Paroxysmal nocturnal hemoglobinuria (PNH): higher sensitivity and validity in diagnosis and serial monitoring by flow cytometric analysis of reticulocytes

por Höchsmann, Britta, Rojewski, Markus, Schrezenmeier, Hubert
Publicado 2011

Relationship of paroxysmal nocturnal hemoglobinuria (PNH) granulocyte clone size to disease burden and risk of major vascular events in untreated patients: results from the Interna...

por Dingli, David, Maciejewski, Jaroslaw P., Larratt, Loree, Go, Ronald S., Höchsmann, Britta, Zu, Ke, Gustovic, Philippe, Kulagin, Alexander D.
Publicado 2023

Deregulation of Factor H by Factor H-Related Protein 1 Depends on Sialylation of Host Surfaces

por Dopler, Arthur, Stibitzky, Selina, Hevey, Rachel, Mannes, Marco, Guariento, Mara, Höchsmann, Britta, Schrezenmeier, Hubert, Ricklin, Daniel, Schmidt, Christoph Q.
Publicado 2021

Development of a disease-specific quality of life questionnaire for patients with aplastic anemia and/or paroxysmal nocturnal hemoglobinuria (QLQ-AA/PNH)—report on phases I and II...

por Groth, Martha, Singer, Susanne, Niedeggen, Cathrin, Petermann-Meyer, Andrea, Röth, Alexander, Schrezenmeier, Hubert, Höchsmann, Britta, Brümmendorf, Tim H., Panse, Jens
Publicado 2016

Design and development of a disease-specific quality of life tool for patients with aplastic anaemia and/or paroxysmal nocturnal haemoglobinuria (QLQ-AA/PNH)—a report on phase III...

por Niedeggen, Cathrin, Singer, Susanne, Groth, Martha, Petermann-Meyer, Andrea, Röth, Alexander, Schrezenmeier, Hubert, Höchsmann, Britta, Brümmendorf, Tim H., Panse, Jens
Publicado 2019

Different Levels of Incomplete Terminal Pathway Inhibition by Eculizumab and the Clinical Response of PNH Patients

por Harder, Markus J., Höchsmann, Britta, Dopler, Arthur, Anliker, Markus, Weinstock, Christof, Skerra, Arne, Simmet, Thomas, Schrezenmeier, Hubert, Schmidt, Christoph Q.
Publicado 2019

Risk factors for thromboembolic events in patients with paroxysmal nocturnal hemoglobinuria (PNH): a nested case–control study in the International PNH Registry

por Höchsmann, Britta, Peffault de Latour, Regis, Hill, Anita, Röth, Alexander, Devos, Timothy, Patriquin, Christopher J., Chou, Wen-Chien, Jain, Deepak, Zu, Ke, Wu, Chuntao, Lee, Jong Wook
Publicado 2023

First line treatment of aplastic anemia with thymoglobuline in Europe and Asia: Outcome of 955 patients treated 2001‐2012

por Bacigalupo, Andrea, Oneto, Rosi, Schrezenmeier, Hubert, Hochsmann, Britta, Dufour, Carlo, Kojima, Seiji, Zhu, Xiaofan, Chen, Xiaojuan, Issaragrisil, Surapol, Chuncharunee, Suporn, Jeong, Dae Chul, Giammarco, Sabrina, Van Lint, Maria Teresa, Zheng, Yizhou, Vallejo, Carlos
Publicado 2018

DNA methylation in PRDM8 is indicative for dyskeratosis congenita

por Weidner, Carola I., Lin, Qiong, Birkhofer, Carina, Gerstenmaier, Uwe, Kaifie, Andrea, Kirschner, Martin, Bruns, Heiko, Balabanov, Stefan, Trummer, Arne, Stockklausner, Clemens, Höchsmann, Britta, Schrezenmeier, Hubert, Wlodarski, Marcin, Panse, Jens, Brümmendorf, Tim H., Beier, Fabian, Wagner, Wolfgang
Publicado 2016

Constitutional PIGA mutations cause a novel subtype of hemochromatosis in patients with neurologic dysfunction

por Muckenthaler, Lena, Marques, Oriana, Colucci, Silvia, Kunz, Joachim, Fabrowski, Piotr, Bast, Thomas, Altamura, Sandro, Höchsmann, Britta, Schrezenmeier, Hubert, Langlotz, Monika, Richter-Pechanska, Paulina, Rausch, Tobias, Hofmeister-Mielke, Nicole, Gunkel, Nikolas, Hentze, Matthias W., Kulozik, Andreas E., Muckenthaler, Martina U.
Publicado 2022

Long-term outcome of a randomized controlled study in patients with newly diagnosed severe aplastic anemia treated with antithymocyte globulin and cyclosporine, with or without gra...

por Tichelli, André, de Latour, Régis Peffault, Passweg, Jakob, Knol-Bout, Cora, Socié, Gérard, Marsh, Judith, Schrezenmeier, Hubert, Höchsmann, Britta, Bacigalupo, Andrea, Samarasinghe, Sujith, Rovó, Alicia, Kulasekararaj, Austin, Röth, Alexander, Eikema, Dirk-Jan, Bosman, Paul, Bader, Peter, Risitano, Antonio, Dufour, Carlo
Publicado 2020

Identification of Adult Patients With Classical Dyskeratosis Congenita or Cryptic Telomere Biology Disorder by Telomere Length Screening Using Age-modified Criteria

por 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., Beier, Fabian
Publicado 2023