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Kidney International Reports
|
March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2011
Advances in Alport syndrome diagnosis using next-generation sequencing
Rosangela Artuso, Chiara Fallerini, Laura Dosa, et al.
Frontiers in Immunology
|
August 6, 2019
Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome
Manuela Colucci, Rita Carsetti, Jessica Serafinelli, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
June 8, 2021
Prevalence of SARS-CoV-2-IgG Antibodies in Children with CKD or Immunosuppression
William Morello, Antonio Mastrangelo, Isabella Guzzo, et al.
Journal of the American Society of Nephrology : JASN
|
May 15, 2012
Rituximab in children with resistant idiopathic nephrotic syndrome
Alberto Magnasco, Pietro Ravani, Alberto Edefonti, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
July 8, 2011
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype
Maddalena Gigante, Gianluca Caridi, Eustacchio Montemurno, et al.
Journal of the American Society of Nephrology : JASN
|
April 23, 2003
Broadening the spectrum of diseases related to podocin mutations
Gianluca Caridi, Roberta Bertelli, Marco Di Duca, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
December 15, 2020
Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression
Antonio Mastrangelo, William Morello, Enrico Vidal, et al.
Journal of the American Society of Nephrology : JASN
|
February 1, 2014
Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome
Piero Ruggenenti, Barbara Ruggiero, Paolo Cravedi, et al.
Human Mutation
|
November 4, 2017
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome
Sergio Daga, Margherita Baldassarri, Caterina Lo Rizzo, et al.
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of 6
Search research articles
Search
Showing results (21-30 of 58) with videos related to
Sort By:
Page
of 6
Kidney International Reports
|
March 19, 2026
Update on Alport Syndrome: The Report of the 2024 International Workshop on Alport Syndrome
Thomas M Oates, Moumita Barua, Susie Gear, et al.
European Journal of Human Genetics : EJHG
|
September 8, 2011
Advances in Alport syndrome diagnosis using next-generation sequencing
Rosangela Artuso, Chiara Fallerini, Laura Dosa, et al.
Frontiers in Immunology
|
August 6, 2019
Prolonged Impairment of Immunological Memory After Anti-CD20 Treatment in Pediatric Idiopathic Nephrotic Syndrome
Manuela Colucci, Rita Carsetti, Jessica Serafinelli, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
June 8, 2021
Prevalence of SARS-CoV-2-IgG Antibodies in Children with CKD or Immunosuppression
William Morello, Antonio Mastrangelo, Isabella Guzzo, et al.
Journal of the American Society of Nephrology : JASN
|
May 15, 2012
Rituximab in children with resistant idiopathic nephrotic syndrome
Alberto Magnasco, Pietro Ravani, Alberto Edefonti, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
July 8, 2011
TRPC6 mutations in children with steroid-resistant nephrotic syndrome and atypical phenotype
Maddalena Gigante, Gianluca Caridi, Eustacchio Montemurno, et al.
Journal of the American Society of Nephrology : JASN
|
April 23, 2003
Broadening the spectrum of diseases related to podocin mutations
Gianluca Caridi, Roberta Bertelli, Marco Di Duca, et al.
Clinical Journal of the American Society of Nephrology : CJASN
|
December 15, 2020
Impact of COVID-19 Pandemic in Children with CKD or Immunosuppression
Antonio Mastrangelo, William Morello, Enrico Vidal, et al.
Journal of the American Society of Nephrology : JASN
|
February 1, 2014
Rituximab in steroid-dependent or frequently relapsing idiopathic nephrotic syndrome
Piero Ruggenenti, Barbara Ruggiero, Paolo Cravedi, et al.
Human Mutation
|
November 4, 2017
Urine-derived podocytes-lineage cells: A promising tool for precision medicine in Alport Syndrome
Sergio Daga, Margherita Baldassarri, Caterina Lo Rizzo, et al.
Page
of 6