Tolerability of Eribulin and correlation between polymorphisms and neuropathy in an unselected population of female patients with metastatic breast cancer: results of the multicenter, single arm, phase IV PAINTER study

Authors: Nicla La Verde, Giovanna Damia, Ornella Garrone, Daniele Santini, Alessandra Fabi, Mariangela Ciccarese, Daniele Giulio Generali, Martina Nunzi, Elena Poletto, Elisa Ferraris, Elisabetta Cretella, Giuseppa Scandurra, Icro Meattini, Alessandro Stefano Bertolini, Luigi Cavanna, Elena Collovà, Emanuela Romagnoli, Eliana Rulli, Lorenzo Legramandi, Federica Guffanti, Annalisa Bramati, Anna Moretti, Alessandra Cassano, Patrizia Vici, Valter Torri, Gabriella Farina, PAINTER investigators

Source: Breast Cancer Research, Vol 24, Iss 1, Pp 1-12 (2022)

Subject Terms: Breast cancer, Eribulin, Neurotoxicity, Polymorphisms, Peripheral neuropathy, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282

File Description: electronic resource

Relation: https://doaj.org/toc/1465-542X

Access URL: https://doaj.org/article/ce3620b6c9374e95a95402fd78331bff

Lipoprotein(a) and family history for cardiovascular disease in paediatric patients: A new frontier in cardiovascular risk stratification. Data from the LIPIGEN paediatric group

Authors: Pederiva, Cristina, Capra, Maria Elena, Biasucci, Giacomo, Banderali, Giuseppe, Fabrizi, Enrico, Gazzotti, Marta, Casula, Manuela, Catapano, Alberico L., Marcello, Arca, Maurizio, Averna, Stefano, Bertolini, Sebastiano, Calandra, Luigi, Catapano Alberico, Patrizia, Tarugi, Fabio, Pellegatta

Source: Atherosclerosis. 349:233-239

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100170818426.0x000001&indx=1&recIds=ETOCvdc_100170818426.0x000001

Lipoprotein(a) Genotype Influences the Clinical Diagnosis of Familial Hypercholesterolemia

Authors: Elena Olmastroni, Marta Gazzotti, Maurizio Averna, Marcello Arca, Patrizia Tarugi, Sebastiano Calandra, Stefano Bertolini, Alberico L. Catapano, Manuela Casula

Source: Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 12, Iss 10 (2023)

Subject Terms: cardiovascular risk, clinical diagnosis, familial hypercholesterolemia, lipoprotein(a), Diseases of the circulatory (Cardiovascular) system, RC666-701

File Description: electronic resource

Relation: https://doaj.org/toc/2047-9980

Access URL: https://doaj.org/article/824df55f452e4ba28aff9a337cba2499

Corrigendum: The role of registers in increasing knowledge and improving management of children and adolescents affected by familial hypercholesterolemia: The LIPIGEN pediatric group

Authors: Marta Gazzotti, Manuela Casula, Stefano Bertolini, Maria Elena Capra, Elena Olmastroni, Alberico Luigi Catapano, Cristina Pederiva, LIPIGEN Paediatric Group

Source: Frontiers in Genetics, Vol 14 (2023)

Subject Terms: familial hypercholesterolemia, pediatric cohort, genetic diagnosis, pathology register, clinical diagnosis, cardiovascular genetics, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2023.1113454/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/ea643da41d71474993702c60d0ccb8b4

Long-term efficacy of lipoprotein apheresis and lomitapide in the treatment of homozygous familial hypercholesterolemia (HoFH): a cross-national retrospective survey

Authors: Laura D’Erasmo, Antonio Gallo, Angelo Baldassare Cefalù, Alessia Di Costanzo, Samir Saheb, Antonina Giammanco, Maurizio Averna, Alessio Buonaiuto, Gabriella Iannuzzo, Giuliana Fortunato, Arturo Puja, Tiziana Montalcini, Chiara Pavanello, Laura Calabresi, Giovanni Battista Vigna, Marco Bucci, Katia Bonomo, Fabio Nota, Tiziana Sampietro, Francesco Sbrana, Patrizia Suppressa, Carlo Sabbà, Fabio Fimiani, Arturo Cesaro, Paolo Calabrò, Silvia Palmisano, Sergio D’Addato, Livia Pisciotta, Stefano Bertolini, Randa Bittar, Olga Kalmykova, Sophie Béliard, Alain Carrié, Marcello Arca, Eric Bruckert

Source: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-12 (2021)

Subject Terms: Homozygous hypercholesterolemia, Lipoprotein apheresis, Lomitapide, LDL, Therapeutics, Genetic disease, Medicine

File Description: electronic resource

Relation: https://doaj.org/toc/1750-1172

Access URL: https://doaj.org/article/d3d61cde509e4a539ecfd7328d4ab9a4

Efficacy of Long-Term Treatment of Autosomal Recessive Hypercholesterolemia With Lomitapide: A Subanalysis of the Pan-European Lomitapide Study

Authors: Laura D’Erasmo, Antonina Giammanco, Patrizia Suppressa, Chiara Pavanello, Gabriella Iannuzzo, Alessia Di Costanzo, Daniele Tramontano, Ilenia Minicocci, Simone Bini, Anja Vogt, Kim Stewards, Jeanine Roeters Van Lennep, Stefano Bertolini, Marcello Arca, the Italian and European Working Group on Lomitapide in HoFH, Maurizio Averna, Eric Boersma, Katia Bonomo, Marco Bucci, Laura Calabresi, Paolo Calabrò, Angelo Baldassare Cefalù, Jaimini Cegla, Arturo Cesaro, Sergio D’Addato, Eugene Daphnis, Maria Donata Di Taranto, Avishay Ellis, Fabio Fimiani, Giuliana Fortunato, Marco Gentile, Meral Kayikcioglu, Genovefa Kolovou, Evangelos Liberopoulos, Karin Littmann, Sergio Martínez-Hervás, Tiziana Montalcini, Fabio Nota, Livia Pisciotta, Arturo Puja, Giovanni José Real, Jeanine Roeters van Lennep, Joost Rutten, Carlo Sabbà, Tiziana Sampietro, Francesco Sbrana, Kim Steward, Fulvio Ventura, Battista Vigna, Shahenaz Walji

Source: Frontiers in Genetics, Vol 13 (2022)

Subject Terms: Real-world study, rare disease, autosomal recessive hypercholesterolaemia, LDL-C, lomitapide, long-term, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.937750/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/c310a706a0ae42eda26ba363b9582898

Lipoprotein(a) Modulates Carotid Atherosclerosis in Metabolic Syndrome

Authors: Anna Laura Cremonini, Andrea Pasta, Federico Carbone, Luca Visconti, Matteo Casula, Edoardo Elia, Aldo Bonaventura, Luca Liberale, Maria Bertolotto, Nathan Artom, Silvia Minetti, Paola Contini, Daniela Verzola, Roberto Pontremoli, Francesca Viazzi, Giorgio Luciano Viviani, Stefano Bertolini, Aldo Pende, Fabrizio Montecucco, Livia Pisciotta

Source: Frontiers in Molecular Biosciences, Vol 9 (2022)

Subject Terms: lipoprotein (a), atherosclerosis, metabolic syndrome, cardiovascular disease, ASCVD, Biology (General), QH301-705.5

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fmolb.2022.854624/full; https://doaj.org/toc/2296-889X

Access URL: https://doaj.org/article/1b5685523d594be69391fc489b7d0d84

The Role of Registers in Increasing Knowledge and Improving Management of Children and Adolescents Affected by Familial Hypercholesterolemia: the LIPIGEN Pediatric Group

Authors: Marta Gazzotti, Manuela Casula, Stefano Bertolini, Maria Elena Capra, Elena Olmastroni, Alberico Luigi Catapano, Cristina Pederiva, the LIPIGEN Paediatric Group, Massimiliano Allevi, Marcello Arca, Renata Auricchio, Maurizio Averna, Davide Baldera, Giuseppe Banderali, Andrea Bartuli, Giacomo Biasucci, Claudio Borghi, Patrizia Bruzzi, Raffaele Buganza, Paola Sabrina Buonuomo, Paolo Calabrò, Sebastiano Calandra, Francesca Carubbi, Arturo Cesaro, Francesco Cipollone, Nadia Citroni, Giuseppe Covetti, Annalaura Cremonini, Sergio D’Addato, Maria Del Ben, Maria Donata Di Taranto, Giuliana Fortunato, Roberto Franceschi, Federica Galimberti, Simonetta Genovesi, Antonina Giammanco, Liliana Grigore, Ornella Guardamagna, Arcangelo Iannuzzi, Gabriella Iannuzzo, Lorenzo Iughetti, Lidia Lascala, Fabiana Locatelli, Sara Madaghiele, Giuseppe Mandraffino, Massimo Raffaele Mannarino, Bucci Marco, Lorenzo Maroni, Ilenia Minicocci, Giuliana Mombelli, Sandro Muntoni, Fabio Nascimbeni, Gianfranco Parati, Angelina Passaro, Chiara Pavanello, Fabio Pellegatta, Francesco Massimo Perla, Matteo Pirro, Livia Pisciotta, Arturo Pujia, Francesco Purrello, Elisabetta Rinaldi, Riccardo Sarzani, Roberto Scicali, Patrizia Suppressa, Patrizia Tarugi, Sabrina Verachtert, Giovanni Battista Vigna, Josè Pablo Werba, Alberto Zambon, Sabina Zambon, Maria Grazia Zenti

Source: Frontiers in Genetics, Vol 13 (2022)

Subject Terms: familial hypercholesterolemia, pediatric cohort, genetic diagnosis, pathology register, clinical diagnosis, cardiovascular genetics, Genetics, QH426-470

File Description: electronic resource

Relation: https://www.frontiersin.org/articles/10.3389/fgene.2022.912510/full; https://doaj.org/toc/1664-8021

Access URL: https://doaj.org/article/89bbc97e24a34c4996186aca15b69866

A multisystem approach by bed-side ultrasound in patients with COVID-19 infection: a case series

Authors: Gabriele Cioni, Ginevra Bellandi, Stefano Bertolini, Giacomo Betti, Wanda Bialek, Angela Fedeli, Marco Antonio Lumini, Roberto Michelotti, Carmelo Muscari, Francesca Pacini, Sabrina Pastacaldi, Rossella Squillante, Francesco Tola, Antonio Vergara, Emiliano Votino, Mauro Zuccotti, Fabio Daviddi

Source: Italian Journal of Medicine (2020)

Subject Terms: COVID-19, ultrasound, pneumonia., Medicine

File Description: electronic resource

Relation: https://italjmed.org/index.php/ijm/article/view/1288; https://doaj.org/toc/1877-9344; https://doaj.org/toc/1877-9352

Access URL: https://doaj.org/article/8aa6f419a9ff4db6bd8465a3ec720f56

Long term substrate reduction therapy with ezetimibe alone or associated with statins in three adult patients with lysosomal acid lipase deficiency

Authors: Maja Di Rocco, Livia Pisciotta, Annalisa Madeo, Marta Bertamino, Stefano Bertolini

Source: Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-6 (2018)

Subject Terms: Lysosomal acid lipase deficiency, Ezetimibe, Substrate reduction therapy, Medicine

File Description: electronic resource

Relation: http://link.springer.com/article/10.1186/s13023-018-0768-8; https://doaj.org/toc/1750-1172

Access URL: https://doaj.org/article/f4db1b1e368b47dea599d297c14f45b9

Clinical characteristics and plasma lipids in subjects with familial combined hypolipidemia: a pooled analysis[S]

Authors: Ilenia Minicocci, Sara Santini, Vito Cantisani, Nathan Stitziel, Sekar Kathiresan, Juan Antonio Arroyo, Gertrudis Martí, Livia Pisciotta, Davide Noto, Angelo B. Cefalù, Marianna Maranghi, Giancarlo Labbadia, Giovanni Pigna, Fabio Pannozzo, Fabrizio Ceci, Ester Ciociola, Stefano Bertolini, Sebastiano Calandra, Patrizia Tarugi, Maurizio Averna, Marcello Arca

Source: Journal of Lipid Research, Vol 54, Iss 12, Pp 3481-3490 (2013)

Subject Terms: ANGPTL3 mutations, angiopoietin-like 3, cardiovascular disease, fatty liver, diabetes mellitus, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520356996; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/5b85b008f28e45d7a8865bda58dd9395

Lipoprotein Glomerulopathy Associated with a Mutation in Apolipoprotein E

Authors: Riccardo Magistroni, Marco Bertolotti, Luciana Furci, Rita Adriana Fano, Marco Leonelli, Livia Pisciotta, Elisa Pellegrini, Laura Calabresi, Stefano Bertolini, Sebastiano Calandra

Source: Clinical Medicine Insights: Case Reports, Vol 2013, Iss 6, Pp 189-196 (2013)

Subject Terms: Medicine (General), R5-920

File Description: electronic resource

Relation: http://www.la-press.com/lipoprotein-glomerulopathy-associated-with-a-mutation-in-apolipoprotei-article-a3989; https://doaj.org/toc/1179-5476

Access URL: https://doaj.org/article/c8d76ff1cf044c4bb46796e24d28398a

Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk

Authors: Sebastiano Calandra, Patrizia Tarugi, Helen E. Speedy, Andrew F. Dean, Stefano Bertolini, Carol C. Shoulders

Source: Journal of Lipid Research, Vol 52, Iss 11, Pp 1885-1926 (2011)

Subject Terms: intestinal sterol absorption and efflux, cellular cholesterol synthesis, lipoprotein assembly, gallstones, LDL uptake, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520350811; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/004457eb37a7421e8f2b1c85c455dc17

Denaturing high-performance liquid chromatography in the detection of ABCA1 gene mutations in familial HDL deficiency

Authors: Tommaso Fasano, Letizia Bocchi, Livia Pisciotta, Stefano Bertolini, Sebastiano Calandra

Source: Journal of Lipid Research, Vol 46, Iss 4, Pp 817-822 (2005)

Subject Terms: high density lipoprotein, ATP binding cassette transporter A1, heteroduplexes, sequence variants, primary hypoalphalipoproteinemia, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520340177; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/3cda3cae15194ee4b3fa77a68d0d15ef

Abnormal splicing of ABCA1 pre-mRNA in Tangier disease due to a IVS2 +5G>C mutation in ABCA1 gene

Authors: Serena Altilia, Livia Pisciotta, Rita Garuti, Patrizia Tarugi, Alfredo Cantafora, Laura Calabresi, Jacopo Tagliabue, Sergio Maccari, Franco Bernini, Ilaria Zanotti, Carlo Vergani, Stefano Bertolini, Sebastiano Calandra

Source: Journal of Lipid Research, Vol 44, Iss 2, Pp 254-264 (2003)

Subject Terms: ABCA1 minigenes, in vitro splicing, donor splice site mutation, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520312128; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/eb6e958ad20e4b4cb77ab5e79e99a6b5

Phenotypic expression of familial hypobetalipoproteinemia in three kindreds with mutations of apolipoprotein B gene

Authors: Patrizia Tarugi, Amedeo Lonardo, Carlo Gabelli, Franca Sala, Giorgia Ballarini, Irene Cortella, Lorenzo Previato, Stefano Bertolini, Renzo Cordera, Sebastiano Calandra

Source: Journal of Lipid Research, Vol 42, Iss 10, Pp 1552-1561 (2001)

Subject Terms: truncated apoBs, fatty liver, lipid malabsorption, carotid atherosclerosis, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520322082; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/78987decb10a424390fe9e32d8e9ebce

Analysis of two duplications of the LDL receptor gene affectingintracellular transport, catabolism, and surface binding of the LDLreceptor

Authors: Dilip.D. Patel, Nicoletta Lelli, Rita Garuti, Salvatore Li Volti, Stefano Bertolini, Brian L. Knight, Sebastiano Calandra

Source: Journal of Lipid Research, Vol 39, Iss 7, Pp 1466-1475 (1998)

Subject Terms: familial hypercholesterolemia, amino acid sequence, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520325281; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/64866ca961af47379d1c2aa2f598c9ea

Simple detection of a point mutation in LDL receptor gene causing familial hypercholesterolemia in southern Italy by allele-specific polymerase chain reaction

Authors: Alfredo Cantafora, Ida Blotta, Elisabetta Mercuri, Sebastiano Calandra, Stefano Bertolini

Source: Journal of Lipid Research, Vol 39, Iss 5, Pp 1101-1105 (1998)

Subject Terms: allele-specific primers, polymerase chain reaction amplification of specific alleles, Biochemistry, QD415-436

File Description: electronic resource

Relation: http://www.sciencedirect.com/science/article/pii/S0022227520338797; https://doaj.org/toc/0022-2275

Access URL: https://doaj.org/article/2dab7a4b5d9249ea99e90d7a844ae4e6

Quantitative polymerase chain reaction and microchip electrophoresis to detect major rearrangements of the low-density lipoprotein receptor gene causing familial hypercholesterolemia.

Authors: Alfredo Cantafora, Ida Blotta, Elisabetta Pino, Livia Pisciotta, Sebastiano Calandra, Stefano Bertolini

Source: Electrophoresis; Nov2004, Vol. 25 Issue 21/22, p3882-3889, 8p

Evaluation of RNA messengers involved in lipid trafficking of human intestinal cells by reverse-transcription polymerase chain reaction with competimer technology and microchip electrophoresis.

Authors: Alfredo Cantàfora, Ida Blotta, Roberto Rivabene, Livia Pisciotta, Stefano Bertolini

Source: Electrophoresis; Nov2003, Vol. 24 Issue 21, p3748-3754, 7p