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Transfusion Medicine (Oxford, England)|March 25, 1998
A new high-molecular-weight glycophorin C variant with a duplication of exon 2 in the glycophorin C geneM Uchikawa, H Tsuneyama, T Onodera, et al.Vox Sanguinis|January 1, 1994
First case of hemolytic disease of the newborn due to anti-Ula antibodiesK Sakuma, H Suzuki, H Ohto, et al.Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine|January 1, 1996
Serological analysis of monoclonal anti-E and -e with Japanese E/e variant red cellsM Uchikawa, C Toyoda, K Shinozaki, et al.Journal of Clinical Epidemiology|October 1, 1996
Family study of acute intermittent porphyria and hereditary coproporphyria in Niigata and Akita Prefectures, JapanH Sasaki, K Kaneko, H Tsuneyama, et al.Blood|January 15, 1998
Molecular cloning and characterization of decay-accelerating factor deficiency in Cromer blood group Inab phenotypeL Wang, M Uchikawa, H Tsuneyama, et al.Vox Sanguinis|September 5, 2015
Weak D alleles in Japanese: a c.960G>A silent mutation in exon 7 of the RHD gene that affects D expressionK Ogasawara, K Sasaki, K Isa, et al.Vox Sanguinis|April 14, 2015
A novel DO null allele with a c.268C>T (p.Gln90Stop) mutation in JapaneseT Onodera, H Tsuneyama, K Ogasawara, et al.Vox Sanguinis|May 31, 2014
JK null alleles identified from Japanese individuals with Jk(a−b−) phenotypeT Onodera, K Sasaki, H Tsuneyama, et al.Transfusion Science|October 18, 2000
Three episodes of delayed hemolytic transfusion reactions due to multiple red cell antibodies, anti-Di, anti-Jk and anti-EH Yasuda, H Ohto, O Yamaguchi, et al.Vox Sanguinis|May 18, 2016
Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD allelesK Isa, K Sasaki, K Ogasawara, et al.Pageof 2