Výsledky vyhledávání - Ralf Knöfler
- Zobrazuji výsledky 1 - 3 z 3
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1
Risk factors for recurrent venous thromboembolism in the European collaborative paediatric database on cerebral venous thrombosis: a multicentre cohort study Autor Gili Kenet, Fenella J. Kirkham, Thomas Niederstadt, Achim Heinecke, Dawn E. Saunders, Monika Stoll, Benjamin Brenner, Christoph Bidlingmaier, Christine Heller, Ralf Knöfler, R. Schobeß, Barbara Zieger, Guillaume Sébire, Ulrike Nowak‐Göttl
Vydáno 2007Artigo -
2
Variants in exons 5 and 6 of ACTB cause syndromic thrombocytopenia Autor Sharissa L. Latham, Nadja Ehmke, P. Reinke, Manuel H. Taft, Dorothee Eicke, Theresia Reindl, Werner Stenzel, Michael J. Lyons, Michael J. Friez, Jennifer A. Lee, Ramona Hecker, Michael C. Frühwald, Kerstin Becker, Teresa Neuhann, Denise Horn, Evelin Schröck, Indra Niehaus, Katharina Sarnow, Konrad Grützmann, Luzie Gawehn, Barbara Klink, Andreas Rump, Christine Chaponnier, Constança Figueiredo, Ralf Knöfler, Dietmar J. Manstein, Nataliya Di Donato
Vydáno 2018Artigo -
3
Distinct pathways for genetic and epigenetic predisposition in familial and bilateral Wilms tumor Autor Jenny Wegert, Silke Appenzeller, Taryn D. Treger, Heike Streitenberger, Barbara Ziegler, Sabrina Bausenwein, Christian Vokuhl, Conor Parks, Eva Jüttner, Susanne Gramlich, Karen Ernestus, Sheena Warman, Jörg Fuchs, Jochen Hubertus, Dietrich von Schweinitz, Birgit Fröhlich, Norbert Jorch, Ralf Knöfler, Carsten Friedrich, Selim Corbacioglu, Michael C. Frühwald, Arnulf Pekrun, Dominik T. Schneider, Jörg Faber, Jana Stursberg, Markus Metzler, Nils Welter, Kathy Pritchard‐Jones, Norbert Graf, Rhoikos Furtwängler, Sam Behjati, Manfred Gessler
Vydáno 2025Artigo
Vyhledávací nástroje:
Související témata
Medicine
Biology
Gene
Genetics
Allele
Atrial fibrillation
Beckwith–Wiedemann syndrome
Bioinformatics
CDKN2A
CHEK2
Cancer
Cancer research
Cohort
Cohort study
Computational biology
Confidence interval
DNA methylation
Epigenetics
Exome sequencing
Exon
Gene expression
Genetic predisposition
Germline
Germline mutation
Hazard ratio
Heparin
Internal medicine
Loss of heterozygosity
Low molecular weight heparin
Mutation