Autor Steinemann, Doris

• 2011 | Konferenzbeitrag (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.
  ​Details  WoS 

• 2011 | Zeitschriftenartikel | 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 
  ​Details  DOI  PMID  PMC  WoS 

• 2012 | Zeitschriftenartikel
  ​ ​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. u.a.​ (2012) 
  American Journal of Medical Genetics Part A, 158A(3) pp. 652​-658​.​ DOI: https://doi.org/10.1002/ajmg.a.34439 
  ​Details  DOI  PMID  PMC  WoS 

• 2013 | Zeitschriftenartikel | 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.  u.a.​ (2013) 
  Journal of Clinical Investigation, 123(3) pp. 1285​-1298​.​ DOI: https://doi.org/10.1172/JCI66854 
  ​Details  DOI  PMID  PMC  WoS 

• 2015 | Zeitschriftenartikel | 
  ​ ​Phenotypic and molecular insights into CASK-related disorders in males​
  Moog, U.; Bierhals, T.; Brand, K.; Bautsch, J.; Biskup, S.; Brune, T. & Denecke, J. u.a.​ (2015) 
  Orphanet Journal of Rare Diseases, 10 art. 44​.​ DOI: https://doi.org/10.1186/s13023-015-0256-3 
  ​Details  DOI  PMID  PMC  WoS 

• 2017 | Konferenzbeitrag (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. u.a.​ (2017)
  Haematologica, 102 ​22nd Congress of the European-Hematology-Association​, Madrid, SPAIN.
  Pavia​: Ferrata Storti Foundation.
  ​Details  WoS 

• 2018 | Zeitschriftenartikel
  ​ ​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. u.a.​ (2018) 
  Haematologica, 103(2) pp. e55​-e58​.​ DOI: https://doi.org/10.3324/haematol.2017.178723 
  ​Details  DOI 

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