Daniela P. Cunha

Fiocruz, RJ, Brazil

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

Inherited IFNAR1 structural deficiency in severe adverse events following yellow fever vaccination.

Inherited IFNAR1 structural deficiency in severe adverse events following yellow fever vaccination.

Journal: Clinical immunology (Orlando, Fla.)

Published: March 19, 2026

Genetic Variants Affect Distinct Metabolic Pathways in Pediatric Multisystem Inflammatory Syndrome and Severe COVID-19.

Genetic Variants Affect Distinct Metabolic Pathways in Pediatric Multisystem Inflammatory Syndrome and Severe COVID-19.

Journal: Journal of medical virology

Published: February 28, 2025

Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel Variant.

Genotype-Phenotype Correlations of Nance-Horan Syndrome in Male and Female Carriers of a Novel Variant.

Journal: Genes

Published: December 05, 2024

FOXP2 Expression and Oral Feeding Success in Preterm Infants: Sex 2 Differences.

FOXP2 Expression and Oral Feeding Success in Preterm Infants: Sex 2 Differences.

Journal: Genes

Published: August 30, 2024

Decidual production of interferon lambda in response to ZIKV persistence: Clinical evidence and in vitro modelling.

Decidual production of interferon lambda in response to ZIKV persistence: Clinical evidence and in vitro modelling.

Journal: Heliyon

Published: December 20, 2023

The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis.

The cost of genetic diagnosis of suspected hereditary pediatric cataracts with whole-exome sequencing from a middle-income country perspective: a mixed costing analysis.

Journal: Journal of community genetics

Published: September 25, 2023

Biotechnological Advances in Gene Therapy of Hematopoietic Stem Cells: Systematic Review and Meta-Analysis.

Biotechnological Advances in Gene Therapy of Hematopoietic Stem Cells: Systematic Review and Meta-Analysis.

Journal: Human gene therapy

Published: August 25, 2023

Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.

Genotypic-Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.

Journal: International journal of molecular sciences

Published: June 27, 2023

Congenital Zika Syndrome Is Associated With Interferon Alfa Receptor 1.

Congenital Zika Syndrome Is Associated With Interferon Alfa Receptor 1.

Journal: Frontiers in immunology

Published: August 25, 2021

The clinical spectrum and immunopathological mechanisms underlying ZIKV-induced neurological manifestations.

The clinical spectrum and immunopathological mechanisms underlying ZIKV-induced neurological manifestations.

Journal: PLoS neglected tropical diseases

Published: August 05, 2021

Chronic Granulomatous Disease and Myelodysplastic Syndrome in a Patient with a Novel Mutation in CYBB.

Chronic Granulomatous Disease and Myelodysplastic Syndrome in a Patient with a Novel Mutation in CYBB.

Journal: Genes

Published: May 25, 2021

Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.

Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.

Journal: Genes

Published: May 25, 2021

Showing 1-12 of 17

Last Updated: 09/26/2026