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Absent X-linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non-coding deletion.
Pediatr Int. 2022 Jan;64(1):e14892. doi: 10.1111/ped.14892.
Pediatr Int. 2022.
PMID: 34145698
A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases.
Ueki M, Yamada M, Ito K, Tozawa Y, Morino S, Horikoshi Y, Takada H, Abdrabou SS, Takezaki S, Kobayashi I, Ariga T.
Ueki M, et al.
Clin Immunol. 2017 Jan;174:24-31. doi: 10.1016/j.clim.2016.11.004. Epub 2016 Nov 14.
Clin Immunol. 2017.
PMID: 27856304
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A deep intronic mutation of c.1166-285 T > G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).
Tozawa Y, Abdrabou SSMA, Nogawa-Chida N, Nishiuchi R, Ishida T, Suzuki Y, Sano H, Kobayashi R, Kishimoto K, Ohara O, Imai K, Naruto T, Kobayashi K, Ariga T, Yamada M.
Tozawa Y, et al. Among authors: abdrabou ssma.
Clin Immunol. 2019 Nov;208:108256. doi: 10.1016/j.clim.2019.108256. Epub 2019 Sep 5.
Clin Immunol. 2019.
PMID: 31494288
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Identification of Germline Non-coding Deletions in XIAP Gene Causing XIAP Deficiency Reveals a Key Promoter Sequence.
Sbihi Z, Tanita K, Bachelet C, Bole C, Jabot-Hanin F, Tores F, Le Loch M, Khodr R, Hoshino A, Lenoir C, Oleastro M, Villa M, Spossito L, Prieto E, Danielian S, Brunet E, Picard C, Taga T, Abdrabou SSMA, Isoda T, Yamada M, Palma A, Kanegane H, Latour S.
Sbihi Z, et al. Among authors: abdrabou ssma.
J Clin Immunol. 2022 Apr;42(3):559-571. doi: 10.1007/s10875-021-01188-z. Epub 2022 Jan 9.
J Clin Immunol. 2022.
PMID: 35000057
Free article.
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Sub-100 nm carriers by template polymerization for drug delivery applications.
Hashim PK, Abdrabou SSMA.
Hashim PK, et al. Among authors: abdrabou ssma.
Nanoscale Horiz. 2024 Apr 29;9(5):693-707. doi: 10.1039/d3nh00491k.
Nanoscale Horiz. 2024.
PMID: 38497369
Review.
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