Cargando…

Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study

BACKGROUND: Prospective research of children receiving heterogeneous vaccines has shown that immunization is not associated with pediatric idiopathic nephrotic syndrome (NS) relapses. However, prospective data concentrating only on influenza (flu) virus vaccines are not available. METHODS: This mult...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ishimori, Shingo, Horinouchi, Tomoko, Fujimura, Junya, Yamamura, Tomohiko, Matsunoshita, Natsuki, Kamiyoshi, Naohiro, Sato, Mai, Ogura, Masao, Kamei, Koichi, Ishikura, Kenji, Iijima, Kazumoto, Nozu, Kandai
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2022
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709736/ https://www.ncbi.nlm.nih.gov/pubmed/36449102 http://dx.doi.org/10.1007/s00467-022-05783-z

Ejemplares similares

An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome
por: Horinouchi, Tomoko, et al.
Publicado: (2022)

Study protocol: mycophenolate mofetil as maintenance therapy after rituximab treatment for childhood-onset, complicated, frequently-relapsing nephrotic syndrome or steroid-dependent nephrotic syndrome: a multicenter double-blind, randomized, placebo-controlled trial (JSKDC07)
por: Horinouchi, Tomoko, et al.
Publicado: (2018)

Rituximab in steroid-sensitive nephrotic syndrome: lessons from clinical trials
por: Iijima, Kazumoto, et al.
Publicado: (2017)

Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases
por: Ishiko, Shinya, et al.
Publicado: (2020)

Rituximab for nephrotic syndrome in children
por: Iijima, Kazumoto, et al.
Publicado: (2016)

Rituximab Treatment for Nephrotic Syndrome in Children
por: Iijima, Kazumoto, et al.
Publicado: (2014)

Influenza virus vaccination in children with nephrotic syndrome: insignificant risk of relapse
por: Ishimori, Shingo, et al.
Publicado: (2020)

Study protocol: multicenter double-blind, randomized, placebo-controlled trial of rituximab for the treatment of childhood-onset early-stage uncomplicated frequently relapsing or steroid-dependent nephrotic syndrome (JSKDC10 trial)
por: Nagano, China, et al.
Publicado: (2019)

Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
por: Inoue, Tomohiko, et al.
Publicado: (2021)

Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
por: Inoue, Tomohiko, et al.
Publicado: (2020)

Three Severe Cases of Viral Infections with Post-Kidney Transplantation Successfully Confirmed by Polymerase Chain Reaction and Flow Cytometry
por: Nakanishi, Keita, et al.
Publicado: (2018)

Study protocol: high-dose mizoribine with prednisolone therapy in short-term relapsing steroid-sensitive nephrotic syndrome to prevent frequent relapse (JSKDC05 trial)
por: Hama, Taketsugu, et al.
Publicado: (2018)

The utility of urinary CD80 as a diagnostic marker in patients with renal diseases
por: Minamikawa, Shogo, et al.
Publicado: (2018)

Clinical and Genetic Characteristics in Patients With Gitelman Syndrome
por: Fujimura, Junya, et al.
Publicado: (2018)

Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome
por: Yamamura, Tomohiko, et al.
Publicado: (2019)

Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children’s primary emergency medical center
por: Morioka, Ichiro, et al.
Publicado: (2017)

Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
por: Nagano, China, et al.
Publicado: (2020)

Genetic background, recent advances in molecular biology, and development of novel therapy in Alport syndrome
por: Nozu, Kandai, et al.
Publicado: (2020)

The Contribution of COL4A5 Splicing Variants to the Pathogenesis of X-Linked Alport Syndrome
por: Yamamura, Tomohiko, et al.
Publicado: (2022)

Extranodal natural killer/T‐cell lymphoma in an 11‐year‐old child
por: Ninchoji, Takeshi, et al.
Publicado: (2020)

Genotype-Phenotype Correlation in WT1 Exon 8 to 9 Missense Variants
por: Nagano, China, et al.
Publicado: (2021)

An in vitro splicing assay reveals the pathogenicity of a novel intronic variant in ATP6V0A4 for autosomal recessive distal renal tubular acidosis
por: Yamamura, Tomohiko, et al.
Publicado: (2017)

Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay
por: Horinouchi, Tomoko, et al.
Publicado: (2020)

Steroid resistant nephrotic syndrome with collapsing focal segmental glomerulosclerosis in a 12-year-old Japanese female after SARS-CoV-2 vaccination
por: Horinouchi, Tomoko, et al.
Publicado: (2023)

Yersinia pseudotuberculosis infection in Kawasaki disease and its clinical characteristics
por: Horinouchi, Tomoko, et al.
Publicado: (2015)

Two cases of idiopathic steroid-resistant nephrotic syndrome complicated with thrombotic microangiopathy
por: Nishi, Kentaro, et al.
Publicado: (2020)

Influenza virus vaccination in pediatric nephrotic syndrome significantly reduces rate of relapse and influenza virus infection as assessed in a nationwide survey
por: Ishimori, Shingo, et al.
Publicado: (2021)

iPSC-derived type IV collagen α5-expressing kidney organoids model Alport syndrome
por: Hirayama, Ryuichiro, et al.
Publicado: (2023)

Diagnostic challenge in a patient with nephropathic juvenile cystinosis: a case report
por: Higashi, Satomi, et al.
Publicado: (2017)

Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene
por: Okada, Eri, et al.
Publicado: (2022)

Systematic Review of Clinical Characteristics and Genotype-Phenotype Correlation in LAMB2-Associated Disease
por: Suzuki, Ryota, et al.
Publicado: (2023)

Treatment of hemolytic uremic syndrome related to Bordetella pertussis infection —is plasma exchange or eculizumab use necessary?
por: Saida, Ken, et al.
Publicado: (2018)

A multicenter randomized trial indicates initial prednisolone treatment for childhood nephrotic syndrome for two months is not inferior to six-month treatment
por: Yoshikawa, Norishige, et al.
Publicado: (2015)

Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay
por: Horinouchi, Tomoko, et al.
Publicado: (2019)

Last Nucleotide Substitutions of COL4A5 Exons Cause Aberrant Splicing
por: Aoto, Yuya, et al.
Publicado: (2021)

Trimerization and Genotype–Phenotype Correlation of COL4A5 Mutants in Alport Syndrome
por: Kamura, Misato, et al.
Publicado: (2020)

A birth of bipartite exon by intragenic deletion
por: Nozu, Kandai, et al.
Publicado: (2017)

A Novel Mutation in a Japanese Family with X-linked Alport Syndrome
por: Abe, Yoshifusa, et al.
Publicado: (2016)

A review of clinical characteristics and genetic backgrounds in Alport syndrome
por: Nozu, Kandai, et al.
Publicado: (2018)

All reported non-canonical splice site variants in GLA cause aberrant splicing
por: Okada, Eri, et al.
Publicado: (2023)

Cannot write session to /tmp/vufind_sessions/sess_j7q5ftreauqrf1a4u8uq4betmg