Pedro H. Cabello
Rio De Janeiro, RJ, Brazil
Last Updated: 09/26/2026
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Found 39 publications
Case Report: New insights about clinical manifestations of patients with GCK genetic variants.
Journal: Frontiers in endocrinology
Published: December 20, 2024
Genomic deletions on 16p11.2 associated with severe obesity in Brazil.
Journal: Frontiers in endocrinology
Published: September 12, 2024
FTO rs17817449 Variant Increases the Risk of Severe Obesity in a Brazilian Cohort: A Case-Control Study.
Journal: Diabetes, metabolic syndrome and obesity : targets and therapy
Published: December 09, 2023
Human N-acetyltransferase 2 (NAT2) gene variability in Brazilian populations from different geographical areas.
Journal: Frontiers in pharmacology
Published: August 16, 2023
What Do We Know about Neonatal Diabetes caused by PDX1 Mutations?
Journal: Current diabetes reviews
Published: July 04, 2023
Outcome of Direct Pulp Capping Using Calcium Hydroxide: A Long-term Retrospective Study.
Journal: Journal of endodontics
Published: July 13, 2022
SH2B1 variants as potential causes of non-syndromic monogenic obesity in a Brazilian cohort.
Journal: Eating and weight disorders : EWD
Published: June 02, 2022
Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil.
Journal: Frontiers in endocrinology
Published: December 01, 2021
Identification of a Rare and Potential Pathogenic MC4R Variant in a Brazilian Patient With Adulthood-Onset Severe Obesity.
Journal: Frontiers in genetics
Published: September 21, 2020
PDX1-MODY: A rare missense mutation as a cause of monogenic diabetes.
Journal: European journal of medical genetics
Published: August 26, 2020
A Rare Potential Pathogenic Variant in the BDNF Gene is Found in a Brazilian Patient with Severe Childhood-Onset Obesity.
Journal: Diabetes, metabolic syndrome and obesity : targets and therapy
Published: June 20, 2020
Last Updated: 09/26/2026