日本における腎臓及び尿路の先天性異常(CAKUT)の網羅的遺伝子解析

Naoya Morisada(Kobe Children's Hospital), Kazumoto Iijima(Kobe Children's Hospital), Ryojiro Tanaka(Kobe Children's Hospital), Mariko Taniguchi‐Ikeda, Shuichi Ito(Yokohama City University), Kenji Ishikura(Kitasato University), Koichi Kamei(National Center For Child Health and Development), Kandai Nozu(Kobe Children's Hospital), Akemi Shono(Kobe University), Hisahide Nishio
日本人類遺伝学会大会プログラム・抄録集
January 1, 2016
Cited by 0

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