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Case Reports in Endocrinology|March 18, 2020
Recurrent Hypoglycemia in a Case of Congenital AnalbuminemiaMartin Litzel, Gianluca Caridi, Francesca Lugani, et al.
Frontiers in Genetics|May 7, 2019
Diagnosis, Phenotype, and Molecular Genetics of Congenital AnalbuminemiaLorenzo Minchiotti, Gianluca Caridi, Monica Campagnoli, et al.
Giornale Italiano Di Nefrologia : Organo Ufficiale Della Societa Italiana Di Nefrologia|October 20, 2015
[Familial Focal Segmental Glomerulosclerosis, a vademecum for clinical nephrologist]Gianluca Caridi, Francesca Lugani, Elisa Bonanni, et al.
Gene Expression|July 3, 2003
The first intron of the human osteopontin gene contains a C/EBP-beta-responsive enhancerFrancesca Giacopelli, Nadia Rosatto, Maria Teresa Divizia, et al.
Pediatric Nephrology (Berlin, Germany)|December 13, 2022
Vaccines and nephrotic syndrome: efficacy and safetyAndrea Angeletti, Francesca Lugani, Edoardo La Porta, et al.
Clinical Kidney Journal|February 10, 2021
Renal involvement and Strømme syndromeGianluca Caridi, Francesca Lugani, Margherita Lerone, et al.
Pediatric Nephrology (Berlin, Germany)|January 30, 2020
Low-dose ofatumumab for multidrug-resistant nephrotic syndrome in children: a randomized placebo-controlled trialPietro Ravani, Isabella Pisani, Monica Bodria, et al.
Pediatric Nephrology (Berlin, Germany)|November 21, 2007
Recurrent lymphomatoid papulosis associated with nephrotic syndrome. An occurrence of uncertain originGian Marco Ghiggeri, Dario Bleid, Alberto Garaventa, et al.
Nephron|July 26, 2002
Expression of nuclear transcription factor PAX2 in renal biopsies of juvenile nephronophthisisLuisa Murer, Gianluca Caridi, Manuela Della Vella, et al.
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|June 28, 2014
mRNA sequencing of a novel NPHS2 intronic mutation in a child with focal and segmental glomerulosclerosisElisa Benetti, Gianluca Caridi, Sonia Centi, et al.
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