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Research Output

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2017
2015

Gelatinases and their tissue inhibitors in metabolic syndrome

Hopps, E., Lo Presti, R., Canino, B., Averna, M., Caimi, G. & Noto, D., 2014. 1 p.

Research output: Contribution to conferenceOther

Oxidative status in metabolic syndrome

Lo Presti, R., Hopps, E., Caimi, G., Averna, M., Canino, B., Noto, D. & Montana, M., 2014. 1 p.

Research output: Contribution to conferenceOther

2013

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

Cefalu', A. B., Valenti, V., 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

42 Citations (Scopus)

CLINICAL CHARACTERISTICS AND PLASMALIPIDS IN SUBJECTS WITH FAMILIALCOMBINED HYPOLIPIDEMIA:A POOLED ANALYSIS

Cefalu', A. B., Averna, M., Pigna, G., Ciociola, E., Arroyo, J. A., Minicocci, I., Calandra, S., Santini, S., Martí, G., Pannozzo, F., Stitziel, N., Kathiresan, S., Pisciotta, L., Ceci, F., Maranghi, M., Cantisani, V., Labbadia, G., Tarugi, P., Bertolini, S., Arca, M. & 1 others, Noto, D., 2013, p. 3481-3490. 10 p.

Research output: Contribution to conferenceOther

29 Citations (Scopus)

LIPIDOMICS OF HUMAN SKIN FIBROBLASTS IN NEIMANN-PICK DISEASE TYPE C

Altieri, G. I., Di Gaudio, F., Averna, M., Palesano, O., Noto, D., Fayer, F. & Indelicato, S., 2013, p. 103-103. 1 p.

Research output: Contribution to conferenceOther

REDUCTION OF CHOLESTEROL WITH NUTRACEUTICAL: RESULTS OF A DOUBLE BLIND STUDY

Altieri, G. I., Giammanco, A., Averna, M., Barbagallo, C. M., Panno, M. D. & Longo, F. M., 2013, p. 97-97. 1 p.

Research output: Contribution to conferenceOther

2012

Prothrombotic gene variants in AMI young women

Averna, M., Cefalu', A. B., Bellia, C. & Ciaccio, M., 2012. 1 p.

Research output: Contribution to conferenceOther

2011

LIPIDOMICS OF FATTY LIVER IN NAFLD AND HCV INFECTION: LIVER SPHYNGOLIPIDS AND FATTYACIDS

Petta, S., Spina, R., Valenti, V., Craxi, A., Averna, M., Altieri, G. I., Greco, M., Noto, D. & Fayer, F., 2011, p. 73-73. 1 p.

Research output: Contribution to conferenceOther

Metabolomic analysis of plasma from Alzheimer disease patients

Greco, M., Monastero, R., Averna, M., Tralongo, P., Cefalu', A. B., Spina, R., Palesano, O., Altieri, G. I., Valenti, V., Cannizzaro, A., Noto, D. & Fayer, F., 2011, p. 61-61. 1 p.

Research output: Contribution to conferenceOther

PREVALENCE OF ANGPTL3 AND APOBGENE MUTATIONS IN SUBJECTS WITHCOMBINED HYPOLIPIDEMIA

Averna, M., Cefalu', A. B., Spina, R., Valenti, V., Noto, D., Fayer, F. & Ditta, M., 2011, p. 99-99. 1 p.

Research output: Contribution to conferenceOther

VASCULOPROTECTIVE FUNCTION OF HDLFROM CETP-DEFICIENT SUBJECTS

Spina, R., Cefalu', A. B., Valenti, V. & Averna, M., 2011, p. 82-82. 1 p.

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

CARDIOVASCULAR RISK FACTORS ANALYSIS OF PEDIATRIC MATABOLIC SYNDROME

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

Research output: Contribution to conferenceOther

FAMILIAL HYPOBETALIPOPROTEINEMIA DUE TO APOLIPOPROTEIN B GENE MUTATIONS CAUSES INTESTINAL FAT ACCUMULATION AND LIPID MALABSORPTION.

Carroccio, A., Averna, M., Cefalu', A. B., Barbagallo, C. M., Notarbartolo, A., Fayer, F., Di Prima, L. & Mina', M., 2007, p. 37-37.

Research output: Contribution to conferenceOther

GENETIC HETEROGENEITY OF SEVERE HYPOBETALIPOPROTEINEMIA

Cefalu', A. B. & Averna, M., 2007, p. S8-S8.

Research output: Contribution to conferenceOther

INTERLEUKIN 6 PLASMA LEVELS PREDICT WITH HIGH SENSITIVITY AND SPECIFICITY CORONARY STENOSIS DETECTED BY CORONARY ANGIOGRAPHY

Cerasola, G., Averna, M., Cefalu', A. B., Barbagallo, C. M., Pernice, V., Notarbartolo, A., Vadala', A., Fayer, F., Maggiore, M., Mina', M. & Pernice, V., 2007, p. S14-S14.

Research output: Contribution to conferenceOther

16 Citations (Scopus)

SHORT APOB TRUNCATIONS SHOW IMPAIRE CHYLOMICRON EXPORT AND ENTEROCYTE TRIGLYCERIDE ACCUMULATION. IN VIVO AND IN VITRO EVIDENCE ON A APOB 28.25 STABLE-TRANSFECTED ENTEROCYTE CELL LINE

Valenti, V., Cefalu', A. B., Averna, M., Notarbartolo, A., Cannizzaro, A., Fayer, F., Barraco, G. & Mina', M., 2007, p. S4-S4. 1 p.

Research output: Contribution to conferenceOther

ΒETA ARRESTIN-2: A NEW “ACTOR” IN THE LDL-R ENDOCYTOSIS?

Cefalu', A. B., Averna, M., Vivona, N., Valenti, V., Spina, R., Notarbartolo, A., Pollaccia, D., Fayer, F. & Mina', M., 2007, p. S26-S26.

Research output: Contribution to conferenceOther

A NOVEL LOSS OF FUNCTION MUTATION OF PCSK9 GENE

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

Research output: Contribution to conferenceOther

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

Cefalu', A. B., Valenti, V., Averna, M., 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

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

COMPOUND HETEROZYGOUS FH AND FDB: IDENTIFICATION OF A SICILIAN FAMILY HARBOURING THE FDB3531 MUTATION AND THE Y398X MUTATION OF THE LDL RECEPTOR GENE.

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

Research output: Contribution to conferenceOther

PREVALENCE OF PCSK9 VARIANTS IN A COHORT OF SUBJECTS WITH HYPOCHOLESTEROLEMIA

Barbagallo, C. M., Valenti, V., Cefalu', A. B., Averna, M., Notarbartolo, A., Pollaccia, D., Fayer, F., Barraco, G. & Mina', M., 2006, p. S16-S16.

Research output: Contribution to conferenceOther

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

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

Research output: Contribution to conferenceOther