FH ALERT: efficacy of a novel approach to identify patients with familial hypercholesterolemia

por Fath, Felix, Bengeser, Andreas, Barresi, Mathias, Binner, Priska, Schwab, Stefanie, Ray, Kausik K., Krämer, Bernhard K., Fraass, Uwe, März, Winfried
Publicado 2021

Severe hypertriglyceridemia in a patient heterozygous for a lipoprotein lipase gene allele with two novel missense variants

por Kassner, Ursula, Salewsky, Bastian, Wühle-Demuth, Marion, Szijarto, Istvan Andras, Grenkowitz, Thomas, Binner, Priska, März, Winfried, Steinhagen-Thiessen, Elisabeth, Demuth, Ilja
Publicado 2015

Variation in the human soluble epoxide hydrolase gene and risk of restenosis after percutaneous coronary intervention

por Kullmann, Silke, Binner, Priska, Rackebrandt, Kirsten, Huge, Andreas, Haltern, Georg, Lankisch, Mark, Füth, Reiner, von Hodenberg, Eberhard, Bestehorn, Hans-Peter, Scheffold, Thomas
Publicado 2009

Six sequence variants on chromosome 9p21.3 are associated with a positive family history of myocardial infarction: a multicenter registry

por Scheffold, Thomas, Kullmann, Silke, Huge, Andreas, Binner, Priska, Ochs, Hermann R, Schöls, Wolfgang, Thale, Joachim, Motz, Wolfgang, Hegge, Franz Josef, Stellbrink, Christoph, Dorsel, Thomas, Gülker, Hartmut, Heuer, Hubertus, Dinh, Wilfried, Stoll, Monika, Haltern, Georg
Publicado 2011

Noncompaction of the Ventricular Myocardium Is Associated with a De Novo Mutation in the β-Myosin Heavy Chain Gene

por Budde, Birgit S., Binner, Priska, Waldmüller, Stephan, Höhne, Wolfgang, Blankenfeldt, Wulf, Hassfeld, Sabine, Brömsen, Jürgen, Dermintzoglou, Anastassia, Wieczorek, Marcus, May, Erik, Kirst, Elisabeth, Selignow, Carmen, Rackebrandt, Kirsten, Müller, Melanie, Goody, Roger S., Vosberg, Hans-Peter, Nürnberg, Peter, Scheffold, Thomas
Publicado 2007