Hydrogen accumulation and diffusion in cylindrical-shaped pipeline steels with coating defects von Auinger, Michael, Büchler, Markus, Schöneich, Hanns-Georg, Gierl-Mayer, Christian, Danninger, Herbert

Volltext

An Industry Experience with Data Sharing von Schmidt, Hendrik, Caldwell, Brent, Mollet, Annette, Leimer, Hanns-Georg, Szucs, Thomas

Volltext

Liquid profiling – circulating nucleic acid diagnostics gains momentum von Holdenrieder, Stefan, Klein, Hanns-Georg, Winter, Christof

Volltext

Performance evaluation of the Elecsys PIVKA‐II and Elecsys AFP assays for hepatocellular carcinoma diagnosis von Chan, Henry L Y, Vogel, Arndt, Berg, Thomas, De Toni, Enrico N, Kudo, Masatoshi, Trojan, Jörg, Eiblmaier, Anja, Klein, Hanns‐Georg, Hegel, Johannes Kolja, Sharma, Ashish, Madin, Kairat, Rolny, Vinzent, Lisy, Marcus‐Rene, Piratvisuth, Teerha

Volltext

Understanding attitudes and behaviors towards cell-free DNA-based noninvasive prenatal testing (NIPT): A survey of European health-care providers von Benachi, Alexandra, Caffrey, Jessica, Calda, Pavel, Carreras, Elena, Jani, Jacques C., Kilby, Mark D., Klein, Hanns-Georg, Rizzo, Giuseppe, Yaron, Yuval

Volltext

Pharmakogenetik und Therapeutisches Drug Monitoring: Diagnostische Bausteine fur die individualisierte Therapie von Klein, Hanns-Georg, Haen, Ekkehard

Volltext

Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis von Büscher, Anja K., Celebi, Nora, Hoyer, Peter F., Klein, Hanns-Georg, Weber, Stefanie, Hoefele, Julia

Volltext

Identification of 47 novel mutations in patients with Alport syndrome and thin basement membrane nephropathy von Weber, Stefanie, Strasser, Katja, Rath, Sabine, Kittke, Achim, Beicht, Sonja, Alberer, Martin, Lange-Sperandio, Bärbel, Hoyer, Peter F., Benz, Marcus R., Ponsel, Sabine, Weber, Lutz T., Klein, Hanns-Georg, Hoefele, Julia

Volltext

German Society for Clinical Chemistry and Laboratory Medicine – areas of expertise: Division reports from the German Congress of Laboratory Medicine 2022 in Mannheim, 13–14 October... von Nauck, Matthias, Holdenrieder, Stefan, Klein, Hanns-Georg, Findeisen, Peter, Winter, Christof, Ceglarek, Uta, Petersmann, Astrid, Klouche, Mariam, Lichtinghagen, Ralf, Biemann, Ronald, Adler, Jakob, Streichert, Thomas, von Meyer, Alexander, Wieland, Eberhard, Hofmann, Walter, Aufenanger, Johannes, Orth, Matthias, Shipkova, Maria, Bidlingmaier, Martin, Birschmann, Ingvild, Blüthner, Martin, Conrad, Karsten, Luppa, Peter B., Kiehntopf, Michael, Bietenbeck, Andreas, Baum, Hannsjörg, Renz, Harald

Volltext

Truncating Wilms Tumor Suppressor Gene 1 Mutation in an XX Female with Adult-Onset Focal Segmental Glomerulosclerosis and Streak Ovaries: A Case Report von Hoefele, Julia, Kemper, Markus J., Schoenermarck, Ulf, Mueller, Susanna, Klein, Hanns-Georg, Lemke, Anja

Volltext

Development and clinical validation of a novel algorithmic score (GAAD) for detecting HCC in prospective cohort studies von Piratvisuth, Teerha, Hou, Jinlin, Tanwandee, Tawesak, Berg, Thomas, Vogel, Arndt, Trojan, Jörg, De Toni, Enrico N, Kudo, Masatoshi, Eiblmaier, Anja, Klein, Hanns-Georg, Hegel, Johannes Kolja, Madin, Kairat, Kroeniger, Konstantin, Sharma, Ashish, Chan, Henry L Y

Volltext

Strong association of a common dihydropyrimidine dehydrogenase gene polymorphism with fluoropyrimidine-related toxicity in cancer patients von Gross, Eva, Busse, Birgit, Riemenschneider, Matthias, Neubauer, Steffi, Seck, Katharina, Klein, Hanns-Georg, Kiechle, Marion, Lordick, Florian, Meindl, Alfons

Volltext

Expanding the mutation spectrum for Fraser syndrome: Identification of a novel heterozygous deletion in FRAS1 von Hoefele, Julia, Wilhelm, Christian, Schiesser, Monika, Mack, Reinhold, Heinrich, Uwe, Weber, Lutz T., Biskup, Saskia, Daumer-Haas, Cornelia, Klein, Hanns-Georg, Rost, Imma

Volltext

Genetic heterogeneity of cytogenetically normal AML with mutations of CEBPA von Konstandin, Nikola P., Pastore, Friederike, Herold, Tobias, Dufour, Annika, Rothenberg-Thurley, Maja, Hinrichsen, Tanja, Ksienzyk, Bianka, Tschuri, Sebastian, Schneider, Stephanie, Hoster, Eva, Berdel, Wolfgang E., Woermann, Bernhard J., Sauerland, Maria C., Braess, Jan, Bohlander, Stefan K., Klein, Hanns-Georg, Hiddemann, Wolfgang, Metzeler, Klaus H., Spiekermann, Karsten

Volltext

Next generation sequencing as a useful tool in the diagnostics of mosaicism in Alport syndrome von Beicht, Sonja, Strobl-Wildemann, Gertrud, Rath, Sabine, Wachter, Oliver, Alberer, Martin, Kaminsky, Elke, Weber, Lutz T., Hinrichsen, Tanja, Klein, Hanns-Georg, Hoefele, Julia

Volltext

Novel KCNH1 Mutations Associated with Epilepsy: Broadening the Phenotypic Spectrum of KCNH1 -Associated Diseases von von Wrede, Randi, Jeub, Monika, Ariöz, Idil, Elger, Christian E, von Voss, Hubertus, Klein, Hanns-Georg, Becker, Albert J, Schoch, Susanne, Surges, Rainer, Kunz, Wolfram S

Volltext

Lessons From the EThIGII Trial: Proper Putative Benefit Assessment of Low-Molecular-Weight Heparin Treatment in M2/ANXA5 Haplotype Carriers von Rogenhofer, Nina, Markoff, Arseni, Wagner, Annett, Klein, Hanns-Georg, Petroff, David, Schleussner, Ekkehard, Thaler, Christian J.

Volltext

Novel PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease (ADPKD) von Hoefele, Julia, Mayer, Karin, Scholz, Manuela, Klein, Hanns-Georg

Volltext

FBN2 gene: new mutations, locus-specific database (Universal Mutation Database FBN2), and genotype-phenotype correlations von Frédéric, Melissa Yana, Monino, Christine, Marschall, Christoph, Hamroun, Dalil, Faivre, Laurence, Jondeau, Guillaume, Klein, Hanns-Georg, Neumann, Luitgard, Gautier, Elodie, Binquet, Christine, Maslen, Cheryl, Godfrey, Maurice, Gupta, Prateek, Milewicz, Dianna, Boileau, Catherine, Claustres, Mireille, Béroud, Christophe, Collod-Béroud, Gwenaëlle

Volltext

Blood oxygenation level-dependent magnetic resonance imaging of the skeletal muscle in patients with peripheral arterial occlusive disease von LEDERMANN, Hans-Peter, SCHULTE, Anja-Carina, HEIDECKER, Hanns-Georg, ASCHWANDEN, Markus, JÄGER, Kurt A, SCHEFFLER, Klaus, STEINBRICH, Wolfgang, BILECEN, Deniz

Volltext