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NPHS2 mutations account for only 15 % of nephrotic syndrome..:

Guaragna, Mara Sanches ; Lutaif, Anna Cristina GB ; Piveta, Cristiane SC...
BMC Medical Genetics. 16 (2015) 1 - p. , 2015

Link: https://doi.org/10.1186/..

2

Characterization of Herpesviridae Family Members, BK Virus,..:

Ferreira Menoni, Silvia Mendonça ; Leon, Lucas Lopes ; de Lima, Rodrigo Gonçalves...
Viruses. 16 (2024) 7 - p. 1017 , 2024

Link: https://doi.org/10.3390/..

3

Funcional analysis of variants in NPHS2 promoter identified..:

Mello, Maricilda Palandi de ; Guerra Júnior, Gil ; Belangero, Vera Maria Santoro...
Revista dos Trabalhos de Iniciação Científica da UNICAMP. , 2019

Link: https://doi.org/10.20396..

4

NPHS2Mutations: A Closer Look to Latin American Countries:

Guaragna, Mara Sanches ; Lutaif, Anna Cristina G. B. ; Maciel-Guerra, Andréa T....
BioMed Research International. 2017 (2017) - p. 1-6 , 2017

Link: https://doi.org/10.1155/..

5

NPHS1 gene mutations confirm congenital nephrotic syndrome ..:

Guaragna, Mara S. ; Cleto, Thaís Lira ; Souza, Marcela Lopes...
Nephrology. 21 (2016) 9 - p. 753-757 , 2016

Link: https://doi.org/10.1111/..

6

Two distinct WT1 mutations identified in patients and relat..:

Guaragna, Mara S. ; Lutaif, Anna Cristina G.B. ; Piveta, Cristiane S.C....
Biochemical and Biophysical Research Communications. 441 (2013) 2 - p. 371-376 , 2013

Link: https://doi.org/10.1016/..

7

APOL1 in an ethnically diverse pediatric population with ne..:

Watanabe, Andreia ; Guaragna, Mara Sanches ; Belangero, Vera Maria Santoro...
Pediatric Nephrology. , 2021

Link: https://doi.org/10.1007/..

8

Promises and pitfalls of whole-exome sequencing exemplified..:

Guaragna, Mara Sanches ; de Brito Lutaif, Anna Cristina Gervásio ; de Souza, Marcela Lopes...
Molecular Genetics and Genomics. 295 (2019) 1 - p. 135-142 , 2019

Link: https://doi.org/10.1007/..

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