Invited commentary to: ADAMTS13 deficiency is associated with abnormal distribution of von Willebrand factor multimers in patients with COVID-19 by Tiffany Pascreau et al. Letter t...

por Lämmle, Bernhard, Rossmann, Heidi
Publicado 2021

A Novel Nonsense Mutation of the AGL Gene in a Romanian Patient with Glycogen Storage Disease Type IIIa

por Zimmermann, Anca, Rossmann, Heidi, Bucerzan, Simona, Grigorescu-Sido, Paula
Publicado 2016

Impact of Glutathione Peroxidase-1 Deficiency on Macrophage Foam Cell Formation and Proliferation: Implications for Atherogenesis

por Cheng, Fei, Torzewski, Michael, Degreif, Adriana, Rossmann, Heidi, Canisius, Antje, Lackner, Karl J.
Publicado 2013

Central Venous Access Devices (CVAD) in Pediatric Oncology Patients—A Single-Center Retrospective Study Over More Than 9 Years

por Beck, Olaf, Muensterer, Oliver, Hofmann, Sarah, Rossmann, Heidi, Poplawski, Alicia, Faber, Jörg, Gödeke, Jan
Publicado 2019

Diagnosis of Hereditary TTP Caused by Homozygosity for a Rare Complex ADAMTS13 Allele After Salmonella Infection in a 43-Year-Old Asylum Seeker

por Wendt, Ralph, Kalbitz, Sven, Otto, Felix, Falter, Tanja, Beige, Joachim, Rossmann, Heidi, Lämmle, Bernhard
Publicado 2021

Comment on “Worldwide Distribution of PK Deficiency: the Defect Seems Mainly Concentrated in West African Countries and the United States”

por Barco, Stefano, Adenaeuer, Anke, Trinchero, Alice, Falter, Tanja, Lackner, Karl J., Lämmle, Bernhard, Rossmann, Heidi
Publicado 2021

Differential Inhibition of Platelet Reactivity by Dual Therapy With Aspirin and Low-Dose Rivaroxaban in Peripheral Arterial Disease: A Pilot Study

por Jurk, Kerstin, Rothenaicher, Korbinian F., Groß, Kathrin, Rossmann, Heidi, Weißer, Gerhard, Schmidtmann, Irene, Münzel, Thomas, Espinola-Klein, Christine
Publicado 2022

Gene variants of osteoprotegerin, estrogen-, calcitonin- and vitamin D-receptor genes and serum markers of bone metabolism in patients with Gaucher disease type 1

por Zimmermann, Anca, Popp, Radu A, Rossmann, Heidi, Bucerzan, Simona, Nascu, Ioana, Leucuta, Daniel, Weber, Matthias M, Grigorescu-Sido, Paula
Publicado 2018

Distribution of estimated glomerular filtration rate and determinants of its age dependent loss in a German population-based study

por Waas, Thomas, Schulz, Andreas, Lotz, Johannes, Rossmann, Heidi, Pfeiffer, Norbert, Beutel, Manfred E., Schmidtmann, Irene, Münzel, Thomas, Wild, Philipp S., Lackner, Karl J.
Publicado 2021

Evidence for the utility of cfDNA plasma concentrations to predict disease severity in COVID-19: a retrospective pilot study

por Hoeter, Katharina, Neuberger, Elmo, Fischer, Susanne, Herbst, Manuel, Juškevičiūtė, Ema, Enders, Kira, Rossmann, Heidi, Sprinzl, Martin F., Simon, Perikles, Bodenstein, Marc, Schaefer, Michael
Publicado 2023

Second MAFA Variant Causing a Phosphorylation Defect in the Transactivation Domain and Familial Insulinomatosis

por Fottner, Christian, Sollfrank, Stefanie, Ghiasi, Mursal, Adenaeuer, Anke, Musholt, Thomas, Schad, Arno, Miederer, Matthias, Schadmand-Fischer, Simin, Weber, Matthias M., Lackner, Karl J., Rossmann, Heidi
Publicado 2022

Novel GATA1 Variant Causing a Bleeding Phenotype Associated with Combined Platelet α-/δ-Storage Pool Deficiency and Mild Dyserythropoiesis Modified by a SLC4A1 Variant

por Jurk, Kerstin, Adenaeuer, Anke, Sollfrank, Stefanie, Groß, Kathrin, Häuser, Friederike, Czwalinna, Andreas, Erkel, Josef, Fritsch, Nele, Marandiuc, Dana, Schaller, Martin, Lackner, Karl J., Rossmann, Heidi, Bergmann, Frauke
Publicado 2022

Evaluation of a laboratory-based high-throughput SARS-CoV-2 antigen assay for non-COVID-19 patient screening at hospital admission

por Häuser, Friederike, Sprinzl, Martin F., Dreis, Kim J., Renzaho, Angelique, Youhanen, Simon, Kremer, Wolfgang M., Podlech, Jürgen, Galle, Peter R., Lackner, Karl J., Rossmann, Heidi, Lemmermann, Niels A.
Publicado 2021

Protective behavior and SARS-CoV-2 infection risk in the population – Results from the Gutenberg COVID-19 study

por Baumkötter, Rieke, Yilmaz, Simge, Zahn, Daniela, Fenzl, Katharina, Prochaska, Jürgen H., Rossmann, Heidi, Schmidtmann, Irene, Schuster, Alexander K., Beutel, Manfred E., Lackner, Karl J., Münzel, Thomas, Wild, Philipp S.
Publicado 2022

A novel von Willebrand factor multimer ratio as marker of disease activity in thrombotic thrombocytopenic purpura

por Falter, Tanja, Rossmann, Heidi, de Waele, Laure, Dekimpe, Charlotte, von Auer, Charis, Müller-Calleja, Nadine, Häuser, Friederike, Degreif, Adriana, Marandiuc, Dana, Messmer, Xavier, Sprinzl, Martin, Lackner, Karl J., Jurk, Kerstin, Vanhoorelbeke, Karen, Lämmle, Bernhard
Publicado 2023

No Evidence for Classic Thrombotic Microangiopathy in COVID-19

por Falter, Tanja, Rossmann, Heidi, Menge, Philipp, Goetje, Jan, Groenwoldt, Steffen, Weinmann, Arndt, Sivanathan, Visvakanth, Schulz, Andreas, Lemmermann, Niels A.W., Danckwardt, Sven, Lackner, Karl J., Galle, Peter R., Scharrer, Inge, Lämmle, Bernhard, Sprinzl, Martin F.
Publicado 2021

Hypermethylation of RAD9A intron 2 in childhood cancer patients, leukemia and tumor cell lines suggest a role for oncogenic transformation

por Galetzka, Danuta, Böck, Julia, Wagner, Lukas, Dittrich, Marcus, Sinizyn, Olesja, Ludwig, Marco, Rossmann, Heidi, Spix, Claudia, Radsak, Markus, Scholz-Kreisel, Peter, Mirsch, Johanna, Linke, Matthias, Brenner, Walburgis, Marron, Manuela, Poplawski, Alicia, Haaf, Thomas, Schmidberger, Heinz, Prawitt, Dirk
Publicado 2022

Pathogenic lipid‐binding antiphospholipid antibodies are associated with severity of COVID‐19

por Hollerbach, Anne, Müller‐Calleja, Nadine, Pedrosa, Denise, Canisius, Antje, Sprinzl, Martin F., Falter, Tanja, Rossmann, Heidi, Bodenstein, Marc, Werner, Christian, Sagoschen, Ingo, Münzel, Thomas, Schreiner, Oliver, Sivanathan, Visvakanth, Reuter, Michael, Niermann, Johannes, Galle, Peter R., Teyton, Luc, Ruf, Wolfram, Lackner, Karl J.
Publicado 2021

Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility

por Zeller, Tanja, Wild, Philipp, Szymczak, Silke, Rotival, Maxime, Schillert, Arne, Castagne, Raphaele, Maouche, Seraya, Germain, Marine, Lackner, Karl, Rossmann, Heidi, Eleftheriadis, Medea, Sinning, Christoph R., Schnabel, Renate B., Lubos, Edith, Mennerich, Detlev, Rust, Werner, Perret, Claire, Proust, Carole, Nicaud, Viviane, Loscalzo, Joseph, Hübner, Norbert, Tregouet, David, Münzel, Thomas, Ziegler, Andreas, Tiret, Laurence, Blankenberg, Stefan, Cambien, François
Publicado 2010

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

por Nuzhat, Nafisa, Van Schil, Kristof, Liakopoulos, Sandra, Bauwens, Miriam, Rey, Alfredo Dueñas, Käseberg, Stephan, Jäger, Melanie, Willer, Jason R., Winter, Jennifer, Truong, Hanh M., Gruartmoner, Nuria, Van Heetvelde, Mattias, Wolf, Joachim, Merget, Robert, Grasshoff-Derr, Sabine, Van Dorpe, Jo, Hoorens, Anne, Stöhr, Heidi, Mansard, Luke, Roux, Anne-Françoise, Langmann, Thomas, Dannhausen, Katharina, Rosenkranz, David, Wissing, Karl M., Van Lint, Michel, Rossmann, Heidi, Häuser, Friederike, Nürnberg, Peter, Thiele, Holger, Zechner, Ulrich, Pearring, Jillian N., De Baere, Elfride, Bolz, Hanno J.
Publicado 2023