Author Steinemann, Doris
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2011 | Conference Abstract
NON-SYNDROMIC THROMBOCYTOPENIA WITH PROPENSITY TO MYELOID MALIGNANCIES DUE TO A DE-NOVO MICRODELETION ON CHROMOSOME 21q INVOLVING RUNX1 - WHAT TO DO NEXT?
Ripperger, T.; Steinemann, D.; Tauscher, M.; Goehring, G.; Haase, D.; Griesinger, F. & Schlegelberger, B. (2011)
Annals of Hematology, 90 pp. S5-S6.
New york: Springer.
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2011 | Journal Article | Letter Note
Managing individuals with propensity to myeloid malignancies due to germline RUNX1 deficiency
Ripperger, T.; Tauscher, M.; Haase, D.; Griesinger, F.; Schlegelberger, B. & Steinemann, D. (2011)
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 96(12) pp. 1892-1894. DOI: https://doi.org/10.3324/haematol.2011.053710
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2012 | Journal Article
Occurrence of acute lymphoblastic leukemia and juvenile myelomonocytic leukemia in a patient with Noonan syndrome carrying the germline PTPN11 mutation p.E139D
Pauli, S.; Steinemann, D.; Dittmann, K.; Wienands, J. ; Shoukier, M.; Moeschner, M. & Burfeind, P. et al. (2012)
American Journal of Medical Genetics Part A, 158A(3) pp. 652-658. DOI: https://doi.org/10.1002/ajmg.a.34439
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2013 | Journal Article | Research Paper
Parthenogenetic stem cells for tissue-engineered heart repair
Didie, M. ; Christalla, P.; Rubart, M.; Muppala, V. ; Doeker, S.; Unsoeld, B. W. & El-Armouche, A. et al. (2013)
Journal of Clinical Investigation, 123(3) pp. 1285-1298. DOI: https://doi.org/10.1172/JCI66854
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2015 | Journal Article |
Phenotypic and molecular insights into CASK-related disorders in males
Moog, U.; Bierhals, T.; Brand, K.; Bautsch, J.; Biskup, S.; Brune, T. & Denecke, J. et al. (2015)
Orphanet Journal of Rare Diseases, 10 art. 44. DOI: https://doi.org/10.1186/s13023-015-0256-3
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2017 | Conference Abstract
IDENTIFICATION OF A NOVEL GERMLINE MECOM / EVI1 VARIANT THAT RUNS IN A PEDIGREE WITH RADIOULNAR SYNOSTOSIS AND AMEGAKARYOCYTIC THROMBOCYTOPENIA AND PREDISPOSES TO ADULT ONSET MYELOID MALIGNANCY
Ripperger, T.; Hofmann, W.; Koch, J. C.; Shirneshan, K.; Haase, D.; Wulf, G. & Issing, P. R. et al. (2017)
Haematologica, 102 22nd Congress of the European-Hematology-Association, Madrid, SPAIN.
Pavia: Ferrata Storti Foundation.
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2018 | Journal Article
MDS1 and EVI1 complex locus (MECOM): a novel candidate gene for hereditary hematological malignancies
Ripperger, T.; Hofmann, W.; Koch, J. C. ; Shirneshan, K. ; Haase, D. ; Wulf, G. & Issing, P. R. et al. (2018)
Haematologica, 103(2) pp. e55-e58. DOI: https://doi.org/10.3324/haematol.2017.178723
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