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Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS)

2021 . Kerz, J. | Schürmann, P. | Rothämel, T. | Dörk, T. | Klintschar, Michael

Pharmacogenetic association of diabetes-associated genetic risk score with rapid progression of coronary artery calcification following treatment with HMG-CoA-reductase inhibitors —results of the Heinz Nixdorf Recall Study

2021 . Pechlivanis, Sonali | Jung, Dominik | Moebus, Susanne | Lehmann, Nils | Mahabadi, Amir A. | Hoffmann, Per | Erbel, Raimund | Nöthen, Markus M. | Bachmann, Hagen

The need for tumor surveillance of children and adolescents with cancer predisposition syndromes: a retrospective cohort study in a tertiary-care children’s hospital

2021 . Huber, Simon | Schimmel, Mareike | Dunstheimer, Désirée | Nemes, Karolina | Richter, Markus | Streble, Joachim | Vollert, Kurt | Walden, Ulrike | Frühwald, Michael C. | Kuhlen, Michaela

Tooth loss and adiposity: possible role of carnitine transporter (OCTN1/2) polymorphisms in women but not in men

2020 . Meisel, Peter | Pagels, Stefanie | Grube, Markus | Jedlitschky, Gabriele | Völzke, Henry | Kocher, Thomas

Post-mortem genetic investigation of cardiac disease–associated genes in sudden infant death syndrome (SIDS) cases

2020 . Köffer, Jasmin | Scheiper-Welling, Stefanie | Verhoff, Marcel A. | Bajanowski, Thomas | Kauferstein, Silke

EGFR and BRAF mutations in inverted sinonasal papilloma — a more complex landscape?

2020 . Zonnur, Sarah | Erbersdobler, Andreas | Schneider, Bjoern

Need for a precise molecular diagnosis in Beckwith-Wiedemann and Silver-Russell syndrome: what has to be considered and why it is important

2020 . Eggermann, Thomas | Brück, Johanna | Knopp, Cordula | Fekete, György | Kratz, Christian | Tasic, Velibor | Kurth, Ingo | Elbracht, Miriam | Eggermann, Katja | Begemann, Matthias