Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Mateus, Martins Prata"'
Autor:
Teresa Adragão, Ana Salomé Pires, José Dias Curto, Rui E. Castro, Cristina Nogueira, Mateus Martins Prata, Ana Beatriz Oliveira, Joaquim Bordalo, Patrícia Branco
Publikováno v:
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
WOS:000299957700048 (Nº de Acesso Web of Science) “Prémio Científico ISCTE-IUL 2013” Background. The ankle-brachial index (ABI) is a noninvasive method to evaluate peripheral artery disease (PAD). ABI 1.3 is a false negative caused by noncompr
Publikováno v:
American Journal of Kidney Diseases. 47:587-592
Hypertension and increased left ventricular mass index (LVMI) have been reported in patients with early stages of autosomal dominant polycystic kidney disease (ADPKD). Whether these abnormalities are associated with diastolic dysfunction in this stag
Autor:
S Silva, E de Almeida, Cristina Resina, João F. Lacerda, Fernando Abreu, José António Lopes, S Gonçalves, Carlos Martins, J A do Carmo, F. Lourenço, Sofia Jorge, Mateus Martins Prata
Publikováno v:
Bone Marrow Transplantation. 42:139-141
Contemporary analysis of the influence of acute kidney injury (AKI) after myeloablative hematopoietic cell transplantation on long-term patient's survival
Autor:
Edgar Almeida, Mateus Martins Prata
Publikováno v:
Nephrology Dialysis Transplantation. 23:1831-1833
The first description of polycystic kidney disease (PKD) in a Portuguese medical journal occurred in 1918 when Dr Custodio Cabeca published a manuscript in Medicina Contemporânea, a medical journal founded in 1883 by Dr Miguel Bombarda (1851–1910)
Autor:
I. Tavora, Dorien J.M. Peters, Mateus Martins Prata, José Ricardo Pinto, João Lavinha, S. De Almeida, Martijn H. Breuning, E de Almeida
Publikováno v:
Human Genetics. 96:83-88
Autosomal dominant polycystic kidney disease is characterized by clinical and genetic heterogeneity. Two loci implicated in the disease have previously been mapped (PKD1 on chromosome 16 and PKD2 on chromosome 4). By two point and multipoint linkage
Publikováno v:
Scopus-Elsevier
Autor:
Mateus Martins Prata, José António Lopes, Mário Raimundo, J A do Carmo, Leonidas C. Resende, João F. Lacerda, Sofia Jorge, F. Lourenço, S Gonçalves, Carlos Martins, J.M.F. Lacerda
Publikováno v:
Bone marrow transplantation. 42(9)
We evaluated retrospectively the incidence of acute kidney injury (AKI), defined by risk, injury, failure, loss and end-stage kidney disease (RIFLE) and its influence on long-term survival, in 82 patients aged 18-60 years who underwent a reduced inte
Autor:
Sara Gonçalves, Maria João Palhano, José António Lopes, Alice Fortes, Paulo R. Fernandes, Mateus Martins Prata, José Barbas, Fernando Abreu
Publikováno v:
NDT Plus
A 17-year-old black African female from Saint Thomas and Prince with growth failure and a 5-year history of frothy urine and periorbitary oedema was referred to our department for evaluation of renal insufficiency. At admission, the patient was hyper
Autor:
Wim, Van Biesen, Francesco, Locatelli, Mateus, Martins Prata, Jean Pierre, Wauters, Alicja, Debska-Slizien, Joan M, Mauri, Kaj, Metsärinne, Gabriel, Mircescu, Kostas C, Siamopoulos, Vianda S, Stel, Eric, Will, Lucia, Del Vecchio, Carmine, Zoccali, Kitty J, Jager
Publikováno v:
Journal of nephrology. 20(5)
Autor:
Lucia, Del Vecchio, Francesco, Locatelli, Mateus, Martins Prata, Jean Pierre, Wauters, Alicja, Debska-Slizien, Joan M, Mauri, Kaj, Metsärinne, Gabriel, Mircescu, Kostas C, Siamopoulos, Vianda S, Stel, Eric, Will, Wim, Van Biesen, Kitty J, Jager, Carmine, Zoccali
Publikováno v:
Journal of nephrology. 20(5)