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223 results on '"Connie M. Westhoff"'

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1. The protean presentations of XK disease (McLeod syndrome): a case series with new observations and updates on previously reported families

2. PIGG defines the Emm blood group system

3. Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

6. Whole-exome sequencing for RH genotyping and alloimmunization risk in children with sickle cell anemia

7. ABO Genotyping finds more A2 to B kidney transplant opportunities than lectin-based subtyping

13. Accurate long-read sequencing allows assembly of the duplicated RHD and RHCE genes harboring variants relevant to blood transfusion

15. Two new Scianna variants causing loss of high prevalence antigens: ERMAP model and 3D analysis of the antigens

17. The use of pluripotent stem cells to generate diagnostic tools for transfusion medicine

18. ABO maternal‐child discordance: Evidence of variable allelic expression and considerations for investigation

19. P-Null Phenotype Due to a Rare Frame-Shift Mutation and with Allo-Anti-PP1Pk Causing a Severe Hemolytic Transfusion Reaction: A Case Report with Clinical Management

21. Disruption of the tumour-associated EMP3 enhances erythroid proliferation and causes the MAM-negative phenotype

22. Multiple GYPB gene deletions associated with the U− phenotype in those of African ancestry

23. Reliability of labeling red cell units with minor antigen historical results and process considerations

24. American Society of Hematology 2020 guidelines for sickle cell disease: transfusion support

25. Red Cell Antigens and Antibodies

28. Anti-Emm, a rare specificity to the high-incidence antigen Emm in an Indian patient defining the new blood group system EMM (ISBT042)

30. Five novel silenced <scp>KEL</scp> *02 alleles

31. An insertion/deletion polymorphism in the KLF1 gene resulting in an In(Lu) phenotype

33. Three new XK alleles; two associated with a McLeod RBC phenotype

34. Severe delayed hemolytic transfusion reaction due to anti-Fy3 in a patient with sickle cell disease undergoing red cell exchange prior to hematopoietic progenitor cell collection for gene therapy

35. Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies

36. Blood group genotyping

37. Use of an in-house trypsin-based method to resolve the interference of daratumumab

38. Screening of blood donors for sickle cell trait using a DNA-based approach: Frequency in a multiethnic donor population

39. Rh alloimmunization in chronically transfused patients with thalassemia receiving RhD, C, E, and K matched transfusions

40. A pair of S-silencing single nucleotide variants cis-linked on GYPB

41. Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles

42. PIGG defines the Emm blood group system

44. A novel RHD*DAU allele with c.1136CT (p.Thr379Met) and c.17CT (p. Pro6Leu)

45. It’s time to phase out 'serologic weak D phenotype' and resolve D types with RHD genotyping including weak D type 4

46. Development and validation of a universal blood donor genotyping platform: A multinational prospective study

47. A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg a

48. Development and evaluation of a transfusion medicine genome wide genotyping array

49. RH genotype matching for transfusion support in sickle cell disease

50. Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study

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