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Page 1
Amino acid sequence homology of monoclonal serum free light chain dimers and tissue deposited light chains in AL amyloidosis: a pilot study.
Goldis R, Kaplan B, Arad M, Dispenzieri A, Dasari S, Kukuy OL, Simon AJ, Dori A, Shavit-Stein E, Ziv T, Murray D, Kourelis T, Gertz MA, Dominissini D, Magen H, Muchtar E. Goldis R, et al. Among authors: simon aj. Clin Chem Lab Med. 2023 Sep 26;62(3):464-471. doi: 10.1515/cclm-2023-0591. Print 2024 Feb 26. Clin Chem Lab Med. 2023. PMID: 37747270
Amyloid Typing in Cardiac Amyloidosis Using Western Blotting.
Kaplan B, Goldis R, Ziv T, Dori A, Magen H, Simon AJ, Volkov A, Maor E, Arad M. Kaplan B, et al. Among authors: simon aj. Isr Med Assoc J. 2024 Mar;26(3):149-156. Isr Med Assoc J. 2024. PMID: 38493325 Free article.
Inherited SLP76 deficiency in humans causes severe combined immunodeficiency, neutrophil and platelet defects.
Lev A, Lee YN, Sun G, Hallumi E, Simon AJ, Zrihen KS, Levy S, Beit Halevi T, Papazian M, Shwartz N, Somekh I, Levy-Mendelovich S, Wolach B, Gavrieli R, Vernitsky H, Barel O, Javasky E, Stauber T, Ma CA, Zhang Y, Amariglio N, Rechavi G, Hendel A, Yablonski D, Milner JD, Somech R. Lev A, et al. Among authors: simon aj. J Exp Med. 2021 Mar 1;218(3):e20201062. doi: 10.1084/jem.20201062. J Exp Med. 2021. PMID: 33231617 Free PMC article.
Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.
Simon AJ, Lev A, Zhang Y, Weiss B, Rylova A, Eyal E, Kol N, Barel O, Cesarkas K, Soudack M, Greenberg-Kushnir N, Rhodes M, Wiest DL, Schiby G, Barshack I, Katz S, Pras E, Poran H, Reznik-Wolf H, Ribakovsky E, Simon C, Hazou W, Sidi Y, Lahad A, Katzir H, Sagie S, Aqeilan HA, Glousker G, Amariglio N, Tzfati Y, Selig S, Rechavi G, Somech R. Simon AJ, et al. Among authors: simon c. J Exp Med. 2016 Jul 25;213(8):1429-40. doi: 10.1084/jem.20151618. Epub 2016 Jul 18. J Exp Med. 2016. PMID: 27432940 Free PMC article.
Exogenous interleukin-2 can rescue in-vitro T cell activation and proliferation in patients with a novel capping protein regulator and myosin 1 linker 2 mutation.
Shamriz O, Simon AJ, Lev A, Megged O, Ledder O, Picard E, Joseph L, Molho-Pessach V, Tal Y, Millman P, Slae M, Somech R, Toker O, Berger M. Shamriz O, et al. Among authors: simon aj. Clin Exp Immunol. 2020 Jun;200(3):215-227. doi: 10.1111/cei.13432. Epub 2020 Apr 18. Clin Exp Immunol. 2020. PMID: 32201938 Free PMC article.
Chronic demodicosis in patients with immune dysregulation: An unexpected infectious manifestation of Signal transducer and activator of transcription (STAT)1 gain-of-function.
Shamriz O, Lev A, Simon AJ, Barel O, Javasky E, Matza-Porges S, Shaulov A, Davidovics Z, Toker O, Somech R, Zlotogorski A, Molho-Pessach V, Tal Y. Shamriz O, et al. Among authors: simon aj. Clin Exp Immunol. 2021 Oct;206(1):56-67. doi: 10.1111/cei.13636. Epub 2021 Jul 12. Clin Exp Immunol. 2021. PMID: 34114647 Free PMC article.
236 results