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Iranian Journal of Kidney Diseases|June 3, 2017
Fourier Transform Infrared Analysis of Urinary Calculi and Metabolic Studies in a Group of Sicilian ChildrenMaria Michela D'Alessandro, Giuseppe Gennaro, Pietro Tralongo, et al.
Italian Journal of Pediatrics|June 17, 2021
Novel SCNN1A gene splicing-site mutation causing autosomal recessive pseudohypoaldosteronism type 1 (PHA1) in two Italian patients belonging to the same small townGregorio Serra, Vincenzo Antona, Maria Michela D'Alessandro, et al.
Clinical Kidney Journal|May 14, 2024
Lumasiran treatment in pediatric patients with PH1: real-world data within a compassionate use program in ItalyFrancesca Taroni, Licia Peruzzi, Germana Longo, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|May 1, 2018
[Atypical Hemolytic Uremic Syndrome: experience of a pediatric center]Rosa Cusumano, Maria Chiara Sapia, Ciro Corrado, et al.
Italian Journal of Pediatrics|November 21, 2022
A novel NF1 mutation in a pediatric patient with renal artery aneurysmIlenia Chillura, Giulia Angela Restivo, Simonetta Callari, et al.
Biomedicines|February 25, 2023
Uromodulin and Vesico-Ureteral Reflux: A Genetic StudySilvio Maringhini, Rosa Cusumano, Ciro Corrado, et al.
Italian Journal of Pediatrics|October 16, 2020
Autosomal recessive polycystic kidney disease: case report of a newborn with rare PKHD1 mutation, rapid renal enlargement and early fatal outcomeGregorio Serra, Giovanni Corsello, Vincenzo Antona, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|May 1, 2018
[Nephrocalcinosis in children]Maria Michela D'Alessandro, Giovanni Pavone, Maria Cristina Castiglione, et al.
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