about
NPHS2 mutations account for only 15% of nephrotic syndrome cases.NPHS1 gene mutations confirm congenital nephrotic syndrome in four Brazilian cases: A novel mutation is described.Collaborative Brazilian Pediatric Renal Transplant Registry (CoBrazPed-RTx): A Report From 2004 to 2013.NPHS2 Mutations: A Closer Look to Latin American Countries.Hypercalcemia in children: three cases report with unusual clinical presentations.Apparent mineralocorticoid excess syndrome in a Brazilian boy caused by the homozygous missense mutation p.R186C in the HSD11B2 gene.Prospective cohort analyzing risk factors for chronic kidney disease progression in children.WT1 Haploinsufficiency Supports Milder Renal Manifestation in Two Patients with Denys-Drash Syndrome.Frasier syndrome: four new cases with unusual presentations.Promises and pitfalls of whole-exome sequencing exemplified by a nephrotic syndrome family
P50
Q35792721-802F6039-8914-4153-AED4-8D6EC0A4F814Q40330789-9BF51F70-B0B8-4D76-A53E-34E6380EF8DDQ40876994-8FD4483F-4716-4C43-BF9F-45AB6D51F3B7Q41141616-A4098B37-134B-4953-B0ED-F9FDE2D6F2CFQ44059160-263AF684-9944-4FC4-91AC-2C09171DB210Q46147309-0F4CE22D-C110-495C-85FF-80A9C6C5EE4BQ49573667-86804825-C7A0-4680-9C87-37AB98DECAD1Q51047892-8FD4ADBA-DACF-4C4F-981E-B4915C6A6CB1Q51282603-C24C46E2-016E-4493-A6AF-B8EAFA297C6EQ90102371-1B3F59D3-3A20-405B-B3CE-EE61C7F23FE7
P50
description
investigador
@es
researcher
@en
name
Vera Maria Santoro Belangero
@en
type
label
Vera Maria Santoro Belangero
@en
prefLabel
Vera Maria Santoro Belangero
@en
P31
P496
0000-0002-6828-5431