Nahum A - Search Results

1

Incidence of typically Severe Primary Immunodeficiency Diseases in Consanguineous and Non-consanguineous Populations.

Broides A, Nahum A, Mandola AB, Rozner L, Pinsk V, Ling G, Yerushalmi B, Levy J, Givon-Lavi N. Broides A, et al. Among authors: nahum a. J Clin Immunol. 2017 Apr;37(3):295-300. doi: 10.1007/s10875-017-0378-6. Epub 2017 Mar 16. J Clin Immunol. 2017. PMID: 28299599

2

Lycopene inhibition of cell cycle progression in breast and endometrial cancer cells is associated with reduction in cyclin D levels and retention of p27(Kip1) in the cyclin E-cdk2 complexes.

Nahum A, Hirsch K, Danilenko M, Watts CK, Prall OW, Levy J, Sharoni Y. Nahum A, et al. Oncogene. 2001 Jun 7;20(26):3428-36. doi: 10.1038/sj.onc.1204452. Oncogene. 2001. PMID: 11423993

3

Fatal combined immunodeficiency associated with heterozygous mutation in STAT1.

Sharfe N, Nahum A, Newell A, Dadi H, Ngan B, Pereira SL, Herbrick JA, Roifman CM. Sharfe N, et al. Among authors: nahum a. J Allergy Clin Immunol. 2014 Mar;133(3):807-17. doi: 10.1016/j.jaci.2013.09.032. Epub 2013 Nov 13. J Allergy Clin Immunol. 2014. PMID: 24239102

4

IL-12 receptor 1β deficiency with features of autoimmunity and photosensitivity.

Ling G, Ling E, Broides A, Poran Feldman H, Levy J, Garty BZ, Nahum A. Ling G, et al. Among authors: nahum a. Autoimmunity. 2016;49(3):143-6. doi: 10.3109/08916934.2015.1134513. Epub 2016 Jan 13. Autoimmunity. 2016. PMID: 26761636 Free article.

5

The clinical and laboratory spectrum of dedicator of cytokinesis 8 immunodeficiency syndrome in patients with a unique mutation.

Broides A, Mandola AB, Levy J, Yerushalmi B, Pinsk V, Eldan M, Shubinsky G, Hadad N, Levy R, Nahum A, Ben-Harosh M, Lev A, Simon A, Somech R. Broides A, et al. Among authors: nahum a. Immunol Res. 2017 Jun;65(3):651-657. doi: 10.1007/s12026-016-8883-x. Immunol Res. 2017. PMID: 28070732

6

First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights.

Rechavi E, Lev A, Simon AJ, Stauber T, Daas S, Saraf-Levy T, Broides A, Nahum A, Marcus N, Hanna S, Stepensky P, Toker O, Dalal I, Etzioni A, Almashanu S, Somech R. Rechavi E, et al. Among authors: nahum a. Front Immunol. 2017 Nov 6;8:1448. doi: 10.3389/fimmu.2017.01448. eCollection 2017. Front Immunol. 2017. PMID: 29167666 Free PMC article.

7

Neutrophil Functions in Immunodeficiency Due to DOCK8 Deficiency.

Mandola AB, Levy J, Nahum A, Hadad N, Levy R, Rylova A, Simon AJ, Lev A, Somech R, Broides A. Mandola AB, et al. Among authors: nahum a. Immunol Invest. 2019 May;48(4):431-439. doi: 10.1080/08820139.2019.1567533. Epub 2019 Jan 28. Immunol Invest. 2019. PMID: 30689480

8

Defining the biological responses of IL-6 by the study of a novel IL-6 receptor chain immunodeficiency.

Nahum A, Sharfe N, Broides A, Dadi H, Naghdi Z, Mandola AB, Vong L, Arbiv A, Dalal I, Brami I, Wormser O, Levy J, Roifman CM. Nahum A, et al. J Allergy Clin Immunol. 2020 Mar;145(3):1011-1015.e6. doi: 10.1016/j.jaci.2019.11.015. Epub 2019 Nov 26. J Allergy Clin Immunol. 2020. PMID: 31778705 No abstract available.

9

Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene: IgG hypergammaglobulinemia with IgA and IgE deficiency.

Nahum A, Somech R, Shubinsky G, Levy J, Broides A. Nahum A, et al. Clin Immunol. 2020 Apr;213:108366. doi: 10.1016/j.clim.2020.108366. Epub 2020 Feb 21. Clin Immunol. 2020. PMID: 32092471

10

A novel zeta-associated protein 70 homozygous mutation causing combined immunodeficiency presenting as neonatal autoimmune hemolytic anemia.

Ling E, Broides A, Ling G, Shubinsky G, Hadad N, Nahum A, Simon AJ, Lev A, Somech R. Ling E, et al. Among authors: nahum a. Immunol Res. 2021 Feb;69(1):100-106. doi: 10.1007/s12026-021-09172-w. Epub 2021 Jan 23. Immunol Res. 2021. PMID: 33484432

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