Search Results - "Lerario, Sarah"

Diet and Physical Activity in Adult Dominant Polycystic Kidney Disease: A Review of the Literature by Capelli, Irene, Lerario, Sarah, Aiello, Valeria, Provenzano, Michele, Di Costanzo, Roberta, Squadrani, Andrea, Vella, Anna, Vicennati, Valentina, Poli, Carolina, La Manna, Gaetano, Baraldi, Olga

“…Autosomal polycystic kidney disease is the most common inherited kidney disease determining 5% of all end-stage kidney disease. The only therapy approved for…”
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Kidney transplantation in systemic sclerosis: Advances in graft, disease, and patient outcome by Maritati, Federica, Provenzano, Michele, Lerario, Sarah, Corradetti, Valeria, Bini, Claudia, Busutti, Marco, Grandinetti, Valeria, Cuna, Vania, La Manna, Gaetano, Comai, Giorgia

“…Systemic sclerosis (SSc) is an immune-mediated rheumatic disease characterized by vascular abnormalities, tissue fibrosis, and inflammation. Renal disease…”
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No evidence of Fabry disease in a patient with the new p.Met70Val GLA gene variant by Capelli, Irene, Di Costanzo, Roberta, Aiello, Valeria, Lerario, Sarah, De Giovanni, Paola, Montevecchi, Marcello, Cerretani, Davide, Donadio, Vincenzo, La Manna, Gaetano, Mignani, Renzo

“…Background Fabry disease (FD) is a rare X‐linked lysosomal storage disorder caused by variants in GLA gene leading to deficient α‐galactosidase A enzyme…”
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Fabry disease: a rare disorder calling for personalized medicine by Lerario, Sarah, Monti, Luigi, Ambrosetti, Irene, Luglio, Agnese, Pietra, Andrea, Aiello, Valeria, Montanari, Francesca, Bellasi, Antonio, Zaza, Gianluigi, Galante, Antonio, Salera, Davide, Capelli, Irene, La Manna, Gaetano, Provenzano, Michele

“…Fabry Disease (FD) is a genetic disease caused by a deficiency in the activity of lysosomal galactosidase A (α-GalA), an enzyme responsible for the catabolism…”
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MO520SARS-COVID19 INFECTION AT VARIOUS STAGES OF KIDNEY DISEASE: A SINGLE CENTRE EXPERIENCE by Napoli, Marianna, Donati, Gabriele, Gasperoni, Lorenzo, Zappulo, Fulvia, Aiello, Valeria, Scrivo, Anna, Busutti, Marco, Ruggeri, Marco, Di Filippo, Federica, Lerario, Sarah, Bini, Claudia, Tondolo, Francesco, Stefanini, Carlo, Comai, Giorgia, La Manna, Gaetano

“…Abstract Background and Aims Several chronic medical conditions appear to increase the risk of severe COVID-19. Chronic kidney disease (CKD) patients have a…”
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No evidence of Fabry disease in a patient with the new p. Met70Val GLA gene variant by Capelli, Irene, Di Costanzo, Roberta, Aiello, Valeria, Lerario, Sarah, De Giovanni, Paola, Montevecchi, Marcello, Cerretani, Davide, Donadio, Vincenzo, La Manna, Gaetano, Mignani, Renzo

“…Abstract Background Fabry disease (FD) is a rare X‐linked lysosomal storage disorder caused by variants in GLA gene leading to deficient α‐galactosidase A…”
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DNAJB11 Mutation in ADPKD Patients: Clinical Characteristics in a Monocentric Cohort by Aiello, Valeria, Ciurli, Francesca, Conti, Amalia, Cristalli, Carlotta Pia, Lerario, Sarah, Montanari, Francesca, Sciascia, Nicola, Vischini, Gisella, Fabbrizio, Benedetta, Di Costanzo, Roberta, Olivucci, Giulia, Pietra, Andrea, Lopez, Antonia, Zambianchi, Loretta, La Manna, Gaetano, Capelli, Irene

“…Autosomal Dominant Polycystic Kidney Disease (ADPKD) is a late-onset cilia-related disorder, characterized by progressive cystic enlargement of the kidneys. It…”
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Current Perspectives in ABO-Incompatible Kidney Transplant by Maritati, Federica, Bini, Claudia, Cuna, Vania, Tondolo, Francesco, Lerario, Sarah, Grandinetti, Valeria, Busutti, Marco, Corradetti, Valeria, La Manna, Gaetano, Comai, Giorgia

“…For a long time, ABO incompatible living donor kidney transplantation has been considered contraindicated, due to the presence of isohemagglutinins, natural…”
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