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- 2008
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Mark
Bendamustine Versus Chlorambucil as First-Line Treatment in B Cell Chronic Lymphocytic Leukemia: An Updated Analysis from An International Phase III Study
(
- Contribution to journal › Published meeting abstract
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Mark
Pre-transplantation confirmatory ABO genotyping reveals a novel non-deletional 0 allele
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.178-178(
- Contribution to journal › Published meeting abstract
-
Mark
Investigation into A antigen expression on O-2 heterozygous group O-labeled red blood cell units
(
- Contribution to journal › Article
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Mark
Clinical aspects and molecular basis of a P phenotype individual from Argentina
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.201-202(
- Contribution to journal › Published meeting abstract
-
Mark
ABO transcript levels in peripheral blood and erythropoietic culture show different allele-related patterns independent of the CBF/NF-Y enhancer motif and multiple novel allele-specific variations in the 5'- and 3'-noncoding regions.
(
- Contribution to journal › Article
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Mark
A partial RH4 phenotype
2008) XXXth International Congress of the International Society of Blood Transfusion In Vox Sanguinis 95(s1). p.70-70(
- Contribution to journal › Published meeting abstract
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Mark
Variability of clinical manifestations of factor VII-deficiency in subjects homozygous or heterozygous for the F7 gene mutation A294V
(
- Contribution to journal › Letter
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Mark
A systematic overview of the first pasteurised VWF/FVIII medicinal product, Haemate P/ Humate -P: history and clinical performance.
(
- Contribution to journal › Scientific review
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Mark
A Randomised Placebo Controlled Study With Melphalan/Prednisone Vs Melphalan/Prednisone/Thalidomide: Quality Of Life And Toxicity
2008) 13th Congress of the European-Hematology-Association In Haematologica-The Hematology Journal 93. p.0209-0209(
- Contribution to journal › Published meeting abstract
-
Mark
Erythroid urea transporter deficiency due to novel JK(null) alleles
(
- Contribution to journal › Article