Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center
- DOI
- 10.6084/m9.figshare.c.8116365.v1
- Published
- 2025
- Container
- Not recorded
- Publisher
- figshare
- Open access
- yes
Credibility signals
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Cite this work
BibTeX
@article{allodium:10.6084/m9.figshare.c.8116365.v1,
title = {Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center},
author = {Sayed, Bayan and Alhuthil, Raghad and Saadeh, Sermin and Al-Shareef, Turki and Alhassoun, Ibrahim and Al-Sabban, Essam},
year = {2025},
doi = {10.6084/m9.figshare.c.8116365.v1},
url = {https://doi.org/10.6084/m9.figshare.c.8116365.v1}
}RIS
TY - JOUR TI - Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center AU - Sayed, Bayan AU - Alhuthil, Raghad AU - Saadeh, Sermin AU - Al-Shareef, Turki AU - Alhassoun, Ibrahim AU - Al-Sabban, Essam PY - 2025 DO - 10.6084/m9.figshare.c.8116365.v1 UR - https://doi.org/10.6084/m9.figshare.c.8116365.v1 ER -
APA
Bayan, S., Raghad, A., Sermin, S., Turki, A., Ibrahim, A., & Essam, A. (2025). Primary hyperoxaluria: insights into its clinical presentation, genetic mutations, and transplantation outcomes in a pediatric population in a tertiary care center. https://doi.org/10.6084/m9.figshare.c.8116365.v1
Source records
- datacite · retrieved 2026-09-26T21:01:59.075Z