Aline D. Riquetto-Costa

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 12 publications

Families' perspectives and the development of an educational program for diabetes in schools.

Families' perspectives and the development of an educational program for diabetes in schools.

Journal: Jornal de pediatria

Published: September 09, 2025

Families' perspectives and the development of an educational program for diabetes in schools.

Families' perspectives and the development of an educational program for diabetes in schools.

Journal: Jornal de pediatria

Published: September 09, 2025

Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia.

Enhancing the diagnostic yield of monogenic diabetes in unresolved cases with early-onset hyperglycemia.

Journal: Communications medicine

Published: January 12, 2024

Phenotypic and molecular reanalysis of a cohort of patients with monogenic diabetes reveals a case of partial lipodystrophy due to the A8344G mutation in the mitochondrial DNA.

Phenotypic and molecular reanalysis of a cohort of patients with monogenic diabetes reveals a case of partial lipodystrophy due to the A8344G mutation in the mitochondrial DNA.

Journal: Archives of endocrinology and metabolism

Published: March 10, 2023

The performance of the MODY calculator in a non-Caucasian, mixed-race population diagnosed with diabetes mellitus before 35 years of age.

The performance of the MODY calculator in a non-Caucasian, mixed-race population diagnosed with diabetes mellitus before 35 years of age.

Journal: Diabetology & metabolic syndrome

Published: November 08, 2022

Genetic and clinical features of neonatal and early onset diabetes mellitus in a tertiary center cohort in Brazil.

Genetic and clinical features of neonatal and early onset diabetes mellitus in a tertiary center cohort in Brazil.

Journal: Clinical genetics

Published: October 15, 2022

Targeted massively parallel sequencing for congenital generalized lipodystrophy.

Targeted massively parallel sequencing for congenital generalized lipodystrophy.

Journal: Archives of endocrinology and metabolism

Published: May 25, 2021

Targeted sequencing identifies novel variants in common and rare MODY genes.

Targeted sequencing identifies novel variants in common and rare MODY genes.

Journal: Molecular genetics & genomic medicine

Published: November 15, 2018

Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell Carcinoma.

Acquired Lipodystrophy Associated With Nivolumab in a Patient With Advanced Renal Cell Carcinoma.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 16, 2018

Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred.

Homozygous and Heterozygous Nuclear Lamin A p.R582C Mutation: Different Lipodystrophic Phenotypes in the Same Kindred.

Journal: Frontiers in endocrinology

Published: March 08, 2018

PDX1 -MODY and dorsal pancreatic agenesis: New phenotype of a rare disease.

PDX1 -MODY and dorsal pancreatic agenesis: New phenotype of a rare disease.

Journal: Clinical genetics

Published: January 31, 2017

Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families.

Clinical application of ACMG-AMP guidelines in HNF1A and GCK variants in a cohort of MODY families.

Journal: Clinical genetics

Published: November 18, 2016

Showing 1-12 of 12

Last Updated: 09/26/2026