| Biologicals in atopic disease in pregnancy: an EAACI position paper B Pfaller, J José Yepes‐Nuñez, I Agache, CA Akdis, M Alsalamah, ... Allergy 76 (1), 71-89, 2021 | 45 | 2021 |
| Transaldolase deficiency: report of 12 new cases and further delineation of the phenotype W Eyaid, T Al Harbi, S Anazi, MMC Wamelink, C Jakobs, M Al Salammah, ... Journal of Inherited Metabolic Disease: Official Journal of the Society for …, 2013 | 40 | 2013 |
| Anaphylaxis to milk after elimination diet for eosinophilic gastrointestinal disease M Alsalamah, M Makhajia, G Somers, M Marcon, D Hummel, J Upton Official journal of the American College of Gastroenterology| ACG 111 (5 …, 2016 | 24 | 2016 |
| Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect … A Asiri, D Alwadaani, M Umair, KM Alhamoudi, MH Almuhanna, A Nasir, ... Genes 12 (2), 294, 2021 | 9 | 2021 |
| Establishing reference ranges for lymphocyte proliferation responses to phytohemagglutinin in patients with T cell dysfunction M Alsalamah, L Vong, L Cimpean, H Dadi LymphoSign Journal 6 (1), 26-30, 2019 | 4 | 2019 |
| Hemophagocytic lymphohistiocytosis in a patient with CD3δ deficiency M Alsalamah, A Sarpal, VM Siu, P Gibson, CA Rupar, M Barton, ... LymphoSign Journal 2 (4), 201-206, 2015 | 3 | 2015 |
| Hemophagocytic lymphohistiocytosis associated with ataxia telangiectasia M Alsalamah, CM Roifman LymphoSign Journal 4 (3), 113-116, 2017 | 1 | 2017 |
| Chapter: SPENCDI Syndrome: Genetic Syndromes A Comprehensive Reference Guide (Nima Rezaei) M Alsalamah, C Roifman | | 2024 |
| Targeted busulfan-based reduced-intensity regimen in mhc class ii deficiency and chronic granulomatous disease: Single center study M Essa, F Alrogi, R Abujoub, E Elbashir, M Alsalamah, S Memon, ... BONE MARROW TRANSPLANTATION 57 (SUPPL 1), 251-252, 2022 | | 2022 |
| Association between NOD2 and autoinflammation presenting as Yellow Nail Syndrome LE Abrego Fuentes, M Alsalamah LymphoSign Journal 9 (3), 67-71, 2022 | | 2022 |
| Case report of a novel mutation in Bruton’s tyrosine kinase gene with confirmed agammaglobulinemia and absent B lymphocytes N Bedaiwy, S Alhamdi, W Al Suwairi, M Alsalamah LymphoSign Journal 9 (1), 1-4, 2022 | | 2022 |
| Causes of False-Positives in Severe Combined Immune Deficiency Newborn Screening based on T-Cell Receptor Excision Circles (TRECs): A single Center Canadian Experience M Alsalamah, C Roifman Canadian Society of Allergy and Clinical Immunology, 2017 | | 2017 |
| Chronic granulomatous disease with an initial presentation of arthritis and oral ulcers M Alsalamah, M Hanna, J Upton LymphoSign Journal 3 (1), 35-40, 2015 | | 2015 |
