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Roser Torra Balcells
Roser Torra Balcells
Fundacio Puigvert
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Unified criteria for ultrasonographic diagnosis of ADPKD
Y Pei, J Obaji, A Dupuis, AD Paterson, R Magistroni, E Dicks, P Parfrey, ...
Journal of the American Society of Nephrology 20 (1), 205-212, 2009
8432009
Comparison of phenotypes of polycystic kidney disease types 1 and 2
N Hateboer, MA v Dijk, N Bogdanova, E Coto, AK Saggar-Malik, ...
The Lancet 353 (9147), 103-107, 1999
7131999
Treatment of Fabry’s disease with the pharmacologic chaperone migalastat
DP Germain, DA Hughes, K Nicholls, DG Bichet, R Giugliani, WR Wilcox, ...
New england journal of medicine 375 (6), 545-555, 2016
5872016
Autosomal-dominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
AB Chapman, O Devuyst, KU Eckardt, RT Gansevoort, T Harris, S Horie, ...
Kidney international 88 (1), 17-27, 2015
5872015
Cellular and subcellular localization of the ARPKD protein; fibrocystin is expressed on primary cilia
CJ Ward, D Yuan, TV Masyuk, X Wang, R Punyashthiti, S Whelan, ...
Human molecular genetics 12 (20), 2703-2710, 2003
3942003
Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy
O Gross, C Licht, HJ Anders, B Hoppe, B Beck, B Tönshoff, B Höcker, ...
Kidney international 81 (5), 494-501, 2012
3742012
Chronic kidney disease is a key risk factor for severe COVID-19: a call to action by the ERA-EDTA
ERACODA Working Group Duivenvoorden Raphaël Franssen Casper FM Hemmelder ...
Nephrology Dialysis Transplantation 36 (1), 87-94, 2021
3592021
Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney …
RT Gansevoort, M Arici, T Benzing, H Birn, G Capasso, A Covic, ...
Nephrology Dialysis Transplantation 31 (3), 337-348, 2016
3172016
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome
S Santín, G Bullich, B Tazón-Vega, R García-Maset, I Giménez, I Silva, ...
Clinical Journal of the American Society of Nephrology 6 (5), 1139-1148, 2011
2832011
Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival—an analysis of data from the ERA-EDTA Registry
EM Spithoven, A Kramer, E Meijer, B Orskov, C Wanner, JM Abad, ...
Nephrology Dialysis Transplantation 29 (suppl_4), iv15-iv25, 2014
2672014
An update for atypical haemolytic uraemic syndrome: diagnosis and treatment. A consensus document
JM Campistol, M Arias, G Ariceta, M Blasco, L Espinosa, M Espinosa, ...
Nefrología (English Edition) 35 (5), 421-447, 2015
2452015
Coordinate expression of the autosomal dominant polycystic kidney disease proteins, polycystin-2 and polycystin-1, in normal and cystic tissue
ACM Ong, CJ Ward, RJ Butler, S Biddolph, C Bowker, R Torra, Y Pei, ...
The American journal of pathology 154 (6), 1721-1729, 1999
2331999
An update for atypical haemolytic uraemic syndrome: diagnosis and treatment. A consensus document
JM Campistol, M Arias Ballesteros, G Ariceta, M Blasco, M Espinosa, ...
Sociedad Española de Nefrología, 2013
1972013
Linkage, clinical features, and prognosis of autosomal dominant polycystic kidney disease types 1 and 2.
R Torra, C Badenas, A Darnell, C Nicolau, V Volpini, L Revert, X Estivill
Journal of the American Society of Nephrology 7 (10), 2142-2151, 1996
1961996
Screening, diagnosis, and management of patients with Fabry disease: conclusions from a “Kidney Disease: Improving Global Outcomes”(KDIGO) Controversies Conference
R Schiffmann, DA Hughes, GE Linthorst, A Ortiz, E Svarstad, DG Warnock, ...
Kidney international 91 (2), 284-293, 2017
1872017
Incompletely penetrant PKD1 alleles mimic the renal manifestations of ARPKD
M Vujic, CM Heyer, E Ars, K Hopp, A Markoff, C Örndal, B Rudenhed, ...
Journal of the American Society of Nephrology 21 (7), 1097-1102, 2010
1822010
Patients with multiple myeloma requiring long‐term dialysis: presenting features, response to therapy, and outcome in a series of 20 cases
R Torra, J Blade, A Cases, J López‐Pedret, E Montserrat, C Rozman, ...
British journal of haematology 91 (4), 854-859, 1995
1761995
Nephrin mutations cause childhood-and adult-onset focal segmental glomerulosclerosis
S Santín, R García-Maset, P Ruíz, I Giménez, I Zamora, A Pena, A Madrid, ...
Kidney international 76 (12), 1268-1276, 2009
1752009
Mutations in theCOL4A4 and COL4A3 genes cause familial benign hematuria
M Praga, B Tazón, L Heidet, C Arrondel, A Armengol, A Andrés, ...
Journal of the American Society of Nephrology 13 (5), 1248-1254, 2002
1662002
Expert consensus guidelines for the genetic diagnosis of Alport syndrome
J Savige, F Ariani, F Mari, M Bruttini, A Renieri, O Gross, C Deltas, ...
Pediatric Nephrology 34, 1175-1189, 2019
1572019
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