Final-year nephrology resident with a strong interest in rare diseases. Working at a national reference center for hereditary amyloidosis in Portugal. Clinical and research work focused on hereditary transthyretin (Val30Met mutation) and AL amyloidosis, with a strong interest in improving cardiorenal outcomes in those multisystemic diseases. Additional interests include IgA nephropathy, minimal changes disease, segmental focal glomerulosclerosis, membranous nephropathy, membranoproliferative glomerulonephritis, vasculitis, lupus nephropathy and autossomic dominant polycystic kidney disease.