Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Paolo Gilles Vercelloni"'
Publikováno v:
La Pediatria Medica e Chirurgica, Vol 34, Iss 4 (2012)
Not available
Externí odkaz:
https://doaj.org/article/257264991a76484caf6c79e17dbec42c
Autor:
Renato Alberto Sinico, Alessandra Palmisano, Federica Maritati, Paolo Gilles Vercelloni, Gina Gregorini, Maria Letizia Urban, Marta Calatroni, Giorgio Trivioli, Augusto Vaglio, Matthias A. Cassia, Alessandra Bettiol, Pasquale Esposito, Corrado Murtas, Paola Romagnani, David Jayne, Davide Gianfreda, Federico Alberici, Gabriella Moroni, Lucio Manenti, Giacomo Emmi, Seerapani Gopaluni
Publikováno v:
Clinical Kidney Journal
Background Although rapidly progressive glomerulonephritis is the main renal phenotype of anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), slow renal disease progression is sometimes observed. These forms have been rarely disc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c537ccf6190658a4cd8d16da98cf803
http://hdl.handle.net/11567/1049793
http://hdl.handle.net/11567/1049793
Autor:
Lucia Sacchi, Augusto Vaglio, Piergiorgio Messa, Mariele Gatto, Francesca Raffiotta, Gabriella Moroni, Andrea Doria, Davide Gianfreda, Maria Letizia Urban, Paolo Gilles Vercelloni, Silvana Quaglini, Margherita Zen, Gloria Costantini, Renato Alberto Sinico, Federico Pieruzzi
Publikováno v:
Annals of the Rheumatic Diseases. 77:1318-1325
ObjectivesTo evaluate changes in demographic, clinical and histological presentation, and prognosis of lupus nephritis (LN) over time.Patients and methodsWe studied a multicentre cohort of 499 patients diagnosed with LN from 1970 to 2016. The 46-year
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b3642d3d0890eff488e86d37c386c3d
https://doi.org/10.1136/annrheumdis-2017-212732
https://doi.org/10.1136/annrheumdis-2017-212732
Autor:
Piergiorgio Messa, Renato Alberto Sinico, Francesca Saccon, Paolo Gilles Vercelloni, Federico Alberici, Giulia Frontini, Mariele Gatto, Valentina Binda, G. Moroni, Francesca Radice, Andrea Doria
Publikováno v:
Annals of the Rheumatic Diseases. 79:351.1-352
Background:Indications to repeat renal biopsy (RB) in lupus nephritis (LN) are not unanimously acknowledged.Objectives:To evaluate the renal outcome of patients with LN undergoing a second RB.Methods:We retrospectively analyzed prospectively collecte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e90b97d219d2306956b2210fa6959f37
https://doi.org/10.1136/annrheumdis-2020-eular.3523
https://doi.org/10.1136/annrheumdis-2020-eular.3523
Autor:
Lucia Sacchi, Mariele Gatto, D. Gainfreda, Francesca Raffiotta, Silvana Quaglini, Augusto Vaglio, G. Moroni, Paolo Gilles Vercelloni, Renato Alberto Sinico, Andrea Doria
Publikováno v:
FRIDAY, 15 JUNE 2018.
Background Lupus nephritis (LN) presentation changed over time following earlier diagnosis and treatment. Objectives To evaluate changes in LN clinical and histological presentation in the last 5 decades. Methods This is a retrospective multicentric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c3bd022813586e77f5dfdaa69e9c273
https://doi.org/10.1136/annrheumdis-2018-eular.7035
https://doi.org/10.1136/annrheumdis-2018-eular.7035
Autor:
Franca Anglani, Dorella Del Prete, G Marra, Cristiana Meloni, Rosalba Cristofaro, Maria Addis, Enrica Tosetto, Paolo Gilles Vercelloni, Maria Antonietta Melis, Monica Ceol
Dent's disease is an X-linked renal tubulopathy caused by mutations mainly affecting the CLCN5 gene. Defects in the OCRL gene, which is usually mutated in patients with Lowe syndrome, have been shown to lead to a Dent-like phenotype called Dent disea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00a38f6ac5f03741fdbf96bfe9d2aa43
https://europepmc.org/articles/PMC3658198/
https://europepmc.org/articles/PMC3658198/
Adenine Phosphoribosyltransferase Deficiency: An Underdiagnosed Cause of Lithiasis and Renal Failure
Autor:
Giuseppe Garigali, Maria Angela Pavesi, Alberto Edefonti, Gianantonio Manzoni, Giuseppina Marra, Lionel Mockel, Irene Ceballos Picot, Paolo Gilles Vercelloni, Giovanni B. Fogazzi
Publikováno v:
JIMD Reports ISBN: 9783642280955
We describe an infant affected by adenine phosphoribosyltransferase (APRT) deficiency diagnosed at 18 months of age with a de novo mutation that has not been previously reported. APRT deficiency is a rare defect of uric acid catabolism that leads to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::563c50c87a31335a96375740c3b5273d
https://doi.org/10.1007/8904_2011_92
https://doi.org/10.1007/8904_2011_92