Everlayny F. Costalonga

Vitoria, ES, Brazil

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 15 publications

Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.

Screening of targeted panel genes in Brazilian patients with primary ovarian insufficiency.

Journal: PloS one

Published: March 03, 2020

Uremic leontiasis ossea.

Uremic leontiasis ossea.

Journal: Endocrine

Published: February 26, 2019

Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation.

Atypical presentation of familial hypomagnesemia with hypercalciuria and nephrocalcinosis in a patient with a new claudin-16 gene mutation.

Journal: Clinical nephrology. Case studies

Published: July 16, 2018

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.

Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.

Journal: Clinical endocrinology

Published: March 05, 2017

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.

FGFR1 and PROKR2 rare variants found in patients with combined pituitary hormone deficiencies.

Journal: Endocrine connections

Published: March 05, 2015

A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).

A homozygous point mutation in the GH1 promoter (c.-223C>T) leads to reduced GH1 expression in siblings with isolated GH deficiency (IGHD).

Journal: European journal of endocrinology

Published: February 09, 2015

Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center.

Frequent development of combined pituitary hormone deficiency in patients initially diagnosed as isolated growth hormone deficiency: a long term follow-up of patients from a single center.

Journal: Pituitary

Published: October 16, 2014

Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism.

Genetic predictors of long-term response to growth hormone (GH) therapy in children with GH deficiency and Turner syndrome: the influence of a SOCS2 polymorphism.

Journal: The Journal of clinical endocrinology and metabolism

Published: June 07, 2014

Sitting-height measures are related to body mass index and blood pressure levels in children.

Sitting-height measures are related to body mass index and blood pressure levels in children.

Journal: Arquivos brasileiros de endocrinologia e metabologia

Published: February 28, 2014

Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren.

Study of the association between 3111T/C polymorphism of the CLOCK gene and the presence of overweight in schoolchildren.

Journal: Jornal de pediatria

Published: August 16, 2013

High blood pressure in children and its correlation with three definitions of obesity in childhood.

High blood pressure in children and its correlation with three definitions of obesity in childhood.

Journal: Arquivos brasileiros de cardiologia

Published: April 13, 2013

The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.

The sitting height/height ratio for age in healthy and short individuals and its potential role in selecting short children for SHOX analysis.

Journal: Hormone research in paediatrics

Published: March 18, 2013

Showing 1-12 of 15

Last Updated: 09/26/2026