Emese Boros
Brussels, BRU, Belgium
Last Updated: 09/26/2026
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Found 22 publications
Phenotypic and genotypic analysis of pediatric patients with congenital isolated growth hormone deficiency resulting from biallelic variants in the GHRHR gene: a Belgian registry study.
Journal: European journal of pediatrics
Published: March 01, 2026
Could increased thiamazole sales among children in Belgium during the pandemic indicate a surge in Graves' disease cases?
Journal: Journal of endocrinological investigation
Published: June 23, 2025
Delayed Thyrotropin Rise in Preterm Newborns: Value of Multiple Screening Samples and of a Detailed Clinical Characterization.
Journal: Thyroid : official journal of the American Thyroid Association
Published: June 11, 2025
Trend in body mass index during childhood in 460 girls with idiopathic central precocious puberty.
Journal: Endocrine connections
Published: May 06, 2025
Hypothyroidism due to biallelic variants in IYD: description of 4 families and a novel variant.
Journal: European journal of endocrinology
Published: May 03, 2024
Near Adult Height and Body Mass Index Changes in Growth Hormone Treated Short Children with Noonan Syndrome: The Belgian Experience.
Journal: Hormone research in paediatrics
Published: December 18, 2023
Childhood craniopharyngioma: a retrospective study of children followed in Hôpital Universitaire de Bruxelles.
Journal: Frontiers in endocrinology
Published: September 19, 2023
Thyrotropin Screening of Newborns: Before or After 72 Hours of Life? Before Discharge or at Home?
Journal: Thyroid : official journal of the American Thyroid Association
Published: August 08, 2023
Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.
Journal: Human reproduction open
Published: June 19, 2023
Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study.
Journal: European journal of endocrinology
Published: April 21, 2023
Genotype-phenotype Description of Vitamin D-dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder Disease.
Journal: The Journal of clinical endocrinology and metabolism
Published: July 22, 2022
Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty.
Journal: Journal of the Endocrine Society
Published: April 14, 2022
Last Updated: 09/26/2026