• 3460 Citations
  • 29 h-Index
19952019

Research output per year

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Research Output

  • 3460 Citations
  • 29 h-Index
  • 131 Article
  • 73 Other
  • 25 Book/Film/Article review
  • 2 Paper

[ANTI-TNF (INFLIXIMAB) TREATMENT IN CROHN DISEASE: SAFETY PROFILE

Cefalu', A. B., Carroccio, A., Di Prima, L., Ambrosiano, G., Di Prima, L., Noto, D., Pirrone, G., Ambrosiano, G., Cefalù, A. B. & Carroccio, A., 2006, In : Recenti Progressi in Medicina. 97, p. 108-112 5 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)
14 Citations (Scopus)
14 Citations (Scopus)

Accumulation of apoE-enriched triglyceride-rich lipoproteins in patients with coronary artery disease.

Rizzo, M; Noto, D; Frasheri, A; Pernice, V; Rubino, A; Pieri, D; Pinto, V; Cefalù, Ab, 2006, In : METABOLISM, CLINICAL AND EXPERIMENTAL. 5, p. - 6 p.

Research output: Contribution to journalArticle

14 Citations (Scopus)

Additive effect of mutations in LDLR and PCSK9 genes on the phenotyoe of familial hypercholesterolemia

Cefalu', A. B., Averna, M., Fresa, R., Cantafora, A., Patel, D., Calandra, S., Pisciotta, L., Bellocchio, A., Tarugi, P., Bertolini, S. & Oliva, C. P., 2006, In : ATHEROSCLEROSIS. 2, p. 433-440 8 p.

Research output: Contribution to journalArticle

77 Citations (Scopus)

Albumin versus solvent/detergent-treated pooled plasma as replacement fluid for long-term plasma exchange therapy in a patient with primary hypertriglyceridemia and recurrent hyperlipidemic pancreatitis

Averna, M., Caruso, C., Cefalu', A. B., Giammanco, A., Barbagallo, C. M., Rizzo, C. M., Rizzo, S., Lima, G. M., Scirè, E., Di Bona, D., Rizzo, S., Caruso, C. & Lima, G. M., 2016, In : Transfusion. p. 755-760 6 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

A Novel APOB Mutation Identified by Exome Sequencing Cosegregates With Steatosis, Liver Cancer, and Hypocholesterolemia.

Averna, M., Valenti, V., Spina, R., Cefalu', A. B., Pirruccello, J. P., Gupta, N., Kathiresan, S., Tarugi, P., Gabriel, S. & Noto, D., 2013, In : Arteriosclerosis, Thrombosis, and Vascular Biology. 33, p. 2021-2025 5 p.

Research output: Contribution to journalArticle

43 Citations (Scopus)

A NOVEL APOB MUTATION IDENTIFIEDBY EXOME SEQUENCING COSEGREGATESWITH STEATOSIS, LIVER CANCERAND HYPOCHOLESTEROLEMIA

Valenti, V., Cefalu', A. B., Altieri, G. I., Palesano, O., Averna, M., Spina, R., Pirruccello, J. P., Gupta, N., Kathiresan, S., Tarugi, P., Gabriel, S. & Fayer, F., 2013, p. 116-116. 1 p.

Research output: Contribution to conferenceOther

43 Citations (Scopus)

A NOVEL COMPOUND HETEROZYGOUS MUTATION OF THE LIPOPROTEIN LIPASE GENE IN A NEWBORN WITH CHYLOMICRONEMIA

Valenti, V., Averna, M., Barbagallo, C. M., Cefalu', A. B., Vivona, N., Notarbartolo, A., Buglino, C. M., Pollaccia, D., Fayer, F., Barraco, G., Onorato, K. & Mina', M., 2005, p. S28-S28.

Research output: Contribution to conferenceOther

A NOVEL LOSS OF FUCTION MUTATION OF PCSK9 GENE IN CAUCASIANS WITH LOW PLASMA LDL-CHOLESTEROL

Cefalu', A. B., Valenti, V., Averna, M. & Pollaccia, D., 2007, p. 15-16.

Research output: Contribution to conferenceOther

A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE

Cefalu', A. B., Averna, M. & Valenti, V., 2006, p. S9-S9.

Research output: Contribution to conferenceOther

A novel loss of function mutation of PCSK9 gene in white subjects with low-plasma low-density lipoprotein cholesterol.

Averna, M., Cefalu', A. B., Valenti, V., Di Leo, E., Guardamagna, O., Tarugi, P., Bonardi, R., Bocchi, L., Fasano, T., Pollaccia, D. & Noto, D., 2007, In : Arteriosclerosis, Thrombosis, and Vascular Biology. 27, p. 677-681 5 p.

Research output: Contribution to journalArticle

104 Citations (Scopus)

A Novel Mutation of the DHCR7 Gene in a Sicilian Compound Heterozygote with Smith-Lemli-Opitz Syndrome

Averna, M., Cefalu', A. B., Pezzino, F. M., Romano, F., Puglisi, A., Longombardo, M. T., Fiore, B., Mattina, T., Travali, S., Brogna, A. & Noto, D., 2005, In : Molecular Diagnosis. 9, p. 201-204 4 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
16 Citations (Scopus)

A novel nonsense mutation in the cept gene in italian Hyperalphalipoproteinemic subjects

Valenti, V., Cefalu', A. B., Averna, M., Barbagallo, C. M., Notarbartolo, A., Buglino, C. M., Fayer, F. & Mina', M., 2004. 1 p.

Research output: Contribution to conferenceOther

A NOVEL NONSENSE MUTATION IN THE CETP GENE IN ITALIAN HYPERALPHALIPOPROTEINEMIC SUBJECTS

Cefalu', A. B., Averna, M., Valenti, V., Barbagallo, C. M., Buglino, C. M., Noto, D., Fayer, F., Gueli, M. C. & Mina', M., 2006, p. 133-134. 2 p.

Research output: Contribution to conferenceOther

A novel putative interactor for the low densitylipoprotein receptor cytoplasmic domain

Gianguzza, F., Ragusa, M. A., Costa, S., Averna, M., Cefalu', A. B., Nicosia, A. & Pollaccia, D., 2010, In : Molecular Medicine Reports. 3 (Marzo/Aprile), p. 341-345 5 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

An unexplained congenital disorder of glycosylation-II in a child with neurohepatic involvement, hypercholesterolemia and hypoceruloplasminemia

Cefalu', A. B., Cisarò, F., Porta, F., Jaeken, J., Pinon, M., Reggiani, S., Lefeber, D. J., Sturiale, L., Spada, M., Rabbone, I., Garozzo, D. & Calvo, P. L., 2018, In : JIMD Reports. 38, p. 97-100 4 p.

Research output: Contribution to journalArticle

23 Citations (Scopus)

ApoE polymorphism in a small Mediterranean island: relationships with plasma lipids, lipoproteins and LDL particle size.

Polizzi, F; Severino, M; Rizzo, M; Vivona, N; Onorato, F; Caldarella, R; Cefalù, Ab; Noto, D; Notarbartolo, A, 2001, In : European Journal of Epidemiology. 17, p. 707-713 7 p.

Research output: Contribution to journalArticle

23 Citations (Scopus)
8 Citations (Scopus)
20 Citations (Scopus)

Association between plasma lipid levels and migraine in subjects aged ≥50 years: preliminary data from the Zabùt Aging Project

Camarda, R., Cefalu', A. B., Camarda, C., Turco Liveri, E., Rosano, R., Monastero, R., Pipia, C. & Monastero R; Pipia C; Cefalù Ab; Turco Liveri E; Rosano R; Camarda R; Camarda C, 2008, In : Neurological Sciences. 29, p. S179-S181

Research output: Contribution to journalArticle

20 Citations (Scopus)
36 Citations (Scopus)

ASSOCIATION OF THE PARAOXONASE-1 Q192R POLYMORPHISM WITH CORONARY ARTERY DISEASE IN AMI PATIENTS, NON AMI CAD AND HEALTHY CONTROLS.

Averna, M., Valenti, V., Novo, G., Cefalu', A. B., Notarbartolo, A., Buglino, C. M., Fayer, F., Barraco, G., Onorato, K., Mina', M. & Davi', V., 2004, p. 313-313.

Research output: Contribution to conferenceOther

Autosomal Recessive Hypercholesterolemia: Long-Term Cardiovascular Outcomes

Cefalu', A. B., Averna, M., Masana, L., Fellin, R., Manzato, E., Sánchez-Hernández, R. M., Sirtori, C., Minicocci, I., Prieto-Matos, P., Vogt, A., Sjouke, B., D'Erasmo, L., Fuentes, F. J., Pavanello, C., Scardapane, M., Real, J. T., Real, J. T., Ascaso, J. F., Lafuente, E. E., Sánchez-Hernández, R. M. & 16 others, Roeters Van Lennep, J. E., Pintus, P., Zambon, S., Harada-Shiba, M., Pes, G. M., Bertolini, S., Calabresi, L., Nicolucci, A., Pocovi, M., Mata, P., Muntoni, S., Zambon, A., Arca, M., Fuentes, F. J., Pacifico, A. A. & Noto, D., 2018, In : Journal of the American College of Cardiology. 71, p. 279-288 10 p.

Research output: Contribution to journalArticle

13 Citations (Scopus)

Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene.

Cefalu', A. B., Averna, M., Rizzo, M., Fiore, Emmanuele, G., Travali, S., Mazzarino, M. C., Brogna, A. & Corsini, A., 2003, In : ATHEROSCLEROSIS. 166, p. 395-400 6 p.

Research output: Contribution to journalArticle

21 Citations (Scopus)

Baseline metabolic disturbances and the twenty-five years risk of incident cancer in a Mediterranean population

Valenti, V., Cefalu', A. B., Averna, M., Giammanco, A., Spina, R., Barbagallo, C. M., Sbordone, Burrascano, Termini, La Seta, Crupi, Cavera, G., Ganci, A. & Noto, D., 2016, In : NMCD. NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES. 26, p. 1020-1025 6 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)

Bassa prevalenza delle LDL aterogene piccole e dense in una popolazione mediterranea

Cefalu', A. B. & Rizzo, M., 2002, In : Italian Heart Journal. 3, p. 118S-118S 1 p.

Research output: Contribution to journalBook/Film/Article review

Bassa prevalenza delle LDL aterogene piccole e dense in una popolazione mediterranea

Cefalu', A. B. & Rizzo, M., 2002, In : Abstract book. 00, p. 89-89 1 p.

Research output: Contribution to journalBook/Film/Article review

BETA-2-GLYCOPROTEIN I IS GROWTH REGULATED AND PLAYS A ROLE AS SURVIVAL FACTOR FOR HEPATOCYTES

Averna, M., Barbagallo, C. M., Cefalu', A. B., Ragusa, M. A., Magro, G., Paravizzini, G., Emmanuele, G., Callari, D., Bartoloni, G., Travali, S., Mazzarino, M. C., Notarbartolo, A., Noto, D. & Emmanuele, G., 2004, In : THE INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY. 36, p. 1297-1305 9 p.

Research output: Contribution to journalArticle

7 Citations (Scopus)

Beyond Statins: New Lipid Lowering Strategies to Reduce Cardiovascular Risk

Cefalu', A. B., Averna, M. & Noto, D., 2014, In : Current Atherosclerosis Reports. 16, p. 414-423 10 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)

CARDIOVASCULAR RISK FACTORS ANALYSIS OF PEDIATRIC MATABOLIC SYNDROME

Averna, M., Cefalu', A. B., Notarbartolo, A., Fertitta, E. & Cardella, G., 2007, p. S5-S5.

Research output: Contribution to conferenceOther

8 Citations (Scopus)

CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction

Cefalu', A. B. & Rizzo, M., 2002, p. 243-243. 1 p.

Research output: Contribution to conferenceOther

CD14 C(-260)>T gene polymorphism is not a risk factor for myocardial infarction

Rizzo, M. & Cefalu', A. B., 2002, p. 86-86. 1 p.

Research output: Contribution to conferenceOther

CEREBROTENDINOUS XANTHOMATOSIS: A SICILIAN FAMILY HARBOURING THE R362C MUTATION IN THE STEROL 27-HYDROXYLASE GENE

Vivona, N., Averna, M., Cefalu', A. B., Barbagallo, C. M., Valenti, V., Notarbartolo, A., Pollaccia, D., Fayer, F., Barraco, G. & Mina', M., 2006, p. S21-S21.

Research output: Contribution to conferenceOther

CETP levels rather than polymorphisms as markers of coronary risk: Healthy athlete with high HDL-C and coronary disease-effectiveness of probucol.

Averna, M., Cefalu', A. B., Baldassarre, D., Calabresi, L., Franceschini, G. & Sirtori, C. R., 2006, In : Atherosclerosis. 186, p. 225-227 3 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

CETP levels rather than polymorphisms as markers of coronary risk: healthy athlete with high HDL-C and coronary disease--effectiveness of probucol.

Averna, M., Cefalu', A. B., Franceschini, G., Sirtori, C. R., Baldassarre, D. & Calabresi, L., 2006, In : ATHEROSCLEROSIS. 1, p. 225-227 3 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

Changes in levels of triglyceride-rich lipoprotein subfractions during dialysis in uremic patients

Rizzo, M. & Cefalu', A. B., 2002, In : Atherosclerosis Supplements. 3, p. 194-194 1 p.

Research output: Contribution to journalBook/Film/Article review

Changes in plasma lipids and low-density lipoprotein peak particle size during and after acute myocardial infarction

Rizzo, M., Cefalu', A. B., Averna, M., Castello, A., Sarullo, F. & Barbagallo, C. M., 2002, In : THE AMERICAN JOURNAL OF CARDIOLOGY. 89, p. 460-462 3 p.

Research output: Contribution to journalArticle

18 Citations (Scopus)

Characterisation of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS): Establishment of an FCS clinical diagnostic score

Cefalu', A. B., Averna, M., Banach, M., D'Erasmo, L., Reiner, Ž., Bruckert, E., Stefanutti, C., Gouni-Berthold, I., Johnson, C., Di Costanzo, A., Hughes, E., Dufour, R., Borén, J., Pintó, X., Hughes, E., Van Lennep, J. R., Van Lennep, J. R., Soran, H., Marçais, C., Stroes, E. & 6 others, Pintó, X., Cramb, R., Arca, M., Moulin, P., Walther, L. A. A-S. & Noto, D., 2018, In : Data in Brief. 21, p. 1334-1336 3 p.

Research output: Contribution to journalArticle

2 Citations (Scopus)