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Said El Shamieh

Showing results (31-40 of 77) with videos related to

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Data in Brief|December 15, 2018
Dataset on significant role of Candesartan on cognitive functions in rats having memory impairment induced by electromagnetic wavesMohamad Nasser, Pia Chedid, Ali Salami, et al.
Drug Metabolism and Personalized Therapy|February 9, 2018
Effect of SLCO1B1 gene polymorphisms and vitamin D on statin-induced myopathyBaraa Alghalyini, Said El Shamieh, Ali Salami, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 16, 2011
Cardiovascular diseases and genome-wide association studiesNdeye Coumba Ndiaye, Mohsen Azimi Nehzad, Said El Shamieh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 2010
Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levelsSaid El Shamieh, Bernard Herbeth, Mohsen Azimi-Nezhad, et al.
Molecular Biology Reports|November 6, 2025
A novel HPS3 pathogenic nonsense variant associated with Hermansky-Pudlak syndrome type 3 and a platelet dysfunctionChahnaz Chouman, Suzana Salhab, Salvatore Martella, et al.
Orphanet Journal of Rare Diseases|April 24, 2022
The research output of rod-cone dystrophy geneticsLama Jaffal, Zamzam Mrad, Mariam Ibrahim, et al.
Ophthalmic Genetics|October 23, 2025
Identification of a novel <i>CABP4</i> frameshift variant and a secondary <i>USH2A</i> missense variant in congenital cone-rod synaptic disorderZahraa Mousawi, Alain Chebly, Joseph Nehme, et al.
Frontiers in Endocrinology|September 4, 2025
Evaluation of vitamin D status, vitamin D receptor expression, and innate immune mediators in COVID-19Ferdos Missilmani, Dima Maarabouni, Elie Salem-Sokhn, et al.
BMC Medical Genomics|May 1, 2023
The genetic landscape of inherited retinal dystrophies in ArabsLama Jaffal, Hawraa Joumaa, Jinane Noureldine, et al.
Ophthalmic Genetics|April 28, 2025
Exploring copy number variations in Lebanese families with rod-cone dystrophy reveals a novel deletion in <i>PRPF31</i> with haploinsufficiencyZahraa Mousawi, Maysa Choukeir, Lama Jaffal, et al.
Pageof 8

Showing results (31-40 of 77) with videos related to

Sort By:
Pageof 8
Data in Brief|December 15, 2018
Dataset on significant role of Candesartan on cognitive functions in rats having memory impairment induced by electromagnetic wavesMohamad Nasser, Pia Chedid, Ali Salami, et al.
Drug Metabolism and Personalized Therapy|February 9, 2018
Effect of SLCO1B1 gene polymorphisms and vitamin D on statin-induced myopathyBaraa Alghalyini, Said El Shamieh, Ali Salami, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 16, 2011
Cardiovascular diseases and genome-wide association studiesNdeye Coumba Ndiaye, Mohsen Azimi Nehzad, Said El Shamieh, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 2010
Human formyl peptide receptor 1 C32T SNP interacts with age and is associated with blood pressure levelsSaid El Shamieh, Bernard Herbeth, Mohsen Azimi-Nezhad, et al.
Molecular Biology Reports|November 6, 2025
A novel HPS3 pathogenic nonsense variant associated with Hermansky-Pudlak syndrome type 3 and a platelet dysfunctionChahnaz Chouman, Suzana Salhab, Salvatore Martella, et al.
Orphanet Journal of Rare Diseases|April 24, 2022
The research output of rod-cone dystrophy geneticsLama Jaffal, Zamzam Mrad, Mariam Ibrahim, et al.
Ophthalmic Genetics|October 23, 2025
Identification of a novel <i>CABP4</i> frameshift variant and a secondary <i>USH2A</i> missense variant in congenital cone-rod synaptic disorderZahraa Mousawi, Alain Chebly, Joseph Nehme, et al.
Frontiers in Endocrinology|September 4, 2025
Evaluation of vitamin D status, vitamin D receptor expression, and innate immune mediators in COVID-19Ferdos Missilmani, Dima Maarabouni, Elie Salem-Sokhn, et al.
BMC Medical Genomics|May 1, 2023
The genetic landscape of inherited retinal dystrophies in ArabsLama Jaffal, Hawraa Joumaa, Jinane Noureldine, et al.
Ophthalmic Genetics|April 28, 2025
Exploring copy number variations in Lebanese families with rod-cone dystrophy reveals a novel deletion in <i>PRPF31</i> with haploinsufficiencyZahraa Mousawi, Maysa Choukeir, Lama Jaffal, et al.
Pageof 8