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Edgar Jost

2PUBLICATIONS

3CO-AUTHORS

Neurology and neuromuscular diseasesHaematology

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Publications (2)

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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

Frequent Collaborators

1 joint publications

Inga Rebecca Heinen

1 joint publications

Thomas Eggermann

1 joint publications

Ingo Kurth

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