Associated Papers
Long-term kidney function stabilization with fludrocortisone in autosomal recessive renal tubular dysgenesis: a case report.
Sugita R et al.
Pediatric Nephrology (berlin, Germany), 2026
41212229 (PubMed )
Supplement: 467_2025_7051_MOESM2_ESM.xlsx › Sheet1
ACE-Dependent Alzheimer's Disease: Circulating ACE Phenotypes in Heterozygous Carriers of Rare ACE Variants.
Mironenko IV et al.
International Journal of Molecular Sciences, 2025
41009662 (PubMed )
Supplement: ijms-26-09099-s001.zip › ijms-3824164-supplementary.pdf
Clinical features and genetic analysis of 15 Chinese children with dent disease.
Li Q et al.
Renal Failure, 2024
Effects of Angiotensin-I-Converting Enzyme (ACE) Mutations Associated with Alzheimer's Disease on Blood ACE Phenotype.
Kryukova OV et al.
Biomedicines, 2024
39457722 (PubMed )
Supplement: biomedicines-12-02410-s001.zip › biomedicines-3224268-supplementary.pdf
Carriers of Heterozygous Loss-of-Function ACE Mutations Are at Risk for Alzheimer's Disease.
Danilov SM et al.
Biomedicines, 2024
38255267 (PubMed )
Supplement: biomedicines-12-00162-s001.zip › biomedicines-2780808-Supplementary.pdf
Spectrum of mutations in the renin-angiotensin system genes in autosomal recessive renal tubular dysgenesis.
Gribouval O et al.
Human Mutation, 2012
Survival over 2 years of autosomal-recessive renal tubular dysgenesis.
Kim SY et al.
Clinical Kidney Journal, 2012
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