Search Results - "Behr, R."
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1
Application of artificial intelligence to the electrocardiogram
Published in European heart journal (07-12-2021)“…Abstract Artificial intelligence (AI) has given the electrocardiogram (ECG) and clinicians reading them super-human diagnostic abilities. Trained without…”
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2
SARS-CoV-2, COVID-19, and inherited arrhythmia syndromes
Published in Heart rhythm (01-09-2020)“…Ever since the first case was reported at the end of 2019, the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the associated coronavirus…”
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3
Fibrosis, Connexin-43, and Conduction Abnormalities in the Brugada Syndrome
Published in Journal of the American College of Cardiology (03-11-2015)“…Abstract Background The right ventricular outflow tract (RVOT) is acknowledged to be responsible for arrhythmogenesis in Brugada syndrome (BrS), but the…”
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4
Pharmacological treatment of acquired QT prolongation and torsades de pointes
Published in British journal of clinical pharmacology (01-03-2016)“…Torsades de pointes (TdP) is a characteristic polymorphic ventricular arrhythmia associated with delayed ventricular repolarization as evidenced on the surface…”
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The involvement of gonadotropin inhibitory hormone and kisspeptin in the metabolic regulation of reproduction
Published in Journal of endocrinology (01-05-2015)“…Recently, kisspeptin (KP) and gonadotropin inhibitory hormone (GnIH), two counteracting neuropeptides, have been acknowledged as significant regulators of…”
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6
Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway?
Published in European heart journal (14-03-2021)“…Abstract Brugada syndrome (BrS) was first described as a primary electrical disorder predisposing to the risk of sudden cardiac death and characterized by…”
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7
Sudden Death and Left Ventricular Involvement in Arrhythmogenic Cardiomyopathy
Published in Circulation (New York, N.Y.) (09-04-2019)“…BACKGROUND:Arrhythmogenic cardiomyopathy (ACM) is an inherited heart muscle disorder characterized by myocardial fibrofatty replacement and an increased risk…”
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8
Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death
Published in American journal of human genetics (05-10-2012)“…Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a devastating inherited disorder characterized by episodic syncope and/or sudden cardiac arrest…”
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9
Quantitative and comparative assessment of dyes and protocols for rapid ex vivo microscopy of fresh tissues
Published in Scientific reports (13-09-2024)“…Using ex vivo microscopy, virtual pathology can improve histological procedures by providing pathology images in near real-time without tissue destruction…”
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10
Genetic testing for inherited cardiac disease
Published in Nature reviews cardiology (01-10-2013)“…Cardiomyopathies and cardiac channelopathies can predispose individuals to sudden cardiac death. The genetics that underlie these phenotypes are complex and…”
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11
Interpretation and actionability of genetic variants in cardiomyopathies: a position statement from the European Society of Cardiology Council on cardiovascular genomics
Published in European heart journal (21-05-2022)“…Abstract This document describes the contribution of clinical criteria to the interpretation of genetic variants using heritable Mendelian cardiomyopathies as…”
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12
Drug-induced arrhythmia: pharmacogenomic prescribing?
Published in European heart journal (01-01-2013)“…Drug-induced Torsades de Pointes is a rare, unpredictable, and life-threatening serious adverse event. It can be caused by both cardiac and non-cardiac drugs…”
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13
Misleading and reliable markers to differentiate between primate testis-derived multipotent stromal cells and spermatogonia in culture
Published in Human reproduction (Oxford) (01-06-2012)“…BACKGROUND Several studies have reported the generation of spermatogonia-derived pluripotent stem cells from human testes. The initial aim of the present study…”
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14
Sudden unexpected death in epilepsy genetics: Molecular diagnostics and prevention
Published in Epilepsia (Copenhagen) (01-01-2016)“…Summary Epidemiologic studies clearly document the public health burden of sudden unexpected death in epilepsy (SUDEP). Clinical and experimental studies have…”
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15
The MUSCLES Extension for Atmospheric Transmission Spectroscopy: UV and X-Ray Host-star Observations for JWST ERS & GTO Targets
Published in The Astronomical journal (01-07-2023)“…Abstract X-ray through infrared spectral energy distributions (SEDs) are essential for understanding a star’s effect on exoplanet atmospheric composition and…”
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16
Towards a 1 V Josephson Arbitrary Waveform Synthesizer
Published in IEEE transactions on applied superconductivity (01-06-2015)“…The establishment at PTB of an AC Josephson voltage standard (Josephson Arbitrary Waveform Synthesizer- JAWS) based on pulse-driven Josephson arrays is focused…”
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17
Primordial germ cells do not migrate along nerve fibres in marmoset monkey and mouse embryos
Published in Reproduction (Cambridge, England) (01-01-2019)“…Primordial germ cells (PGCs) are the embryonic precursors of spermatozoa and eggs. In mammals, PGCs arise early in embryonic development and migrate from their…”
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18
Mechanism of the effects of sodium channel blockade on the arrhythmogenic substrate of Brugada syndrome
Published in Heart rhythm (01-03-2022)“…The mechanisms by which sodium channel blockade and high-rate pacing modify electrogram (EGM) substrates of Brugada syndrome (BrS) have not been elucidated…”
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19
The Radiation Environments of Middle-aged F-type Stars
Published in The Astrophysical journal (01-10-2023)“…Abstract Far-ultraviolet (FUV) emission lines from dwarf stars are important driving sources of photochemistry in planetary atmospheres. Properly interpreting…”
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AZFa Y gene, DDX3Y, evolved novel testis transcript variants in primates with proximal 3´UTR polyadenylation for germ cell specific translation
Published in Scientific reports (27-05-2022)“…Translational control is a major level of gene expression regulation in the male germ line. DDX3Y located in the AZFa region of the human Y chromosome encodes…”
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