Renata C. Scalco

Sao Paulo, SP 05403000, Brazil

Last Updated: 09/26/2026

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Found 20 publications

Two adult 46,XY sisters with female-like phenotype due to a novel homozygous LHCGR splice-site variant.

Two adult 46,XY sisters with female-like phenotype due to a novel homozygous LHCGR splice-site variant.

Journal: JCEM case reports

Published: February 27, 2026

Long-term growth hormone therapy improves adult height in children with Indian hedgehog (IHH)-related short stature.

Long-term growth hormone therapy improves adult height in children with Indian hedgehog (IHH)-related short stature.

Journal: Hormone research in paediatrics

Published: January 26, 2026

Diagnostic yield of genetic testing in children with short stature: a systematic review.

Diagnostic yield of genetic testing in children with short stature: a systematic review.

Journal: European journal of endocrinology

Published: October 16, 2025

Non-RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome.

Non-RASopathy Genetic Syndromes Identified as the Molecular Cause of Disease in Patients Previously Diagnosed With Noonan Syndrome.

Journal: American journal of medical genetics. Part A

Published: May 08, 2025

Exome sequencing of patients with syndromic tall stature reveals four novel candidate genes.

Exome sequencing of patients with syndromic tall stature reveals four novel candidate genes.

Journal: Endocrine connections

Published: March 10, 2025

Response to Recombinant Human Growth Hormone Therapy in Short Children Born at Very Low Birth Weight.

Response to Recombinant Human Growth Hormone Therapy in Short Children Born at Very Low Birth Weight.

Journal: Hormone research in paediatrics

Published: July 22, 2024

Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability.

Identification of a second genetic alteration in patients with SHOX deficiency individuals: a potential explanation for phenotype variability.

Journal: European journal of endocrinology

Published: May 10, 2023

Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature.

Diagnostic yield of a multigene sequencing approach in children classified as idiopathic short stature.

Journal: Endocrine connections

Published: October 04, 2022

Adult Height of Patients with SHOX Haploinsufficiency with or without GH Therapy: A Real-World Single-Center Study.

Adult Height of Patients with SHOX Haploinsufficiency with or without GH Therapy: A Real-World Single-Center Study.

Journal: Hormone research in paediatrics

Published: February 03, 2022

Hormone resistance and short stature: A journey through the pathways of hormone signaling.

Hormone resistance and short stature: A journey through the pathways of hormone signaling.

Journal: Molecular and cellular endocrinology

Published: January 15, 2021

Adult Height in 299 Patients with Turner Syndrome with or without Growth Hormone Therapy: Results and Literature Review.

Adult Height in 299 Patients with Turner Syndrome with or without Growth Hormone Therapy: Results and Literature Review.

Journal: Hormone research in paediatrics

Published: December 30, 2020

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome.

ESR1 polymorphism (rs2234693) influences femoral bone mass in patients with Turner syndrome.

Journal: Endocrine connections

Published: October 28, 2019

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Last Updated: 09/26/2026