Wagner T - Search Results

1

Aberrant ABO B Phenotype with Irregular Anti-B Caused by a Para-Bombay FUT1 Mutation.

Matzhold EM, Wagner T, Drexler C, Schönbacher M, Körmöczi GF. Matzhold EM, et al. Among authors: wagner t. Transfus Med Hemother. 2020 Feb;47(1):94-97. doi: 10.1159/000499724. Epub 2019 Apr 29. Transfus Med Hemother. 2020. PMID: 32110200 Free PMC article.

2

A novel ABO O allele caused by a large deletion covering two exons of the ABO gene identified in a Caucasian family showing discrepant ABO blood typing results.

Matzhold EM, Drexler C, Wagner T. Matzhold EM, et al. Among authors: wagner t. Transfusion. 2016 Nov;56(11):2739-2743. doi: 10.1111/trf.13768. Epub 2016 Aug 21. Transfusion. 2016. PMID: 27546586

3

A 24-base pair deletion in the ABO gene causes a hereditary splice site defect: a novel mechanism underlying ABO blood group O.

Matzhold EM, Drexler C, Wagner A, Bernecker C, Pessentheiner A, Bogner-Strauß JG, Helmberg W, Wagner T. Matzhold EM, et al. Among authors: wagner a, wagner t. Transfusion. 2020 Jul;60(7):1564-1572. doi: 10.1111/trf.15907. Epub 2020 Jun 4. Transfusion. 2020. PMID: 32500601 Free PMC article.

4

Ethical Issues and Management of Fetal Hemolytic Anemia Caused by Anti-Rh17 in a Multipara with Rare -D- Phenotype.

Torreiter PP, Macher S, Matzhold EM, Resch B, Klaritsch P, Körmöczi GF, Polin H, Neuhold L, Schönbacher M, Schlenke P, Wagner T. Torreiter PP, et al. Among authors: wagner t. Transfus Med Hemother. 2021 May;48(3):183-187. doi: 10.1159/000513124. Epub 2021 Jan 5. Transfus Med Hemother. 2021. PMID: 34177424 Free PMC article.

5

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. Transfusion. 2005 Apr;45(4):520-6. doi: 10.1111/j.0041-1132.2005.04256.x. Transfusion. 2005. PMID: 15819672

6

Tetragametic chimerism detected in a healthy woman with mixed-field agglutination reactions in ABO blood grouping.

Drexler C, Glock B, Vadon M, Staudacher E, Dauber EM, Ulrich S, Reisacher RB, Mayr WR, Lanzer G, Wagner T. Drexler C, et al. Among authors: wagner t. Transfusion. 2005 May;45(5):698-703. doi: 10.1111/j.1537-2995.2005.04304.x. Transfusion. 2005. PMID: 15847657

7

Genetic diversity of KELnull and KELel: a nationwide Austrian survey.

Körmöczi GF, Wagner T, Jungbauer C, Vadon M, Ahrens N, Moll W, Mühlbacher A, Ozgül-Gülce S, Kleinrath T, Kilga-Nogler S, Schönitzer D, Gassner C. Körmöczi GF, et al. Among authors: wagner t. Transfusion. 2007 Apr;47(4):703-14. doi: 10.1111/j.1537-2995.2007.01174.x. Transfusion. 2007. PMID: 17381630

8

Identification of 14 new alleles at the fucosyltransferase 1, 2, and 3 loci in Styrian blood donors, Austria.

Matzhold EM, Helmberg W, Wagner T, Drexler C, Ulrich S, Winkler A, Lanzer G. Matzhold EM, et al. Among authors: wagner t. Transfusion. 2009 Oct;49(10):2097-108. doi: 10.1111/j.1537-2995.2009.02293.x. Epub 2009 Jun 30. Transfusion. 2009. PMID: 19572973

9

Novel ABO gene variants caused by missense mutations in Exon 7 leading to discrepant ABO blood typing results.

Matzhold EM, Wagner A, Drexler C, Wagner T. Matzhold EM, et al. Among authors: wagner a, wagner t. Transfusion. 2015 Jun;55(6 Pt 2):1589-90. doi: 10.1111/trf.13025. Epub 2015 Apr 9. Transfusion. 2015. PMID: 25855329 No abstract available.

10

RHD Tyr311Stop encoded by a novel nonsense mutation.

Polin H, Matzhold EM, Schlenke P, Gabriel C, Danzer M, Wagner T. Polin H, et al. Among authors: wagner t. Transfusion. 2016 Sep;56(9):2389-90. doi: 10.1111/trf.13702. Epub 2016 Jun 28. Transfusion. 2016. PMID: 27351456 No abstract available.

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