Meshaal SS - Search Results

1

Clinical and immunological features of four patients with activation-induced cytidine deaminase deficiency: Renal amyloidosis and other presentations.

Meshaal SS, El Hawary RE, Abd Elaziz DS, Eldash A, Darwish R, Erfan A, Lotfy S, Saad MM, Chohayeb EA, Nagy MS, Alkady R, Boutros JA, Galal NM, Elmarsafy AM. Meshaal SS, et al. Ann Hum Genet. 2025 Jan;89(1):47-53. doi: 10.1111/ahg.12583. Epub 2024 Nov 8. Ann Hum Genet. 2025. PMID: 39513285

2

Cernunnos deficiency: Further delineation in 5 Egyptian patients.

El Hawary R, Meshaal S, Lotfy S, Abd Elaziz D, Alkady R, Eldash A, Erfan A, Chohayeb E, Saad M, Darwish R, Boutros J, Galal N, Elmarsafy A. El Hawary R, et al. Eur J Med Genet. 2023 Oct;66(10):104840. doi: 10.1016/j.ejmg.2023.104840. Epub 2023 Sep 11. Eur J Med Genet. 2023. PMID: 37703920

3

Analysis of Clinical, Immunological and Molecular Features of Leukocyte Adhesion Deficiency Type I in Egyptian Children.

Saad MM, Alkady R, Eldash A, El Hawary RE, Meshaal SS, Galal NM, Elmarsafy AM. Saad MM, et al. Among authors: meshaal ss. J Clin Immunol. 2024 Apr 5;44(4):92. doi: 10.1007/s10875-024-01693-x. J Clin Immunol. 2024. PMID: 38578558 Free PMC article.

4

Study of naïve and memory cells in a cohort of Egyptian chronic granulomatous disease patients.

El Hawary R, Meshaal S, Nagy D, Fikry I, Alkady R, Abd Elaziz D, Galal N, Boutros J, Elmarsafy A, Jan Farid R. El Hawary R, et al. J Recept Signal Transduct Res. 2015;35(5):423-8. doi: 10.3109/10799893.2014.996818. Epub 2015 Mar 23. J Recept Signal Transduct Res. 2015. PMID: 25798665

5

Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt.

Meshaal S, El Hawary R, Elsharkawy M, Mousa RK, Farid RJ, Abd Elaziz D, Alkady R, Galal N, Massaad MJ, Boutros J, Elmarsafy A. Meshaal S, et al. Clin Immunol. 2015 Jun;158(2):167-73. doi: 10.1016/j.clim.2015.04.003. Epub 2015 Apr 11. Clin Immunol. 2015. PMID: 25869295

6

Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.

Galal N, Meshaal S, Elhawary R, ElAziz DA, Alkady R, Lotfy S, Eldash A, Boutros J, Elmarsafy A. Galal N, et al. J Clin Immunol. 2016 Oct;36(7):649-55. doi: 10.1007/s10875-016-0314-1. Epub 2016 Aug 2. J Clin Immunol. 2016. PMID: 27484503 Review.

7

Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt.

El Hawary RE, Meshaal SS, Abd Elaziz DS, Elsharkawy MA, Alkady RS, Lotfy S, El-Sheikhah A, Hassan A, Galal NM, Boutros JA, Elmarsafy AM. El Hawary RE, et al. Among authors: meshaal ss. Mol Diagn Ther. 2017 Dec;21(6):677-684. doi: 10.1007/s40291-017-0297-5. Mol Diagn Ther. 2017. PMID: 28900865

8

Diagnosis of DOCK8 deficiency using Flow cytometry Biomarkers: an Egyptian Center experience.

Meshaal SS, El Hawary RE, Eldash A, Grimbacher B, Camacho-Ordonez N, Abd Elaziz DS, Galal NM, Boutros JA, Shawky SM, Elmarsafy AM. Meshaal SS, et al. Clin Immunol. 2018 Oct;195:36-44. doi: 10.1016/j.clim.2018.07.011. Epub 2018 Jul 24. Clin Immunol. 2018. PMID: 30048691

9

MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes.

El Hawary RE, Mauracher AA, Meshaal SS, Eldash A, Abd Elaziz DS, Alkady R, Lotfy S, Opitz L, Galal NM, Boutros JA, Pachlopnik Schmid J, Elmarsafy AM. El Hawary RE, et al. Among authors: meshaal ss. J Allergy Clin Immunol Pract. 2019 Mar;7(3):856-863. doi: 10.1016/j.jaip.2018.07.046. Epub 2018 Aug 28. J Allergy Clin Immunol Pract. 2019. PMID: 30170160

10

Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients.

Meshaal S, El Hawary R, Adel R, Abd Elaziz D, Erfan A, Lotfy S, Hafez M, Hassan M, Johnson M, Rojas-Restrepo J, Gamez-Diaz L, Grimbacher B, Shoman W, Abdelmeguid Y, Boutros J, Galal N, El-Guindy N, Elmarsafy A. Meshaal S, et al. J Clin Immunol. 2020 Aug;40(6):820-832. doi: 10.1007/s10875-020-00799-2. Epub 2020 Jun 6. J Clin Immunol. 2020. PMID: 32506362

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