Edgar Jost
3PUBLICATIONS
13CO-AUTHORS
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Publications (3)
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|Mar 14, 2022
Novel homozygous nonsense mutation in the P5'N-1 coding gene as an alternative cause for hereditary anemia with basophilic stippling.Martin Kirschner, Inga Rebecca Heinen, Steffen Koschmieder
|May 05, 2017
Perioperative intravenous immunoglobulin treatment in a patient with severe acquired von Willebrand syndrome: case report and review of the literature.Eva Jennes, Dorothee Guggenberger, Rainer Zotz
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Frequent Collaborators
1 joint publications
Inga Rebecca Heinen
1 joint publications
Thomas Eggermann
1 joint publications
Ingo Kurth
1 joint publications
Noëlle Sieg
1 joint publications
Ruth Flümann
1 joint publications
Jan-Michel Heger
1 joint publications
Peter Borchmann
1 joint publications
Boris Böll
1 joint publications
Udo Holtick
1 joint publications
Michael Hallek