Publications

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2019
Galal, N., M. Ohida, S. Meshaal, and D. A. E. etal, "Targeted Screening for Primary Immunodeficiency disorders in the neonatal period and early infancy", African Health Sciences, vol. 19, pp. 1449-1459, 2019. afhs1901-1449.pdf
2018
Hawary, R. E. E., A. A. Mauracher, S. S. Meshaal, A. Eldash, and D. A. S. Elaziz, MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes, , 2018. mhc_ii.pdf
Tucci, F., V. Calbi, F. Barzaghi, M. Migliavacca, and F. Ferrua, "Successful Treatment With Ledipasvir/ Sofosbuvir in an Infant With Severe Combined Immunodeficiency Caused by Adenosine Deaminase Deficiency With HCV Allowed Gene Therapy with Strimvelis", Hepatology, vol. 68, issue 6, pp. 2434-2437, 2018. tucci_et_al-2018-hepatology-1.pdf
2017
Hawary, R. E., S. Meshaal, D. A. Elaziz, R. Alkady, S. Lotfy, A. El-Sheikhah, A. Hassan, N. Galal, J. Boutros, A. ELmarsafy, et al., "Genetic Counseling in Primary Immunodeficiency Disorders: An Emerging Experience in Egypt", Molecular Diagnosis & Therapy, vol. 21, pp. 677-684, 2017. genetic_counseling_in_pid.pdf
2015
Meshaal, S., R. E. Hawarya, M. Elsharkawy, R. K. Mousa, R. J. Farid, D. A. Elaziz, R. Alkady, N. Galal, M. J. Massaad, J. Boutros, et al., "Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt", Clinical Immunology, pp. 158-167, 2015.
2014
Elaziz, D. A. S., A. ELmarsafy, S. S. Meshaal, M. Hafez, and N. Galal, "CD4+ CD25+ cells in type 1 diabetic patients with other autoimmune manifestations ", JAR, issue 5, pp. 647-655, 2014. jar.pdf
Meshaal, S., R. E. Hawary, A. E. Marsafi, N. Galal, R. Alkady, J. Boutros, and D. A. Elaziz, "Chronic granulomatous disease: Review of a cohort of Egyptian patients", Allergol Immunopathol, 2014.
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