Lior Carmon
Weizmann Science Park
Ness Ziona, M, Israel
Ness Ziona, M, Israel
Last Updated: 09/26/2026
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Found 21 publications
Xq26.2 Contiguous Gene Deletion Involving FRMD7 and IGSF1: Highly Penetrant Infantile Nystagmus with Variable Endocrine Involvement.
Journal: Genes
Published: July 15, 2026
Growth Patterns in MPS IVA and MPS IIIA: A Longitudinal Single-Center Study.
Journal: Journal of clinical medicine
Published: April 19, 2026
A lethal form of ASCC3 disease: Severe global developmental delay, axial hypotonia, hypoplasia of corpus callosum, hypothyroidism, and micropenis.
Journal: HGG advances
Published: January 23, 2026
Diagnosis of Growth Hormone Deficiency in Children: Comparative Performance of Arginine Versus Glucagon as the First Stimulation Test.
Journal: Clinical endocrinology
Published: January 16, 2026
Successful Salvage of Ventriculoperitoneal Shunt Using Rifampicin in Staphylococcus epidermidis Infection.
Journal: The Israel Medical Association journal : IMAJ
Published: October 28, 2025
Assessment of Long-Term Knowledge Retention in Children with Type 1 Diabetes and Their Families: A Pilot Study.
Journal: Children (Basel, Switzerland)
Published: June 04, 2025
Impact of COVID-19 outbreak on the seasonality and incidence of type 1 diabetes mellitus: A nationwide cohort study.
Journal: World journal of diabetes
Published: April 24, 2025
Diagnostic Yield of Critical Sample and Elective Fast-Test in Children After a Hypoglycemic Event: Experience From a Single Center in Israel.
Journal: Indian pediatrics
Published: March 07, 2024
GH treatment in pediatric Down syndrome: a systematic review and mini meta-analysis.
Journal: Frontiers in endocrinology
Published: January 01, 2023
GHRH-GH-IGF1 axis in pediatric Down syndrome: A systematic review and mini meta-analysis.
Journal: Frontiers in pediatrics
Published: December 27, 2022
Hypoparathyroidism-retardation-dysmorphism syndrome-Clinical insights from a large longitudinal cohort in a single medical center.
Journal: Frontiers in pediatrics
Published: April 09, 2022
TSHB R75G is a founder variant and prevalent cause of low or undetectable TSH in Indian Jews.
Journal: European thyroid journal
Published: November 08, 2021
Last Updated: 09/26/2026