Items where Author is "Thol, F."
![]() | Up a level |
Article
Schlenk, R. F. and Weber, D. and Herr, W. and Wulf, G. and Salih, H. R. and Derigs, H. G. and Kuendgen, A. and Ringhoffer, M. and Hertenstein, B. and Martens, U. M. and Griesshammer, M. and Bernhard, H. and Krauter, J. and Girschikofsky, M. and Wolf, D. and Lange, E. and Westermann, J. and Koller, E. and Kremers, S. and Wattad, M. and Heuser, M. and Thol, F. and Goehring, G. and Haase, D. and Teleanu, V and Gaidzik, V and Benner, A. and Doehner, K. and Ganser, A. and Paschka, P. and Doehner, H. (2019) Randomized phase-II trial evaluating induction therapy with idarubicin and etoposide plus sequential or concurrent azacitidine and maintenance therapy with azacitidine. LEUKEMIA, 33 (8). pp. 1923-1933. ISSN 0887-6924, 1476-5551
Other
Beier, F. and Kirschner, M. and Bouillon, A-S and Halfmeyer, I and Ferreira, Ventura M. and Kricheldorf, K. and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Radsak, M. and Ayuk, F. A. and Corbacioglu, S. and Hoechsmann, B. and Wilk, C. M. and Hinze, C. and Chromik, J. and Egle, A. and Bittenbring, J. T. and Eggermann, T. and Kurth, I and Koschmieder, S. and Schemionek, M. and Isfort, S. and Panse, J. and Bruemmendorf, T. H. (2018) Identification of patients with classical and/or cryptic dyskeratosis congenita (DKC) by telomere length screening using different percentiles - results from the Aachen telomeropathy registry. KARGER, BASEL.
Kirschner, M. and Bouillon, A. -S. and Ferreira, Ventura M. and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Blau, W. and Ayuk, F. A. and Corbacioglu, S. and Schrezenmeier, H. and Manz, M. and Ebel, L. and Koschmieder, S. and Schemionek, M. and Isfort, S. and Panse, J. and Brmmendorf, T. H. and Beier, F. (2017) Heterozygous RTEL1 variants are associated with bone marrow failure in cryptic dyskeratosis congenita - first results from the Aachen telomere registry. KARGER, BASEL.
Beier, F. and Kirschner, M. and Bouillon, A. -S. and Halfmeyer, I. and Ferreira, M. S. Ventura and Maurer, A. and Wilop, S. and Thol, F. and Roeth, A. and Platzbecker, U. and Blau, W. and Ayuk, F. A. and Corbacioglu, S. and Schrezenmeier, H. and Manz, M. G. and Eggermann, T. and Zerres, K. and Koschmieder, S. and Schmemionek, M. and Isfort, S. and Panse, J. and Bruemmendorf, T. H. (2017) TELOMERE LENGTH SCREENING TRIGGERED BY CLINICAL SUSPICION FOR CLASSICAL AND/OR CRYPTIC DYSKERATOSIS CONGENITA - PROSPECTIVE RESULTS FROM THE AACHEN TELOMEROPATHY REGISTRY. FERRATA STORTI FOUNDATION, PAVIA.

