Osnat Admoni
Afula, Z, Israel
Last Updated: 09/26/2026
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Found 11 publications
The natural course of newborns with transient congenital hypothyroidism.
Journal: Endocrine connections
Published: July 02, 2024
Clinical and Molecular Characteristics and Long-term Follow-up of Children With Pseudohypoparathyroidism Type IA.
Journal: The Journal of clinical endocrinology and metabolism
Published: April 14, 2023
Youth-onset type 2 diabetes in Israel: A national cohort.
Journal: Pediatric diabetes
Published: November 22, 2021
Long-Term Outcome of Patients with TPO Mutations.
Journal: Journal of clinical medicine
Published: July 22, 2021
The evolving role of whole-exome sequencing in the management of disorders of sex development.
Journal: Endocrine connections
Published: May 09, 2021
Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood.
Journal: Frontiers in endocrinology
Published: March 15, 2020
A novel HSD17B3 gene mutation in a 46,XY female-phenotype newborn identified by whole-exome sequencing.
Journal: Clinical endocrinology
Published: June 16, 2017
A Novel Mutation (S54C) of the PAX8 Gene in a Family with Congenital Hypothyroidism and a High Proportion of Affected Individuals.
Journal: Hormone research in paediatrics
Published: December 29, 2015
Novel microdeletions affecting the GNAS locus in pseudohypoparathyroidism: characterization of the underlying mechanisms.
Journal: The Journal of clinical endocrinology and metabolism
Published: January 17, 2015
Long-term outcome of loss-of-function mutations in thyrotropin receptor gene.
Journal: Thyroid : official journal of the American Thyroid Association
Published: January 06, 2015
Ghrelin and growth hormone secretagogue receptor (GHSR) genes are not commonly involved in growth or weight abnormalities in an Israeli pediatric population.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 11, 2012
Showing 1-11 of 11
Last Updated: 09/26/2026