Petershofen EK - Search Results

1

Weak D type 1.1 exemplifies another complexity in weak D genotyping.

Doescher A, Flegel WA, Petershofen EK, Bauerfeind U, Wagner FF. Doescher A, et al. Among authors: petershofen ek. Transfusion. 2005 Oct;45(10):1568-73. doi: 10.1111/j.1537-2995.2005.00585.x. Transfusion. 2005. PMID: 16181206

2

RHCE-D-CE hybrid genes can cause false-negative DNA typing of the Rh e antigen.

Hundhausen T, Petershofen EK, Doescher A, Bauerfeind U, Müller TH, Schunter F. Hundhausen T, et al. Among authors: petershofen ek. Vox Sang. 2002 Oct;83(3):268-72. doi: 10.1046/j.1423-0410.2002.00220.x. Vox Sang. 2002. PMID: 12366772

3

Presence of RHD in serologically D-, C/E+ individuals: a European multicenter study.

Gassner C, Doescher A, Drnovsek TD, Rozman P, Eicher NI, Legler TJ, Lukin S, Garritsen H, Kleinrath T, Egger B, Ehling R, Körmöczi GF, Kilga-Nogler S, Schoenitzer D, Petershofen EK. Gassner C, et al. Among authors: petershofen ek. Transfusion. 2005 Apr;45(4):527-38. doi: 10.1111/j.0041-1132.2004.04211.x. Transfusion. 2005. PMID: 15819673

4

In-frame triplet deletions in RHD alter the D antigen phenotype.

Flegel WA, Eicher NI, Doescher A, Hustinx H, Gowland P, Mansouri Taleghani B, Petershofen EK, Bauerfeind U, Ernst M, von Zabern I, Schrezenmeier H, Wagner FF. Flegel WA, et al. Among authors: petershofen ek. Transfusion. 2006 Dec;46(12):2156-61. doi: 10.1111/j.1537-2995.2006.01046.x. Transfusion. 2006. PMID: 17176329

5

Cost-efficient sequence-specific priming-polymerase chain reaction screening for blood donors with rare phenotypes.

Wagner FF, Bittner R, Petershofen EK, Doescher A, Müller TH. Wagner FF, et al. Among authors: petershofen ek. Transfusion. 2008 Jun;48(6):1169-73. doi: 10.1111/j.1537-2995.2008.01682.x. Epub 2008 Apr 15. Transfusion. 2008. PMID: 18422854

6

RHCE alleles detected after weak and/or discrepant results in automated Rh blood grouping of blood donors in Northern Germany.

Döscher A, Vogt C, Bittner R, Gerdes I, Petershofen EK, Wagner FF. Döscher A, et al. Among authors: petershofen ek. Transfusion. 2009 Sep;49(9):1803-11. doi: 10.1111/j.1537-2995.2009.02221.x. Epub 2009 May 18. Transfusion. 2009. PMID: 19453979

7

Evaluation of single-nucleotide polymorphisms as internal controls in prenatal diagnosis of fetal blood groups.

Doescher A, Petershofen EK, Wagner FF, Schunter M, Müller TH. Doescher A, et al. Among authors: petershofen ek. Transfusion. 2013 Feb;53(2):353-62. doi: 10.1111/j.1537-2995.2012.03738.x. Epub 2012 Jun 13. Transfusion. 2013. PMID: 22691192

8

Platelet recovery and survival measured in patients by quantitative polymerase chain reaction of mitochondrial DNA.

Doescher A, Petershofen EK, Hertenstein B, Kraemer D, Casper J, Schmidt JP, Müller TH. Doescher A, et al. Among authors: petershofen ek. Transfusion. 2015 Jan;55(1):55-63. doi: 10.1111/trf.12778. Epub 2014 Jul 23. Transfusion. 2015. PMID: 25056505 Clinical Trial.

9

The Glass Slide Extraction System Snap Card Improves Non-Invasive Prenatal Genotyping in Pregnancies with Antibodies.

Adamczyk T, Doescher A, Haydock PV, Aldrich R, Petershofen EK, Müller TH. Adamczyk T, et al. Among authors: petershofen ek. Transfus Med Hemother. 2015 Nov;42(6):379-84. doi: 10.1159/000441542. Epub 2015 Oct 26. Transfus Med Hemother. 2015. PMID: 26733769 Free PMC article.

10

Evaluation of droplet digital PCR for quantification of residual leucocytes in red blood cell concentrates.

Doescher A, Loges U, Petershofen EK, Müller TH. Doescher A, et al. Among authors: petershofen ek. Vox Sang. 2017 Nov;112(8):744-750. doi: 10.1111/vox.12566. Epub 2017 Oct 2. Vox Sang. 2017. PMID: 28967676

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