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Refinado por: Nome da Publicação: Atherosclerosis remover
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1
The contemporary management of patients with homozygous familial hypercholesterolemia: The experience of the Italian Lipigen registry and a systematic review of the literature
The contemporary management of patients with homozygous familial hypercholesterolemia: The experience of the Italian Lipigen registry and a systematic review of the literature
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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 literature

D'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]

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2
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 horizon
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 horizon
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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 horizon

BERTOLINI, S ; PISCIOTTA, L ; SERI, M ; CUSANO, R ; CANTAFORA, A ; CALABRESI, L ; FRANCESCHINI, G ; RAVAZZOLO, R ; CALANDRA, S

Atherosclerosis, 2001, Vol.154 (3), p.599-605 [Periódico revisado por pares]

Amsterdam: Elsevier

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3
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma
Changes of the main isoform of human apolipoprotein A-I following incubation of plasma
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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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4
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic golgi apparatus and plasma
Isoforms of rat apolipoprotein A-I isolated from the lipoproteins of hepatic golgi apparatus and plasma
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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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5
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
A point mutation in ABC1 gene in a patient with severe premature coronary heart disease and mild clinical phenotype of Tangier disease
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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

Bertolini, 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 Ltd

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6
Separation of the isoprotein forms of apoprotein A-I of rat, rabbit and human HDL by combined isoelectrofocusing and SDS-polyacrylamide gel electrophoresis
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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7
C11 Two novel mutations in exon 4 of LDL-receptor gene causing familial hypercholesterolemia (FH) in northern Italy
C11 Two novel mutations in exon 4 of LDL-receptor gene causing familial hypercholesterolemia (FH) in northern Italy
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C11 Two novel mutations in exon 4 of LDL-receptor gene causing familial hypercholesterolemia (FH) in northern Italy

Bertolini, S ; Rolleri, M ; Trovatello, G ; Masturzo ; Elicio, N ; Martini, S ; Previato, L ; Calandra, S

Atherosclerosis, 1999-07, Vol.145, p.S3-S3 [Periódico revisado por pares]

Elsevier Ireland Ltd

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8
A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease
A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease
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A point mutation in ABC1 gene in a patient with a severe premature chd and a mild phenotype of tangier disease

Bertolini, 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.V

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9
C10 Clinical comparison between LDL-R gene mutations which cause no receptor synthesis or truncated receptors and LDL-R gene missense mutations
C10 Clinical comparison between LDL-R gene mutations which cause no receptor synthesis or truncated receptors and LDL-R gene missense mutations
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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 mutations

Fascetti, V ; Rolleri, M ; Cantafora, A ; Motti, C ; Averna, M ; Carru, C ; Garuti, R ; Calandra, S ; Bertolini, S

Atherosclerosis, 1999-07, Vol.145, p.S3-S3 [Periódico revisado por pares]

Elsevier Ireland Ltd

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10
FH clusters in Southern Italy
FH clusters in Southern Italy
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FH clusters in Southern Italy

Fascetti, 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 Ltd

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