Výsledky vyhledávání - "Anders Krogh Broendberg"

Akademický článek

Outcome after out-of-hospital cardiac arrest in patients with ischaemic and non-ischaemic heart disease: A Danish tertiary-center cohort study

Autor: Marie-Louise Beier Guldfeldt, Tanja Charlotte Frederiksen, Anders Krogh Broendberg, Morten Krogh Christiansen, Henrik Kjaerulf Jensen

Publikováno v: International Journal of Cardiology: Heart & Vasculature, Vol 41, Iss , Pp 101059- (2022)

Background: Mortality following out-of-hospital cardiac arrest (OHCA) is high, and studies on return to work show varying results. It remains uncertain whether mortality and return to work differs between patients with ischaemic heart disease (IHD) a

Externí odkaz: https://doaj.org/article/3a3169c95ac645f0b76b4078dff578e8

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Akademický článek

Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene

Autor: Anders Krogh Broendberg, MD, Lisbeth Noerum Pedersen, MSc, PhD, Jens Cosedis Nielsen, MD, DMSc, PhD, Henrik Kjaerulf Jensen, MD, DMSc, PhD

Publikováno v: HeartRhythm Case Reports, Vol 2, Iss 3, Pp 261-264 (2016)

Externí odkaz: https://doaj.org/article/9d6c5ba322e347c298ee7dc900f267f0

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Akademický článek

Ankyrin-2 variants associated with idiopathic ventricular fibrillation storm in patients with intermittent early repolarization pattern

Autor: Anders Krogh Broendberg, MD, Lisbeth Noerum Pedersen, Msc, PhD, Jens Cosedis Nielsen, MD, DMSc, PhD, Henrik Kjaerulf Jensen, MD, DMSc, PhD

Publikováno v: HeartRhythm Case Reports, Vol 1, Iss 5, Pp 337-341 (2015)

Externí odkaz: https://doaj.org/article/59481048350a404481fd69550b47635e

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The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes

Autor: Kirstine Calloe, Michelle Geryk, Kristine Freude, Jacqueline A Treat, Victoria A Vold, Henriette Reventlow S Frederiksen, Anders Krogh Broendberg, Tanja Charlotte Frederiksen, Henrik K Jensen, Jonathan M Cordeiro

Publikováno v: Calloe, K, Geryk, M, Freude, K, Treat, J A, Vold, V A, Frederiksen, H R S, Broendberg, A K, Frederiksen, T C, Jensen, H K & Cordeiro, J M 2022, ' The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes ', Europace, vol. 24, no. 12, pp. 2015–2027 . https://doi.org/10.1093/europace/euac090

Aims Variants in SCN5A encoding Nav1.5 are associated with cardiac arrhythmias. We aimed to determine the mechanism by which c.638G>A in SCNA5 resulting in p.Gly213Asp (G213D) in Nav1.5 altered Na+ channel function and how flecainide corrected the de

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85b744baf01ac9143dffcf92964a0a7d
https://doi.org/10.1093/europace/euac090

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Cardiac ryanodine receptor calcium release deficiency syndrome

Publikováno v: Digital.CSIC. Repositorio Institucional del CSIC
instname
Science Translational Medicine, 13(579):eaba7287. American Association for the Advancement of Science
Sun, B, Yao, J, Ni, M, Wei, J, Zhong, X, Guo, W, Zhang, L, Wang, R, Belke, D, Chen, Y X, Lieve, K V V, Broendberg, A K, Roston, T M, Blankoff, I, Kammeraad, J A, Von Alvensleben, J C, Lazarte, J, Vallmitjana, A, Bohne, L J, Rose, R A, Benitez, R, Hove-Madsen, L, Napolitano, C, Hegele, R A, Fill, M, Sanatani, S, Wilde, A A M, Roberts, J D, Priori, S G, Jensen, H K & Chen, S R W 2021, ' Cardiac ryanodine receptor calcium release deficiency syndrome ', Science Translational Medicine, vol. 13, no. 579, eaba7287 . https://doi.org/10.1126/scitranslmed.aba7287
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Science Translational Medicine
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Science translational medicine, 13(579):eaba7287. American Association for the Advancement of Science

Cardiac ryanodine receptor (RyR2) gain-of-function mutations cause catecholaminergic polymorphic ventricular tachycardia, a condition characterized by prominent ventricular ectopy in response to catecholamine stress, which can be reproduced on exerci

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d0eac87fccf6badb97aa1c081b5aeea
https://doi.org/10.1126/scitranslmed.aba7287

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Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Na v 1.5 gain-of-function mutation (G213D)

Autor: Anders Krogh Broendberg, Maria de los Angeles Tejada, Lisbeth Nørum Pedersen, Alex H. Christensen, Søren Friis, Henrik Jensen, Morten S. Olesen, Morten B. Thomsen, Kirstine Calloe, Henning Bundgaard

Publikováno v: Calloe, K, Broendberg, A K, Christensen, A H, Pedersen, L N, Olesen, M S, de Los Angeles Tejada, M, Friis, S, Thomsen, M B, Bundgaard, H & Jensen, H K 2018, ' Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Na1.5 gain-of-function mutation (G213D) ', International Journal of Cardiology, vol. 257, pp. 160-167 . https://doi.org/10.1016/j.ijcard.2017.11.095

BACKGROUND: SCN5A mutations can lead to different cardiac diseases. Recently, SCN5A mutations have been linked to the clinical entity multifocal ectopic Purkinje-related premature contractions (MEPPC) characterized by ventricular ectopy and dilated c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a6fa96586e71fc2ff8d491517447de1
https://doi.org/10.1016/j.ijcard.2017.11.095

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Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene

Autor: Lisbeth Noerum Pedersen, Anders Krogh Broendberg, Jens Cosedis Nielsen, Henrik Jensen

Publikováno v: HeartRhythm Case Reports, Vol 2, Iss 3, Pp 261-264 (2016)
Krogh Brøndberg, A, Pedersen, L N, Nielsen, J C & Jensen, H K 2016, ' Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene ', HeartRhythm Case Reports, vol. 2, no. 3, pp. 261-264 . https://doi.org/10.1016/j.hrcr.2016.02.008
HeartRhythm Case Reports

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2df869e7e466e6b41fb6ad0bad564355
https://doi.org/10.1016/j.hrcr.2016.02.008

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Implantable cardioverter defibrillator therapy and device-related complications in young patients with inherited cardiomyopathies or channelopathies: a 17-year cohort study

Autor: Henrik Jensen, Lærke D D Petersen, Morten Krogh Christiansen, Lisbeth Nørum Pedersen, Jens Nielsen, Anders Krogh Broendberg

Publikováno v: Petersen, L D D, Christiansen, M K, Pedersen, L N, Nielsen, J C, Broendberg, A K & Jensen, H K 2018, ' Implantable cardioverter defibrillator therapy and device-related complications in young patients with inherited cardiomyopathies or channelopathies: a 17-year cohort study ', Europace, vol. 20, no. 11, pp. 1849-1855 . https://doi.org/10.1093/europace/euy081

Aims: To quantify appropriate and inappropriate therapy and complications related to implantable cardioverter-defibrillator (ICD) treatment in young patients receiving an ICD for a hereditary cardiomyopathy or channelopathy.Methods and results: This

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0a16cc128df649e1b5f47beb48fbd73
https://pure.au.dk/portal/da/publications/implantable-cardioverter-defibrillator-therapy-and-devicerelated-complications-in-young-patients-with-inherited-cardiomyopathies-or-channelopathies-a-17year-cohort-study(3a232463-178b-44a5-8886-369cdad8a9e7).html

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Outcome of clinical management in relatives of sudden cardiac death victims

Autor: Anders Krogh Broendberg, Katrine M. Müllertz, Henrik Jensen, Morten Krogh Christiansen, Lisbeth Nørum Pedersen

Publikováno v: Müllertz, K M, Christiansen, M K, Broendberg, A K, Pedersen, L N & Jensen, H K 2018, ' Outcome of clinical management in relatives of sudden cardiac death victims ', International Journal of Cardiology, vol. 262, pp. 45-50 . https://doi.org/10.1016/j.ijcard.2018.03.022

BACKGROUND: International guidelines recommend clinical assessment of the surviving first-degree relatives of sudden cardiac death (SCD) victims to identify a probable cause of death and protect surviving relatives. Only few studies have reported the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dede1ded971a0ecc7632aafba337f9c7
https://pubmed.ncbi.nlm.nih.gov/29598884

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Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias

Autor: Lisbeth Noerum Pedersen, Morten Krogh Christiansen, Henrik Jensen, Anders Krogh Broendberg, Jens Cosedis Nielsen

Publikováno v: Broendberg, A K, Christiansen, M K, Nielsen, J C, Pedersen, L N & Jensen, H K 2018, ' Targeted next generation sequencing in a young population with suspected inherited malignant cardiac arrhythmias ', European Journal of Human Genetics, vol. 26, no. 3, pp. 303-313 . https://doi.org/10.1038/s41431-017-0060-8

Aborted sudden cardiac death in the young often is due to inherited heart disease. However, the clinical phenotype in these patients is not always evident. The aim of this study was to identify pathogenic molecular genetic variants in a population wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daa6eb16f81b6a862ab244436ce1c597
https://pubmed.ncbi.nlm.nih.gov/29343803

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