Musa Alharbi

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells

Marjorie Côte, Mickaël Ménager, Agathe Burgess et al. · Journal of Clinical Investigation · 2009 · 349 citations · Full text

Life Sciences, Genetics, Immunology +13

Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: Report from the constitutional mismatch repair deficiency consortium

Doua Bakry, Melyssa Aronson, Carol Durno et al. · European Journal of Cancer · 2014 · 235 citations

Life Sciences, Genetics, Molecular Genetics +16

Survival Benefit for Individuals With Constitutional Mismatch Repair Deficiency Undergoing Surveillance

Carol Durno, Ayse B. Ercan, Vanessa Bianchi et al. · Journal of Clinical Oncology · 2021 · 101 citations · Full text

Medicine, Oncology, Dna Repair +16

Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency

Musa Alharbi, Nahla Ali Mobark, Latifa AlMubarak et al. · The Oncologist · 2018 · 72 citations · Full text

Medicine, Oncology, Pediatrics +17

Gastrointestinal Findings in the Largest Series of Patients With Hereditary Biallelic Mismatch Repair Deficiency Syndrome: Report from the International Consortium

Melyssa Aronson, Steven Gallinger, Zane Cohen et al. · The American Journal of Gastroenterology · 2016 · 47 citations

Medicine, Genetics, Oncology +17