Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center

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Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2025-10-28
DOI
https://doi.org/10.1186/s13023-025-04082-8
Citations
1
Primary Topic
Kidney Stones and Urolithiasis Treatments
Type
article
Field-Weighted Citation Impact
1.52
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article

Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center

Raghad Alhuthil, Sermin Saadeh, Ibrahim A. Al-Hassoun, Essam Al‐Sabban et al.
1 citations
Orphanet Journal of Rare Diseases
Kidney Stones and Urolithiasis Treatments
1.52
article

Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center

Raghad Alhuthil, Sermin Saadeh, Ibrahim A. Al-Hassoun, Essam Al‐Sabban, Turki Alshareef, Bilqees Sayed
article en
1 citations

Abstract

No abstract available for this paper.
Orphanet Journal of Rare DiseasesVol. 20(1)
King Faisal Specialist Hospital & Research Centre (SA)
Openalex Percentile: Top 13%
Kidney Stones and Urolithiasis Treatments
1.52
DOIOpen Access PDFOpenAlex
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