Campos R. Galvao

Barretos, SP, Brazil

Last Updated: 09/26/2026

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Found 12 publications

Living with alveolar capillary dysplasia with misalignment of the pulmonary veins-case report.

Living with alveolar capillary dysplasia with misalignment of the pulmonary veins-case report.

Journal: Pediatric pulmonology
Published: June 18, 2024

The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?

The history of families at-risk for hereditary breast and ovarian cancer: what are the impacts of genetic counseling and testing?

Journal: Frontiers in psychology
Published: October 03, 2023

Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

Functional pri-miR-34b/c rs4938723 and KRAS 3'UTR rs61764370 SNPs: Novel phenotype modifiers in Li-Fraumeni Syndrome?

Journal: Gene
Published: July 25, 2023

Cost-Effectiveness of BRCA 1/2 Genetic Test and Preventive Strategies: Using Real-World Data From an Upper-Middle Income Country.

Cost-Effectiveness of BRCA 1/2 Genetic Test and Preventive Strategies: Using Real-World Data From an Upper-Middle Income Country.

Journal: Frontiers in oncology
Published: May 23, 2022

Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.

Whole-Exome Sequencing Identifies Pathogenic Germline Variants in Patients with Lynch-Like Syndrome.

Journal: Cancers
Published: April 13, 2022

Cancer risk-reducing surgery: Brazilian society of surgical oncology guideline part 1 (gynecology and breast).

Cancer risk-reducing surgery: Brazilian society of surgical oncology guideline part 1 (gynecology and breast).

Journal: Journal of surgical oncology
Published: January 07, 2022

Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome.

Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome.

Journal: Cancer genetics
Published: June 18, 2020

Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients.

Using Co-segregation and Loss of Heterozygosity Analysis to Define the Pathogenicity of Unclassified Variants in Hereditary Breast Cancer Patients.

Journal: Frontiers in oncology
Published: June 10, 2020

MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers.

MIR605 rs2043556 is associated with the occurrence of multiple primary tumors in TP53 p.(Arg337His) mutation carriers.

Journal: Cancer genetics
Published: August 09, 2019

TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling.

TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling.

Journal: Familial cancer
Published: July 20, 2019

The Brazilian TP53 mutation (R337H) and sarcomas.

The Brazilian TP53 mutation (R337H) and sarcomas.

Journal: PloS one
Published: July 17, 2019

Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis.

Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis.

Journal: PloS one
Published: March 08, 2017
Showing 1-12 of 12

Last Updated: 09/26/2026