P. Aidery

发表

Pressure Overload by Transverse Aortic Constriction Induces Maladaptive Hypertrophy in a Titin-Truncated Mouse Model

M. Gawaz, R. Harvey, M. Feneley, 2015, BioMed research international.

Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.

H. Katus, Dierk Thomas, P. Schweizer, 2011, Biochimica et biophysica acta.

Resumption of Antiplatelet Therapy after Major Bleeding

K. Huber, J. Collet, R. Storey, 2022, Thrombosis and Haemostasis.

Identification and functional characterization of the novel human ether-a-go-go-related gene (hERG) R744P mutant associated with hereditary long QT syndrome 2.

H. Katus, Dierk Thomas, P. Schweizer, 2012, Biochemical and biophysical research communications.

Personalized Medicine Approach in a DCM Patient with LMNA Mutation Reveals Dysregulation of mTOR Signaling

M. V. van Zandvoort, K. Klingel, K. Witte, 2022, Journal of personalized medicine.

Autoimmune Heparin-Induced Thrombocytopenia after Transcatheter Aortic Valve Implantation: Successful Treatment with Adjunct High-Dose Intravenous Immunoglobulin

O. Borst, M. Gawaz, R. Riessen, 2019, TH Open.

Inhibition of miR-208b improves cardiac function in titin-based dilated cardiomyopathy.

M. Gawaz, C. Sticht, R. Kandolf, 2017, International journal of cardiology.

Impaired ion channel function related to a common KCNQ1 mutation - implications for risk stratification in long QT syndrome 1.

H. Katus, Dierk Thomas, P. Schweizer, 2012, Gene.

Dysregulated IER3 Expression is Associated with Enhanced Apoptosis in Titin-Based Dilated Cardiomyopathy

M. Gawaz, Qifeng Zhou, S. Labeit, 2017, International journal of molecular sciences.

Thrombozytenaggregationshemmung nach Koronarintervention (PCI)

P. Aidery, T. Geisler, 2023, Kardiologie up2date.

Biophysical properties of mutant KCNQ1 S277L channels linked to hereditary long QT syndrome with phenotypic variability.

H. Katus, Dierk Thomas, P. Schweizer, 2011, Biochimica et biophysica acta.