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Pediatric Research|April 9, 2005
NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanismsGianluca Caridi, Francesco Perfumo, Gian Marco GhiggeriPediatric Nephrology (Berlin, Germany)|July 31, 2007
Teaching molecular genetics: chapter 4-positional cloning of genetic disordersAldamaria Puliti, Gianluca Caridi, Roberto Ravazzolo, et al.Pediatric Nephrology (Berlin, Germany)|August 26, 2009
Five cases of severe vesico-ureteric reflux in a family with an X-linked compatible traitMitra Naseri, Gian Marco Ghiggeri, Gianluca Caridi, et al.Clinical Journal of the American Society of Nephrology : CJASN|November 21, 2015
Anti-CD20 Antibodies for Idiopathic Nephrotic Syndrome in ChildrenPietro Ravani, Alice Bonanni, Roberta Rossi, et al.Frontiers in Medicine|June 27, 2018
Molecular and Cellular Mechanisms for Proteinuria in Minimal Change DiseaseRoberta Bertelli, Alice Bonanni, Gianluca Caridi, et al.Clinical Nephrology|February 10, 2018
A novel UMOD gene mutation associated with chronic kidney failure at a young ageNicolina Stefania Carucci, Gianluca Caridi, Francesca Lugani, et al.Biochimica Et Biophysica Acta|April 25, 2013
Congenital analbuminaemia: molecular defects and biochemical and clinical aspectsLorenzo Minchiotti, Monica Galliano, Gianluca Caridi, et al.International Journal of Molecular Sciences|February 15, 2022
Variations in the Human Serum Albumin Gene: Molecular and Functional AspectsGianluca Caridi, Francesca Lugani, Andrea Angeletti, et al.Annals of Clinical Biochemistry|November 7, 2015
A novel splicing mutation in the albumin gene (c.270+1G>T) causes analbuminaemia in a German infantGianluca Caridi, Wolfgang Thomas, Monica Campagnoli, et al.Pediatric Nephrology (Berlin, Germany)|December 11, 2008
Familial forms of nephrotic syndromeGianluca Caridi, Antonella Trivelli, Simone Sanna-Cherchi, et al.Pageof 11