Catarina Lundin

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2021
Mark Evolution of P-wave indices during long-term follow-up as markers of atrial substrate progression in arrhythmogenic right ventricular cardiomyopathy
Baturova, Maria A. ^LU ; Svensson, Anneli ; Aneq, Meriam Åström ; Svendsen, Jesper H. ; Risum, Niels ; Sherina, Valeriia ; Bundgaard, Henning ; Meurling, Carl ^LU ; Lundin, Catarina ^LU and Carlson, Jonas ^LU , et al. (2021) In Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology 23(1). p.29-37
- Contribution to journal › Article
2020
Mark Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Walsh, Roddy ; Lahrouchi, Najim ; Tadros, Rafik ; Kyndt, Florence ; Glinge, Charlotte ; Postema, Pieter G. ; Amin, Ahmad S. ; Nannenberg, Eline A. ; Ware, James S. and Whiffin, Nicola , et al. (2020) In Genetics in Medicine
- Contribution to journal › Article
2019
Mark Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort
Chaudhry, U. ^LU ; Platonov, P. G. ^LU ; Rubulis, A. ; Bergfeldt, L. ; Jensen, S. M. ; Lundin, C. ^LU and Borgquist, R. ^LU (2019) In Journal of Electrocardiology 56. p.46-51
- Contribution to journal › Article
Mark Danon disease presenting with early onset of hypertrophic cardiomyopathy and peripheral pigmentary retinal dystrophy in a female with a de novo novel mosaic mutation in the LAMP2 gene
Meinert, Monika ^LU ; Englund, Elisabet ^LU ; Hedberg-Oldfors, Carola ; Oldfors, Anders ; Kornhall, Björn ^LU ; Lundin, Catarina ^LU and Wittström, Elisabeth ^LU (2019) In Ophthalmic Genetics 40(3). p.227-236
- Contribution to journal › Article
2016
Mark Rare novel variants in the ZIC3 gene cause X-linked heterotaxy
Paulussen, Aimee D C ; Steyls, Anja ; Vanoevelen, Jo ; Van Tienen, Florence H J ; Krapels, Ingrid P C ; Claes, Godelieve R F ; Chocron, Sonja ; Velter, Crool ; Tan-Sindhunata, Gita M. and Lundin, Catarina ^LU , et al. (2016) In European Journal of Human Genetics 24(12). p.1783-1791
- Contribution to journal › Article
2014
Mark Constitutional and somatic deletions of the Williams-Beuren syndrome critical region in Non-Hodgkin Lymphoma
Guenat, David ; Quentin, Samuel ; Rizzari, Carmelo ; Lundin, Catarina ^LU ; Coliva, Tiziana ; Edery, Patrick ; Fryssira, Helen ; Bermont, Laurent ; Ferrand, Christophe and Soulier, Jean , et al. (2014) In Journal of Hematology & Oncology 7.
- Contribution to journal › Letter
Mark Clinical and genetic features of pediatric acute lymphoblastic leukemia in Down syndrome in the Nordic countries
Lundin, Catarina ^LU ; Forestier, Erik ; Andersen, Mette Klarskov ; Autio, Kirsi ; Barbany, Gisela ; Cavelier, Lucia ; Golovleva, Irina ; Heim, Sverre ; Heinonen, Kristiina and Hovland, Randi , et al. (2014) In Journal of Hematology & Oncology 7.
- Contribution to journal › Article
2013
Mark Submicroscopic genomic imbalances in burkitt lymphomas/leukemias: Association with age and further evidence that 8q24/MYC translocations are not sufficient for leukemogenesis.
Lundin, Catarina ^LU ; Hjorth, Lars ^LU ; Behrendtz, Mikael ; Ehinger, Mats ^LU ; Biloglav, Andrea ^LU and Johansson, Bertil ^LU (2013) In Genes, Chromosomes and Cancer 52(4). p.370-377
- Contribution to journal › Article
Mark Novel Mutation in the KCNJ2 Gene Is Associated with a Malignant Arrhythmic Phenotype of Andersen-Tawil Syndrome.
Fernlund, Eva ^LU ; Lundin, Catarina ^LU ; Hertervig, Eva ^LU ; Kongstad Rasmussen, Ole ^LU ; Alders, M and Platonov, Pyotr ^LU (2013) In Annals of Noninvasive Electrocardiology 18(5). p.471-478
- Contribution to journal › Article
2012
Mark High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome.
Lundin, Catarina ^LU ; Hjorth, Lars ^LU ; Behrendtz, Mikael ; Nordgren, Ann ; Palmqvist, Lars ; Andersen, Mette Klarskov ; Biloglav, Andrea ^LU ; Forestier, Erik ; Paulsson, Kajsa ^LU and Johansson, Bertil ^LU (2012) In Genes, Chromosomes and Cancer 51. p.196-206
- Contribution to journal › Article

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