PISCIOTTA, LIVIA

PISCIOTTA, LIVIA  

100007 - Dipartimento di Medicina interna e specialità mediche  

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A 33-year-old man with nephrotic syndrome and lecithin-cholesterol acyltransferase (LCAT) deficiency. Description of two new mutations in the LCAT gene 1-gen-2004 Frasca', Gm; Soverini, L; Tampieri, E; Franceschini, G; Calabresi, L; Pisciotta, Livia; Preda, P; Vangelista, A; Stefoni, S; Bertolini, Stefano
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla) 1-gen-2015 Pisciotta, Livia; Vitali, Cecilia; Favari, Elda; Fossa, Paola; Adorni, Maria Pia; Leone, Daniela; Artom, Nathan; Fresa, Raffaele; Calabresi, Laura; Calandra, Sebastiano; Bertolini, Stefano
A novel mutation of the apolipoprotein A-I gene in a family with familial combined hyperlipidemia 1-gen-2008 Pisciotta, Livia; Fasano, T.; Calabresi, L.; Bellocchio, A.; Fresa, R.; Borrini, C.; Calandra, S.; Bertolini, Stefano
A novel sequence variant in APOA5 gene found in patients with severe hypertriglyceridemia. 1-gen-2006 Priore Oliva, C; Tarugi, P; Calandra, S; Pisciotta, Livia; Bellocchio, A; Bertolini, Stefano; Guardamagna, O; Schaap, Fg
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease 1-gen-2001 Bertolini, Stefano; Pisciotta, Livia; Seri, M; Cusano, R; Cantafora, A; Calabresi, L; Franceschini, G; Ravazzolo, Roberto; Calandra, S.
A silent mutation of Niemann-Pick C1-like 1 and apolipoprotein E4 modulate cholesterol absorption in primary hyperlipidemias. 1-gen-2013 Lupattelli, G; Pisciotta, Livia; De Vuono, S; Siepi, D; Bellocchio, A; Melis, F; Bertolini, Stefano; Pirro, M; Mannarino, E.
A successful term pregnancy with severe hypertriglyceridaemia and acute pancreatitis. Clinical management and review of the literature 1-gen-2019 Perrone, S.; Brunelli, R.; Perrone, G.; Zannini, I.; Galoppi, P.; Di Giacomo, S.; Morozzi, C.; Pisciotta, L.; Stefanutti, C.
A three month-old infant with severe hyperchylomicronemia: molecular diagnosis and extracorporeal treatment. 1-gen-2013 Stefanutti, C; Gozzer, M; Pisciotta, Livia; D'Eufemia, P; Bosco, G; Morozzi, C; Papadia, F; Shafii, M; Di Giacomo, S; Bertolini, Stefano
A “de novo” mutation of the LDL-receptor gene as the cause of familial hypercholesterolemia. 1-gen-2002 Pisciotta, Livia; Cantafora, A; DE STEFANO, Francesco; Langheim, S; Calandra, S; Bertolini, Stefano
Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene 1-gen-2003 Altilia, S; Pisciotta, Livia; Garuti, R; Tarugi, P.; Cantafora, A.; Calabresi, L; Tagliabue, J; Maccari, S; Bernini, F; Vergani, C; Bertolini, Stefano; Calandra, S.
Additive effect of mutations in LDLR and PCSK9 genes on the phenotype of familial hypercholesterolemia 1-gen-2006 Pisciotta, Livia; Oliva, Cp; Cefalu, Ab; Noto, D; Bellocchio, A; Fresa, R; Cantafora, A; Patel, D; Averna, M; Tarugi, P; Calandra, S; Bertolini, Stefano
Among biomarkers of neutrophil activity, matrix metalloproteinases 8 independently predicts remission of metabolic syndrome 1-gen-2022 Carbone, Federico; Elia, Edoardo; Casula, Matteo; Bonaventura, Aldo; Bertolotto, Maria; Minetti, Silvia; Artom, Nathan; Camici, Giovanni G; Contini, Paola; Pontremoli, Roberto; Viazzi, Francesca; Bertolini, Stefano; Pende, Aldo; Pisciotta, Livia; Montecucco, Fabrizio; Liberale, Luca
An apparent inconsistency in parent to offspring transmission of point mutations of LDLR gene in familial hypercholesterolemia. 1-gen-2009 Rabacchi, C; Wunsch, A; Ghisellini, M; Marino, M; Pisciotta, Livia; Bertolini, Stefano; Calandra, S.
Appropriateness criteria for the management of lipid-lowering therapy with alirocumab in high cardiovascular risk patients. The opinion of a multidisciplinary group of Italian experts 1-gen-2020 Lettino, M.; Zambon, A.; Musumeci, G.; Arca, M.; Bilato, C.; Brunetti, N. D.; Calabro, P.; Casu, G.; Chiarella, F.; Faggiano, P.; Ferlini, M.; Guardigli, G.; Imbalzano, E.; Indolfi, C.; Marcucci, R.; Menozzi, A.; Mureddu, G. F.; Filardi, P. P.; Pirro, M.; Pisciotta, L.; Scherillo, M.; Suppressa, P.; Uguccioni, M.; Varbella, F.; Gentile, L.; Rapezzi, C.; Averna, M.
Autosomal recessive hypercholesterolemia (ARH) and homozygous familial hypercholesterolemia (FH): a phenotypic comparison. 1-gen-2006 Pisciotta, Livia; Oliva, Cp; Pes, Gm; DI SCALA, L; Bellocchio, A; Fresa, R; Cantafora, A; Arca, M; Calandra, S; Bertolini, Stefano
Baseline hs-CRP predicts hypertension remission in metabolic syndrome 1-gen-2019 Carbone, F; Elia, E; Casula, M; Bonaventura, A; Liberale, L; Bertolotto, M; Artom, N; Minetti, S; Dallegri, F; Contini, P; Verzola, D; Pontremoli, R; Viazzi, F; L Viviani, G; Bertolini, S; Pende, A; Pisciotta, L; Montecucco, F
Beta-sitosterolaemia: a new nonsense mutation in the ABCG5 gene. 1-gen-2007 Mannucci, L; Guardamagna, O; Bertucci, P; Pisciotta, Livia; Liberatoscioli, L; Bertolini, Stefano; Irace, C; Gnasso, A; Federici, G; Cortese, C.
Beta-thalassemia is a modifying factor of the clinical expression of familial hypercholesterolemia. 1-gen-2004 Calandra, S; Bertolini, Stefano; Pes, Gm; Deiana, L; Tarugi, P; Pisciotta, Livia; Li Volti, S; Li Volti, G; Maccarone, C.
Carotid ultrasonography in the assessment of cardiovascular risk 1-gen-2015 Pende, Aldo; Artom, Nathan; Pistocchi, Giovanni; Pisciotta, Livia; Dallegri, Franco
Changes in the expression of cytokeratins and nuclear matrix proteins are correlated with the level of differentiation in human prostate cancer 1-gen-2000 Alberti, I; Barboro, P; Barbesino, M; Sanna, P; Pisciotta, Livia; Parodi, Silvio; Nicolo', G; Boccardo, Francesco; Galli, S; Patrone, E; Balbi, C.