Zobrazeno 1 - 10
of 266
pro vyhledávání: '"Frank Weidemann"'
Autor:
Mengjia Chen, Dan Liu, Frank Weidemann, Björn Daniel Lengenfelder, Georg Ertl, Kai Hu, Stefan Frantz, Peter Nordbeck
Publikováno v:
ESC Heart Failure, Vol 8, Iss 6, Pp 5248-5258 (2021)
Abstract Aims This study aimed to identify echocardiographic determinants of left ventricular thrombus (LVT) formation after acute anterior myocardial infarction (MI). Methods and results This case–control study comprised 55 acute anterior MI patie
Externí odkaz:
https://doaj.org/article/c0f7fb174317489fbeddbecef6598b5d
Publikováno v:
Endocrine Connections, Vol 10, Iss 3, Pp 358-370 (2021)
Objective: The usefulness of routine calcitonin measurement for early detection of medullary thyroid carcinoma (MTC) in patients with nodular thyroid disease (NTD) has been investigated in various studies. Recently, a Cochrane review has been publish
Externí odkaz:
https://doaj.org/article/de41bbc39e3c4e5798cf0b21647daf6c
Autor:
Christoph Wanner, Ulla Feldt‐Rasmussen, Ana Jovanovic, Aleš Linhart, Meng Yang, Elvira Ponce, Eva Brand, Dominique P. Germain, Derralynn A. Hughes, John L. Jefferies, Ana Maria Martins, Albina Nowak, Bojan Vujkovac, Frank Weidemann, Michael L. West, Alberto Ortiz
Publikováno v:
ESC Heart Failure, Vol 7, Iss 3, Pp 825-834 (2020)
Abstract Aims Long‐term treatment effect studies in large female Fabry patient groups are challenging to design because of phenotype heterogeneity and lack of appropriate comparison groups, and have not been reported. We compared long‐term cardio
Externí odkaz:
https://doaj.org/article/d245bf80912e439eb9ef9a86af5c8b32
Autor:
Robert J. Hopkin, Ulla Feldt-Rasmussen, Dominique P. Germain, Ana Jovanovic, Ana Maria Martins, Kathleen Nicholls, Alberto Ortiz, Juan Politei, Elvira Ponce, Carmen Varas, Frank Weidemann, Meng Yang, William R. Wilcox
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 25, Iss , Pp 100670- (2020)
Background: Fabry disease is an inherited disorder of glycolipid metabolism with progressive involvement of multiple organs, including the gastrointestinal tract, in classically affected male patients. Clinical presentations in males with later-onset
Externí odkaz:
https://doaj.org/article/539b308254b24c07ac41d8b8ceeb4b74
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 3, p 1887 (2022)
Fabry disease is an X-linked lysosomal multisystem storage disorder induced by a mutation in the alpha-galactosidase A (GLA) gene. Reduced activity or deficiency of alpha-galactosidase A (AGAL) leads to escalating storage of intracellular globotriaos
Externí odkaz:
https://doaj.org/article/243c9997e76946b0a486611fbd8b4fbd
Autor:
Florian Sagmeister, Sebastian Herrmann, Tobias Gassenmaier, Peter Bernhardt, Volker Rasche, Andreas Liebold, Frank Weidemann, Horst Brunner, Meinrad Beer
Publikováno v:
Journal of International Medical Research, Vol 48 (2020)
Objective To assess the influence of pressure recovery (PR)-corrected haemodynamic parameters on outcome in patients with aortic stenosis. Methods Aortic stenosis severity parameters were corrected for PR (increase in static pressure due to decreasin
Externí odkaz:
https://doaj.org/article/3bc339b474d749c6a244b23d2269854a
Autor:
Irfan Vardarli, Manuel Weber, Christoph Rischpler, Dagmar Führer, Ken Herrmann, Frank Weidemann
Publikováno v:
Journal of Clinical Medicine, Vol 10, Iss 14, p 3026 (2021)
Fabry disease is a multisystem X-linked lysosomal storage disorder caused by a mutation in the alpha-galactosidase A gene. Deficiency or reduced activity of alpha-galactosidase A (GLA) is leading to progressive intracellular accumulation of globotria
Externí odkaz:
https://doaj.org/article/3b61acee6e234dfeade6565a6e5766f4
Autor:
Tim Salinger, Kai Hu, Dan Liu, Scharoch Taleh, Sebastian Herrmann, Daniel Oder, Daniel Gensler, Jonas Müntze, Georg Ertl, Kristina Lorenz, Stefan Frantz, Frank Weidemann, Peter Nordbeck
Publikováno v:
Cardiology Research and Practice, Vol 2018 (2018)
Background. Fast progression of the transaortic mean gradient (Pmean) is relevant for clinical decision making of valve replacement in patients with moderate and severe aortic stenosis (AS) patients. However, there is currently little knowledge regar
Externí odkaz:
https://doaj.org/article/aae630471bbc4cdda469f2c35c48818d
Autor:
Nora Seydelmann, Dan Liu, Johannes Krämer, Christiane Drechsler, Kai Hu, Peter Nordbeck, Andreas Schneider, Stefan Störk, Bart Bijnens, Georg Ertl, Christoph Wanner, Frank Weidemann
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 5, Iss 6 (2016)
BackgroundHigh‐sensitivity troponin (hs‐TNT), a biomarker of myocardial damage, might be useful for assessing fibrosis in Fabry cardiomyopathy. We performed a prospective analysis of hs‐TNT as a biomarker for myocardial changes in Fabry patient
Externí odkaz:
https://doaj.org/article/ce1a874371604977bf9a85d8ac8b5726
Autor:
Nurcan Üçeyler, Nils Schröter, Waldemar Kafke, Daniela Kramer, Christoph Wanner, Frank Weidemann, Claudia Sommer
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0166484 (2016)
The X-chromosomally linked life-limiting Fabry disease (FD) is associated with deposits of the sphingolipid globotriaosylceramide 3 (Gb3) in various tissues. Skin is easily accessible and may be used as an additional diagnostic and follow-up medium.
Externí odkaz:
https://doaj.org/article/895b79f75aa841f09d8cc67a7701d967