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A novel EXT2 mutation in a consanguineous family with severe developmental delay, microcephaly, seizures, feeding difficulties, and osteopenia extends the phenotypic spectrum of autosomal recessive EXT2-related syndrome (AREXT2).
El-Bazzal L, Atkinson A, Gillart AC, Obeid M, Delague V, Mégarbané A. El-Bazzal L, et al. Among authors: obeid m. Eur J Med Genet. 2019 Apr;62(4):259-264. doi: 10.1016/j.ejmg.2018.07.025. Epub 2018 Jul 31. Eur J Med Genet. 2019. PMID: 30075207
Protein-based nanomaterials: a new tool for targeted drug delivery.
Aljabali AA, Rezigue M, Alsharedeh RH, Obeid MA, Mishra V, Serrano-Aroca Á, El-Tanani M, Tambuwala MM. Aljabali AA, et al. Among authors: obeid ma. Ther Deliv. 2022 Aug 4. doi: 10.4155/tde-2021-0091. Online ahead of print. Ther Deliv. 2022. PMID: 35924586 Free article. Review.
Recent updates in curcumin delivery.
Obeid MA, Alsaadi M, Aljabali AA. Obeid MA, et al. J Liposome Res. 2022 Jun 14:1-12. doi: 10.1080/08982104.2022.2086567. Online ahead of print. J Liposome Res. 2022. PMID: 35699160 Review.
Humoral Responses Against Variants of Concern by COVID-19 mRNA Vaccines in Immunocompromised Patients.
Obeid M, Suffiotti M, Pellaton C, Bouchaab H, Cairoli A, Salvadé V, Stevenel C, Hottinger R, Pythoud C, Coutechier L, Molinari L, Trono D, Ribi C, Gottardo R, Fenwick C, Pascual M, Duchosal MA, Peters S, Pantaleo G. Obeid M, et al. JAMA Oncol. 2022 May 1;8(5):e220446. doi: 10.1001/jamaoncol.2022.0446. Epub 2022 May 19. JAMA Oncol. 2022. PMID: 35271706 Free PMC article.
212 results