1 A better trend was obtained also among combined liver-kidney transplantations in ADPKD .
2 However, long-term clinical outcomes of ADPKD patients on PD remain unclear.
3 Conclusions: Population whole-genome sequencing suggests a higher than expected prevalence of ADPKD - associated mutations.
4 Conclusion: Peritoneal dialysis is a suitable renal replacement therapy option for ADPKD patients.
5 Our investigation highlights major limitations of WES in ADPKD genetic diagnosis.
6 Substantial rare variation exists in genes with potential for phenotype modification in ADPKD .
7 This study explored potential mechanisms underlying resistance to FGF23 in ADPKD .
8 Thus, higher salt, but not higher protein intake may be detrimental in ADPKD .
9 Significant interfamilial and intrafamilial renal disease variability in ADPKD has been well documented.
10 The a allele might have a negative influence on the progression of ADPKD .
11 These findings have important health care and economic implications in following patients with ADPKD .
12 These preliminary results have potential important implications for cardiovascular and renal protection in ADPKD .
13 Methods: An epidemiological study involving 513 ADPKD subjects was performed.
14 In general, these modalities are reliable for the diagnosis of ADPKD in older individuals.
15 Impairment of endothelial function has been observed in ADPKD patients.
16 However, the relative contribution of JAK-STAT family members in promoting proliferation in ADPKD is unknown.
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