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Roser Torra

Showing results (31-40 of 161) with videos related to

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Clinical Kidney Journal|March 14, 2019
Podocyturia: why it may have added value in rare diseasesMaria Dolores Sanchez-Niño, Maria Vanessa Perez-Gomez, Lara Valiño-Rivas, et al.
Nefrologia|July 25, 2024
Genetic study in young patients with chronic kidney disease stage G5 from unknown etiology. The GENSEN study designMiquel Blasco, Borja Quiroga, José M García-Aznar, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|June 27, 2017
A review on autosomal dominant tubulointerstitial kidney diseaseNadia Ayasreh Fierro, Rosa Miquel Rodríguez, Ana Matamala Gastón, et al.
Clinical Kidney Journal|August 7, 2019
MYH9-related disease: it does exist, may be more frequent than you think and requires specific therapyRaul Fernandez-Prado, Sol Maria Carriazo-Julio, Roser Torra, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 7, 2008
Prevalence of cysts in seminal tract and abnormal semen parameters in patients with autosomal dominant polycystic kidney diseaseRoser Torra, Joaquim Sarquella, Jordi Calabia, et al.
Clinical Kidney Journal|April 17, 2024
'The forgotten sex': gender disparities in kidney diseaseKate I Stevens, Francesca Mallamaci, Alberto Ortiz, et al.
European Journal of Human Genetics : EJHG|June 16, 2005
Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotypeElisabet Ars, Bárbara Tazón-Vega, Patricia Ruiz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2026
The updated global burden of chronic kidney disease: one death every 20 secondsAlberto Ortiz, Jennifer S Lees, Roser Torra, et al.
Orphanet Journal of Rare Diseases|November 13, 2012
Assessing the effectiveness of rapamycin on angiomyolipoma in tuberous sclerosis: a two years trialCristina Cabrera-López, Teresa Martí, Violeta Catalá, et al.
Orphanet Journal of Rare Diseases|January 8, 2025
Clinical management of female patients with Fabry disease based on expert consensusEva Brand, Aleš Linhart, Patrick Deegan, et al.
Pageof 17

Showing results (31-40 of 161) with videos related to

Sort By:
Pageof 17
Clinical Kidney Journal|March 14, 2019
Podocyturia: why it may have added value in rare diseasesMaria Dolores Sanchez-Niño, Maria Vanessa Perez-Gomez, Lara Valiño-Rivas, et al.
Nefrologia|July 25, 2024
Genetic study in young patients with chronic kidney disease stage G5 from unknown etiology. The GENSEN study designMiquel Blasco, Borja Quiroga, José M García-Aznar, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia|June 27, 2017
A review on autosomal dominant tubulointerstitial kidney diseaseNadia Ayasreh Fierro, Rosa Miquel Rodríguez, Ana Matamala Gastón, et al.
Clinical Kidney Journal|August 7, 2019
MYH9-related disease: it does exist, may be more frequent than you think and requires specific therapyRaul Fernandez-Prado, Sol Maria Carriazo-Julio, Roser Torra, et al.
Clinical Journal of the American Society of Nephrology : CJASN|March 7, 2008
Prevalence of cysts in seminal tract and abnormal semen parameters in patients with autosomal dominant polycystic kidney diseaseRoser Torra, Joaquim Sarquella, Jordi Calabia, et al.
Clinical Kidney Journal|April 17, 2024
'The forgotten sex': gender disparities in kidney diseaseKate I Stevens, Francesca Mallamaci, Alberto Ortiz, et al.
European Journal of Human Genetics : EJHG|June 16, 2005
Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotypeElisabet Ars, Bárbara Tazón-Vega, Patricia Ruiz, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|February 25, 2026
The updated global burden of chronic kidney disease: one death every 20 secondsAlberto Ortiz, Jennifer S Lees, Roser Torra, et al.
Orphanet Journal of Rare Diseases|November 13, 2012
Assessing the effectiveness of rapamycin on angiomyolipoma in tuberous sclerosis: a two years trialCristina Cabrera-López, Teresa Martí, Violeta Catalá, et al.
Orphanet Journal of Rare Diseases|January 8, 2025
Clinical management of female patients with Fabry disease based on expert consensusEva Brand, Aleš Linhart, Patrick Deegan, et al.
Pageof 17