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1. A Founder Mutation in EHD1 Presents with Tubular Proteinuria and Deafness. Issue 4 (April 2022)

4. MO910CHANGE IN BODY COMPOSITION MEASURED BY BIOIMPEDANCE SPECTROSCOPY AFTER COVID19 LOCKDOWN IN HAEMODIALYSIS PATIENTS. (29th May 2021)

6. Severe congenital nephrogenic diabetes insipidus in a compound heterozygote with a new large deletion of the AQP2 gene. A case report. Issue 4 (19th February 2019)