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Molecular Genetics and Metabolism Reports
|
August 17, 2021
Long-term follow-up of renal function in patients treated with migalastat for Fabry disease
Daniel G Bichet, Roser Torra, Eric Wallace, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
March 19, 2011
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome
Sheila Santín, Gemma Bullich, Bárbara Tazón-Vega, et al.
Human Vaccines
|
February 9, 2011
Epidemiological analysis of severe hospitalized 2009 pandemic influenza A (H1N1) cases in Catalonia, Spain
Neus Cardeñosa, Anna Rodés, Núria Follia, et al.
Orphanet Journal of Rare Diseases
|
February 9, 2022
Do clinical guidelines facilitate or impede drivers of treatment in Fabry disease?
Derralynn A Hughes, Patrício Aguiar, Olivier Lidove, et al.
Nefrologia
|
November 15, 2019
Recommendations for the management of renal involvement in the tuberous sclerosis complex
Gema Ariceta, María José Buj, Mónica Furlano, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
July 31, 2013
Familial chronic interstitial nephropathy with hyperuricaemia caused by the UMOD gene
Nadia Ayasreh-Fierro, Elisabet Ars-Criach, Vanesa Lopes-Martín, et al.
Medicine
|
December 9, 2016
Renal volume and cardiovascular risk assessment in normotensive autosomal dominant polycystic kidney disease patients
Laia Sans, Julio Pascual, Aleksandar Radosevic, et al.
Molecular Genetics and Metabolism Reports
|
December 22, 2021
Corrigendum to "Long-term follow-up of renal function in patients treated with migalastat for Fabry disease" [Bichet et al., MGM Reports; 28 (2021) 100786]
Daniel G Bichet, Roser Torra, Eric Wallace, et al.
Stem Cell Research
|
December 17, 2017
Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS)
Bernd Kuebler, Begoña Aran, Laia Miquel-Serra, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
October 16, 2010
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome
Sheila Santín, Bárbara Tazón-Vega, Irene Silva, et al.
Page
of 17
Search research articles
Search
Showing results (61-70 of 161) with videos related to
Sort By:
Page
of 17
Molecular Genetics and Metabolism Reports
|
August 17, 2021
Long-term follow-up of renal function in patients treated with migalastat for Fabry disease
Daniel G Bichet, Roser Torra, Eric Wallace, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
March 19, 2011
Clinical utility of genetic testing in children and adults with steroid-resistant nephrotic syndrome
Sheila Santín, Gemma Bullich, Bárbara Tazón-Vega, et al.
Human Vaccines
|
February 9, 2011
Epidemiological analysis of severe hospitalized 2009 pandemic influenza A (H1N1) cases in Catalonia, Spain
Neus Cardeñosa, Anna Rodés, Núria Follia, et al.
Orphanet Journal of Rare Diseases
|
February 9, 2022
Do clinical guidelines facilitate or impede drivers of treatment in Fabry disease?
Derralynn A Hughes, Patrício Aguiar, Olivier Lidove, et al.
Nefrologia
|
November 15, 2019
Recommendations for the management of renal involvement in the tuberous sclerosis complex
Gema Ariceta, María José Buj, Mónica Furlano, et al.
Nefrologia : Publicacion Oficial De La Sociedad Espanola Nefrologia
|
July 31, 2013
Familial chronic interstitial nephropathy with hyperuricaemia caused by the UMOD gene
Nadia Ayasreh-Fierro, Elisabet Ars-Criach, Vanesa Lopes-Martín, et al.
Medicine
|
December 9, 2016
Renal volume and cardiovascular risk assessment in normotensive autosomal dominant polycystic kidney disease patients
Laia Sans, Julio Pascual, Aleksandar Radosevic, et al.
Molecular Genetics and Metabolism Reports
|
December 22, 2021
Corrigendum to "Long-term follow-up of renal function in patients treated with migalastat for Fabry disease" [Bichet et al., MGM Reports; 28 (2021) 100786]
Daniel G Bichet, Roser Torra, Eric Wallace, et al.
Stem Cell Research
|
December 17, 2017
Integration-free induced pluripotent stem cells derived from a patient with autosomal recessive Alport syndrome (ARAS)
Bernd Kuebler, Begoña Aran, Laia Miquel-Serra, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
October 16, 2010
Clinical value of NPHS2 analysis in early- and adult-onset steroid-resistant nephrotic syndrome
Sheila Santín, Bárbara Tazón-Vega, Irene Silva, et al.
Page
of 17