Diagnostic gain of cardiac MR in patients with premature ventricular complexes and structurally normal hearts on echocardiography

Autor: T Ahmed, S Aagaard-Nilsen, O G Anfinsen, F Hegbom, T Holm, G Bosse, T Edvardsen, E Kongsgaard, L A Dejgaard, M Korseberg Stokke

Publikováno v: Europace. 25

Funding Acknowledgements Type of funding sources: Public Institution(s). Main funding source(s): KG Jebsen Centre for Cardiac Research, University of Oslo, Oslo, Norway Background An important part of the diagnostic evaluation of patients with premat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::902633414144e4bcb1c22405f5be67a2
https://doi.org/10.1093/europace/euad122.633

Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia

Autor: Lilian Bomme Ousager, Anette Drøhse Kjeldsen, Katrine S. Aagaard, Martin Jakob Larsen, Klaus Brusgaard, Emilie B. Lester, Pernille Mathiesen Tørring, Ieva Miceikaite

Publikováno v: Molecular Genetics & Genomic Medicine, Vol 8, Iss 11, Pp n/a-n/a (2020)
Aagaard, K S, Brusgaard, K, Miceikaite, I, Larsen, M J, Kjeldsen, A D, Lester, E B, Ousager, L B & Tørring, P M 2020, ' Chromosomal translocation disrupting the SMAD4 gene resulting in the combined phenotype of Juvenile polyposis syndrome and Hereditary Hemorrhagic Telangiectasia ', Molecular Genetics and Genomic Medicine, vol. 8, no. 11, e1498 . https://doi.org/10.1002/mgg3.1498
Molecular Genetics & Genomic Medicine

Background Patients with germline variants in SMAD4 can present symptoms of both juvenile polyposis syndrome (JPS) and Hereditary Hemorrhagic Telangiectasia (HHT): JP‐HHT syndrome. Next‐Generation Sequencing (NGS) techniques disclose causative se

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61fcfc12b56672a105be32f086b1ebb6
https://doaj.org/article/f725ae3adc49493f95c49b3543b04589

Comorbidity among HHT patients and their controls in a 20 years follow-up period

Autor: Anette Drøhse Kjeldsen, Pernille Mathiesen Tørring, Katrine S. Aagaard, Anders Green

Publikováno v: Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-9 (2018)
Aagaard, K S, Kjeldsen, A D, Tørring, P M & Green, A 2018, ' Comorbidity among HHT patients and their controls in a 20 years follow-up period ', Orphanet Journal of Rare Diseases, vol. 13, 223 . https://doi.org/10.1186/s13023-018-0962-8

Background Hereditary Haemorrhagic Telangiectasia (HHT) is an autosomal dominant genetic disorder with a wide variety of clinical manifestations due to the presence of multiple arteriovenous malformations in various tissues and organs. Objective To s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f482c4eed80072a9a770066f39daa5b3
http://europepmc.org/articles/PMC6295040

Changes in Greenland’s peripheral glaciers linked to the North Atlantic Oscillation

Autor: Shfaqat Abbas Khan, Horst Machguth, Kurt H. Kjær, A Lütt, Yannick Peings, Niels J. Korsgaard, Jason E. Box, S. Aagaard, John Cappelen, Anders A. Bjørk, Kristian K. Kjeldsen, Camilla S. Andresen, Nicolaj K. Larsen, William Colgan

Publikováno v: Bjørk, A A, Aagaard, S, Lütt, A, Khan, S A, Box, J E, Kjeldsen, K K, Larsen, N K, Korsgaard, N J, Cappelen, J, Colgan, W T, Machguth, H, Andresen, C S, Peings, Y & Kjær, K H 2018, ' Changes in Greenland’s peripheral glaciers linked to the North Atlantic Oscillation ', Nature Climate Change, vol. 8, pp. 48-52 . https://doi.org/10.1038/s41558-017-0029-1

Glaciers and ice caps peripheral to the main Greenland Ice Sheet contribute markedly to sea-level rise 1–3 . Their changes and variability, however, have been difficult to quantify on multi-decadal timescales due to an absence of long-term data 4 .

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e424d6195faf44176c53815226eb1d4
http://doc.rero.ch/record/309007/files/mac_cgp.pdf

Neonatal epicardial-derived progenitors aquire myogenic traits in skeletal muscle, but not cardiac muscle

Autor: Gunnhildur Asta Traustadottir, Suganya Ganesalingam, Søren P. Sheikh, Charlotte Harken Jensen, Katrine S. Aagaard, Ditte Caroline Andersen, Ida Skovrind, Rikke Helin Johnsen

Publikováno v: Andersen, D C, Jensen, C H, Skovrind, I, Johnsen, R H, Traustadottir, G A, Aagaard, K S, Ganesalingam, S & Sheikh, S P 2016, ' Neonatal epicardial-derived progenitors aquire myogenic traits in skeletal muscle, but not cardiac muscle ', International Journal of Cardiology, vol. 222, pp. 448-456 . https://doi.org/10.1016/j.ijcard.2016.07.165

BACKGROUND/OBJECTIVES: Epicardium-derived progenitor cells (EPDCs) differentiate into all heart cell types in the embryonic heart, yet their differentiation into cardiomyocytes in the adult heart is limited and poorly described. This may be due to EP

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::99577f86dd7af4fcae0750549b80c149
https://pubmed.ncbi.nlm.nih.gov/27505332