Vinicius N. Brito

Sao Paulo, SP, Brazil

Last Updated: 09/26/2026

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Found 58 publications

Phenotypic Variability of Males with Loss-of-Function Mutations of MKRN3: A Case Report and Literature Review.

Phenotypic Variability of Males with Loss-of-Function Mutations of MKRN3: A Case Report and Literature Review.

Journal: Hormone research in paediatrics

Published: July 11, 2025

Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series.

Peripheral precocious puberty in girls with McCune-Albright syndrome: a case series.

Journal: Archives of endocrinology and metabolism

Published: May 14, 2025

Unraveling the Complexity of Primary Ovarian Insufficiency Genetics.

Unraveling the Complexity of Primary Ovarian Insufficiency Genetics.

Journal: The Journal of clinical endocrinology and metabolism

Published: April 08, 2025

Single-session music therapy reduces anxiety and depression among hospitalized adults in an endocrinology ward.

Single-session music therapy reduces anxiety and depression among hospitalized adults in an endocrinology ward.

Journal: Clinics (Sao Paulo, Brazil)

Published: October 23, 2024

Genetic Investigation of Regulatory Regions of MKRN3 and DLK1 Genes in Children with Central Precocious Puberty.

Genetic Investigation of Regulatory Regions of MKRN3 and DLK1 Genes in Children with Central Precocious Puberty.

Journal: Hormone research in paediatrics

Published: September 26, 2024

The genetic etiology is a relevant cause of central precocious puberty.

The genetic etiology is a relevant cause of central precocious puberty.

Journal: European journal of endocrinology

Published: March 02, 2024

Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels.

Familial central precocious puberty due to DLK1 deficiency: novel genetic findings and relevance of serum DLK1 levels.

Journal: European journal of endocrinology

Published: June 05, 2023

Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study.

Rare variants in the MECP2 gene in girls with central precocious puberty: a translational cohort study.

Journal: The lancet. Diabetes & endocrinology

Published: November 19, 2022

Sexuality and fertility desire in a large cohort of individuals with 46, XY differences in sex development.

Sexuality and fertility desire in a large cohort of individuals with 46, XY differences in sex development.

Journal: Clinics (Sao Paulo, Brazil)

Published: November 11, 2022

Arterial Stiffness in Transgender Men Receiving Long-term Testosterone Therapy.

Arterial Stiffness in Transgender Men Receiving Long-term Testosterone Therapy.

Journal: Journal of the Endocrine Society

Published: October 20, 2022

Clinical and Genetic Characterization of Familial Central Precocious Puberty.

Clinical and Genetic Characterization of Familial Central Precocious Puberty.

Journal: The Journal of clinical endocrinology and metabolism

Published: October 13, 2022

The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty.

The Congenital and Acquired Mechanisms Implicated in the Etiology of Central Precocious Puberty.

Journal: Endocrine reviews

Published: February 24, 2022

Showing 1-12 of 58

Last Updated: 09/26/2026