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Journal of Pediatric Urology
|
February 1, 2016
Renal function tests also exist
Margarita Monge-Zamorano, María Isabel Luis-Yanes, Víctor García-Nieto
Pediatric Nephrology (Berlin, Germany)
|
June 19, 2017
How best to quantify and express the levels of substances in the urine?
Víctor M García-Nieto, María Isabel Luis-Yanes, Pedro Arango-Sancho
Pediatric Nephrology (Berlin, Germany)
|
August 30, 2011
Effect of thiazides on bone mineral density in children with idiopathic hypercalciuria
Víctor García-Nieto, Margarita Monge-Zamorano, Montserrat González-García, et al.
Advances in Therapy
|
May 25, 2020
Correction to: Panel Discussion: Some Aspects of the Management of Patients with X-Linked Hypophosphataemic Rickets
José-Vicente Torregrosa, Jaime Sánchez Del Pozo, María Isabel Luis Yanes, et al.
Anales De Pediatria
|
December 30, 2019
[Kidney function tests at the crossroads]
Víctor M García Nieto, María Isabel Luis Yanes, Patricia Tejera Carreño, et al.
Indian Journal of Pediatrics
|
May 13, 2021
Imaging in Febrile Urinary Tract Infections - Area of Debate: Correspondence
Víctor M García-Nieto, Margarita Monge-Zamorano, María Isabel Luis-Yanes, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 20, 2009
Determination of Clara cell protein urinary elimination as a marker of tubular dysfunction
Ascensión Martín-Granado, Carmen Vázquez-Moncholí, María Isabel Luis-Yanes, et al.
World Journal of Pediatrics : WJP
|
May 8, 2014
Decreased concentrating capacity in children with febrile urinary tract infection and normal 99mTc-dimercaptosuccinic acid scan: does medullonephritis exist?
Víctor García-Nieto, Silvia González-Cerrato, María Isabel Luis-Yanes, et al.
Nefrologia
|
June 5, 2019
The idiopathic hypercalciuria reviewed. Metabolic abnormality or disease?
Víctor M García Nieto, María Isabel Luis Yanes, Patricia Tejera Carreño, et al.
Nefrologia
|
June 24, 2020
Presence of compound heterozygous mutations in the PHKD1 gene in an asymptomatic patient
María Isabel Luis-Yanes, Georgina Martínez Gómez, Carolina Tapia-Romero, et al.
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Search research articles
Search
Showing results (1-10 of 25) with videos related to
Sort By:
Page
of 3
Journal of Pediatric Urology
|
February 1, 2016
Renal function tests also exist
Margarita Monge-Zamorano, María Isabel Luis-Yanes, Víctor García-Nieto
Pediatric Nephrology (Berlin, Germany)
|
June 19, 2017
How best to quantify and express the levels of substances in the urine?
Víctor M García-Nieto, María Isabel Luis-Yanes, Pedro Arango-Sancho
Pediatric Nephrology (Berlin, Germany)
|
August 30, 2011
Effect of thiazides on bone mineral density in children with idiopathic hypercalciuria
Víctor García-Nieto, Margarita Monge-Zamorano, Montserrat González-García, et al.
Advances in Therapy
|
May 25, 2020
Correction to: Panel Discussion: Some Aspects of the Management of Patients with X-Linked Hypophosphataemic Rickets
José-Vicente Torregrosa, Jaime Sánchez Del Pozo, María Isabel Luis Yanes, et al.
Anales De Pediatria
|
December 30, 2019
[Kidney function tests at the crossroads]
Víctor M García Nieto, María Isabel Luis Yanes, Patricia Tejera Carreño, et al.
Indian Journal of Pediatrics
|
May 13, 2021
Imaging in Febrile Urinary Tract Infections - Area of Debate: Correspondence
Víctor M García-Nieto, Margarita Monge-Zamorano, María Isabel Luis-Yanes, et al.
Pediatric Nephrology (Berlin, Germany)
|
January 20, 2009
Determination of Clara cell protein urinary elimination as a marker of tubular dysfunction
Ascensión Martín-Granado, Carmen Vázquez-Moncholí, María Isabel Luis-Yanes, et al.
World Journal of Pediatrics : WJP
|
May 8, 2014
Decreased concentrating capacity in children with febrile urinary tract infection and normal 99mTc-dimercaptosuccinic acid scan: does medullonephritis exist?
Víctor García-Nieto, Silvia González-Cerrato, María Isabel Luis-Yanes, et al.
Nefrologia
|
June 5, 2019
The idiopathic hypercalciuria reviewed. Metabolic abnormality or disease?
Víctor M García Nieto, María Isabel Luis Yanes, Patricia Tejera Carreño, et al.
Nefrologia
|
June 24, 2020
Presence of compound heterozygous mutations in the PHKD1 gene in an asymptomatic patient
María Isabel Luis-Yanes, Georgina Martínez Gómez, Carolina Tapia-Romero, et al.
Page
of 3