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Entries of Koschmieder, Steffen on the publication server
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Number of items: 3.
2023
Tometten, Mareike, Kirschner, Martin, Meyer, Robert, Begemann, Matthias, Halfmeyer, Insa, Vieri, Margherita, Kricheldorf, Kim, Maurer, Angela, Platzbecker, Uwe, Radsak, Markus, Schafhausen, Philippe, Corbacioglu, Selim, Höchsmann, Britta, Matthias Wilk, C., Hinze, Claas, Chromik, Jörg, Heuser, Michael, Kreuter, Michael, Koschmieder, Steffen, Panse, Jens, Isfort, Susanne, Kurth, Ingo, Brümmendorf, Tim H. and Beier, Fabian
(2023)
Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria.
HemaSphere 7 (5), e874.
Fulltext not available.
2021
Kirschner, Martin, do Ó Hartmann, Nicole, Parmentier, Stefani, Hart, Christina, Henze, Larissa, Bisping, Guido, Griesshammer, Martin, Langer, Florian, Pabinger-Fasching, Ingrid, Matzdorff, Axel, Riess, Hanno and Koschmieder, Steffen
(2021)
Primary Thromboprophylaxis in Patients with Malignancies: Daily Practice Recommendations by the Hemostasis Working Party of the German Society of Hematology and Medical Oncology (DGHO), the Society of Thrombosis and Hemostasis Research (GTH), and the Austrian Society of Hematology and Oncology (ÖGHO).
Cancers 13 (12), p. 2905.
Fulltext not available.
2018
Kirschner, Martin, Maurer, Angela, Wlodarski, Marcin W., Ventura Ferreira, Monica S., Bouillon, Anne-Sophie, Halfmeyer, Insa, Blau, Wolfgang, Kreuter, Michael, Rosewich, Martin, Corbacioglu, Selim, Beck, Joachim, Schwarz, Michaela, Bittenbring, Jörg, Radsak, Markus P., Wilk, Christian Matthias 
, Koschmieder, Steffen, Begemann, Matthias, Kurth, Ingo , Schemionek, Mirle, Brümmendorf, Tim H. and Beier, Fabian
(2018)
Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.
Leukemia 32 (8), pp. 1762-1767.
Fulltext not available.
, Koschmieder, Steffen, Begemann, Matthias, Kurth, Ingo , Schemionek, Mirle, Brümmendorf, Tim H. and Beier, Fabian
(2018)
Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita.
Leukemia 32 (8), pp. 1762-1767.
Fulltext not available.
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