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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1966 2
1967 2
1970 1
1971 1
1973 2
1975 1
1976 2
1978 1
1986 1
1989 1
1997 1
1998 1
2000 1
2003 1
2004 1
2005 1
2007 1
2008 1
2009 1
2011 3
2012 1
2013 1
2015 1
2016 2
2021 1
2024 0

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31 results

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Page 1
[Hypertrophic cardiomyopathy].
Scheffold T, Binner P, Erdmann J, Schunkert H; Mitglieder des Teilprojekts 5 im Kompetenznetz Herzinsuffizienz. Scheffold T, et al. Among authors: binner p. Herz. 2005 Sep;30(6):550-7. doi: 10.1007/s00059-005-2731-4. Herz. 2005. PMID: 16170688 Review. German.
Development of the research department.
Binner PR. Binner PR. Milbank Mem Fund Q. 1966 Jan;44(1):Suppl:313-9. Milbank Mem Fund Q. 1966. PMID: 5907664 No abstract available.
Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia.
Grenkowitz T, Kassner U, Wühle-Demuth M, Salewsky B, Rosada A, Zemojtel T, Hopfenmüller W, Isermann B, Borucki K, Heigl F, Laufs U, Wagner S, Kleber ME, Binner P, März W, Steinhagen-Thiessen E, Demuth I. Grenkowitz T, et al. Among authors: binner p. Atherosclerosis. 2016 Oct;253:88-93. doi: 10.1016/j.atherosclerosis.2016.08.037. Epub 2016 Aug 26. Atherosclerosis. 2016. PMID: 27596133
Hox genes in the honey bee Apis mellifera.
Walldorf U, Binner P, Fleig R. Walldorf U, et al. Among authors: binner p. Dev Genes Evol. 2000 Oct;210(10):483-92. doi: 10.1007/s004270000091. Dev Genes Evol. 2000. PMID: 11180797
Lipoprotein Apheresis for Lipoprotein(a)-Associated Cardiovascular Disease: Prospective 5 Years of Follow-Up and Apolipoprotein(a) Characterization.
Roeseler E, Julius U, Heigl F, Spitthoever R, Heutling D, Breitenberger P, Leebmann J, Lehmacher W, Kamstrup PR, Nordestgaard BG, Maerz W, Noureen A, Schmidt K, Kronenberg F, Heibges A, Klingel R; Pro(a)LiFe-Study Group. Roeseler E, et al. Arterioscler Thromb Vasc Biol. 2016 Sep;36(9):2019-27. doi: 10.1161/ATVBAHA.116.307983. Epub 2016 Jul 14. Arterioscler Thromb Vasc Biol. 2016. PMID: 27417585
Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy.
Geier C, Perrot A, Ozcelik C, Binner P, Counsell D, Hoffmann K, Pilz B, Martiniak Y, Gehmlich K, van der Ven PF, Fürst DO, Vornwald A, von Hodenberg E, Nürnberg P, Scheffold T, Dietz R, Osterziel KJ. Geier C, et al. Among authors: binner p. Circulation. 2003 Mar 18;107(10):1390-5. doi: 10.1161/01.cir.0000056522.82563.5f. Circulation. 2003. PMID: 12642359
High-density oligonucleotide-based resequencing assay for mutations causing syndromic and non-syndromic forms of thoracic aortic aneurysms and dissections.
Kathiravel U, Keyser B, Hoffjan S, Kötting J, Müller M, Sivalingam S, Bonin M, Arslan-Kirchner M, von Kodolitsch Y, Binner P, Scheffold T, Stuhrmann M, Waldmüller S. Kathiravel U, et al. Among authors: binner p. Mol Cell Probes. 2013 Apr;27(2):103-8. doi: 10.1016/j.mcp.2012.10.002. Epub 2012 Nov 6. Mol Cell Probes. 2013. PMID: 23142374
31 results