Publications from the RaDaR database

A role for OCRL in glomerular function and disease

Year: 2019

Journal:

Pediatric Nephrology

Databases:

RaDaR

High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults

Year: 2019

Journal:

Kidney International

Databases:

RaDaR

Molecular stratification of idiopathic nephrotic syndrome

Year: 2019

Journal:

Nature Reviews Nephrology

Databases:

RaDaR

TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways

Year: 2019

Journal:

The American Journal of Human Genetics

Databases:

RaDaR

Treatment and long-term outcome in primary distal renal tubular acidosis

Year: 2019

Journal:

Nephrology Dialysis Transplantation

Databases:

RaDaR

G33(P) Overview of rare renal diseases at a paediatric renal centre through the national registry of rare kidney diseases (RaDaR) in the united kingdom

Year: 2018

Journal:

Archives of disease in childhood

Authors:

J Kainth, Larissa Kerecuk, Maria Kokocinska, Melanie Dillon, Sharon Parkes

Databases:

RaDaR

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management

Year: 2017

Journal:

Kidney International

Databases:

RaDaR

IgA nephropathy: driving innovation with a rare renal disease registry

Year: 2017

Journal:

Journal of Kidney Care

Databases:

RaDaR

Clinical and Genetic Analysis of Patients with Cystinuria in the United Kingdom

Year: 2015

Journal:

Clinical Journal of the American Society of Nephrology

Databases:

RaDaR