Gianluca Caridi
Gianluca Caridi
Istituto Giannina Gaslini IRCCS
Email verificata su - Home page
Citata da
Citata da
Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens
K Kiryluk, Y Li, F Scolari, S Sanna-Cherchi, M Choi, M Verbitsky, D Fasel, ...
Nature genetics 46 (11), 1187-1196, 2014
Renal outcome in patients with congenital anomalies of the kidney and urinary tract
S Sanna-Cherchi, P Ravani, V Corbani, S Parodi, R Haupt, G Piaggio, ...
Kidney international 76 (5), 528-533, 2009
IgA nephropathy, the most common cause of glomerulonephritis, is linked to 6q22–23
AG Gharavi, Y Yan, F Scolari, FP Schena, GM Frasca, GM Ghiggeri, ...
Nature genetics 26 (3), 354-357, 2000
Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium.
M Seri, R Cusano, S Gangarossa, G Caridi, D Bordo, L Nigro, ...
Nature genetics 26 (1), 103-105, 2000
COQ2 nephropathy: a newly described inherited mitochondriopathy with primary renal involvement
F Diomedi-Camassei, S Di Giandomenico, FM Santorelli, G Caridi, ...
Journal of the American Society of Nephrology 18 (10), 2773-2780, 2007
Allelism of MCKD, FJHN and GCKD caused by impairment of uromodulin export dynamics
L Rampoldi, G Caridi, D Santon, F Boaretto, I Bernascone, G Lamorte, ...
Human molecular genetics 12 (24), 3369-3384, 2003
Prevalence, genetics, and clinical features of patients carrying podocin mutations in steroid-resistant nonfamilial focal segmental glomerulosclerosis
G Caridi, R Bertelli, A Carrea, M Di Duca, P Catarsi, M Artero, M Carraro, ...
Journal of the American Society of Nephrology 12 (12), 2742-2746, 2001
Copy-number disorders are a common cause of congenital kidney malformations
S Sanna-Cherchi, K Kiryluk, KE Burgess, M Bodria, MG Sampson, ...
The American Journal of Human Genetics 91 (6), 987-997, 2012
Broadening the spectrum of diseases related to podocin mutations
G Caridi, R Bertelli, M Di Duca, M Dagnino, F Emma, AO Muda, F Scolari, ...
Journal of the American Society of Nephrology 14 (5), 1278-1286, 2003
AHI1 is required for photoreceptor outer segment development and is a modifier for retinal degeneration in nephronophthisis
CM Louie, G Caridi, VS Lopes, F Brancati, A Kispert, MA Lancaster, ...
Nature genetics 42 (2), 175-180, 2010
Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin
R Bertelli, F Ginevri, G Caridi, M Dagnino, S Sandrini, M Di Duca, F Emma, ...
American journal of kidney diseases 41 (6), 1314-1321, 2003
Whole-exome sequencing in adults with chronic kidney disease: a pilot study
S Lata, M Marasa, Y Li, DA Fasel, E Groopman, V Jobanputra, H Rasouly, ...
Annals of internal medicine 168 (2), 100-109, 2018
Genetic approaches to human renal agenesis/hypoplasia and dysplasia
S Sanna-Cherchi, G Caridi, PL Weng, F Scolari, F Perfumo, AG Gharavi, ...
Pediatric nephrology 22, 1675-1684, 2007
Uromodulin storage diseases: clinical aspects and mechanisms
F Scolari, G Caridi, L Rampoldi, R Tardanico, C Izzi, D Pirulli, A Amoroso, ...
American journal of kidney diseases 44 (6), 987-999, 2004
Genotype–phenotype associations in WT1 glomerulopathy
BS Lipska, B Ranchin, P Iatropoulos, J Gellermann, A Melk, F Ozaltin, ...
Kidney international 85 (5), 1169-1178, 2014
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
M Gigante, P Pontrelli, E Montemurno, L Roca, F Aucella, R Penza, ...
Nephrology Dialysis Transplantation 24 (6), 1858-1864, 2009
NPHS2 (Podocin) mutations in nephrotic syndrome. Clinical spectrum and fine mechanisms
G Caridi, F Perfumo, GM Ghiggeri
Pediatric research 57 (7), 54-61, 2005
Mutations in DSTYK and Dominant Urinary Tract Malformations
S Sanna-Cherchi, RV Sampogna, N Papeta, KE Burgess, SN Nees, ...
New England Journal of Medicine 369 (7), 621-629, 2013
Rituximab is a safe and effective long-term treatment for children with steroid and calcineurin inhibitor–dependent idiopathic nephrotic syndrome
P Ravani, A Ponticelli, C Siciliano, A Fornoni, A Magnasco, F Sica, ...
Kidney international 84 (5), 1025-1033, 2013
Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)
GM Ghiggeri, G Caridi, U Magrini, A Sessa, A Savoia, M Seri, A Pecci, ...
American Journal of Kidney Diseases 41 (1), 95-104, 2003
Il sistema al momento non pu˛ eseguire l'operazione. Riprova pi¨ tardi.
Articoli 1–20