Nathalia M. Andrade
Sao Paulo, SP, Brazil
Last Updated: 09/26/2026
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Found 8 publications
Deleterious variants in intolerant genes reveal new candidates for self-limited delayed puberty.
Journal: European journal of endocrinology
Published: January 19, 2025
Clinical Characteristics of Children with THRA Mutations: Variable Phenotype and Good Response to Recombinant Human Growth Hormone Therapy.
Journal: Hormone research in paediatrics
Published: January 26, 2024
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
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
Delayed Puberty Phenotype Observed in Noonan Syndrome Is More Pronounced in Girls than Boys.
Journal: Hormone research in paediatrics
Published: October 29, 2021
Update on new GH-IGF axis genetic defects.
Journal: Archives of endocrinology and metabolism
Published: September 03, 2019
Genetic causes of isolated short stature.
Journal: Archives of endocrinology and metabolism
Published: November 29, 2018
Does the Intensity of IGG4 Immunostaining Have a Correlation with the Clinical Presentation of Riedel's Thyroiditis?
Journal: Case reports in endocrinology
Published: December 17, 2017
Showing 1-8 of 8
Last Updated: 09/26/2026