Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Flora Puteo"'
Autor:
Enrico Verrina, Stefano Picca, Fabio Paglialonga, Bruno Gianoglio, Enrico Vidal, Flora Puteo, Carmine Pecoraro, Maria Teresa Saravo, Silvia Consolo, Alberto Edefonti
Publikováno v:
Pediatric Nephrology. 31:833-841
Chronic haemodialysis (HD) in small children has not been adequately investigated.This was a retrospective investigation of the use of chronic HD in 21 children aged 2 years (n = 12 aged1 year) who were registered in the Italian Pediatric Dialysis Re
Autor:
Giovanni Messina, Giuseppe Castellano, Mario Giordano, Loreto Gesualdo, Flora Puteo, Tommaso Depalo, Claretta Divella, R. Bellantuono, V Colella
Publikováno v:
Pediatrics. 130:e1385-e1388
Genetic mutations in complement components are associated with the development of atypical hemolytic uremic syndrome (aHUS), a rare disease with high morbidity rate triggered by infections or unidentified factors. The uncontrolled activation of the a
Autor:
Albina, Tummolo, Vincenzo, Colella, Rosa, Bellantuono, Mario, Giordano, Giovanni, Messina, Flora, Puteo, Palma, Sorino, Tommaso, De Palo
Publikováno v:
Giornale italiano di nefrologia : organo ufficiale della Societa italiana di nefrologia. 29
Apheresis procedures are used in children to treat an increasing number of conditions by removing different types of substances from the bloodstream. In a previous study we evaluated the first results of our experience in children, emphasizing the so
Autor:
Tommaso Depalo, D. A. Caringella, Rocco Marzolla, Mario Giordano, Flora Puteo, Lucio Scianaro
Publikováno v:
Pediatric radiology. 37(7)
Contrast-enhanced voiding urosonography (VUS) is becoming more widely used for the diagnosis of vesicoureteric reflux (VUR), but until now its use has only been accepted for first diagnosis in females and in the follow-up of children, including boys,
Autor:
Enrico Vidal, Rosa Maria Roperto, Bruno Gianoglio, Roberto Chimenz, Francesca Mencarelli, Flora Puteo, Alberto Edefonti, Enrico Verrina, Carmine Pecoraro, Germana Longo, Silvio Maringhini, Giovanna Leozappa, Ilse-Maria Ratsch
Publikováno v:
Nephrology Dialysis Transplantation. 30:iii663-iii663
Publikováno v:
Pediatric Nephrology. 9:672-672
Autor:
Giuseppe Grandaliano, Loreto Gesualdo, Mario Giordano, Giuseppe Stefano Netti, Luisa Santangelo, Vincenza Carbone, Sterpeta Diella, Flora Puteo, Maddalena Gigante
Publikováno v:
BMC Nephrology
Background Schimke immuno-osseous dysplasia (SIOD, OMIM #242900) is an autosomal-recessive pleiotropic disorder characterized by spondyloepiphyseal dysplasia, renal dysfunction and T-cell immunodeficiency. SIOD is caused by mutations in the gene SMAR