Shimaa Abdrabou

Shimaa Abdrabou

Hokkaido University - Sapporo / Japan
Medical and Health Sciences / Pediatrics and Child Health
AD Scientific Index ID: 4812469
北海道大学
person_outline Shimaa Abdrabou's MOST POPULAR ARTICLES
1-) A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases M Ueki, M Yamada, K Ito, Y Tozawa, S Morino, Y Horikoshi, H Takada, ... Clinical Immunology 174, 24-31, 2017 182017
2-) A deep intronic mutation of c. 1166-285 T> G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM) Y Tozawa, SSMA Abdrabou, N Nogawa-Chida, R Nishiuchi, T Ishida, ... Clinical Immunology 208, 108256, 2019 142019
3-) Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence Z Sbihi, K Tanita, C Bachelet, C Bole, F Jabot-Hanin, F Tores, M Le Loch, ... Journal of Clinical Immunology 42 (3), 559-571, 2022 32022
4-) Absent X‐linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non‐coding deletionSSMA Abdrabou, N Toita, S Ichihara, Y Tozawa, M Takahashi, S Fujiwara, ...Pediatrics International 64 (1), e14892, 202232022
5-) Sub-100 nm carriers by template polymerization for drug delivery applications.PK Hashim, SSMA AbdrabouNanoscale Horizons, 202412024