Birgit Stallmeyer

Birgit Stallmeyer

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Birgit Stallmeyer

Birgit Stallmeyer

Publications by authors named "Birgit Stallmeyer"

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Cardiac α-Actin (ACTC1) Gene Mutation Causes Atrial-Septal Defects Associated With Late-Onset Dilated Cardiomyopathy.

Circ Genom Precis Med 2019 Aug 20;12(8):e002491. Epub 2019 Aug 20.

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine (C.F., S.D., B.S., Ellen Schulze-Bahr, S.P., G.S., A.U., Eric Schulze-Bahr), University Hospital Münster.

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http://dx.doi.org/10.1161/CIRCGEN.119.002491DOI Listing
August 2019

Familial Sinus Node Disease Caused by a Gain of GIRK (G-Protein Activated Inwardly Rectifying K Channel) Channel Function.

Circ Genom Precis Med 2019 Jan;12(1):e002238

Department of Cardiovascular Medicine, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Germany (J.K., B.S., S.Z., G.S., E.S.-B.).

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https://www.ahajournals.org/doi/10.1161/CIRCGEN.118.002238
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http://dx.doi.org/10.1161/CIRCGEN.118.002238DOI Listing
January 2019

Impact of presynaptic sympathetic imbalance in long-QT syndrome by positron emission tomography.

Heart 2018 02 1;104(4):332-339. Epub 2017 Sep 1.

Department of Cardiovascular Medicine, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Münster, Germany.

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http://heart.bmj.com/lookup/doi/10.1136/heartjnl-2017-311667
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http://dx.doi.org/10.1136/heartjnl-2017-311667DOI Listing
February 2018

A Mutation in the G-Protein Gene Causes Familial Sinus Node and Atrioventricular Conduction Dysfunction.

Circ Res 2017 May 20;120(10):e33-e44. Epub 2017 Feb 20.

From the Institute for Genetics of Heart Diseases, Department of Cardiology and Angiology, University Hospital Muenster, Germany (B.S., J.K., S.Z., C.F., E.S.-B., G.S., E.S.-B.); Department of Pediatric Cardiology (S.K.) and Department of General Pediatrics (S.R.), University Children's Hospital Muenster, Germany; and Institute for Physiology and Pathophysiology, Vegetative Physiology, Philipps University of Marburg, Germany (K.V., S.R., L.A.M., N.D.).

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http://dx.doi.org/10.1161/CIRCRESAHA.116.310112DOI Listing
May 2017

(Tpeak - Tend)/QRS and (Tpeak - Tend)/(QT × QRS) as risk markers in Brugada syndrome: authors' reply.

Europace 2017 04;19(4):696-697

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Gebäude D3, Münster D-48149, Germany.

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http://dx.doi.org/10.1093/europace/euw210DOI Listing
April 2017

Tpeak-Tend interval and Tpeak-Tend/QT ratio in patients with Brugada syndrome.

Europace 2016 Dec 3;18(12):1866-1872. Epub 2016 Mar 3.

Department of Cardiovascular Medicine, Institute for Genetics of Heart Diseases (IfGH), University Hospital Münster, Albert-Schweitzer-Campus 1, Gebäude D3, D-48149 Münster, Germany.

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http://dx.doi.org/10.1093/europace/euw033DOI Listing
December 2016

Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction.

Basic Res Cardiol 2016 Mar 23;111(2):14. Epub 2016 Jan 23.

Human Stem Cell Pluripotency Group, Max Planck Institute for Molecular Biomedicine, 48149, Münster, Germany.

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http://dx.doi.org/10.1007/s00395-016-0530-0DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4724360PMC
March 2016

Cardiovascular disease and sudden cardiac death: between genetics and genomics.

Eur Heart J 2015 Jul 8;36(26):1643-5. Epub 2015 May 8.

Institute for Genetics of Heart Diseases (IFGH), Department of Cardiovascular Medicine, University Hospital Münster, Germany Interdisciplinary Center for Clinical Research (IZKF), University Hospital Münster, Germany Collaborative Research Centre 656 'Molecular Cardiovascular Imaging' of the University of Münster, Germany

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http://eurheartj.oxfordjournals.org/content/ehj/early/2015/0
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http://eurheartj.oxfordjournals.org/lookup/doi/10.1093/eurhe
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http://dx.doi.org/10.1093/eurheartj/ehv173DOI Listing
July 2015

Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2.

Circ Cardiovasc Genet 2015 Jun 3;8(3):447-456. Epub 2015 Mar 3.

Department of Clinical and Experimental Cardiology (I.C.R.M.K., P.G.P., J.B., T.T.K., A.A.M.W., C.R.B.), Department of Clinical Epidemiology, Biostatistics and Bioinformatics (I.C.R.M.K., M.W.T.T.), and Department of Clinical Genetics (N.H.), Academic Medical Center, Amsterdam, the Netherlands; ICIN (Netherlands Heart Institute) (J.B., A.A.M.W., C.R.B.), Utrecht, the Netherlands; Institut National de la Santé et de la Recherche Médicale (INSERM) Unité Mixte de Recherche (UMR) 1087, L'Institut du Thorax, Nantes, France (J.B., J.-J.S.); Centre National de la Recherche Scientifique (CNRS) UMR 6291, Nantes, France (J.B., J.-J.S.); Université de Nantes, Nantes, France (J.B., J.-J.S.); Department of Medicine I, University Hospital Munich, Campus Grosshadern and Innenstadt, Ludwig-Maximilians University, Munich, Germany (M.F.S., B.M.B., S.K.); German Center for Cardiovascular Research (DZHK), Munich Heart Alliance, Munich, Germany (S.K.T.M.); Institute for Genetics of Heart Diseases, Department of Cardiovascular Medicine, University Hospital Münster, Münster, Germany (S.Z., A.H., B.S., E.S.-B.); Interdisciplinary Centre for Clinical Research (IZKF) of the University of Münster, Münster, Germany (S.Z., A.H., B.S., E.S.-B.); Institute of Bioinformatics and Systems Biology (A.P.), and Institute of Human Genetics (A.P., P.L., T.M.), Helmholtz Zentrum München, Neuherberg, Germany; Institute of Human Genetics, Technische Universität München, Munich, Germany (A.P., P.L., T.M.); Department of Medicine (R.J.M., N.H.B.), Department of Molecular and Cellular Pharmacology (R.J.M., N.H.B.), and Hussmann Institute of Human Genomics (R.J.M., N.H.B.), University of Miami Miller School of Medicine, FL; Department of Medicine and Pharmacology, Vanderbilt University School of Medicine, Nashville, TN (D.M.R.); Princess Al-Jawhara Al-Brahim Centre of Excellence in Research of Hereditary Disorders, Jeddah, Kingdom of Saudi Arabia (A.A.M.W.); and Centre Hospitalier Universitaire (CHU) Nantes, L'Institut du Thorax, Service de Cardiologie, Nantes, France (J.-J.S.).

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http://dx.doi.org/10.1161/CIRCGENETICS.114.000785DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4770255PMC
June 2015

Gain-of-function mutations in the calcium channel CACNA1C (Cav1.2) cause non-syndromic long-QT but not Timothy syndrome.

J Mol Cell Cardiol 2015 Mar 26;80:186-95. Epub 2015 Jan 26.

Institute of Physiology and Pathophysiology, Vegetative Physiology, Philipps-University of Marburg, Deutschhausstr. 1-2, 35037 Marburg, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.yjmcc.2015.01.002DOI Listing
March 2015

First report on an inotropic peptide activating tetrodotoxin-sensitive, "neuronal" sodium currents in the heart.

Circ Heart Fail 2015 Jan 25;8(1):79-88. Epub 2014 Nov 25.

From the Department of Cardiovascular Medicine (P.K., L.F., S.N., L.F.), Department of Pharmacology and Toxicology (J.K., J.S.S., F.U.M., W.S., U.K.), and Department of Cardiovascular Medicine, Institute for Genetics of Heart Disease (IfGH) (B.S., E.S.-B.), Hospital of the University of Muenster, Muenster, Germany; Center for Cardiovascular Sciences, School of Clinical and Experimental Medicine, and SWBH NHS Trust, University of Birmingham, Birmingham, United Kingdom (P.K., L.F.); Technion Israel Institute of Technology, Haifa, Israel (T.T.); Department of Animal and Cell Biology, Institute of Life Sciences, The Hebrew University of Jerusalem, Jerusalem, Israel (T.T., N.N., E.Z.); Department of Pharmacology and Toxicology, Faculty of Pharmacy, Comenius University in Bratislava, Bratislava, Slovak Republic (J.K.); Department of Neurology, and Division of Neuropathophysiology, Institute of Physiology I (P.E.) and Institute of Physiology I (T.K., T.B.), University of Muenster, Muenster, Germany; and Department of Clinical and Interventional Angiology, Asklepios Clinic St. Georg, Hamburg, Germany (S.N.).

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http://dx.doi.org/10.1161/CIRCHEARTFAILURE.113.001066DOI Listing
January 2015

Non dominant-negative KCNJ2 gene mutations leading to Andersen-Tawil syndrome with an isolated cardiac phenotype.

Basic Res Cardiol 2013 May 5;108(3):353. Epub 2013 May 5.

Institut für Physiologie und Pathophysiologie, Vegetative Physiologie, Philipps-University Marburg, Deutschhausstraße 1-2, 35037 Marburg, Germany.

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http://dx.doi.org/10.1007/s00395-013-0353-1DOI Listing
May 2013

Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel.

Cell Physiol Biochem 2012 11;29(5-6):809-18. Epub 2012 May 11.

Biochemistry I - Cation Channel Group, Ruhr University Bochum, Bochum, Germany.

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http://dx.doi.org/10.1159/000178470DOI Listing
November 2012

Inherited long QT syndrome: clinical manifestation, genetic diagnostics, and therapy.

Herzschrittmacherther Elektrophysiol 2012 Sep 21;23(3):211-9. Epub 2012 Sep 21.

Institute for Genetics of Heart Diseases (IfGH), Department of Cardiovascular Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Gebäude D3, 48149, Münster, Germany.

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http://link.springer.com/10.1007/s00399-012-0232-8
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http://dx.doi.org/10.1007/s00399-012-0232-8DOI Listing
September 2012

Identification of novel mutations in LMNA associated with familial forms of dilated cardiomyopathy.

Genet Test Mol Biomarkers 2012 Jun 6;16(6):543-9. Epub 2012 Jan 6.

Institut für Genetik von Herzerkrankungen (IfGH), Universitätsklinik Münster, Münster, Germany.

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http://dx.doi.org/10.1089/gtmb.2011.0214DOI Listing
June 2012

A homozygous SCN5A mutation in a severe, recessive type of cardiac conduction disease.

Hum Mutat 2010 Aug;31(8):E1609-21

Experimental Neuropediatrics, University Medical Center Hamburg-Eppendorf, Germany.

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http://dx.doi.org/10.1002/humu.21302DOI Listing
August 2010

Impaired endocytosis of the ion channel TRPM4 is associated with human progressive familial heart block type I.

J Clin Invest 2009 Sep 24;119(9):2737-44. Epub 2009 Aug 24.

Institut für Neurale Signalverarbeitung, Zentrum für Molekulare Neurobiologie, Universität Hamburg, Hamburg, Germany.

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http://dx.doi.org/10.1172/JCI38292DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2735920PMC
September 2009

Genes causing inherited forms of cardiomyopathies. A current compendium.

Herz 2009 Mar;34(2):98-109

Department of Cardiology and Angiology, University Hospital Münster, Münster, Germany.

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http://dx.doi.org/10.1007/s00059-009-3215-8DOI Listing
March 2009

PKC delta-induced activation of MAPK pathway is required for bFGF-stimulated proliferation of coronary smooth muscle cells.

Cardiovasc Res 2005 Jul 12;67(1):142-50. Epub 2005 Apr 12.

Leibniz-Institute for Arteriosclerosis Research, University of Münster, Domagkstr. 3, 48149 Münster, Germany.

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http://dx.doi.org/10.1016/j.cardiores.2005.03.009DOI Listing
July 2005

Regulation of eNOS in normal and diabetes-impaired skin repair: implications for tissue regeneration.

Nitric Oxide 2002 Mar;6(2):168-77

Pharmazentrum Frankfurt, Klinikum der Johann Wolfgang Goethe-Universität, Theodor-Stern-Kai 7, D-60590 Frankfurt am Main, Germany.

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http://dx.doi.org/10.1006/niox.2001.0407DOI Listing
March 2002