Collagen type IV (α3-α4) nephropathy: from isolated haematuria to renal failureTORRA, Roser; TAZON-VEGA, Barbara; ARS, Elisabet et al.Nephrology, dialysis, transplantation (Print). 2004, Vol 19, Num 10, pp 2429-2432, issn 0931-0509, 4 p.Article

Increased prevalence of polycystic kidney disease type 2 among elderly polycystic patientsTORRA, Roser; BADENAS, Cèlia; PEREZ-OLLER, Laureano et al.American journal of kidney diseases. 2000, Vol 36, Num 4, pp 728-734, issn 0272-6386Article

Nephrin mutations cause childhood- and adult-onset focal segmental glomeruloscierosisSANTIN, Sheila; GARCIA-MASET, Rafael; COBO, Maria Angeles et al.Kidney international. 2009, Vol 76, Num 12, pp 1268-1276, issn 0085-2538, 9 p.Article

Genetic testing for X-linked alport syndrome by direct sequencing of COL4A5 cDNA from hair root RNA samplesTAZON-VEGA, Barbara; ARS, Elisabet; BURSET, Moisès et al.American journal of kidney diseases. 2007, Vol 50, Num 2, pp 257-269, issn 0272-6386, 13 p.Article

Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary ciliaWARD, Christopher J; YUAN, David; HARRIS, Peter C et al.Human molecular genetics (Print). 2003, Vol 12, Num 20, pp 2703-2710, issn 0964-6906, 8 p.Article

Incompletely Penetrant PKD1 Alleles Mimic the Renal Manifestations of ARPKDVUJIC, Mihailo; HEYER, Christina M; BOGDANOVA, Nadja et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 7, pp 1097-1102, issn 1046-6673, 6 p.Article

Haplotype analysis improves molecular diagnostics of Autosomal recessive polycystic kidney diseaseCONSUGAR, Mark B; ANDERSON, Sarah A; HILDEBRANDT, Friedhelm et al.American journal of kidney diseases. 2005, Vol 45, Num 1, pp 77-87, issn 0272-6386, 11 p.Article

Autosomal recessive Alport's syndrome and benign familial hematuria are Collagen type IV diseasesTAZON VEGA, Barbara; BADENAS, Cèlia; ARS, Elisabet et al.American journal of kidney diseases. 2003, Vol 42, Num 5, pp 952-959, issn 0272-6386, 8 p.Article

Mutations in the COL4A4 and COL4A3 genes cause familial benign hematuriaBADENAS, Cèlia; PRAGA, Manuel; DAVILA, Sonia et al.Journal of the American Society of Nephrology. 2002, Vol 13, Num 5, pp 1248-1254, issn 1046-6673Article

TRPC6 mutational analysis in a large cohort of patients with focal segmental glomerulosclerosisSANTIN, Sheila; ARS, Elisabet; PENA, Antonia et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 10, pp 3089-3096, issn 0931-0509, 8 p.Article

Very Low-Molecular-Mass Fragments of Albumin in the Plasma of Patients With Focal Segmental GlomerulosclerosisLOPEZ HELLIN, Joan; BECH-SERRA, Joan J; NIETO, Jose L et al.American journal of kidney diseases. 2009, Vol 54, Num 5, pp 871-880, issn 0272-6386, 10 p.Article

Ciclosporin-induced hypertension is associated with increased sodium transporter of the loop of Henle (NKCC2)ESTEVA-FONT, Cristina; ARS, Elisabet; FERNANDEZ-LLAMA, Patricia et al.Nephrology, dialysis, transplantation (Print). 2007, Vol 22, Num 10, pp 2810-2816, issn 0931-0509, 7 p.Article

Study of candidate genes affecting the progression of renal disease in autosomal dominant polycystic kidney disease type 1TAZON-VEGA, Barbara; VILARDELL, Mireia; PEREZ-OLLER, Laureano et al.Nephrology, dialysis, transplantation (Print). 2007, Vol 22, Num 6, pp 1567-1577, issn 0931-0509, 11 p.Article

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancyGROSS, Oliver; LICHT, Christoph; KONRAD, Martin et al.Kidney international. 2012, Vol 81, Num 5, pp 494-501, issn 0085-2538, 8 p.Article

Are Sodium Transporters in Urinary Exosomes Reliable Markers of Tubular Sodium Reabsorption in Hypertensive Patients?ESTEVA-FONT, Cristina; XIAOYAN WANG; FERNANDEZ-LLAMA, Patricia et al.The Nephron journals. 2010, Vol 114, Num 3, issn 1660-8151, p25-p34Article

Genotype-renal function correlation in type 2 autosomal dominant polycystic kidney diseaseMAGISTRONI, Riccardo; NING HE; COTO, Eliecer et al.Journal of the American Society of Nephrology. 2003, Vol 14, Num 5, pp 1164-1174, issn 1046-6673, 11 p.Article

A complete mutation screen of PKHD1 in autosomal-recessive polycystic kidney disease (ARPKD) pedigreesROSSETTI, Sandro; TORRA, Roser; COTO, Eliecer et al.Kidney international. 2003, Vol 64, Num 2, pp 391-403, issn 0085-2538, 13 p.Article

Incidence of renal failure and nephroprotection by RAAS inhibition in heterozygous carriers of X-chromosomal and autosomal recessive Alport mutationsTEMME, Johanna; PETERS, Frederick; GROSS, Oliver et al.Kidney international. 2012, Vol 81, Num 8, pp 779-783, issn 0085-2538, 5 p.Article

Genetic Variation of DKK3 May Modify Renal Disease Severity in ADPKDLIU, Michelle; SHI, Sally; PIERIDES, Alkis et al.Journal of the American Society of Nephrology. 2010, Vol 21, Num 9, pp 1510-1520, issn 1046-6673, 11 p.Article

Stem cell therapy for Alport syndrome : the hope beyond the hypeGROSS, Oliver; BORZA, Dorin-Bogdan; COSGROVE, Dominic et al.Nephrology, dialysis, transplantation (Print). 2009, Vol 24, Num 3, pp 731-734, issn 0931-0509, 4 p.Article

Unified Criteria for Ultrasonographic Diagnosis of ADPKDPEI, York; OBAJI, James; SAN MILLAN, Jose L et al.Journal of the American Society of Nephrology. 2009, Vol 20, Num 1, pp 205-212, issn 1046-6673, 8 p.Article

Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotypeARS, Elisabet; TAZON-VEGA, Barbara; RUIZ, Patricia et al.European journal of human genetics. 2005, Vol 13, Num 9, pp 1040-1046, issn 1018-4813, 7 p.Article