0028f442e4b6298a38a9da3fa71e7
Autor:
Rita Veríssimo, Estela Nogueira, João Bernardo, Marta Pereira, Cristina P. Abreu, Noelia Lopez, Cristina Resina, Patrícia Matias, José António Lopes, Patrícia Branco, Luísa Pinto
Publikováno v:
Clinical Nephrology – Case Studies. 10:32-36
Autor:
Sofia Jorge, Catarina Silveira, Márcia Rodrigues, Iolanda Godinho, Estela Nogueira, José António Lopes
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS ADTKD represents a recently described group of kidney diseases, characterized by chronic interstitial nephritis (CIN), in most cases hereditary, with an autosomal dominant inheritance pattern, subclassified according to its geneti
Autor:
Filipe Marques, Onassis Silva, Cristina Outerelo, Noélia Lopez, Paulo Fernandes, Estela Nogueira, Sofia Jorge, Joana Gameiro, José António Lopes
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS Percutaneous renal biopsy is a fundamental technique for the diagnosis of numerous renal pathologies. However, it is an invasive technique that requires operator experience and is associated with adverse outcomes. Bleeding complic
Publikováno v:
Nephron. 145:188-191
Atypical hemolytic uremic syndrome (aHUS) is a rare disease. It results from the dysregulation of the alternative complement pathway on the cell surface which causes endothelial damage. Increasing evidence links, these abnormalities to mutations in g