Clinical spectrum of primary hyperoxaluria type 1: Experience of a tertiary center. [electronic resource]
Producer: 20180425Description: 176-182 p. digitalISSN:- 1872-9177
- Adult
- Child
- Child, Preschool
- Cohort Studies
- Consanguinity
- Egypt
- Female
- Humans
- Hyperoxaluria, Primary -- diagnosis
- Infant
- Kidney Failure, Chronic -- genetics
- Male
- Mutation
- Nephrocalcinosis -- diagnosis
- Nephrolithiasis -- diagnosis
- Phenotype
- Pyridoxine -- therapeutic use
- Retrospective Studies
- Risk Factors
- Tertiary Care Centers
- Transaminases -- genetics
- Treatment Outcome
- Vitamin B Complex
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.