Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Priska Binner"'
Autor:
Felix Fath, Andreas Bengeser, Mathias Barresi, Priska Binner, Stefanie Schwab, Kausik K. Ray, Bernhard K. Krämer, Uwe Fraass, Winfried März
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract Diagnosis rates of familial hypercholesterolemia (FH) remain low. We implemented FH ALERT to assess whether alerting physicians for the possibility of FH impacted additional diagnostic activity. The study was conducted from SYNLAB laboratory
Externí odkaz:
https://doaj.org/article/aac64c0164f74964a410a58cae874fbf
Autor:
Birgit S Budde, Priska Binner, Stephan Waldmüller, Wolfgang Höhne, Wulf Blankenfeldt, Sabine Hassfeld, Jürgen Brömsen, Anastassia Dermintzoglou, Marcus Wieczorek, Erik May, Elisabeth Kirst, Carmen Selignow, Kirsten Rackebrandt, Melanie Müller, Roger S Goody, Hans-Peter Vosberg, Peter Nürnberg, Thomas Scheffold
Publikováno v:
PLoS ONE, Vol 2, Iss 12, p e1362 (2007)
Noncompaction of the ventricular myocardium (NVM) is the morphological hallmark of a rare familial or sporadic unclassified heart disease of heterogeneous origin. NVM results presumably from a congenital developmental error and has been traced back t
Externí odkaz:
https://doaj.org/article/aea1aa68f40a4223bf737555eeecb32d
Autor:
Andreas Bengeser, Kausik K. Ray, Priska Binner, Felix Fath, Uwe Fraass, Winfried März, Mathias Barresi, Bernhard K. Krämer, Stefanie Schwab
Publikováno v:
Scientific Reports
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Diagnosis rates of familial hypercholesterolemia (FH) remain low. We implemented FH ALERT to assess whether alerting physicians for the possibility of FH impacted additional diagnostic activity. The study was conducted from SYNLAB laboratory Weiden (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aaecbd47bc4360ea591a7921ae89364
https://doi.org/10.1038/s41598-021-99961-y
https://doi.org/10.1038/s41598-021-99961-y
Autor:
Uwe Fraass, Mathias Barresi, Andreas Bengeser, Stefanie Schwab, Felix Fath, Bernhard K. Krämer, Winfried März, Kausik K. Ray, Priska Binner
Background and aimsDiagnosis rates of familial hypercholesterolemia (FH) remain low. We implemented FH ALERT to assess whether alerting physicians for the possibility of FH impacted additional diagnostic activity.MethodsThe study was conducted from S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1e37e86054b2ab99a6040ba511ab1595
https://doi.org/10.21203/rs.3.rs-108034/v1
https://doi.org/10.21203/rs.3.rs-108034/v1
Autor:
F. Bardey, Ursula Kassner, Elisabeth Steinhagen-Thiessen, Priska Binner, S. Schwab, Dominik Spira, Thomas Bobbert, Joachim Spranger, Ilja Demuth, Winfried März, L. Rieck
Publikováno v:
Atherosclerosis. 315:e43
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a2c506a64da80e04b527aa2d185a4a21
https://doi.org/10.1016/j.atherosclerosis.2020.10.138
https://doi.org/10.1016/j.atherosclerosis.2020.10.138
Autor:
István András Szijártó, Winfried März, Bastian Salewsky, Ursula Kassner, Elisabeth Steinhagen-Thiessen, Priska Binner, Ilja Demuth, Thomas Grenkowitz, Marion Wühle-Demuth
Publikováno v:
European Journal of Human Genetics
Rare monogenic hyperchylomicronemia is caused by loss-of-function mutations in genes involved in the catabolism of triglyceride-rich lipoproteins, including the lipoprotein lipase gene, LPL. Clinical hallmarks of this condition are eruptive xanthomas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17c7152676e8ab46a5571714e0922862
https://doi.org/10.1038/ejhg.2014.295
https://doi.org/10.1038/ejhg.2014.295
Autor:
Damian Counsell, Dieter O. Fürst, Bernhard Pilz, Eberhard von Hodenberg, Karl Josef Osterziel, Andreas Perrot, Cemil Özcelik, Arnold Vornwald, Priska Binner, Rainer Dietz, Yvonne Martiniak, Peter F.M. van der Ven, Katrin Hoffmann, Christian Geier, Katja Gehmlich, Thomas Scheffold, Peter Nürnberg
Background— Muscle LIM protein (MLP) is an essential nuclear regulator of myogenic differentiation. Additionally, it may act as an integrator of protein assembly of the actin-based cytoskeleton. MLP-knockout mice develop a marked cardiac hypertroph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::099ffd6c85a6e829273fe713cba0c6aa
https://doi.org/10.1161/01.cir.0000056522.82563.5f
https://doi.org/10.1161/01.cir.0000056522.82563.5f
Autor:
Eberhard Roeseler, Ulrich Julius, Franz Heigl, Ralf Spitthoever, Dennis Heutling, Paul Breitenberger, Josef Leebmann, Walter Lehmacher, Pia R. Kamstrup, Børge G. Nordestgaard, Winfried Maerz, Asma Noureen, Konrad Schmidt, Florian Kronenberg, Andreas Heibges, Reinhard Klingel, Volker Schettler, Thomas Benzing, Hildegard Christ, Sabine Wehner, Ines Schulz-Merkel, Ralf Kuehn, Albrecht Wagner, Wilfried Dschietzig, Claudia Ernst, Michael Koziolek, Johannes Bunia, Peter Kulzer, Klaus-Dieter Kraenzle, Markus Toelle, Gerhard Riechers, Christine Kuehnel, Tobias Marsen, Christina Saehn, Jens Ringel, Harald Messner, Andreas Oehring, Carsten Schuerfeld, Michael Wintergalen, Falko Neumann, Harald Kaul, Martin Haesner, Juergen Passfall, Andrea Benschneider, Stefan Heidenreich, Winfried März, Ruediger Klaes, Priska Binner, Hans Dieplinger, Gertraud Erhart, Cordula Fassbender
Publikováno v:
Arteriosclerosis, thrombosis, and vascular biology. 36(9)
Objective— Lipoprotein(a)-hyperlipoproteinemia (Lp(a)-HLP) along with progressive cardiovascular disease has been approved as indication for regular lipoprotein apheresis (LA) in Germany since 2008. We aimed to study the long-term preventive effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f20ef915d7985d3248ac62a72c4137a
https://pubmed.ncbi.nlm.nih.gov/27417585
https://pubmed.ncbi.nlm.nih.gov/27417585
Autor:
Priska Binner, Thomas Grenkowitz, Stephan Wagner, Winfried März, Ulrich Laufs, Franz Heigl, Katrin Borucki, Adrian Rosada, Marcus E. Kleber, Berend Isermann, Ursula Kassner, Tomasz Zemojtel, Elisabeth Steinhagen-Thiessen, Marion Wühle-Demuth, Ilja Demuth, Werner Hopfenmüller, Bastian Salewsky
Publikováno v:
Atherosclerosis
Background and aims Autosomal-dominant familial hypercholesterolemia (FH) is characterized by elevated plasma levels of low-density lipoprotein cholesterol (LDL-C) and a dramatically increased risk to develop cardiovascular disease (CVD). Mutations i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd9c8a85faa4c6b130b448da9fe01b1c
https://hdl.handle.net/21.11116/0000-0004-6888-E
https://hdl.handle.net/21.11116/0000-0004-6888-E
Autor:
G. Gelbrich, Andreas Perrot, Heribert Schunkert, Wulf Blankenfeldt, Vera Regitz-Zagrosek, Rolf Wachter, T. Brodherr, Christian Geier, Bernhard Maisch, M. Farr, Markus Loeffler, Hendrik Milting, N. Schulze-Waltrup, Cemil Oezcelik, B. Jurmann, Bernd Timmermann, S. Scheer, Richard Reinhardt, A. Dermintzoglou, W. Zeh, Thomas Scheffold, J. Boergel, J. Haremza, Jeanette Erdmann, S. Pankuweit, Karl-Josef Osterziel, S. Waldmueller, J. Schoenberger, Priska Binner
Publikováno v:
European Journal of Heart Failure. 13:1185-1192
Aims Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) can both be due to mutations in the genes encoding β-myosin heavy chain (MYH7) or cardiac myosin-binding protein C (MYBPC3). The aim of the present study was to determine the pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ff1994847b7ed6e2aa8c8bae35f9711
https://doi.org/10.1093/eurjhf/hfr074
https://doi.org/10.1093/eurjhf/hfr074