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Ophthalmic Genetics|March 30, 2023
Whole-exome screening for primary congenital glaucoma in LebanonNadine J Makhoul, Zahi Wehbi, Dalia El Hadi, et al.
New Microbes and New Infections|September 3, 2020
Are two consecutive negative RT-PCR results enough to rule out COVID-19?R Waked, J Makhoul, G Saliba, et al.
Annals of Human Genetics|January 11, 2005
Genetic heterogeneity of Beta thalassemia in Lebanon reflects historic and recent population migrationN J Makhoul, R S Wells, H Kaspar, et al.
Frontiers in Neurology|March 7, 2019
Developmental Comparison of Ceramide in Wild-Type and Cln3 Δ Mouse Brains and SeraSally El-Sitt, Jihane Soueid, Jamal Al Ali, et al.
Scientific Reports|January 9, 2016
RYR2, PTDSS1 and AREG genes are implicated in a Lebanese population-based study of copy number variation in autismJihane Soueid, Silva Kourtian, Nadine J Makhoul, et al.
Cells|May 13, 2025
Expanded Phenotype of the Cln6 Mouse ModelVictoria Chaoul, Sara Saab, Omar Shmoury, et al.
Prenatal Diagnosis|March 15, 2006
The consanguinity effect on QF-PCR diagnosis of autosomal anomaliesMichel B Choueiri, Nadine J Makhoul, Tony G Zreik, et al.
Nutrition & Metabolism|June 21, 2013
Prediabetic changes in gene expression induced by aspartame and monosodium glutamate in Trans fat-fed C57Bl/6 J miceKate S Collison, Nadine J Makhoul, Marya Z Zaidi, et al.
Cells|August 16, 2020
Exogenous Flupirtine as Potential Treatment for CLN3 DiseaseKatia Maalouf, Joelle Makoukji, Sara Saab, et al.
Genes & Nutrition|December 7, 2011
Nutrigenomics of hepatic steatosis in a feline model: effect of monosodium glutamate, fructose, and Trans-fat feedingKate S Collison, Marya Z Zaidi, Soad M Saleh, et al.
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