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Meanings of adpkd in anglès

rus
поликистоз почек
portuguès
doença do rim policístico
espanyol
enfermedad poliquística renal
català
poliquistosi renal autosòmica dominant
Wikidata

Human disease.

        Related terms
        poliquistosi renal autosòmica dominant
        Synonyms
        Examples for "autosomal dominant pkd"
        Examples for "autosomal dominant pkd"
        1
        An enhancement of these protective interventions in this autosomal dominant PKD model was not demonstrated with the combined treatment.
        Pubmed
        1
        Cerebral aneurysms are sometimes associated with inherited diseases like autosomal dominant polycystic kidney disease.
        Pubmed
        2
        An intriguing feature of autosomal dominant polycystic kidney disease (ADPKD) is the focal and sporadic nature of individual cyst formation.
        Pubmed
        3
        In light of the parallels between cancer and autosomal dominant polycystic kidney disease (ADPKD), the latter is currently being studied as a metabolic disease.
        Pubmed
        4
        The rate at which autosomal dominant polycystic kidney disease (ADPKD) progresses to end-stage renal disease varies widely and is determined by genetic and non-genetic factors.
        Pubmed
        5
        Background and purpose: Autosomal dominant polycystic kidney disease is associated with an increased risk of intracranial aneurysms.
        Pubmed
        Usage of adpkd in anglès
        1
        A better trend was obtained also among combined liver-kidney transplantations in ADPKD.
        Pubmed
        2
        However, long-term clinical outcomes of ADPKD patients on PD remain unclear.
        Pubmed
        3
        Conclusions: Population whole-genome sequencing suggests a higher than expected prevalence of ADPKD-associated mutations.
        Pubmed
        4
        Conclusion: Peritoneal dialysis is a suitable renal replacement therapy option for ADPKD patients.
        Pubmed
        5
        Our investigation highlights major limitations of WES in ADPKD genetic diagnosis.
        Pubmed
        6
        Substantial rare variation exists in genes with potential for phenotype modification in ADPKD.
        Pubmed
        7
        This study explored potential mechanisms underlying resistance to FGF23 in ADPKD.
        Pubmed
        8
        Thus, higher salt, but not higher protein intake may be detrimental in ADPKD.
        Pubmed
        9
        Significant interfamilial and intrafamilial renal disease variability in ADPKD has been well documented.
        Pubmed
        10
        The a allele might have a negative influence on the progression of ADPKD.
        Pubmed
        11
        These findings have important health care and economic implications in following patients with ADPKD.
        Pubmed
        12
        These preliminary results have potential important implications for cardiovascular and renal protection in ADPKD.
        Pubmed
        13
        Methods: An epidemiological study involving 513 ADPKD subjects was performed.
        Pubmed
        14
        In general, these modalities are reliable for the diagnosis of ADPKD in older individuals.
        Pubmed
        15
        Impairment of endothelial function has been observed in ADPKD patients.
        Pubmed
        16
        However, the relative contribution of JAK-STAT family members in promoting proliferation in ADPKD is unknown.
        Pubmed
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        Translations for adpkd
        Adpkd through the time