Ghadir Assad-Elias
Haifa, HA 32000, Israel
Last Updated: 09/26/2026
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Found 11 publications
CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.
Journal: European journal of endocrinology
Published: March 23, 2026
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
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
Case Report: Neonatal Diabetes Mellitus Caused by a Novel GLIS3 Mutation in Twins.
Journal: Frontiers in endocrinology
Published: February 28, 2021
Maturity onset diabetes of the young type 2 (MODY2): Insight from an extended family.
Journal: Diabetes research and clinical practice
Published: January 18, 2021
Case Report: Severe Hypocalcemic Episodes Due to Autoimmune Enteropathy.
Journal: Frontiers in endocrinology
Published: December 22, 2020
High Prevalence of Hearing Impairment in Primary Congenital Hypothyroidism.
Journal: European thyroid journal
Published: April 23, 2020
Long-Term Follow-Up and Outcomes of Autoimmune Thyroiditis in Childhood.
Journal: Frontiers in endocrinology
Published: March 15, 2020
Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review.
Journal: Pediatric endocrinology reviews : PER
Published: July 29, 2016
Showing 1-11 of 11
Last Updated: 09/26/2026