Abdullah Alangari

Revisiting Human IL-12Rβ1 Deficiency

Ludovic de Beaucoudrey, Arina Samarina, Jacinta Bustamante et al. · Medicine · 2010 · 379 citations · Full text

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 · 346 citations · Full text

Immunology, Pathology, Cell Death +18

Herpes simplex encephalitis in children with autosomal recessive and dominant TRIF deficiency

Vanessa Sancho‐Shimizu, Rebeca Pérez de Diego, Lazaro Lorenzo et al. · Journal of Clinical Investigation · 2011 · 301 citations · Full text

Autoimmune Disease, Unrelated Hse Children, Pathogenesis +14

LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency

Abdullah Alangari, Abdulrahman Alsultan, Nouran Adly et al. · Journal of Allergy and Clinical Immunology · 2012 · 244 citations · Full text

Primary Immunodeficiency, Immunogenetics, Autoimmune Disease +12

Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA

Louis‐Marie Charbonnier, Erin Janssen, Janet Chou et al. · Journal of Allergy and Clinical Immunology · 2014 · 241 citations · Full text

Immunodeficiencies, Genetics, Immunology +16