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European Thyroid Journal|January 4, 2022
TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian JewsDavid Shaki, Marina Eskin-Schwartz, Noam Hadar, et al.
Indian Pediatrics|March 7, 2024
Diagnostic Yield of Critical Sample and Elective Fast-Test in Children After a Hypoglycemic Event: Experience From a Single Center in IsraelLior Carmon, Ran Hazan, Eli Hershkovitz, et al.
The Journal of Clinical Endocrinology and Metabolism|November 5, 2020
Multiple Endocrine Deficiencies are Common in Hypoparathyroidism-Retardation-Dysmorphism SyndromeOdeya David, Galia Barash, Rotem Agur, et al.
Frontiers in Pediatrics|March 13, 2023
GHRH-GH-IGF1 axis in pediatric Down syndrome: A systematic review and mini meta-analysisDavid Shaki, Eli Hershkovitz, Shai Tamam, et al.
Children (Basel, Switzerland)|August 28, 2025
Assessment of Long-Term Knowledge Retention in Children with Type 1 Diabetes and Their Families: A Pilot StudyLior Carmon, Eli Hershkovitz, David Shaki, et al.
Journal of Clinical Medicine|June 12, 2026
Growth Patterns in MPS IVA and MPS IIIA: A Longitudinal Single-Center StudyLior Carmon, Majd Nassar, Daphna Idan, et al.
Frontiers in Endocrinology|May 8, 2023
GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysisDavid Shaki, Eli Hershkovitz, Shai Tamam, et al.
Frontiers in Pediatrics|August 8, 2022
Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical centerOdeya David, Rotem Agur, Rosa Novoa, et al.
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