Klaus Lechner was affiliated with the Medical University of Vienna in Austria during their scientific career. Their research contributions are documented primarily through publications in collaboration with several fellow researchers.
Among their published work, the notable paper titled "Molecular defect (Gla+ 14----Lys) and its functional consequences in a hereditary factor X deficiency (factor X Vorarlberg)" was published in 2021. This work appeared in the UNC Libraries and involved research into molecular defects associated with hereditary blood coagulation disorders.
The frequent co-authors who collaborated with Klaus Lechner on scientific output include:
The publication venues for their work are characterized by a presence in:
Lechner's research career, while primarily linked to this documented study, shows cooperation across specialists in hematology and molecular biology fields, reflecting interdisciplinary engagement within medical sciences.
Stephen G. O'Brien;François Guilhot;Richard A. Larson;Insa Gathmann
Francesco Rodeghiero;Roberto Stasi;Terry Gernsheimer;Marc Michel
Paul A. Kyrle;Erich Minar;Mirko Hirschl;Christine Bialonczyk
David Green;Klaus Lechner
Peter Valent;Eva Spanblochl;Wolfgang R. Sperr;Christian Sillaber
Robert Pirker;Josef Wallner;Klaus Geissler;Werner Linkesch
B. Habermalz;S. Sauerland;G. Decker;B. Delaitre
Klaus Lechner;Ulrich Jäger
Gerhard Heil;Dieter Hoelzer;Miguel A. Sanz;Klaus Lechner
S. Eichinger;A. Stümpflen;M. Hirschl;C. Bialonczyk
Andrea Berer;Johannes Stöckl;Otto Majdic;Thomas Wagner
P Valent;LK Ashman;W Hinterberger;F Eckersberger
P Valent;G Schmidt;J Besemer;P Mayer
Hans-Peter Horny;Christian Sillaber;David Menke;Edwin Kaiserling
P Valent;J Besemer;M Muhm;O Majdic
S Eichinger;I Pabinger;A Stümpflen;M Hirschl
I. Pabinger;H. Grafenhofer;A. Kaider;P. A. Kyrle
Peter Valent;Cem Akin;Wolfgang R. Sperr;Hans P. Horny
S Panzer;G Kronik;K Lechner;P Bettelheim
Ingrid Pabinger;Helga Grafenhofer;Paul A. Kyrle;Peter Quehenberger
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