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Increased prevalence of kidney cysts in individuals carrying heterozygous COL4A3 or COL4A4 pathogenic variants.
Published in:
Nephrology Dialysis Transplantation, 2024, v. 39, n. 9, p. 1442, doi. 10.1093/ndt/gfae031
By:
- Furlano, Mónica;
- Pilco-Teran, Melissa;
- Pybus, Marc;
- Martínez, Víctor;
- Aza-Carmona, Miriam;
- Peris, Asunción Rius;
- Pérez-Gomez, Vanessa;
- Berná, Gerson;
- Mazon, Jaime;
- Hernández, Jonathan;
- Arizón, Leonor Fayos de;
- Viera, Elizabet;
- Gich, Ignasi;
- Pérez, Hugo Vergara;
- Gomá-Garcés, Elena;
- Dolon, José Luis Albero;
- Ars, Elisabet;
- Torra, Roser
Publication type:
Article
Clinical utility of genetic testing in early-onset kidney disease: seven genes are the main players.
Published in:
Nephrology Dialysis Transplantation, 2022, v. 37, n. 4, p. 687, doi. 10.1093/ndt/gfab019
By:
- Domingo-Gallego, Andrea;
- Pybus, Marc;
- Bullich, Gemma;
- Furlano, Mónica;
- Ejarque-Vila, Laia;
- Lorente-Grandoso, Laura;
- Ruiz, Patricia;
- Fraga, Gloria;
- González, Mercedes López;
- Piñero-Fernández, Juan Alberto;
- Rodríguez-Peña, Lidia;
- Llano-Rivas, Isabel;
- Sáez, Raquel;
- Bujons-Tur, Anna;
- Ariceta, Gema;
- Guirado, Lluis;
- Torra, Roser;
- Ars, Elisabet
Publication type:
Article
New therapeutic options for Alport syndrome.
Published in:
Nephrology Dialysis Transplantation, 2019, v. 34, n. 8, p. 1272, doi. 10.1093/ndt/gfz131
By:
- Torra, Roser;
- Furlano, Mónica
Publication type:
Article
The Benefits of Early versus Late Therapeutic Intervention in Fabry Disease.
Published in:
2022
By:
- Furlano, Mónica;
- Ars, Elisabet;
- Matamala, Anna;
- Brossa, Vicens;
- Martí, Joan;
- Prado-Venegas, Maria del;
- Crespi, Jaume;
- Roe, Esther;
- Torra, Roser
Publication type:
Case Study
Respuesta a Comentarios sobre el Documento de Consenso de Poliquistosis Renal Autosómica Dominante de la SENefro.
Published in:
Nefrologia, 2023, v. 43, n. 1, p. 152, doi. 10.1016/j.nefro.2022.07.002
By:
- Ortiz, Alberto;
- Ars, Elisabet;
- Bernis, Carmen;
- Fraga, Gloria;
- Furlano, Mónica;
- Martínez, Víctor;
- Martins, Judith;
- Pérez-Gómez, Maria Vanessa;
- Rodríguez-Pérez, José Carlos;
- Sans, Laia;
- Torra, Roser
Publication type:
Article
Consensus document on autosomal dominant polycystic kindey disease from the Spanish Working Group on Inherited Kindey Diseases. Review 2020.
Published in:
Nefrologia, 2022, v. 42, n. 4, p. 367, doi. 10.1016/j.nefroe.2022.11.011
By:
- Ars, Elisabet;
- Bernis, Carmen;
- Fraga, Gloria;
- Furlano, Mónica;
- Martínez, Víctor;
- Martins, Judith;
- Ortiz, Alberto;
- Pérez-Gómez, Maria Vanessa
Publication type:
Article
Kidneys also speak Spanish: Initiatives towards standardisation of our nephrology nomenclature.
Published in:
Nefrologia, 2022, v. 42, n. 3, p. 223, doi. 10.1016/j.nefroe.2022.09.003
By:
- Bover, Jordi;
- Bosch, Ricardo;
- Górriz, José Luis;
- Ureña, Pablo;
- Ortiz, Alberto;
- daSilva, Iara;
- García-Trabanino, Ramón A.;
- Hueso, Miguel;
- Trinidad, Pedro;
- Jara, Aquiles;
- Furlano, Mónica;
- Gelpi, Rosana;
- Vila-Santandreu, Ana;
- Restrepo, César A.;
- Sánchez-Baya, Maya;
- Arana, Carolt;
- Goicoechea, Marián;
- Coll, Verónica;
- Segura, Julián;
- Gutiérrez, Orlando
Publication type:
Article
Los riñones también hablan español.
Published in:
Nefrologia, 2021, v. 41, n. 2, p. 225, doi. 10.1016/j.nefro.2020.11.002
By:
- Bover, Jordi;
- Bosch, Ricardo;
- Ureña, Pablo;
- Trinidad, Pedro;
- Jara, Aquiles;
- Luis Górriz, José;
- Furlano, Mónica;
- García-Trabanino, Ramón A.;
- Gelpi, Rosana;
- Ortiz, Alberto;
- Restrepo, César A.;
- Sánchez-Baya, Maya;
- Arana, Carolt;
- Goicoechea, Marián;
- Coll, Verónica;
- Segura, Julián;
- Gutiérrez, Orlando;
- Sánchez, Emilio;
- Ferreiro, Alejandro;
- García-Maset, Rafael
Publication type:
Article
Recomendaciones de manejo de la afectación renal en el complejo esclerosis tuberosa.
Published in:
Nefrologia, 2020, v. 40, n. 2, p. 142, doi. 10.1016/j.nefro.2019.07.002
By:
- Ariceta, Gema;
- Buj, María José;
- Furlano, Mónica;
- Martínez, Víctor;
- Matamala, Anna;
- Morales, Montserrat;
- Robles, Nicolás Roberto;
- Sansh, Laia;
- Villacampa, Felipe;
- Torra, Roser
Publication type:
Article
Nefropatía asociada a mutación del gen MYH9.
Published in:
Nefrologia, 2019, v. 39, n. 2, p. 133, doi. 10.1016/j.nefro.2018.08.008
By:
- Furlano, Mónica;
- Torra, Roser;
- Ars, Elisabet;
- Ayasreh, Nadia;
- Ballarín, José;
- Arlandis, Rosa;
- del Prado Venegas, María;
- Novelli, Silvana;
- Remacha, Ángel;
- Crespi, Jaume;
- Bullich, Gemma;
- Ruiz, Patricia;
- Lorente, Laura;
- Matamala, Anna
Publication type:
Article
Sangrado de angiomiolipoma renal en paciente con síndrome de genes contiguos (TSC2/PKD1) tras 17 años de tratamiento renal sustitutivo.
Published in:
Nefrologia, 2017, v. 37, n. 1, p. 87, doi. 10.1016/j.nefro.2016.04.007
By:
- Furlano, Mónica;
- Barreiro, Yaima;
- Martí, Teresa;
- Facundo, Carme;
- Ruiz-García, César;
- DaSilva, Iara;
- Ayasreh, Nadia;
- Cabrera-López, Cristina;
- Ballarín, José;
- Ars, Elisabet;
- Torra, Roser
Publication type:
Article
Tables for estimating the glomerular filtration rate using the new CKD-EPI equation from serum creatinine concentration.
Published in:
Nefrologia, 2014, v. 34, n. 2, p. 223, doi. 10.3265/Nefrologia.pre2013.Dec.12226
By:
- Canal, Cristina;
- Pellicer, Rodrigo;
- Facundo, Carme;
- Gràcia-García, Silvia;
- Montañés-Bermúdez, Rosario;
- Ruiz-García, César;
- Furlano, Mónica;
- Da Silva, Iara Karlla;
- Ballarín, José A.;
- Bover, Jordi
Publication type:
Article
Creatine Kinase Elevation in Autosomal Dominant Polycystic Kidney Disease Patients on Tolvaptan Treatment.
Published in:
Nephron, 2023, v. 147, n. 3/4, p. 152, doi. 10.1159/000526368
By:
- Rodríguez-Espinosa, Diana;
- Broseta, José Jesús;
- Bastida, Carla;
- Álvarez-Mora, María Isabel;
- Nicolau, Carlos;
- Alvarez, Cristina;
- Agraz-Pamplona, Irene;
- Sánchez-Baya, Maya;
- Furlano, Mónica;
- Ruiz, César;
- Quintana, Luis F.;
- Piñeiro, Gastón J.;
- Poch, Esteban;
- Torra-Balcells, Roser;
- Blasco, Miquel
Publication type:
Article
Autosomal dominant polycystic kidney disease in young adults.
Published in:
Clinical Kidney Journal, 2023, v. 16, n. 6, p. 985, doi. 10.1093/ckj/sfac251
By:
- Martínez, Víctor;
- Furlano, Mónica;
- Sans, Laia;
- Pulido, Lissett;
- García, Rebeca;
- Pérez-Gómez, María Vanessa;
- Sánchez-Rodríguez, Jinny;
- Blasco, Miquel;
- Castro-Alonso, Cristina;
- Fernández-Fresnedo, Gema;
- Robles, Nicolás Roberto;
- Valenzuela, María Pau;
- Naranjo, Javier;
- Martín, Nadia;
- Pilco, Melissa;
- Agraz-Pamplona, Irene;
- González-Rodríguez, Juan David;
- Panizo, Nayara;
- Fraga, Gloria;
- Fernández, Loreto
Publication type:
Article
Comparative analysis of tools to predict rapid progression in autosomal dominant polycystic kidney disease.
Published in:
Clinical Kidney Journal, 2022, v. 15, n. 5, p. 912, doi. 10.1093/ckj/sfab293
By:
- Naranjo, Javier;
- Furlano, Mónica;
- Torres, Ferran;
- Hernandez, Jonathan;
- Pybus, Marc;
- Ejarque, Laia;
- Cordoba, Christian;
- Guirado, Lluis;
- Ars, Elisabet;
- Torra, Roser
Publication type:
Article
Autosomal dominant polycystic kidney disease: possibly the least silent cause of chronic kidney disease.
Published in:
Clinical Kidney Journal, 2021, v. 14, n. 11, p. 2281, doi. 10.1093/ckj/sfab132
By:
- Torra, Roser;
- Pérez-Gómez, Maria Vanessa;
- Furlano, Mónica
Publication type:
Article
Genetic kidney diseases as an underrecognized cause of chronic kidney disease: the key role of international registry reports.
Published in:
Clinical Kidney Journal, 2021, v. 14, n. 8, p. 1879, doi. 10.1093/ckj/sfab056
By:
- Torra, Roser;
- Furlano, Mónica;
- Ortiz, Alberto;
- Ars, Elisabet
Publication type:
Article
Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression.
Published in:
2018
By:
- Furlano, Mónica;
- Loscos, Irene;
- Martí, Teresa;
- Bullich, Gemma;
- Ayasreh, Nadia;
- Rius, Asunción;
- Roca, Lourdes;
- Ballarín, José;
- Ars, Elisabet;
- Torra, Roser
Publication type:
journal article
Novel homozygous OSGEP gene pathogenic variants in two unrelated patients with Galloway-Mowat syndrome: case report and review of the literature.
Published in:
2019
By:
- Domingo-Gallego, Andrea;
- Furlano, Mónica;
- Pybus, Marc;
- Barraca, Daniel;
- Martínez, Ana Belén;
- Mora Muñoz, Emiliano;
- Torra, Roser;
- Ars, Elisabet
Publication type:
journal article
A Mild Presentation of X-Linked Hypophosphatemia Caused by a Non-Canonical Splice Site Variant in the PHEX Gene.
Published in:
2024
By:
- Fraga, Gloria;
- Herreros, M. Alba;
- Pybus, Marc;
- Aza-Carmona, Miriam;
- Pilco-Teran, Melissa;
- Furlano, Mónica;
- García-Borau, M. José;
- Torra, Roser;
- Ars, Elisabet
Publication type:
Case Study
Lanthanum carbonate for the control of hyperphosphatemia in chronic renal failure patients: a new oral powder formulation — safety, efficacy, and patient adherence.
Published in:
Patient Preference & Adherence, 2013, v. 7, p. 1147, doi. 10.2147/PPA.S31694
By:
- Lloret, Mª Jesús;
- Ruiz-García, César;
- DaSilva, Iara;
- Furlano, Mónica;
- Barreiro, Yaima;
- Ballarín, José;
- Bover, Jordi
Publication type:
Article

Found: 21