Lv0
0 积分 2024-01-06 加入
The frequency of Fabry disease with the E66Q variant in the ?-galactosidase A gene in Japanese dialysis patients: a case report and a literature review
2天前
求助中
Prevalence of Fabry disease in patients with chronic kidney disease: A systematic review and meta-analysis
9天前
已完结
Genotype, phenotype and disease severity reflected by serum LysoGb3 levels in patients with Fabry disease
15天前
已完结
Genetic Management Algorithm in High-Risk Fabry Disease Cases; Especially in Female Indexes with Mutations
15天前
已完结
Fabry disease: Biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution
15天前
已完结
Fabry disease: Detection of undiagnosed hemodialysis patients and identification of a “renal variant” phenotype1
15天前
已完结
GLA variation p.E66Q identified as the genetic etiology of Fabry disease using exome sequencing
15天前
已完结
Fabry Disease with Genetic Variants of Unknown Significance and Concomitant Immunoglobulin A Nephropathy
1个月前
已完结
Glucose induced regulation of iron transporters implicates kidney iron accumulation
2个月前
已完结
Clinical and pathological factors associated with progression of diabetic nephropathy
2个月前
已完结
皖公网安备34019202002308
