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PHYOX2: a pivotal randomized study of nedosiran in primary hyperoxaluria type 1 or 2
3小时前
待确认
Inherited conditions resulting in nephrolithiasis
5小时前
已完结
Phenotype-Genotype Correlations and Estimated Carrier Frequencies of Primary Hyperoxaluria
5小时前
已完结
Genotype–phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome
5小时前
已完结
Clinical practice recommendations for primary hyperoxaluria: an expert consensus statement from ERKNet and OxalEurope
5小时前
已完结
Novel therapeutic approaches for the primary hyperoxalurias
3天前
已完结
Primary hyperoxaluria in infants
9天前
已完结
Advances in the enzymology and molecular genetics of primary hyperoxaluria type 1. Prospects for gene therapy
11天前
已完结
How We Treat Primary Hyperoxaluria Type 1
11天前
已关闭
Lumasiran, an RNAi Therapeutic for Primary Hyperoxaluria Type 1
11天前
已完结
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