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IQSEC2 mutation associated with epilepsy, intellectual disability, and autism results in hyperexcitability of patient-derived neurons and deficient synaptic transmission.
Brant B, Stern T, Shekhidem HA, Mizrahi L, Rosh I, Stern Y, Ofer P, Asleh A, Umanah GKE, Jada R, Levy NS, Levy AP, Stern S. Brant B, et al. Among authors: levy ap, levy ns. Mol Psychiatry. 2021 Dec;26(12):7498-7508. doi: 10.1038/s41380-021-01281-0. Epub 2021 Sep 17. Mol Psychiatry. 2021. PMID: 34535765 Free PMC article.
Restoration of blood flow by using continuous perimuscular infiltration of plasmid DNA encoding subterranean mole rat Spalax ehrenbergi VEGF.
Roguin A, Avivi A, Nitecki S, Rubinstein I, Levy NS, Abassi ZA, Resnick MB, Lache O, Melamed-Frank M, Joel A, Hoffman A, Nevo E, Levy AP. Roguin A, et al. Among authors: levy ap, levy ns. Proc Natl Acad Sci U S A. 2003 Apr 15;100(8):4644-8. doi: 10.1073/pnas.0330833100. Epub 2003 Apr 2. Proc Natl Acad Sci U S A. 2003. PMID: 12672967 Free PMC article.
Role of haptoglobin phenotype in end-stage kidney disease.
Burbea Z, Nakhoul F, Rosenberg S, Zoabi R, Skorecki K, Hochberg I, Miller-Lotan R, Benchetrit S, Weissgarten J, Knecht A, Tovbin D, Levy NS, Levy AP. Burbea Z, et al. Among authors: levy ap, levy ns. Nephron Exp Nephrol. 2004;97(2):e71-6. doi: 10.1159/000078408. Nephron Exp Nephrol. 2004. PMID: 15218325
ELISA for determination of the haptoglobin phenotype.
Levy NS, Levy AP. Levy NS, et al. Among authors: levy ap. Clin Chem. 2004 Nov;50(11):2148-50. doi: 10.1373/clinchem.2004.038547. Clin Chem. 2004. PMID: 15502083 No abstract available.
174 results