OC8 High Prevalence Ofwt1gene Mutations in Patients With Steroid-Resistant Nephrotic Syndrome

doi 10.1136/archdischild-2019-epa.8
Full Text
Abstract

Available in full text

Date
Authors
Publisher

BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health

Related search

Mutations in KIRREL1, a Slit Diaphragm Component, Cause Steroid-Resistant Nephrotic Syndrome

Kidney International
Nephrology
2019English

Current Understandings in Treating Children With Steroid-Resistant Nephrotic Syndrome

Pediatric Nephrology
Child HealthPediatricsPerinatologyNephrology
2020English

Chapter 4: Steroid-Resistant Nephrotic Syndrome in Children

Kidney International Supplements
Nephrology
2012English

Histopathological Diagnosis of Steroid Resistant Nephrotic Syndrome in Children

Annals of King Edward Medical University
2016English

Steroid-Resistant Nephrotic Syndrome: Past and Current Perspectives

Pediatric Health, Medicine and Therapeutics
2017English

Focal Glomerulosclerosis--A Progressive Lesion Associated With Steroid-Resistant Nephrotic Syndrome.

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1971English

NPHS2 Gene Mutation and Polymorphisms in Indonesian Children With Steroid-Resistant Nephrotic Syndrome

Open Journal of Pediatrics
2015English

Long-Term Therapy With Cyclosporine and Alternate-Day Prednisone in Patients With Idiopathic Steroid Resistant Nephrotic Syndrome (SRNS)

Pediatric Review: International Journal of Pediatric Research
2018English

A Trial of Kampo Medicine for Treating Steroid-Resistant Nephrotic Syndrome.

Kampo Medicine
1990English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy