Dominique Beckers
Namur, WAL 5000, Belgium
Last Updated: 09/26/2026
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Found 23 publications
Early loss and progressive deterioration of glucagon responses to hypoglycemia in children with type 1 diabetes.
Journal: BMJ open diabetes research & care
Published: March 16, 2026
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
Clinical Characterization of Atypical Diabetes: Insights from the GENEPEDIAB Study into the Spectrum Between Type 1 and Monogenic Diabetes.
Journal: Cells
Published: January 09, 2026
Prevalence and Changes in Genetic and Clinical Characteristics in Growth Hormone-Treated Belgian Girls with Turner Syndrome: A Study from the BELGROW Registry.
Journal: Hormone research in paediatrics
Published: August 19, 2025
Etiology, histology, and long-term outcome of bilateral testicular regression: a large Belgian series.
Journal: Human reproduction open
Published: June 19, 2023
A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms.
A New Tool to Identify Pediatric Patients with Atypical Diabetes Associated with Gene Polymorphisms.
Journal: Diabetes & metabolism journal
Published: May 26, 2023
Growth response of syndromic versus non-syndromic children born small for gestational age (SGA) to growth hormone therapy: a Belgian study.
Journal: Frontiers in endocrinology
Published: November 30, 2022
IGF1 haploinsufficiency in children with short stature: a case series.
Journal: European journal of endocrinology
Published: March 12, 2021
Long-term mortality after childhood growth hormone treatment: the SAGhE cohort study.
Journal: The lancet. Diabetes & endocrinology
Published: February 13, 2020
DNA Methylation Profiling and Genomic Analysis in 20 Children with Short Stature Who Were Born Small for Gestational Age.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 30, 2020
A Novel Phenotype Combining Primary Ovarian Insufficiency Growth Retardation and Pilomatricomas With MCM8 Mutation.
Journal: The Journal of clinical endocrinology and metabolism
Published: October 09, 2019
Last Updated: 09/26/2026