Lv4
710 积分 2024-09-15 加入
Apparent Mineralocorticoid Excess in the Pediatric Population: Report of a Novel Pathogenic Variant of the 11β-HSD2 Gene and Systematic Review of the Literature
1天前
求助中
Oral administration of oxalate-enriched spinach extract as an improved methodology for the induction of dietary hyperoxaluric nephrocalcinosis in experimental rats
2天前
已完结
A complicated case of calcium urolithiasis in a carrier of SLC7A9 gene mutation responsible for cystinuria
3天前
求助中
Genotype-Phenotype correlation of distal renal tubular acidosis in Tunisia
3天前
求助中
[New Mutation of CYP24A1 in a Case of Idiopathic Infantile Hypercalcemia Diagnosed in Adulthood]
3天前
求助中
A Report of Claudin-19 Mutation Causing Nephrocalcinosis and End-Stage Kidney Disease from Iran
3天前
求助中
Long term tapering versus standard prednisolone treatment for first episode of childhood nephrotic syndrome: phase III randomised controlled trial and economic evaluation
13天前
已关闭
A Report of Claudin-19 Mutation Causing Nephrocalcinosis and End-Stage Kidney Disease from Iran
20天前
已关闭
Molecular and clinical studies of Dents disease in Japan: biochemical examination and renal ultrasonography do not predict carrier state
24天前
已完结
Dents disease: identification of a novel mutation in the renal chloride channel CLCN5
24天前
已关闭
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