Publications

Export 41 results:
Sort by: Author Title Type [ Year (Desc)]
2023
, "Cernunnos deficiency: Further delineation in 5 Egyptian patients", Eur J Med Genet ., vol. 66 (10), 2023.
, "Chronic Granulomatous Disease: a Cohort of 173 Patients-10-Years Single Center Experience from Egypt", Journal of Clinical Immunology, vol. 43 (8), 2023.
, "The Middle East and North Africa Diagnosis and Management Guidelines for Inborn Errors of Immunity", J Allergy Clin Immunol Pract ., vol. 11 (1), 2023.
2022
, "Allergic manifestations of inborn errors of immunity and their impact on the diagnosis: A worldwide study", World Allergy Organ J ., vol. 15 (6), 2022.
, "Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021", Front Immunol . , vol. 13, 2022.
, "Flow cytometry optimizing the diagnostic approach in inborn errors of immunity: experience from Egypt", Allergy Asthma Clin Immunol . , vol. 18 (1), 2022.
, Genetic Testing in Egyptian Patients with Inborn Errors of Immunity: a Single-Center Experience, , pp. 1051-1070, 2022.
, "Resistant psoriasis associated with LRBA deficiency: A case report", J Dtsch Dermatol Ges ., 2022.
, "A Rose Amongst the Thorns: the Mission of the J Project in a Conflictual World", Journal of Clinical Immunology, pp. 1151-1155, 2022.
2021
, "Genetic Analysis of a Cohort of 275 Patients with Hyper-IgE Syndromes and/or Chronic Mucocutaneous Candidiasis", Journal of Clinical Immunology, issue 41 (8), pp. 1804-1838, 2021.
, "Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations", JACI, issue 148(5), pp. 1332, 2021.
, "Simple Measurement of IgA Predicts Immunity and Mortality in Ataxia-Telangiectasia", Journal of Clinical Immunology, pp. 1878-1892, 2021.
2020
, "Clinical Phenotypes and Immunological Characteristics of 18 Egyptian LRBA Deficiency Patients.", J Clin immunol, issue doi: 10.1007/s10875-020-00799-2., 2020.
, "The Konya Declaration for Patients with Primary Immunodeficiencies. Maródi L; J Project Study Group.", J Clin immunol, issue doi: 10.1007/s10875-020-00797-4., 2020.
2019
, "Imaging of Bronchial Pathology in Antibody Deficiency: Data from the European Chest CT Group.", J Clin Immunol, issue Dec 13, 2019.
, "MHC-II Deficiency Among Egyptians: Novel Mutations and Unique Phenotypes.", J Allergy Clin Immunol Pract, 2019.
, "T cell mitochondrial dysfunction and lymphopenia in DOCK2-deficient patients", JACI, vol. 144(1), 2019.
, "Targeted screening for primary immunodeficiency disorders in the neonatal period and early infancy", Afr Health Sci, vol. 19(1), 2019.
, "X-linked agammaglobulinemia (XLA): Phenotype, diagnosis, and therapeutic challenges around the world", World Allergy Journal, vol. 12(3): 100018., 2019.
2018
, Diagnosis of DOCK8 deficiency using Flow cytometry Biomarkers: an Egyptian Center experience., , 2018.
, "Poliovirus excretion following vaccination with live poliovirus vaccine in patients with primary immunodeficiency disorders: clinicians' perspectives in the endgame plan for polio eradication", BMC Res Notes, vol. 11 (1), issue Oct 11;11(1):, pp. 717, 2018.
2017
, "Genetic counselling in Primary Immunodeficiency Disorders:An Emerging Experience in Egypt", Mol Diag Ther, 2017.
, "Targeted Gene Panel Sequencing for Early-onset Inflammatory Bowel Disease and Chronic Diarrhea", Inflamm Bowel Dis, vol. 23, issue 12, pp. 2109-2120, 2017.
2016
Galal, N., S. Meshaal, R. E. Hawary, D. A. Elaziz, R. Alkady, S. Lotfy, A. Eldash, J. Boutros, and A. ELmarsafy, "Patterns of Primary Immunodeficiency Disorders Among a Highly Consanguineous Population: Cairo University Pediatric Hospital's 5-Year Experience.", Journal of clinical immunology, 2016 Aug 2. Abstract

INTRODUCTION: Primary immunodeficiency disorders (PIDs) are heterogeneous disorders that mainly present with severe, persistent, unusual, or recurrent infections in childhood. Reports from different parts of the world indicate a difference between Western and Eastern populations.

AIM: The aim of this study was to report on the different patterns of PIDs and identify subgroup characteristics in a highly consanguineous population in Egypt.

METHODS: We performed a retrospective chart review for children below 18 years diagnosed with PID at Cairo University Pediatric Hospital from 2010 to 2014.

RESULTS: Four hundred seventy-six children were diagnosed with PID disorders. Major categories included combined immunodeficiency disorders, which constituted a large proportion (30 %) of cases, along with predominantly antibody disorders (18 %) followed by syndromic combined disorders (16.8 %), phagocytic disorders (13.2 %), immune dysregulation disorders (10.5 %), and autoinflammatory disorders (9 %).

CONCLUSION: PIDs have different patterns within inbred populations with high consanguinity.

Hamooda, M., "Anti -cyclic Citrullinated peptide antibodies in children with Juvenile Idiopathic Arthritis", Electron Physician, 2016.
Tourism