Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Diletta, Duranti"'
Publikováno v:
Nephrology and Renal Diseases. 6
Autor:
Guendalina Vaggelli, Simona Dei, Sara Fabbroni, Danilo Tacconi, Pasqualino Magliocca, Gianluca Viti, Silvana Gervino, Diletta Duranti, Monica Mazzierli, Erica Mazzeschi, Alessandro Tartaglia Polcini, Monica Cortesi, Angelo Galano, Manuela Mafucci, Agostino Ognibene, Paola Sanchini, Alessandro Pancrazzi, Maria Lorubbio, Antonio D'Urso, Emanuela Tripodo
Publikováno v:
Clinical Biochemistry
Background Since February 2019, Italian hospitals registered COVID-19 (COronaVIrus Disease 19) cases more often than the rest of the country. During this epidemic, health authorities requested swab tests, whileseeking new patient paths. Methods A dua
Autor:
Ennio Duranti, Marco Bagnati, Filomena Panza, Ralli Chiara, Giorgio Bellomo, Diletta Duranti, Matteo Basile
Publikováno v:
Archives of Renal Diseases and Management. :001-005
The uremic syndrome is provoked by a progressive number of compounds that are normally excreted by kidneys in healthy individuals. Indoxylsulphate (IXS) and p-cresylsulphate (PCS), have been found increased in subjects with end stage renal disease (E
Autor:
Filomena Panza, Giorgio Bellomo, Chiara Ralli, Patrizio Imperiali, Ennio Duranti, Diletta Duranti, Marco Bagnati, Matteo Basile
Publikováno v:
Journal of Clinical & Experimental Nephrology.
Introduction: The adsorbing capacity of membranes can be considered the third dimension of the depurative action of dialysis: diffusion, convection and adsorption. Some metabolites are almost totally bound to albumin, so, regardless of their molecula
Autor:
Ennio Duranti, Diletta Duranti
Publikováno v:
Journal of Vaccines & Vaccination.
Patients undergoing hemodialysis often present with a reduced response to anti-hepatitis B virus (anti-HBV) vaccination. The soluble form of CD40 (sCD40) is elevated in hemodialysis patients and this has been shown to correlate with lack of response
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 27(5)
We present the case of a 65-year-old male patient without any family history of renal or hepatic disease. He had been on maintenance hemodialysis for 4 months because of autosomal recessive polycystic kidney disease. At the start of the hemodialysis