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Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy
Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy
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Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy

Caridi, Gianluca ; Lugani, Francesca ; Dagnino, Monica ; Gigante, Maddalena ; Iolascon, Achille ; Falco, Mariateresa ; Graziano, Claudio ; Benetti, Elisa ; Dugo, Mauro ; Del Prete, Dorella ; Granata, Antonio ; Borracelli, Donella ; Moggia, Elisabetta ; Quaglia, Marco ; Rinaldi, Rita ; Gesualdo, Loreto ; Ghiggeri, Gian Marco

Nephrology, dialysis, transplantation, 2014-09, Vol.29 Suppl 4 (suppl 4), p.iv80-iv86 [Periódico revisado por pares]

England

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2
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)
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CD2AP mutations are associated with sporadic nephrotic syndrome and focal segmental glomerulosclerosis (FSGS)

Gigante, Maddalena ; Pontrelli, Paola ; Montemurno, Eustacchio ; Roca, Leonarda ; Aucella, Filippo ; Penza, Rosa ; Caridi, Gianluca ; Ranieri, Elena ; Ghiggeri, Gian Marco ; Gesualdo, Loreto

Nephrology, dialysis, transplantation, 2009-06, Vol.24 (6), p.1858-1864 [Periódico revisado por pares]

Oxford: Oxford University Press

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3
Sex difference in cardiovascular risk in patients with chronic kidney disease: pooled analysis of four cohort studies
Sex difference in cardiovascular risk in patients with chronic kidney disease: pooled analysis of four cohort studies
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Sex difference in cardiovascular risk in patients with chronic kidney disease: pooled analysis of four cohort studies

Borrelli, Silvio ; Garofalo, Carlo ; Gabbai, Francis B ; Liberti, Maria Elena ; Chiodini, Paolo ; Simeon, Vittorio ; De Nicola, Luca ; Minutolo, Roberto

Nephrology, dialysis, transplantation, 2023-02, Vol.38 (10), p.2213-2221 [Periódico revisado por pares]

England: Oxford University Press

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4
P0831HIGH SERUM ALKALINE PHOSPHATASE PREDICTS THE RISK OF CKD PROGRESSION: EFFECT NODIFICATION BY THE GFR
P0831HIGH SERUM ALKALINE PHOSPHATASE PREDICTS THE RISK OF CKD PROGRESSION: EFFECT NODIFICATION BY THE GFR
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P0831HIGH SERUM ALKALINE PHOSPHATASE PREDICTS THE RISK OF CKD PROGRESSION: EFFECT NODIFICATION BY THE GFR

Mallamaci, Francesca ; D'arrigo, Graziella ; Marino, F ; Caridi, Graziella ; Parlongo, Giovanna ; Leonardis, Daniela ; Pizzini, Patrizia ; Cutrupi, Sebastiano ; Pisano, Anna ; Tripepi, Giovanni Luigi ; Kalantar-Zadeh, Kamyar ; Zoccali, Carmine

Nephrology, dialysis, transplantation, 2020-06, Vol.35 (Supplement_3) [Periódico revisado por pares]

Oxford University Press

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5
P0824QUALITY OF LIFE (QOL) DURING THE COURSE OF CKD: A LONGITUDINAL STUDY
P0824QUALITY OF LIFE (QOL) DURING THE COURSE OF CKD: A LONGITUDINAL STUDY
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P0824QUALITY OF LIFE (QOL) DURING THE COURSE OF CKD: A LONGITUDINAL STUDY

D'arrigo, Graziella ; Marino, Carmela ; Leonardis, Daniela ; Pizzini, Patrizia ; Caridi, Graziella ; Parlongo, Giovanna ; Marino, F ; Tripepi, Giovanni Luigi ; Zoccali, Carmine ; Mallamaci, Francesca

Nephrology, dialysis, transplantation, 2020-06, Vol.35 (Supplement_3) [Periódico revisado por pares]

Oxford University Press

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6
Genetic risk factors in typical haemolytic uraemic syndrome
Genetic risk factors in typical haemolytic uraemic syndrome
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Genetic risk factors in typical haemolytic uraemic syndrome

Taranta, Anna ; Gianviti, Alessandra ; Palma, Alessia ; De Luca, Veronica ; Mannucci, Liliana ; Procaccino, Maria Antonietta ; Ghiggeri, Gian Marco ; Caridi, Gianluca ; Fruci, Doriana ; Ferracuti, Silvia ; Ferretti, Alfonso ; Pecoraro, Carmine ; Gaido, Maurizio ; Penza, Rosa ; Edefonti, Alberto ; Murer, Luisa ; Tozzi, Alberto E. ; Emma, Francesco

Nephrology, dialysis, transplantation, 2009-06, Vol.24 (6), p.1851-1857 [Periódico revisado por pares]

Oxford: Oxford University Press

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7
Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy
Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy
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Stop codon at arginine 586 is the prevalent nephronopthisis type 1 mutation in Italy

Caridi, Gianluca ; Dagnino, Monica ; Trivelli, Antonella ; Emma, Francesco ; Perfumo, Francesco ; Ghiggeri, Gian Marco

Nephrology, dialysis, transplantation, 2006-08, Vol.21 (8), p.2301-2303 [Periódico revisado por pares]

Oxford: Oxford University Press

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8
Lack of cardiac anomalies in children with NPHS2 mutations
Lack of cardiac anomalies in children with NPHS2 mutations
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Lack of cardiac anomalies in children with NPHS2 mutations

Caridi, Gianluca ; Dagnino, Monica ; Carrea, Alba ; Massella, Laura ; Amore, Alessandro ; Emma, Francesco ; Coppo, Rosanna ; Perfumo, Francesco ; Ghiggeri, Gian Marco

Nephrology, dialysis, transplantation, 2007-05, Vol.22 (5), p.1477-1479 [Periódico revisado por pares]

England: Oxford University Press

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9
Autosomal dominant medullary cystic disease : a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus
Autosomal dominant medullary cystic disease : a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus
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Autosomal dominant medullary cystic disease : a disorder with variable clinical pictures and exclusion of linkage with the NPH1 locus

SCOLARI, F ; GHIGGERI, G. M ; VIOLA, B. F ; BOSSINI, N ; PRATI, E ; GUSMANO, R ; MAIORCA, R ; CASARI, G ; AMOROSO, A ; PUZZER, D ; CARIDI, G. L ; VALZORIO, B ; TARDANICO, R ; VIZZARDI, V ; SAVOLDI, S

Nephrology, dialysis, transplantation, 1998-10, Vol.13 (10), p.2536-2546 [Periódico revisado por pares]

Oxford: Oxford University Press

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10
Glomerulocystic kidney disease in a family
Glomerulocystic kidney disease in a family
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Glomerulocystic kidney disease in a family

Gusmano, Rosanna ; Caridi, Gianluca ; Marini, Monica ; Perfumo, Francesco ; Ghiggeri, Gian Marco ; Piaggio, Giorgio ; Ceccherini, Isabella ; Seri, Marco

Nephrology, dialysis, transplantation, 2002-05, Vol.17 (5), p.813-818 [Periódico revisado por pares]

Oxford: Oxford University Press

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