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American Journal of Nephrology
|
October 23, 2018
Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression
Mónica Furlano, Irene Loscos, Teresa Martí, et al.
Clinical Kidney Journal
|
December 4, 2023
Artificial intelligence: a new field of knowledge for nephrologists?
Leonor Fayos De Arizón, Elizabeth R Viera, Melissa Pilco, et al.
Case Reports in Genetics
|
January 9, 2023
The Benefits of Early versus Late Therapeutic Intervention in Fabry Disease
Mónica Furlano, Elisabet Ars, Anna Matamala, et al.
Nefrologia
|
February 14, 2025
Indications for genetic testing in adults with focal segmental glomerulosclerosis
Melissa Pilco-Terán, Amir Shabaka, Mónica Furlano, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 23, 2013
HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy
Gemma Bullich, José Ballarín, Artur Oliver, et al.
Journal of Clinical Medicine
|
November 9, 2024
Acute Myeloid Leukemia as a Trigger for Hemolytic-Uremic Syndrome
Jonas El Bachouti, Anna Domínguez-Guasch, Yolanda Arce, et al.
BMC Medical Genetics
|
June 17, 2015
Insight into response to mTOR inhibition when PKD1 and TSC2 are mutated
Cristina Cabrera-López, Gemma Bullich, Teresa Martí, et al.
Clinical Kidney Journal
|
March 6, 2026
Unravelling sex-specific differences in autosomal dominant polycystic kidney disease: a multiorgan perspective
Mónica Furlano, Adria Tinoco, Diego Toso, et al.
Medicina Clinica
|
January 20, 2019
Clinical profile of women diagnosed with Fabry disease non receiving enzyme replacement therapy
Miguel Ángel Barba-Romero, Joaquin Serena, Josep Maria Puig, et al.
Clinical Kidney Journal
|
March 21, 2025
When should the nephrologist think about genetics in patients with glomerular diseases?
Roser Torra, Xoana Barros, Montserrat Díaz-Encarnación, et al.
Page
of 17
Search research articles
Search
Showing results (51-60 of 161) with videos related to
Sort By:
Page
of 17
American Journal of Nephrology
|
October 23, 2018
Autosomal Dominant Polycystic Kidney Disease: Clinical Assessment of Rapid Progression
Mónica Furlano, Irene Loscos, Teresa Martí, et al.
Clinical Kidney Journal
|
December 4, 2023
Artificial intelligence: a new field of knowledge for nephrologists?
Leonor Fayos De Arizón, Elizabeth R Viera, Melissa Pilco, et al.
Case Reports in Genetics
|
January 9, 2023
The Benefits of Early versus Late Therapeutic Intervention in Fabry Disease
Mónica Furlano, Elisabet Ars, Anna Matamala, et al.
Nefrologia
|
February 14, 2025
Indications for genetic testing in adults with focal segmental glomerulosclerosis
Melissa Pilco-Terán, Amir Shabaka, Mónica Furlano, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
November 23, 2013
HLA-DQA1 and PLA2R1 polymorphisms and risk of idiopathic membranous nephropathy
Gemma Bullich, José Ballarín, Artur Oliver, et al.
Journal of Clinical Medicine
|
November 9, 2024
Acute Myeloid Leukemia as a Trigger for Hemolytic-Uremic Syndrome
Jonas El Bachouti, Anna Domínguez-Guasch, Yolanda Arce, et al.
BMC Medical Genetics
|
June 17, 2015
Insight into response to mTOR inhibition when PKD1 and TSC2 are mutated
Cristina Cabrera-López, Gemma Bullich, Teresa Martí, et al.
Clinical Kidney Journal
|
March 6, 2026
Unravelling sex-specific differences in autosomal dominant polycystic kidney disease: a multiorgan perspective
Mónica Furlano, Adria Tinoco, Diego Toso, et al.
Medicina Clinica
|
January 20, 2019
Clinical profile of women diagnosed with Fabry disease non receiving enzyme replacement therapy
Miguel Ángel Barba-Romero, Joaquin Serena, Josep Maria Puig, et al.
Clinical Kidney Journal
|
March 21, 2025
When should the nephrologist think about genetics in patients with glomerular diseases?
Roser Torra, Xoana Barros, Montserrat Díaz-Encarnación, et al.
Page
of 17