Michel Massaad
Faculty of Medicine, American University of Beirut
74 papers found
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Cadherin 17 mutation associated with leaky severe combined immune deficiency is corrected by HSCT
Download from ashpublications.orgDOCK8 and STAT3 dependent inhibition of IgE isotype switching by TLR9 ligation in human B cells
UploadEpidermodysplasia verruciformis as a manifestation of ARTEMIS deficiency in a young adult
UploadDeficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity
Download from doi.orgA DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton
Download from doi.orgSpectrum of Phenotypes Associated with Mutations in LRBA
UploadA missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency
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