Found: 10
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High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Family study of a Swiss patient uncovered a novel genetic basis for the S-s-U+(var) phenotype.
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Family study of a Swiss patient uncovered a novel genetic basis for the S−s− U+<sup>var</sup> phenotype.
- Published in:
- Transfusion, 2014, v. 54, n. 11, p. 2941, doi. 10.1111/trf.12681
- By:
- Publication type:
- Article
Identification of novel silent KEL alleles causing KEL:-5 (Ko) phenotype or discordance between KEL:1,-2 phenotype/KEL*01/02 genotype.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Molecular background of novel silent RHCE alleles.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2990, doi. 10.1111/trf.12023
- By:
- Publication type:
- Article
Identification of novel silent KEL alleles causing KEL:−5 ( Ko) phenotype or discordance between KEL:1,−2 phenotype/ KEL*01/02 genotype.
- Published in:
- Transfusion, 2013, v. 53, n. 11pt2, p. 2859, doi. 10.1111/trf.12206
- By:
- Publication type:
- Article
Antibodies to co-trimoxazole (trimethoprim and/or sulfamethoxazole) related to the presence of the drug in a commercial low-ionic-strength solution.
- Published in:
- Transfusion, 2012, v. 52, n. 4, p. 844, doi. 10.1111/j.1537-2995.2011.03327.x
- By:
- Publication type:
- Article
Anti-D investigations in individuals expressing weak D Type 1 or weak D Type 2: allo- or autoantibodies?
- Published in:
- Transfusion, 2011, v. 51, n. 12, p. 2679, doi. 10.1111/j.1537-2995.2011.03207.x
- By:
- Publication type:
- Article
Analysis of RhCE variants among 806 individuals in France: considerations for transfusion safety, with emphasis on patients with sickle cell disease.
- Published in:
- Transfusion, 2011, v. 51, n. 6, p. 1249, doi. 10.1111/j.1537-2995.2010.02970.x
- By:
- Publication type:
- Article
Heterogeneous molecular background of the weak C, VS+, hr<sup>B</sup>–, Hr<sup>B</sup>– phenotype in black persons.
- Published in:
- Transfusion, 2009, v. 49, n. 3, p. 495, doi. 10.1111/j.1537-2995.2008.02005.x
- By:
- Publication type:
- Article