نتائج البحث - "Paola Alessandrini"

1

Functional Lecithin: Cholesterol Acyltransferase Is Not Required for Efficient Atheroprotection in Humans

المؤلفون: Laura Calabresi, Damiano Baldassarre, Samuela Castelnuovo, Paola Conca, Letizia Bocchi, Chiara Candini, Beatrice Frigerio, Mauro Amato, Cesare R. Sirtori, Paola Alessandrini, Marcello Arca, Giuliano Boscutti, Luigi Cattin, Loreto Gesualdo, Tiziana Sampietro, Gaetano Vaudo, Fabrizio Veglia, Sebastiano Calandra, Guido Franceschini

المساهمون: Calabresi, L., Baldassarre, D., Castelnuovo, S., Conca, P., Bocchi, L., Candini, C., Frigerio, B., Amato, M., Sirtori, C. R., Alessandrini, P., Arca, M., Boscutti, G., Cattin, Luigi, Gesualdo, L., Sampietro, T., Vaudo, G., Veglia, F., Calandra, S., Franceschini, G.

المصدر: Circulation. 120:628-635

مصطلحات موضوعية: lipoproteins, atherosclerosi, atherosclerosis, genetics, imaging, Physiology (medical), atherosclerosis • genetics • imaging • lipoproteins, genetic, Cardiology and Cardiovascular Medicine

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db78e79b1efcf5e4da55abf7a3686857Test
https://doi.org/10.1161/circulationaha.108.848143Test

2

Hypertriglyceridemia is associated with increased insulin resistance in subjects with normal glucose tolerance: Evaluation in a large cohort of subjects assessed with the 1999 World Health Organization criteria for the classification of diabetes

المؤلفون: G. Bittolo-Bon, Paola Alessandrini, M Pais, P. Gallina, G. Cazzolato, E Moro

المصدر: Metabolism. 52:616-619

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffd2187fbdb0591eecd2f7c5dc5d8586Test
https://doi.org/10.1053/meta.2003.50102Test

3

دورية أكاديمية

Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency

المؤلفون: Livia Pisciotta, Roberto Miccoli, Alfredo Cantafora, Patrizia Tarugi, Paola Alessandrini, Gabriele Bittolo Bon, Claudio Cortese, Sebastiano Calandra, Stefano Bertolini, Laura Calabresi, Guido Franceschini

المساهمون: Livia Pisciotta, Roberto Miccoli, Alfredo Cantafora, Laura Calabresi, Patrizia Tarugi, Paola Alessandrini, Gabriele Bittolo Bon, Guido Franceschini, Claudio Cortese, Sebastiano Calandra, Stefano Bertolini

مصطلحات موضوعية: Settore BIO/14 - Farmacologia

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/12818417; info:eu-repo/semantics/altIdentifier/wos/WOS:000182343600019; volume:167; issue:2; firstpage:335; lastpage:345; journal:ATHEROSCLEROSIS SUPPLEMENTS; http://hdl.handle.net/2434/11238Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-0038801308

الإتاحة: https://doi.org/10.1016/S0021-9150Test(03)00020-0
http://hdl.handle.net/2434/11238Test

View record in BASE

4

A modified ACCO for Class II nonextraction treatment

المؤلفون: B Giuliano, Maino, Paola, Alessandrini, Paola, Mura

المصدر: Journal of clinical orthodontics : JCO. 40(10)

مصطلحات موضوعية: Orthodontic Appliances, Removable, Acrylic Resins, Extraoral Traction Appliances, Humans, Orthodontic Appliance Design, Female, Malocclusion, Angle Class II, Child, Orthodontics, Corrective

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::31e4e6a1de6f21a364c37aee3ed51713Test
https://pubmed.ncbi.nlm.nih.gov/17062913Test

5

The molecular basis of lecithin: Cholesterol acyltransferase deficiency syndromes: A comprehensive study of molecular and biochemical findings in 13 unrelated Italian families

مصطلحات موضوعية: Adult, Male, Very low-density lipoprotein, medicine.medical_specialty, Genotype, Apolipoprotein B, Lipoproteins, Sterol O-acyltransferase, Gene Dosage, Biology, Diagnosis, Differential, Phosphatidylcholine-Sterol O-Acyltransferase, chemistry.chemical_compound, Corneal Opacity, Lecithin Cholesterol Acyltransferase Deficiency, Internal medicine, medicine, Humans, Fish-Eye Disease, Triglycerides, Aged, Family Health, Lecithin cholesterol acyltransferase deficiency, cholesterol acyltransferase deficiency • fish eye disease • high-density lipoproteins • lecithin:cholesterol acyltransferase • mutation [familial lecithin], Esterification, Cholesterol, Middle Aged, Atherosclerosis, medicine.disease, Pedigree, Endocrinology, Italy, chemistry, Mutation, biology.protein, Female, lipids (amino acids, peptides, and proteins), Phosphatidylcholine—sterol O-acyltransferase, Cardiology and Cardiovascular Medicine, Lipoprotein

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::347cf4d4cde66daf077119df1ed15644Test
https://hdl.handle.net/11380/636978Test

6

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

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

المساهمون: L PISCIOTTA, I HAMILTON-CRAIG, P TARUGI, A BELLOCCHIO, T FASANO, P ALESSANDRINI, G BITTOLO BON, D SIEPI, E MANNARINO, L CATTIN, M AVERNA, CEFALU' AB, A CANTAFORA, S CALANDRA, S BERTOLINI

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Heterozygote, Settore MED/09 - Medicina Interna, Apolipoprotein B, Adolescent, Premature coronary artery disease, Tangier disease, Coronary Disease, Biology, Gene mutation, medicine.disease_cause, Compound heterozygosity, Internal medicine, Genotype, ABCA1 gene, medicine, Humans, Child, Hypoalphalipoproteinemia, Selection Bias, Aged, Apolipoproteins B, Genetics, Mutation, Familial defective Apo B (FDB), Apolipoprotein A-I, Cholesterol, HDL, nutritional and metabolic diseases, Middle Aged, medicine.disease, Lipoprotein lipase, Familial HDL deficiency, Endocrinology, Child, Preschool, biology.protein, lipids (amino acids, peptides, and proteins), Allelic heterogeneity, ATP-Binding Cassette Transporters, Female, Cardiology and Cardiovascular Medicine, ATP Binding Cassette Transporter 1