L
Luisa Murer
Researcher at University of Padua
Publications - 136
Citations - 5133
Luisa Murer is an academic researcher from University of Padua. The author has contributed to research in topics: Transplantation & Kidney. The author has an hindex of 36, co-authored 135 publications receiving 4369 citations. Previous affiliations of Luisa Murer include Boston Children's Hospital & University of Milan.
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Journal ArticleDOI
COQ2 Nephropathy: A Newly Described Inherited Mitochondriopathy with Primary Renal Involvement
Francesca Diomedi-Camassei,Silvia Di Giandomenico,Filippo M. Santorelli,Gianluca Caridi,Fiorella Piemonte,Giovanni Montini,Gian Marco Ghiggeri,Luisa Murer,Laura Barisoni,Anna Pastore,Andrea Onetti Muda,Marialuisa Valente,Enrico Bertini,Francesco Emma +13 more
TL;DR: It is suggested that inherited COQ2 mutations cause a primary glomerular disease with renal lesions that vary in severity and are not necessarily associated with neurological signs.
Journal ArticleDOI
Antibiotic treatment for pyelonephritis in children: multicentre randomised controlled non-inferiority trial
Giovanni Montini,Antonella Toffolo,Pietro Zucchetta,Roberto Dall'Amico,Daniela Gobber,Alessandro Calderan,F. Maschio,Luigi Pavanello,Pier Paolo Molinari,Dante Scorrano,Sergio Zanchetta,Walburga Cassar,Paolo Brisotto,Andrea Corsini,Stefano Sartori,Liviana Da Dalt,Luisa Murer,Graziella Zacchello +17 more
TL;DR: Treatment with oral antibiotics is as effective as parenteral then oral treatment in the management of the first episode of clinical pyelonephritis in children.
Journal ArticleDOI
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: A CoQ10-responsive condition
Leonardo Salviati,Sabrina Sacconi,Luisa Murer,Graziella Zacchello,L. Franceschini,A. M. Laverda,Giuseppe Basso,Catarina M. Quinzii,Corrado Angelini,Michio Hirano,Ali Naini,Plácido Navas,Salvatore DiMauro,Giovanni Montini +13 more
TL;DR: A 33-month-old boy who presented with corticosteroid-resistant nephrotic syndrome in whom progressive encephalomyopathy later developed was reported, and CoQ10 was decreased both in muscle and in fibroblasts.
Journal ArticleDOI
Broadening the Spectrum of Diseases Related to Podocin Mutations
Gianluca Caridi,Roberta Bertelli,Marco Di Duca,Monica Dagnino,Francesco Emma,Andrea Onetti Muda,Francesco Scolari,Nunzia Miglietti,Gianna Mazzucco,Luisa Murer,Alba Carrea,Laura Massella,Gianfranco Rizzoni,Francesco Perfumo,Gian Marco Ghiggeri +14 more
TL;DR: The clinical features of sporadic nephrotic syndrome due to podocin mutations (homozygous and heterozygous) in a representative population with broad phenotype, including patients with good response to drugs are outlined.
Journal ArticleDOI
Short-Term Effects of Rituximab in Children with Steroid- and Calcineurin-Dependent Nephrotic Syndrome: A Randomized Controlled Trial
Pietro Ravani,Alberto Magnasco,Alberto Edefonti,Luisa Murer,Rossella Rossi,Luciana Ghio,Elisa Benetti,Floriana Scozzola,Andrea Pasini,Nadia Dallera,Felice Sica,Mirco Belingheri,Francesco Scolari,Gian Marco Ghiggeri +13 more
TL;DR: Rituximab and lower doses of prednisone and calcineurin inhibitors are noninferior to standard therapy in maintaining short-term remission in children with INS dependent on both drugs and allow their temporary withdrawal.