Association between the clinical presentation of congenital anomalies of the kidney and urinary tract (CAKUT) and gene mutations: an analysis of 66 patients at a single institution

Sho Ishiwa(National Center For Child Health and Development), Kenji Ishikura(Kitasato University), Kazumoto Iijima(Kobe Children's Hospital), Toru Kanamori(National Center For Child Health and Development), Kentaro Nishi(National Center For Child Health and Development), Shuichi Ito(Yokohama City University), Mika Okutsu(National Center For Child Health and Development), Koichi Kamei(National Center For Child Health and Development), Naoya Morisada(Kobe Children's Hospital), Mai Sato(Kyoto University), Motomichi Kosuga(National Center For Child Health and Development), Kandai Nozu(Kobe Children's Hospital), Mayumi Sako(National Center For Child Health and Development), Masao Ogura(Hokkaido University Hospital)
Pediatric Nephrology
April 1, 2019
10.1007/s00467-019-04230-w
Cited by 37

Related Papers

Rituximab for childhood-onset, complicated, frequently relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicentre, double-blind, randomised, placebo-controlled trial
|The Lancet|2014|450
IPNA clinical practice recommendations for the diagnosis and management of children with steroid-sensitive nephrotic syndrome
|Pediatric Nephrology|2022|278
Creatinine-based equation to estimate the glomerular filtration rate in Japanese children and adolescents with chronic kidney disease
|Clinical and Experimental Nephrology|2013|267
Epidemiology of pediatric chronic kidney disease/kidney failure: learning from registries and cohort studies
|Pediatric Nephrology|2021|149
A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment
|Kidney International|2014|135