Legler TJ - Search Results

1

Molecular and serologic characterization of DWI, a novel "high-grade" partial D.

Körmöczi GF, Legler TJ, Daniels GL, Green CA, Struckmann R, Jungbauer C, Moser S, Flexer M, Schönitzer D, Panzer S, Gassner C. Körmöczi GF, et al. Among authors: legler tj. Transfusion. 2004 Apr;44(4):575-80. doi: 10.1111/j.1537-2995.2003.03318.x. Transfusion. 2004. PMID: 15043574

2

Testing for the D zygosity with three different methods revealed altered Rhesus boxes and a new weak D type.

Perco P, Shao CP, Mayr WR, Panzer S, Legler TJ. Perco P, et al. Among authors: legler tj. Transfusion. 2003 Mar;43(3):335-9. doi: 10.1046/j.1537-2995.2003.00313.x. Transfusion. 2003. PMID: 12675718

3

Anti-D immunization by DEL red blood cells.

Wagner T, Körmöczi GF, Buchta C, Vadon M, Lanzer G, Mayr WR, Legler TJ. Wagner T, et al. Among authors: legler tj. Transfusion. 2005 Apr;45(4):520-6. doi: 10.1111/j.0041-1132.2005.04256.x. Transfusion. 2005. PMID: 15819672

4

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: legler tj. Transfusion. 2005 Apr;45(4):527-38. doi: 10.1111/j.0041-1132.2004.04211.x. Transfusion. 2005. PMID: 15819673

5

A comprehensive analysis of DEL types: partial DEL individuals are prone to anti-D alloimmunization.

Körmöczi GF, Gassner C, Shao CP, Uchikawa M, Legler TJ. Körmöczi GF, et al. Among authors: legler tj. Transfusion. 2005 Oct;45(10):1561-7. doi: 10.1111/j.1537-2995.2005.00584.x. Transfusion. 2005. PMID: 16181205

6

RHD variants in Flanders, Belgium.

Van Sandt VS, Gassner C, Emonds MP, Legler TJ, Mahieu S, Körmöczi GF. Van Sandt VS, et al. Among authors: legler tj. Transfusion. 2015 Jun;55(6 Pt 2):1411-7. doi: 10.1111/trf.12947. Epub 2014 Nov 21. Transfusion. 2015. PMID: 25413499

7

Mosaicism due to myeloid lineage restricted loss of heterozygosity as cause of spontaneous Rh phenotype splitting.

Körmöczi GF, Dauber EM, Haas OA, Legler TJ, Clausen FB, Fritsch G, Raderer M, Buchta C, Petzer AL, Schönitzer D, Mayr WR, Gassner C. Körmöczi GF, et al. Among authors: legler tj. Blood. 2007 Sep 15;110(6):2148-57. doi: 10.1182/blood-2007-01-068106. Epub 2007 May 30. Blood. 2007. PMID: 17537994 Free article.

8

RHD sequencing: a new tool for decision making on transfusion therapy and provision of Rh prophylaxis.

Legler TJ, Maas JH, Köhler M, Wagner T, Daniels GL, Perco P, Panzer S. Legler TJ, et al. Transfus Med. 2001 Oct;11(5):383-8. doi: 10.1046/j.1365-3148.2001.00327.x. Transfus Med. 2001. PMID: 11696232

9

Somatic mosaicisms of chromosome 1 at two different stages of ontogenetic development detected by Rh blood group discrepancies.

Dauber EM, Mayr WR, Hustinx H, Schönbacher M, Budde H, Legler TJ, König M, Haas OA, Fritsch G, Körmöczi GF. Dauber EM, et al. Among authors: legler tj. Haematologica. 2019 Mar;104(3):632-638. doi: 10.3324/haematol.2018.201293. Epub 2018 Sep 20. Haematologica. 2019. PMID: 30237270 Free PMC article.

10

RHD genotyping in weak D phenotypes by multiple polymerase chain reactions.

Legler TJ, Maas JH, Blaschke V, Malekan M, Ohto H, Lynen R, Bustami N, Schwartz DW, Mayr WR, Köhler M, Panzer S. Legler TJ, et al. Transfusion. 1998 May;38(5):434-40. doi: 10.1046/j.1537-2995.1998.38598297211.x. Transfusion. 1998. PMID: 9633555

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