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Anzahl der Publikationen: 5
Zeitschriftenartikel
Schopohl, D.; Bidlingmaier, C.; Herzig, D.; Klamroth, R.; Kurnik, K.; Rublee, D.; Schramm, W.; Schwarzkopf, L. und Berger, K.
(2018):
Prospects for research in haemophilia with real‐world data—An analysis of German registry and secondary data.
In: Haemophilia, Bd. 24, Nr. 4: S. 584-594
Oldenburg, J.; Khair, K.; Mazzucconi, M. G.; Parra, R.; Kurnik, K.; Huth-Kühne, A.; Klamroth, R.; Steinitz-Trost, K. N.; Brondke, H. und Gringeri, A.
(2017):
Real World Prospective Data on Bleeding Frequency in 1,000 Patients with Hemophilia a - is the Goal of Zero Bleeds Achievable?
In: Haemophilia, Bd. 23: S. 16-17
Berger, K.; Schopohl, D.; Lowe, G.; Holme, P. A.; Tait, R. C.; Combescure, C.; Rauchensteiner, S. und Klamroth, R.
(2016):
How to compare cardiovascular disease and risk factors in elderly patients with haemophilia with the general population.
In: Haemophilia, Bd. 22, Nr. 5, E406-E416
Huth-Kuehne, A.; Klamroth, R.; Khair, K.; Kurnik, K.; Mazzucconi, M. G.; Parra, R.; Tsakiris, D. A.; Franch, L. Abad; Brondke, H.; Steinitz-Trost, K.; Gringeri, A. und Oldenburg, J.
(2016):
Striving for a Bleed Free World - An Interim Analysis from the AHEAD Study.
In: Haemophilia, Bd. 22: S. 62
Berger, K.; Eichler, H.; Escuriola-Ettinghausen, C.; Holstein, K.; Klamroth, R.; Königs, C.; Kurnik, K.; Oldenburg, J.; Scholz, U.; Schramm, W. und Tiede, A.
(2016):
Haemophilia care: Which outcomes should be determined in clinical routine care and are adequate for access requirements.
In: Oncology Research and Treatment, Bd. 39: S. 153