Zobrazeno 1 - 10 of 115 pro vyhledávání: '"Giuliano Barsotti"'
2
Very low-protein diet plus ketoacids in chronic kidney disease and risk of death during end-stage renal disease: a historical cohort controlled study
Autor: Mauro Pezzotta, Adamasco Cupisti, Giorgina Barbara Piccoli, Roberto Minutolo, Biagio Di Iorio, Luca De Nicola, Giuliano Barsotti, Battista Fabio Viola, Vincenzo Bellizzi, Paolo Chiodini
Publikováno v: Nephrology Dialysis Transplantation. 30:71-77
BACKGROUND Very low-protein intake during chronic kidney disease (CKD) improves metabolic disorders and may delay dialysis start without compromising nutritional status, but concerns have been raised on a possible negative effect on survival during d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::661a89016eef7262631222809daa75e9
https://doi.org/10.1093/ndt/gfu251
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3
A case of pheochromocytoma presenting as secondary hyperaldosteronism, hyperparathyroidism, diabetes and proteinuric renal disease
Autor: Davide Carrara, Alessandra Bacca, Matteo Bernini, Giuliano Barsotti, Antonio Giuseppe Naccarato, Valentina Carli, Ilaria Farnesi, Giuseppe Casto, Adamasco Cupisti, Giampaolo Bernini
Publikováno v: Nephrology Dialysis Transplantation. 26:1104-1107
A 35-year-old woman was admitted to the Nephrology and Dialysis Unit of Pisa University for hypertension, hypokalaemia, renal impairment, proteinuria and hyperglycaemia. plasma renin activity (PRA) and plasma aldosterone were elevated, but Doppler ul
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf68e5efcb9ecd5633be831be06b4e0b
https://doi.org/10.1093/ndt/gfq747
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4
Lipoprotein glomerulopathy: first report of 2 not consanguineous Italian men from the same town
Autor: Giuliano Barsotti, P Lorusso, Niccola Funel, Giovanna Pasquariello, Maurizio Innocenti, Francesca Minnei, A. Pasquariello
Publikováno v: Journal of Nephrology. 24:381-385
It is well known that the abnormal accumulation of lipids can occur in kidneys of patients affected by some metabolic disorders due either to inherited enzymatic deficiency or to an acquired lipid alteration as in nephrotic syndrome. Lipoprotein glom
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::647f5d28bc18a3a410c81d4d93c48c69
https://doi.org/10.5301/jn.2011.7772
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Plný text Recenzováno Digitální knihovna AV ČR
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