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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
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
Attainment of 2019 ESC/EAS lipid targets in a cohort of high and very-high risk subjects identified through cardiology and laboratory databases
Attainment of 2019 ESC/EAS lipid targets in a cohort of high and very-high risk subjects identified through cardiology and laboratory databases
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Attainment of 2019 ESC/EAS lipid targets in a cohort of high and very-high risk subjects identified through cardiology and laboratory databases

Canovi, S. ; Bonelli, E. ; Foracchia, M. ; Trenti, C. ; Negri, E.A. ; Colaiori, I. ; Guiducci, V. ; Calandra, S. ; Bertolini, S. ; Fasano, T.

Atherosclerosis, 2021-08, Vol.331, p.e282-e283 [Periódico revisado por pares]

Elsevier B.V

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3
Clinical and genetic features of familial hypercholesterolemia in pediatric patients: The lipigen Study
Clinical and genetic features of familial hypercholesterolemia in pediatric patients: The lipigen Study
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Clinical and genetic features of familial hypercholesterolemia in pediatric patients: The lipigen Study

Casula, M. ; Plastina, A. ; Galimberti, F. ; Arca, M. ; Averna, M. ; Bertolini, S. ; Calandra, S. ; Tarugi, P. ; Catapano, A.L.

Atherosclerosis, 2018-08, Vol.275, p.e98-e99 [Periódico revisado por pares]

Elsevier B.V

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4
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol
Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol
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Identification and characterization of novel loss of function mutations in ATP-binding cassette transporter A1 in patients with low plasma high-density lipoprotein cholesterol

Candini, C ; Schimmel, A.W ; Peter, J ; Bochem, A.E ; Holleboom, A.G ; Vergeer, M ; Dullaart, R.P.F ; Dallinga-Thie, G.M ; Hovingh, G.K ; Khoo, K.L ; Fasano, T ; Bocchi, L ; Calandra, S ; Kuivenhoven, J.A ; Motazacker, M.M

Atherosclerosis, 2010-12, Vol.213 (2), p.492-498 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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5
Evaluation of serum cholesterol efflux capacity in diabetic compared to healthy subjects
Evaluation of serum cholesterol efflux capacity in diabetic compared to healthy subjects
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Evaluation of serum cholesterol efflux capacity in diabetic compared to healthy subjects

Adorni, M.P ; Favari, E ; Ronda, N ; Zimetti, F ; Ardigò, D ; Franzini, L ; Manfredini, M ; Calandra, S ; Cicero, A.F.G ; Vigna, G.B ; Zavaroni, I ; Bernini, F

Atherosclerosis, 2014-08, Vol.235 (2), p.e181-e181 [Periódico revisado por pares]

Elsevier Ireland Ltd

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6
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia
Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia
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Genetic polymorphisms affecting the phenotypic expression of familial hypercholesterolemia

Bertolini, Stefano ; Pisciotta, Livia ; Di Scala, Lilla ; Langheim, Silvia ; Bellocchio, Antonella ; Masturzo, Paola ; Cantafora, Alfredo ; Martini, Scipione ; Averna, Maurizio ; Pes, Gianni ; Stefanutti, Claudio ; Calandra, Sebastiano

Atherosclerosis, 2004-05, Vol.174 (1), p.57-65 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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7
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes
Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes
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Combined monogenic hypercholesterolemia and hypoalphalipoproteinemia caused by mutations in LDL-R and LCAT genes

Pisciotta, Livia ; Calabresi, Laura ; Lupattelli, Graziana ; Siepi, Donatella ; Mannarino, Massimo Raffaele ; Moleri, Elsa ; Bellocchio, Antonella ; Cantafora, Alfredo ; Tarugi, Patrizia ; Calandra, Sebastiano ; Bertolini, Stefano

Atherosclerosis, 2005-09, Vol.182 (1), p.153-159 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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8
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders
Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders
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Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders

Pisciotta, Livia ; Hamilton-Craig, Ian ; Tarugi, Patrizia ; Bellocchio, Antonella ; Fasano, Tommaso ; Alessandrini, Paola ; Bon, Gabriele Bittolo ; Siepi, Donatella ; Mannarino, Elmo ; Cattin, Luigi ; Averna, Maurizio ; Cefalù, Angelo Balassare ; Cantafora, Alfredo ; Calandra, Sebastiano ; Bertolini, Stefano

Atherosclerosis, 2004-02, Vol.172 (2), p.309-320 [Periódico revisado por pares]

Amsterdam: Elsevier Ireland Ltd

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9
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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10
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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