Zobrazeno 1 - 4
of 4
pro vyhledávání: '"A. Wålinder Österberg"'
Autor:
Anna Wålinder Österberg, Ingegerd Östman-Smith, Henrik Green, Cecilia Gunnarsson, Mats Fredrikson, Petru Liuba, Eva Fernlund
Publikováno v:
Journal of Cardiovascular Development and Disease, Vol 11, Iss 4, p 105 (2024)
Background: Any difference in biomarkers between genotype-positive individuals with overt hypertrophic cardiomyopathy (HCM), and genotype-positive but phenotype-negative individuals (G+P-) in HCM-associated pathways might shed light on pathophysiolog
Externí odkaz:
https://doaj.org/article/929412b96f7b42c49081ef5a7bfee495
Autor:
Ingegerd Östman-Smith, Cecilia Gunnarsson, Anna Wålinder Österberg, Marcus Carlsson, Robert Jablonowski, Eva Fernlund, Petru Liuba, Henrik Gréen
Publikováno v:
Pediatric Cardiology. 42:492-500
An ECG risk-score has been described that predicts high risk of subsequent cardiac arrest in young patients with hypertrophic cardiomyopathy (HCM). Myocardial fibrosis measured by cardiac magnetic resonance (CMR) late gadolinium enhancement (LGE) als
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1802c27a6b6a82fbe8dd2568170bb352
https://doi.org/10.1007/s00246-020-02506-9
https://doi.org/10.1007/s00246-020-02506-9
Autor:
Anna Wålinder, Österberg, Ingegerd, Östman-Smith, Robert, Jablonowski, Marcus, Carlsson, Henrik, Green, Cecilia, Gunnarsson, Petru, Liuba, Eva, Fernlund
Publikováno v:
Pediatric cardiology. 42(3)
An ECG risk-score has been described that predicts high risk of subsequent cardiac arrest in young patients with hypertrophic cardiomyopathy (HCM). Myocardial fibrosis measured by cardiac magnetic resonance (CMR) late gadolinium enhancement (LGE) als
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4545ba7cc608edeb53faa085ac08e31
https://pubmed.ncbi.nlm.nih.gov/33515326
https://pubmed.ncbi.nlm.nih.gov/33515326
Autor:
A. Wålinder Österberg, Cecilia Gunnarsson, Kjell Jansson, M. Gustafsson, Eva I. Fernlund, E. Kuchinskaya
Publikováno v:
Pediatric Cardiology
Familial dilated cardiomyopathy is a rare cause of dilated cardiomyopathy (DCM), especially in childhood. Our aim was to describe the clinical course and the genetic variants in a family where the proband was a four-month-old infant presenting with r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a4ea9667adc7be8581de5aaf2fb8a6f
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-139519
http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-139519
