Nadine J. Makhoul
Beirut, BA 11072020, Lebanon
Last Updated: 09/26/2026
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Found 13 publications
Novel TRIP12 variants in two Lebanese patients with neurodevelopmental delay.
Journal: BMC medical genomics
Published: October 27, 2025
Downregulation of AKT-mediated p27Kip1 phosphorylation with shift to sphingomyelin synthesis in CLN3 disease.
Journal: IBRO neuroscience reports
Published: March 18, 2025
Whole-exome screening for primary congenital glaucoma in Lebanon.
Journal: Ophthalmic genetics
Published: March 30, 2023
Sex differences in gene expression with galactosylceramide treatment in Cln3Δex7/8 mice.
Journal: PloS one
Published: January 10, 2020
Exogenous Galactosylceramide as Potential Treatment for CLN3 Disease.
Journal: Annals of neurology
Published: March 29, 2019
Developmental Comparison of Ceramide in Wild-Type and Cln3 Δex7/8 Mouse Brains and Sera.
Journal: Frontiers in neurology
Published: November 01, 2018
Candidate Genes for Inherited Autism Susceptibility in the Lebanese Population.
Journal: Scientific reports
Published: November 11, 2016
Gene expression profiling of breast cancer in Lebanese women.
Journal: Scientific reports
Published: August 22, 2016
Association between CLN3 (Neuronal Ceroid Lipofuscinosis, CLN3 Type) Gene Expression and Clinical Characteristics of Breast Cancer Patients.
Journal: Frontiers in oncology
Published: August 20, 2015
Last Updated: 09/26/2026