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• Article

  Anti-PCSK9 treatment: Is ultra-low LDL always good?

  Giammanco, A., Averna, M., Barbagallo, C. M., Cefalu', A. B. & Noto, D., 2018, In: Cardiovascular Research.

  Research output: Contribution to journal › Article › peer-review

  • oxidized low density lipoprotein
  • Lipids
  • Proprotein Convertases
  • Cholesterol
  • Monoclonal Antibodies
  5 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 journal › Article › peer-review

  • Congenital disorder of glycosylation type II
  • Glycosylation
  • Familial apoceruloplasmin deficiency
  • Hypercholesterolemia
  • Genes

• Association between familial hypobetalipoproteinemia and the risk of diabetes. Is this the other side of the cholesterol–diabetes connection? A systematic review of literature

  Cefalu', A. B., Barbagallo, C. M., Averna, M., Noto, D., Tarugi, P., Averna, M. R., Arca, M. & Noto, D., 2017, In: Acta Diabetologica. 54, p. 111-122 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Familial Hypobetalipoproteinemia
  • Diabetes Mellitus
  • Systematic Reviews
  • Hyperlipoproteinemia Type II
  • LDL Cholesterol
  10 Citations (Scopus)

• Automated untargeted stable isotope assisted lipidomics of liver cells on high glucose shows alteration of sphingolipid kinetics

  Cefalu', A. B., Scrimali, C., Spina, R. & Di Gaudio, F., 2020, In: BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS. 1865, p. 158656- 8 p.

  Research output: Contribution to journal › Article › peer-review

  1 Citation (Scopus)

• 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., Sirtori, C., Pavanello, C., Scardapane, M., Real, J. T., Real, J. T., Ascaso, J. F., Lafuente, E. E. & 18 others, Sánchez-Hernández, R. M., Sirtori, C., 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 journal › Article › peer-review

  • Autosomal Recessive Hypercholesterolemia
  • LDL Cholesterol
  • BMS201038
  • Cardiovascular Diseases
  • Ezetimibe
  16 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., Di Costanzo, A., Van Lennep, J. R., Van Lennep, J. R., Soran, H., Marçais, C. & 7 others, Stroes, E., 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 journal › Article › peer-review

  • Hyperlipoproteinemia Type I
  • Genotype
  2 Citations (Scopus)

• Circulating Molecular Chaperones in Subjects with Amnestic Mild Cognitive Impairment and Alzheimer's Disease: Data from the Zabùt Aging Project

  Cefalu', A. B., Monastero, R., Caruso Bavisotto, C., Cappello, F., Restivo, V., Marino Gammazza, A., Accardi, G. & Baschi, R., 2018, In: Journal of Alzheimer's Disease. p. 1-12 12 p.

  Research output: Contribution to journal › Article › peer-review

  • Molecular Chaperones
  • Cognitive Dysfunction
  • Alzheimer Disease
  • Sicily
  • Italy

• Clinical and biochemical characteristics of individuals with low cholesterol syndromes: A comparison between familial hypobetalipoproteinemia and familial combined hypolipidemia

  Cefalu', A. B., Averna, M., Spina, R., Minicocci, I., D'Erasmo, L., Polito, L., Di Costanzo, A., Di Costanzo, A., Di Leo, E., Cantisani, V., Tarugi, P., Arca, M. & Noto, D., 2017, In: Journal of Clinical Lipidology. 11, p. 1234-1242 9 p.

  Research output: Contribution to journal › Article › peer-review

  • Familial Hypobetalipoproteinemia
  • Apolipoproteins B
  • Cholesterol
  • Mutation
  • LDL Cholesterol
  10 Citations (Scopus)

• Effectiveness and safety of lomitapide in a patient with familial chylomicronemia syndrome

  Averna, M., Cabibi, D., Barbagallo, C. M., Cefalu', A. B., Spina, R. & Noto, D., 2020, In: ENDOCRINE. 7 p.

  Research output: Contribution to journal › Article › peer-review

• Efficacy of Lomitapide in the Treatment of Familial Homozygous Hypercholesterolemia: Results of a Real-World Clinical Experience in Italy

  Averna, M., Cefalu', A. B., Giammanco, A., Suppressa, P., Calabrò, P., Sbrana, F., Vigna, G. B., Sirtori, C., D’Erasmo, L., Sirtori, C., Pavanello, C., Medde, P., Sirtori, C., Bigazzi, F., Pintus, P., Sampietro, T., Sileo, F., Natale, F., Sabbà, C., Calabresi, L. & 4 others, Arca, M., Bucci, M., Bonomo, K. & Noto, D., 2017, In: Advances in Therapy. 34, p. 1200-1210 11 p.

  Research output: Contribution to journal › Article › peer-review

  • BMS201038
  • Hyperlipoproteinemia Type II
  • Italy
  • oxidized low density lipoprotein
  • Cholesterol
  24 Citations (Scopus)

• Evaluation of the performance of Dutch Lipid Clinic Network score in an Italian FH population: The LIPIGEN study

  Cefalu', A. B., Spina, R., Averna, M. & Noto, D., 2018, In: ATHEROSCLEROSIS. 277, p. 413-418 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Hyperlipoproteinemia Type II
  • Lipids
  • Population
  • Premature Birth
  • oxidized low density lipoprotein
  18 Citations (Scopus)

• Familial hypercholesterolemia: The Italian Atherosclerosis Society Network (LIPIGEN)

  Averna, M., Barbagallo, C. M., Cefalu', A. B., Averna, M., Spina, R. & Noto, D., 2017, In: Atherosclerosis Supplements. 29, p. 11-16 6 p.

  Research output: Contribution to journal › Article › peer-review

  • Hyperlipoproteinemia Type II
  • Inborn Genetic Diseases
  • Atherosclerosis
  • Lipids
  • Dyslipidemias
  25 Citations (Scopus)

• Genetic epidemiology of autosomal recessive hypercholesterolemia in Sicily: Identification by next-generation sequencing of a new kindred

  Scrimali, C., Spina, R., Cefalu', A. B., Giammanco, A., Valenti, V., Ingrassia, V., Averna, M., Barbagallo, C. M., Misiano, G., Monastero, R., Valenti, V., Spina, R., Cefalù, A. B., Ingrassia, V., Misiano, G., Averna, M. R., Noto, D. & Baschi, R., 2018, In: Journal of Clinical Lipidology. 12, p. 145-151 7 p.

  Research output: Contribution to journal › Article › peer-review

  • Autosomal Recessive Hypercholesterolemia
  • Sicily
  • Molecular Epidemiology
  • Italy
  • Hyperlipoproteinemia Type II
  6 Citations (Scopus)

• Homozygous familial hypercholesterolemia in Italy: Clinical and molecular features

  Cefalu', A. B., Averna, M., Suppressa, P., Trenti, C., Calabrò, P., Rabacchi, C., Sbrana, F., Casula, M., D'Erasmo, L., D'Addato, S., Calandra, S., Pavanello, C., Ripoli, C., Ibba, A., Pasta, A., Negri, E. A., Buonuomo, P. S., Pisciotta, L., Zenti, M. G., Sampietro, T. & 10 others, Sileo, F., Bartuli, A., Iannuzzo, G., Cicero, A., Tarugi, P., Bertolini, S., Catapano, A. L., Arca, M., Bucci, M. & Fasano, T., 2020, In: ATHEROSCLEROSIS. 312, p. 72-78 7 p.

  Research output: Contribution to journal › Article › peer-review

  1 Citation (Scopus)

• Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): Expert panel recommendations and proposal of an “FCS score”

  Averna, M., Cefalu', A. B., 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., Di Costanzo, A., Van Lennep, J. R., Van Lennep, J. R., Alvarez-Sala Walther, L. A., Soran, H. & 7 others, Marçais, C., Stroes, E., Pintó, X., Cramb, R., Arca, M., Moulin, P. & Noto, D., 2018, In: ATHEROSCLEROSIS. 275, p. 265-272 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Hyperlipoproteinemia Type I
  • Pancreatitis
  • Triglycerides
  • Lipoprotein Lipase
  • Hypertriglyceridemia
  40 Citations (Scopus)

• Identification of a novel LMF1 nonsense mutation responsible for severe hypertriglyceridemia by targeted next-generation sequencing

  Scrimali, C., Spina, R., Averna, M., Misiano, G., Altieri, G. I., Barbagallo, C. M., Palesano, O., Cocorullo, G., Cefalu', A. B., Giammanco, A., Valenti, V., Ingrassia, V., Valenti, V., Spina, R., Cefalù, A. B., Ingrassia, V., Scrimali, C., Misiano, G., Averna, M. R., Ganci, A. & 2 others, Noto, D. & Fayer, F., 2017, In: Journal of Clinical Lipidology. 11, p. 272-281 10 p.

  Research output: Contribution to journal › Article › peer-review

  • Nonsense Codon
  • Hypertriglyceridemia
  • Mutation
  • Triglycerides
  • Exons
  13 Citations (Scopus)

• Lack of Correlation of Plasma HDL With Fecal Cholesterol and Plasma Cholesterol Efflux Capacity Suggests Importance of HDL Functionality in Attenuation of Atherosclerosis

  Cefalu', A. B., Srivastava, N., Averna, M. & Srivastava, R. A. K., 2018, In: Frontiers in Physiology. 9

  Research output: Contribution to journal › Article › peer-review

  • Atherosclerosis
  • Cholesterol
  • HDL Cholesterol
  • Peroxisome Proliferator-Activated Receptors
  • Risk Reduction Behavior
  6 Citations (Scopus)

• NPC1L1 and ABCG5/8 induction explain synergistic fecal cholesterol excretion in ob/ob mice co-treated with PPAR-α and LXR agonists

  Averna, M., Cefalu', A. B., Srivastava, N. S. & Srivastava, R. A. K., 2020, In: Molecular and Cellular Biochemistry. 473, p. 247-262 16 p.

  Research output: Contribution to journal › Article › peer-review

• Rapid degradation of ABCA1 protein following cAMP withdrawal and treatment with PKA inhibitor suggests ABCA1 is a short-lived protein primarily regulated at the transcriptional level

  Cefalu', A. B., Averna, M. & Srivastava, R. A. K., 2020, In: Journal of Diabetes and Metabolic Disorders. 19, p. 363-371 9 p.

  Research output: Contribution to journal › Article › peer-review

• Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study

  Cefalu', A. B., Averna, M., Spina, R. & Noto, D., 2017, In: Atherosclerosis Supplements. 29, p. 17-24 8 p.

  Research output: Contribution to journal › Article › peer-review

  • Hyperlipoproteinemia Type II
  • Mutation
  • Heterozygote
  • Apolipoproteins E
  • Italy
  30 Citations (Scopus)

• Therapeutic options for homozygous familial hypercholesterolemia: the role of Lomitapide

  Cefalu', A. B., Giammanco, A., Averna, M. & Noto, D., 2020, In: Current Medicinal Chemistry. 27, p. 3773-3783 11 p.

  Research output: Contribution to journal › Article › peer-review

  • BMS201038
  • microsomal triglyceride transfer protein
  • Hyperlipoproteinemia Type II
  • Liver
  • Apolipoproteins B
  1 Citation (Scopus)
• Other

  Genotypic and phenotypic characterization of patients with autosomal dominant hypercholesterolemia in sicily

  Valenti, V., Giammanco, A., Scrimali, C., Cefalu', A. B., Ingrassia, V., Altieri, G. I., Barbagallo, C. M., Spina, R., Averna, M., Misiano, G., Ganci, A., Noto, D. & Fayer, F., 2017, p. e235-. 1 p.

  Research output: Contribution to conference › Other › peer-review

  • Sicily
  • Hyperlipoproteinemia Type II
  • Mutation
  • Xanthomatosis
  • Tendons