| Clinical utility of NGS diagnosis and disease stratification in a multiethnic primary ciliary dyskinesia cohort MR Fassad, MP Patel, A Shoemark, T Cullup, J Hayward, M Dixon, ... Journal of Medical Genetics 57 (5), 322-330, 2020 | 70 | 2020 |
| Clinical phenotypes and immunological characteristics of 18 Egyptian LRBA deficiency patients S Meshaal, R El Hawary, R Adel, D Abd Elaziz, A Erfan, S Lotfy, M Hafez, ... Journal of Clinical Immunology 40, 820-832, 2020 | 27 | 2020 |
| Immunoglobulin, glucocorticoid, or combination therapy for multisystem inflammatory syndrome in children: a propensity-weighted cohort study S Channon-Wells, O Vito, AJ McArdle, EG Seaby, H Patel, P Shah, ... The Lancet Rheumatology 5 (4), e184-e199, 2023 | 26 | 2023 |
| Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia MR Fassad, WI Shoman, H Morsy, MP Patel, N Radwan, L Jenkins, ... Clinical Genetics 97 (3), 509-515, 2020 | 25 | 2020 |
| Physicians' knowledge and practice concerning diagnosis and management of anaphylaxis: The situation in Egypt ZA El-Sayed, R El-Owaidy, SM Hussein, D Hossam, IH El-Sawi, A Adel, ... African Journal of Emergency Medicine 11 (4), 464-470, 2021 | 14 | 2021 |
| First Egyptian patient with STING-associated vasculopathy with onset in infancy W Shoman, Y El Chazli, I ElSawy, JI Aróstegui Scandinavian Journal of Rheumatology 48 (4), 338-339, 2019 | 9 | 2019 |
| Hemophagocytic lymphohistiocytosis in a child with sickle cell disease W Shoman, Y El Chazli, A Elsharkawy, N Mikhael, A Deghaidy, ... Hematol Transfus Int J 6 (5), 180-182, 2018 | 4 | 2018 |
| Lipoid proteinosis: Novel ECM1 pathogenic variants and intrafamilial variability in four unrelated Arab families M Li, J Fischer, S Safwat, W Shoman, YE Chazli, S Alter, C Has, E Abdalla Pediatric dermatology 40 (1), 113-119, 2023 | 1 | 2023 |
| Infection and colonization pattern in children with chronic granulomatous disease: a prospective cohort study HA Abdelaty, GF Eldriny, AA Galal, SAEF Arafa, W Shoman Senses and Sciences 9 (1), 2022 | 1 | 2022 |
| Soluble il-2 receptor alpha in cerebrospinal fluid of children with hemophagocytic lymphohistiocytosis Y El Chazli, A Elsharkawy, N Mikhael, M Abd El-Maksoud, W Shoman, ... PEDIATRIC BLOOD & CANCER 66, S12-S13, 2019 | 1 | 2019 |
| Fever of unknown origin in pediatrics: causes and clinical characteristics in a single centre experience W Shoman, A Galal, AM Elshishiny, E Hamza Egyptian Pediatric Association Gazette 72 (1), 65, 2024 | | 2024 |
| Evaluation of screening tools for primary ciliary dyskinesia in Egypt: single center study AG Elbanna, W Shoman, MAR Elheneidy, I Elsawy, A Kantar, N Fasseeh Multidisciplinary Respiratory Medicine 19 (1), 966, 2024 | | 2024 |
| Primary ciliary dyskinesia in Egypt: First report of cilia ultrastructural defects and novel genetic variants W Shoman, AG Elbanna, MR Fassad, MAR Elheneidy, L Petrarca, ... Pediatric Pulmonology 59 (6), 1578-1588, 2024 | | 2024 |
| Clinical and laboratory spectrum of hereditary angioedema in a group of Egyptian children: a cross sectional study M Almalky, RM El Shabrawy, NAM Gheetah, HM Elkady, NS Osman, ... Egyptian Pediatric Association Gazette 72 (1), 19, 2024 | | 2024 |
| Impact of Primary Ciliary Dyskinesia Clinical Features on Time Lag to Diagnosis in Egypt: A Retrospective Cohort Study AG Elbanna, W Shoman, M Elheneidy, I Elsawy, N Fasseeh Senses and Sciences 10 (2), 112-119, 2023 | | 2023 |
| Insight into gastrointestinal manifestations of some pediatric autoinflammatory disorders WI Shoman The Egyptian Journal of Pediatric Allergy and Immunology 21 (1), 2-8, 2023 | | 2023 |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN EGYPTIAN CHILDREN: SINGLE CENTER EXPERIENCE Y El Chazli, A Elsharkawy, M Abd El-Maksoud, W Shoman, N Mikhael PEDIATRIC BLOOD & CANCER 67, S9-S9, 2020 | | 2020 |
| HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS: A MISSED DIAGNOSIS IN CHILDREN WITH NEUROLOGICAL MANIFESTATIONS Y El Chazli, M Abd El-Maksoud, A Elsharkawy, W Shoman, N Mikhael, ... PEDIATRIC BLOOD & CANCER 67, S9-S9, 2020 | | 2020 |
| Targeted NGS in primary ciliary dyskinesia: expanding mutation spectrum and novel dynein-related gene discovery MR Fassad, A Shoemark, J Hayward, M Patel, P le Borgne, F Koll, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 796-797, 2019 | | 2019 |
| Genetic analysis in Egyptian patients with Chediak-Higashi syndrome reveals novel LYST mutations NS Radwan, JYW Lee, A El-Sharkawy, W Shoman, YF Elchazly, ... BRITISH JOURNAL OF DERMATOLOGY 178 (6), E424-E424, 2018 | | 2018 |
