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Structured, Harmonized, and Interoperable Integration of Clinical Routine Data to Compute Heart Failure Risk Scores.
Sommer KK, Amr A, Bavendiek U, Beierle F, Brunecker P, Dathe H, Eils J, Ertl M, Fette G, Gietzelt M, Heidecker B, Hellenkamp K, Heuschmann P, Hoos JDE, Kesztyüs T, Kerwagen F, Kindermann A, Krefting D, Landmesser U, Marschollek M, Meder B, Merzweiler A, Prasser F, Pryss R, Richter J, Schneider P, Störk S, Dieterich C. Sommer KK, et al. Among authors: amr a. Life (Basel). 2022 May 18;12(5):749. doi: 10.3390/life12050749. Life (Basel). 2022. PMID: 35629415 Free PMC article.
Personalized Computer Simulation of Diastolic Function in Heart Failure.
Amr A, Kayvanpour E, Sedaghat-Hamedani F, Passerini T, Mihalef V, Lai A, Neumann D, Georgescu B, Buss S, Mereles D, Zitron E, Posch AE, Würstle M, Mansi T, Katus HA, Meder B. Amr A, et al. Genomics Proteomics Bioinformatics. 2016 Aug;14(4):244-52. doi: 10.1016/j.gpb.2016.04.006. Epub 2016 Jul 29. Genomics Proteomics Bioinformatics. 2016. PMID: 27477449 Free PMC article.
Clinical genetics and outcome of left ventricular non-compaction cardiomyopathy.
Sedaghat-Hamedani F, Haas J, Zhu F, Geier C, Kayvanpour E, Liss M, Lai A, Frese K, Pribe-Wolferts R, Amr A, Li DT, Samani OS, Carstensen A, Bordalo DM, Müller M, Fischer C, Shao J, Wang J, Nie M, Yuan L, Haßfeld S, Schwartz C, Zhou M, Zhou Z, Shu Y, Wang M, Huang K, Zeng Q, Cheng L, Fehlmann T, Ehlermann P, Keller A, Dieterich C, Streckfuß-Bömeke K, Liao Y, Gotthardt M, Katus HA, Meder B. Sedaghat-Hamedani F, et al. Among authors: amr a. Eur Heart J. 2017 Dec 7;38(46):3449-3460. doi: 10.1093/eurheartj/ehx545. Eur Heart J. 2017. PMID: 29029073
The chameleon of cardiology: cardiac sarcoidosis before and after heart transplantation.
Sedaghat-Hamedani F, Kayvanpour E, Hamed S, Frankenstein L, Riffel J, Gi WT, Amr A, Shirvani Samani O, Haas J, Miersch T, Herpel E, Kreusser MM, Ehlermann P, Katus HA, Meder B. Sedaghat-Hamedani F, et al. Among authors: amr a. ESC Heart Fail. 2020 Apr;7(2):692-696. doi: 10.1002/ehf2.12581. Epub 2019 Dec 5. ESC Heart Fail. 2020. PMID: 31802644 Free PMC article.
Genotype Complements the Phenotype: Identification of the Pathogenicity of an LMNA Splice Variant by Nanopore Long-Read Sequencing in a Large DCM Family.
Sedaghat-Hamedani F, Rebs S, Kayvanpour E, Zhu C, Amr A, Müller M, Haas J, Wu J, Steinmetz LM, Ehlermann P, Streckfuss-Bömeke K, Frey N, Meder B. Sedaghat-Hamedani F, et al. Among authors: amr a. Int J Mol Sci. 2022 Oct 13;23(20):12230. doi: 10.3390/ijms232012230. Int J Mol Sci. 2022. PMID: 36293084 Free PMC article.
214 results