Cargando…
Clinical analysis of 13 children with primary hyperoxaluria type 1
A retrospective statistical analysis of primary hyperoxaluria type 1 (PH1) in children from June 2016 to May 2019 was carried out to discover its clinical and molecular biological characteristics. Patients were divided into two groups (infant and noninfant) according to clinic type. There were 13 pe...
Autores principales: | Lin, Jin-ai, Liao, Xin, Wu, Wenlin, Xiao, Lixia, Liu, Longshan, Qiu, Jiang |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8416882/ https://www.ncbi.nlm.nih.gov/pubmed/33721035 http://dx.doi.org/10.1007/s00240-021-01249-3 |
Ejemplares similares
-
Primary Hyperoxaluria
por: Harambat, Jérôme, et al.
Publicado: (2011) -
Clinical and Genetic Profile of Indian Children with Primary Hyperoxaluria
por: Pinapala, A., et al.
Publicado: (2017) -
Treatment of primary hyperoxaluria type 1
por: Gupta, Asheeta, et al.
Publicado: (2022) -
Primary Hyperoxaluria Type 1 in 18 Children: Genotyping and Outcome
por: Al Riyami, Mohamed S., et al.
Publicado: (2015) -
Determinants of Kidney Failure in Primary Hyperoxaluria Type 1: Findings of the European Hyperoxaluria Consortium
por: Metry, Elisabeth L., et al.
Publicado: (2023)