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Kidney International
|
December 23, 2016
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Anne Blanchard, Detlef Bockenhauer, Davide Bolignano, et al.
Kidney International
|
January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders
Martin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 1, 2025
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40
Stijn Wigerinck, Pieter Schellekens, Byron H Smith, et al.
The Journal of Clinical Investigation
|
August 27, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencing
Omid Sadeghi-Alavijeh, Melanie My Chan, Gabriel T Doctor, et al.
Nature Reviews. Nephrology
|
October 22, 2024
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)
Elena Levtchenko, Gema Ariceta, Olga Arguedas Flores, et al.
European Journal of Nutrition
|
September 28, 2022
Comment to "Recommendation on an updated standardization of serum magnesium reference ranges"
Jeroen H F de Baaij, Detlef Bockenhauer, Felix Claverie-Martin, et al.
The Journal of Physiology
|
February 9, 2011
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome
Dorothy A Thompson, Sally Feather, Horia C Stanescu, et al.
Kidney International Reports
|
June 25, 2021
Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy
Mallory L Downie, Sanjana Gupta, Mehmet C Tekman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 23, 2018
Progression of Mineral Ion Abnormalities in Patients With Jansen Metaphyseal Chondrodysplasia
Hiroshi Saito, Hiroshi Noda, Philippe Gatault, et al.
The New England Journal of Medicine
|
April 20, 2012
Integrin α3 mutations with kidney, lung, and skin disease
Cristina Has, Giuseppina Spartà, Dimitra Kiritsi, et al.
Page
of 24
Search research articles
Search
Showing results (141-150 of 233) with videos related to
Sort By:
Page
of 24
Kidney International
|
December 23, 2016
Gitelman syndrome: consensus and guidance from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference
Anne Blanchard, Detlef Bockenhauer, Davide Bolignano, et al.
Kidney International
|
January 29, 2021
Diagnosis and management of Bartter syndrome: executive summary of the consensus and recommendations from the European Rare Kidney Disease Reference Network Working Group for Tubular Disorders
Martin Konrad, Tom Nijenhuis, Gema Ariceta, et al.
Pediatric Nephrology (Berlin, Germany)
|
February 1, 2025
Characteristics of patients with autosomal polycystic kidney disease reaching kidney failure by age 40
Stijn Wigerinck, Pieter Schellekens, Byron H Smith, et al.
The Journal of Clinical Investigation
|
August 27, 2024
Quantifying variant contributions in cystic kidney disease using national-scale whole-genome sequencing
Omid Sadeghi-Alavijeh, Melanie My Chan, Gabriel T Doctor, et al.
Nature Reviews. Nephrology
|
October 22, 2024
International expert consensus statement on the diagnosis and management of congenital nephrogenic diabetes insipidus (arginine vasopressin resistance)
Elena Levtchenko, Gema Ariceta, Olga Arguedas Flores, et al.
European Journal of Nutrition
|
September 28, 2022
Comment to "Recommendation on an updated standardization of serum magnesium reference ranges"
Jeroen H F de Baaij, Detlef Bockenhauer, Felix Claverie-Martin, et al.
The Journal of Physiology
|
February 9, 2011
Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome
Dorothy A Thompson, Sally Feather, Horia C Stanescu, et al.
Kidney International Reports
|
June 25, 2021
Identification of a Locus on the X Chromosome Linked to Familial Membranous Nephropathy
Mallory L Downie, Sanjana Gupta, Mehmet C Tekman, et al.
The Journal of Clinical Endocrinology and Metabolism
|
May 23, 2018
Progression of Mineral Ion Abnormalities in Patients With Jansen Metaphyseal Chondrodysplasia
Hiroshi Saito, Hiroshi Noda, Philippe Gatault, et al.
The New England Journal of Medicine
|
April 20, 2012
Integrin α3 mutations with kidney, lung, and skin disease
Cristina Has, Giuseppina Spartà, Dimitra Kiritsi, et al.
Page
of 24