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1 |
Material Type: Artigo
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The contemporary management of patients with homozygous familial hypercholesterolemia: The experience of the Italian Lipigen registry and a systematic review of the literatureD'Erasmo, L. ; Bini, S. ; Casula, M. ; D'Elia, S. ; Gazzotti, M. ; Bertolini†, S. ; Calandra, S. ; Tarugi, P. ; Averna, M. ; Catapano, A. ; Arca, M.Atherosclerosis, 2023-08, Vol.379, p.S67 [Periódico revisado por pares]Texto completo disponível |
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2 |
Material Type: Artigo
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A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease: Genetics and atherosclerosis: broadening the horizonBERTOLINI, S ; PISCIOTTA, L ; SERI, M ; CUSANO, R ; CANTAFORA, A ; CALABRESI, L ; FRANCESCHINI, G ; RAVAZZOLO, R ; CALANDRA, SAtherosclerosis, 2001, Vol.154 (3), p.599-605 [Periódico revisado por pares]Amsterdam: ElsevierTexto completo disponível |
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3 |
Material Type: Artigo
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Changes of the main isoform of human apolipoprotein A-I following incubation of plasmaGhisellini, M. ; Pecorari, M. ; Calandra, S.Atherosclerosis, 1986-03, Vol.59 (3), p.247-256 [Periódico revisado por pares]Amsterdam: Elsevier Ireland LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic golgi apparatus and plasmaTarugi, P. ; Ghisellini, M. ; Pecorari, M. ; Brugni, N. ; Calandra, S.Atherosclerosis, 1985-08, Vol.56 (2), p.189-198 [Periódico revisado por pares]Amsterdam: Elsevier Ireland LtdTexto completo disponível |
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5 |
Material Type: Artigo
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A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier diseaseBertolini, S. ; Pisciotta, L. ; Seri, M. ; Cusano, R. ; Cantafora, A. ; Calabresi, L. ; Franceschini, G. ; Ravazzolo, R. ; Calandra, S.Atherosclerosis, 2001-02, Vol.154 (3), p.599-605 [Periódico revisado por pares]Ireland: Elsevier Ireland LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresisCalandra, S. ; Tarugi, P. ; Ghisellini, M.Atherosclerosis, 1984-02, Vol.50 (2), p.209-221 [Periódico revisado por pares]Amsterdam: Elsevier Ireland LtdTexto completo disponível |
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7 |
Material Type: Artigo
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C11 Two novel mutations in exon 4 of LDL-receptor gene causing familial hypercholesterolemia (FH) in northern ItalyBertolini, S ; Rolleri, M ; Trovatello, G ; Masturzo ; Elicio, N ; Martini, S ; Previato, L ; Calandra, SAtherosclerosis, 1999-07, Vol.145, p.S3-S3 [Periódico revisado por pares]Elsevier Ireland LtdTexto completo disponível |
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8 |
Material Type: Artigo
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A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier diseaseBertolini, S. ; Pisciotta, L. ; Seri, M. ; Cusano, R. ; Cantafora, A. ; Calabresi, L. ; Franceschini, G. ; Ravazzolo, R. ; Calandra, S.Atherosclerosis, 2000-07, Vol.151 (1), p.311-311 [Periódico revisado por pares]Elsevier B.VTexto completo disponível |
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9 |
Material Type: Artigo
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C10 Clinical comparison between LDL-R gene mutations which cause no receptor synthesis or truncated receptors and LDL-R gene missense mutationsFascetti, V ; Rolleri, M ; Cantafora, A ; Motti, C ; Averna, M ; Carru, C ; Garuti, R ; Calandra, S ; Bertolini, SAtherosclerosis, 1999-07, Vol.145, p.S3-S3 [Periódico revisado por pares]Elsevier Ireland LtdTexto completo disponível |
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10 |
Material Type: Artigo
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FH clusters in Southern ItalyFascetti, V. ; Rolleri, M. ; Guido, V. ; Trovatello, G. ; Masturzo, P. ; Garuti, R. ; Motti, C. ; Cortese, C. ; Cantafora, A. ; Calandra, S. ; Bertolini, S.Atherosclerosis, 1997-12, Vol.135, p.S12-S12 [Periódico revisado por pares]Elsevier Ireland LtdTexto completo disponível |