Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Luigi Francesco Pio Morrone"'
Autor:
Maria Rosaria De Cagna, Vincenza Colucci, Arcangelo Di Maggio, Norma Notaristefano, Francesca Cianciotta, Katia Danza, Francesca Salvatore, Anna Santoniccolo, Salvatore Giovanni Lanzillotta, Maria Antonietta Perniola, Anna Lisa Marangi, Luigi Francesco Pio Morrone, Marilina Tampoia
Publikováno v:
Clinical and Experimental Nephrology. 27:445-453
Autor:
Vincenzo Antonio Panuccio, Rocco Tripepi, Maria Carmela Versace, Domenico Russo, Luigi Francesco Pio Morrone, Maria Cristina Mereu, Giovanni Luigi Tripepi, Carlo Alfieri
Publikováno v:
Nephrology Dialysis Transplantation. 37
BACKGROUND AND AIMS Though the current dialysis population is characterized by a better survival, there is a greater burden of cardiovascular comorbidities. These two factors together expose patients to a greater number of diagnostic and therapeutic
Publikováno v:
Scopus-Elsevier
Context.—Because of a marked increase in the number of requests for antinuclear antibodies, anti–extractable nuclear antigen antibodies, and anti–double-stranded DNA antibodies for the diagnosis of autoimmune rheumatic disease, guidelines have
Autor:
Gigante, M., Ranieri, E., Cerullo, G., Calabresi, L., Iolascon, A., Assmann, G., Luigi Francesco Pio MORRONE, Pisciotta, L., Schena, F. P., Gesualdo, L.
Publikováno v:
Scopus-Elsevier
Familial lecithin:cholesterol acyltransferase (LCAT) deficiency is an autosomal recessive disorder of lipoprotein metabolism, resulting from loss of function of lecithin:cholesterol acyltransferase (LCAT; EC 2.3.1.43), a key enzyme in extracellular c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5e54391bb9973927d8dd754efca9dc7e
http://hdl.handle.net/11588/474818
http://hdl.handle.net/11588/474818
Autor:
Luigi Francesco Pio MORRONE, Capurso, D., D Elia, F., Di Paolo, S., Grandaliano, G., Marangi, A. L., Schena, A., Stallone, G., Tarantino, G.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::3efae52694bd62efdf1fcf9b0a40075c
http://www.scopus.com/inward/record.url?eid=2-s2.0-1842834885&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-1842834885&partnerID=MN8TOARS
Autor:
Luigi Francesco Pio MORRONE, Ettorre, G. C., Passavanti, G., Tampoia, M., Schiavone, P., Coratelli, P.
Publikováno v:
Scopus-Elsevier
Europe PubMed Central
Europe PubMed Central
Brown tumors are unusual but serious complications of renal osteodystrophy, and can be successfully treated by parathyroidectomy or by pharmacological treatment of hyperparathyroidism. Brown tumors in patients with severe hyperparathyroidism (HPT) se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::853313aeb8bbc91ae061cc7b725aed9b
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035186840&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0035186840&partnerID=MN8TOARS