Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lisbeth Noerum Pedersen"'
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
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
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
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
https://doi.org/10.1016/j.hrcr.2016.02.008
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
https://pubmed.ncbi.nlm.nih.gov/29343803
Autor:
Anders Krogh Broendberg, Jesper Vandborg Bjerre, Finn Lund Henriksen, Henrik Jensen, Jens Kristensen, Henning Bundgaard, Lisbeth Noerum Pedersen, Jens Cosedis Nielsen
Publikováno v:
Broendberg, A K, Nielsen, J C, Bjerre, J, Pedersen, L N, Kristensen, J, Henriksen, F L, Bundgaard, H & Jensen, H K 2017, ' Nationwide experience of catecholaminergic polymorphic ventricular tachycardia caused by RyR2 mutations ', Heart, vol. 103, no. 12, pp. 901-909 . https://doi.org/10.1136/heartjnl-2016-310509
OBJECTIVE: The aim of this study was to characterise disease penetrance, course of disease and use of antiarrhythmic medication and implantable cardioverter-defibrillator (ICD) therapy in a Danish nationwide cohort of patients with catecholaminergic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64a1a58ac3bfa94f95ae0a775ebabd8d
https://pubmed.ncbi.nlm.nih.gov/28302685
https://pubmed.ncbi.nlm.nih.gov/28302685
Autor:
Anders Krogh Broendberg, Henrik Jensen, Morten Krogh Christiansen, Kasper Thorsen, Lisbeth Noerum Pedersen
Publikováno v:
EP Europace. 18:i156-i156
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb45ef98a6a83082a2f36c63cd71a810
https://doi.org/10.1093/europace/18.suppl_1.i156
https://doi.org/10.1093/europace/18.suppl_1.i156