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1
Predictive factors of survival and intrahepatic recurrence of hepatocellular carcinoma in cirrhosis after percutaneous ethanol injection: analysis of 71 patients
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Predictive factors of survival and intrahepatic recurrence of hepatocellular carcinoma in cirrhosis after percutaneous ethanol injection: analysis of 71 patients

Castellano, Luigi ; Calandra, Maria ; Blanco, Camillo Del Vecchio ; de Sio, Ilario

Journal of hepatology, 1997-11, Vol.27 (5), p.862-870 [Periódico revisado por pares]

Oxford: Elsevier B.V

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2
Prevalence of gallstone disease and related risk factors in 889 diabetic subjects of Southern Italy
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Artigo
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Prevalence of gallstone disease and related risk factors in 889 diabetic subjects of Southern Italy

Gentile, S. ; Castellano, L. ; de Sio, I. ; Calandra, M. ; Torchio, P. ; Corrao, G. ; Del Vecchio Blanco, C.

Digestive and liver disease, 2004-10, Vol.36 (10), p.698-699 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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3
Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene
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Artigo
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Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene

Rabacchi, Claudio, PhD ; D'Addato, Sergio, MD ; Palmisano, Silvia, MD ; Lucchi, Tiziano, MD ; Bertolini, Stefano, MD ; Calandra, Sebastiano, MD ; Tarugi, Patrizia, PhD

Journal of clinical lipidology, 2016-07, Vol.10 (4), p.915-921.e4 [Periódico revisado por pares]

United States: Elsevier Inc

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4
The Type of LDLR Gene Mutation Predicts Cardiovascular Risk in Children with Familial Hypercholesterolemia
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Artigo
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The Type of LDLR Gene Mutation Predicts Cardiovascular Risk in Children with Familial Hypercholesterolemia

Guardamagna, Ornella, MD ; Restagno, Gabriella, MD ; Rolfo, Elio, MD ; Pederiva, Cristina, MD ; Martini, Scipione, MD ; Abello, Francesca, MD ; Baracco, Viviana, MD ; Pisciotta, Livia, MD ; Pino, Elisabetta, MD ; Calandra, Sebastiano, MD ; Bertolini, Stefano, MD

The Journal of pediatrics, 2009-08, Vol.155 (2), p.199-204.e2 [Periódico revisado por pares]

Maryland Heights, MO: Mosby, Inc

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5
Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis
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Artigo
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Novel mutations in the GPIHBP1 gene identified in 2 patients with recurrent acute pancreatitis

Ariza, María José, PhD ; Martínez-Hernández, Pedro Luis, MD, PhD ; Ibarretxe, Daiana, MD ; Rabacchi, Claudio, PhD ; Rioja, José, PhD ; Grande-Aragón, Cristina, PhD ; Plana, Nuria, MD, PhD ; Tarugi, Patrizia, PhD ; Olivecrona, Gunilla, PhD ; Calandra, Sebastiano, MD ; Valdivielso, Pedro, MD, PhD

Journal of clinical lipidology, 2016, Vol.10 (1), p.92-100.e1 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma
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Artigo
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Changes of the main isoform of human apolipoprotein A-I following incubation of plasma

Ghisellini, M. ; Pecorari, M. ; Calandra, S.

Atherosclerosis, 1986-03, Vol.59 (3), p.247-256 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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7
Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations
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Phenotypic variability in 4 homozygous familial hypercholesterolemia siblings compound heterozygous for LDLR mutations

Rabacchi, Claudio, PhD ; Bigazzi, Federico, PhD ; Puntoni, Mariarita, PhD ; Sbrana, Francesco, MD ; Sampietro, Tiziana, MD ; Tarugi, Patrizia, PhD ; Bertolini, Stefano, MD ; Calandra, Sebastiano, MD

Journal of clinical lipidology, 2016-07, Vol.10 (4), p.944-952.e1 [Periódico revisado por pares]

United States: Elsevier Inc

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8
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic golgi apparatus and plasma
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Artigo
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Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic golgi apparatus and plasma

Tarugi, 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 Ltd

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9
A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla )
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Artigo
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A complex phenotype in a child with familial HDL deficiency due to a novel frameshift mutation in APOA1 gene (apoA-IGuastalla )

Pisciotta, Livia, MD ; Vitali, Cecilia, PhD ; Favari, Elda, PhD ; Fossa, Paola, PhD ; Adorni, Maria Pia, PhD ; Leone, Daniela, PhD ; Artom, Nathan, MD ; Fresa, Raffaele, LabTech ; Calabresi, Laura, PhD ; Calandra, Sebastiano, MD ; Bertolini, Stefano, MD

Journal of clinical lipidology, 2015-11, Vol.9 (6), p.837-846 [Periódico revisado por pares]

United States: Elsevier Inc

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10
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis
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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 electrophoresis

Calandra, S. ; Tarugi, P. ; Ghisellini, M.

Atherosclerosis, 1984-02, Vol.50 (2), p.209-221 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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