Zobrazeno 101 - 110
of 124
pro vyhledávání: '"Francesco Scolari"'
Autor:
Roberto Zubani, Alessandra Pola, Francesco Scolari, Pietro Ravani, Simona Guerini, Silvana Savoldi, Rosario Maiorca, Ezio Movilli, Fabio Malberti
Atheroembolic renal disease (AERD) is part of a multisystemic disease accompanied by high cardiovascular comorbidity and mortality. Interrelationships between traditional risk factors for atherosclerosis, vascular comorbidities, precipitating factors
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34297b178755a40582cfddc8960d9e03
http://hdl.handle.net/11379/24564
http://hdl.handle.net/11379/24564
Autor:
Maurizio Bruschi, Laura Santucci, Landino Allegri, Gian Marco Ghiggeri, Corrado Murtas, Marco Prunotto, Giovanni Candiano, Maria Luisa Carnevali, Francesco Scolari
Publikováno v:
Clinical Kidney Journal
Autor:
Giuliano Brunori, Ezio Movilli, Francesco Scolari, Rosario Maiorca, Giovanni Cancarini, Corrado Camerini, Nicoletta Pertica
American guidelines for the management of renal anemia by recombinant human erythropoietin (rHuEPO) recommend collecting a predialysis blood sample to evaluate hemoglobin (Hb) and hematocrit (Hct) levels in hemodialysis patients. Although a predialys
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fd87def2c1ad4043f47b6f6fc33a748
http://hdl.handle.net/11379/22756
http://hdl.handle.net/11379/22756
Autor:
Nicola Bossini, Manuela Baronio, Silvana Savoldi, Franco Franceschini, Roberto Cattaneo, Rosario Maiorca, Francesco Scolari, Ilaria Cavazzana, B. Valzorio, Consuela Mazzucchelli, S. Mombelloni, Battista Fabio Viola
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 16(12)
Background. Primary Sjogren's syndrome is a connective tissue disorder affecting primarily the lacrimal and salivary glands, resulting in xerophtalmia and xerostomia. Extraglandular manifestations are frequent and may include renal involvement. Metho
Autor:
Battista Fabio Viola, Alessandra Pola, Ezio Movilli, Roberta Zani, Rosario Maiorca, Regina Tardanico, Francesco Scolari
Cholesterol crystal embolism, sometimes separately designated atheroembolism, is an increasing and still underdiagnosed cause of renal dysfunction antemortem in elderly patients. Renal cholesterol crystal embolization, also known as atheroembolic ren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::735e4c69d55148df23ab83c0b0b6bc87
http://hdl.handle.net/11379/24501
http://hdl.handle.net/11379/24501
Autor:
Gianluca Caridi, Antonio Amoroso, Battista Fabio Viola, Gian Marco Ghiggeri, Rosanna Gusmano, Nicola Bossini, Silvana Savoldi, Regina Tardanico, Daniela Puzzer, Valerio Vizzardi, Prati E, Giorgio Casari, Francesco Scolari, Rosario Maiorca, B. Valzorio
Publikováno v:
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association. 13(10)
failure. The exclusion of linkage to the NPH1 locus suggests the existence of an MCD responsible locus, Background. The nephronophthisis‐medullary cystic disease (NPH/MCD) complex represents a heterogen- still to be mapped. eous group of hereditary
Autor:
Nicola Bossini, Battista Fabio Viola, Silvana Savoldi, Rosario Maiorca, Roberto Zubani, Silvio Sandrini, L Morassi, Regina Tardanico, Francesco Scolari
Publikováno v:
Transplantation proceedings. 30(5)
IN THE CYCLOSPORINE era, short-term results of renal transplantation have dramatically improved; however, the rate of graft loss in the long-term has only marginally improved. Progressive and irreversible decline in renal function suggests a continuo
Autor:
Francesco Scolari, Patricia L. Weng, Gianluca Caridi, Gian Marco Ghiggeri, Francesco Perfumo, Ali G. Gharavi, Simone Sanna-Cherchi
Publikováno v:
Pediatric Nephrology. 22:1685-1686
Table 2 shows some of the principal human malformation syndromes with kidney hypoplasia/dysplasia. The branchio-oto-renal syndrome is caused by mutations of EYA1, SIX1 or SIX5 genes and not SIX2. We apologize for the mistake in the article.