Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Ulla Wedén"'
Autor:
Cecilia Linde, Mattias Ekström, Maria J. Eriksson, Eva Maret, Håkan Wallén, Patrik Lyngå, Ulla Wedén, Carin Cabrera, Ulrika Löfström, Jenny Stenudd, Lars H. Lund, Bengt Persson, Hans Persson, Camilla Hage, for the Stockholm County/Karolinska Institutet 4D heart failure investigators
Publikováno v:
ESC Heart Failure, Vol 9, Iss 4, Pp 2125-2138 (2022)
Abstract Aim We present the baseline characteristics of the PREFERS Stockholm epidemiological study on the natural history and course of new onset heart failure (HF) aiming to improve phenotyping focusing on HF with preserved left ventricular ejectio
Externí odkaz:
https://doaj.org/article/72d9ecccb1b54bfeb4535da0c9c16a91
Autor:
Hanna Arnesson, Lisbeth Tranebjærg, Anna-Carin Rehnman, Niklas Dahl, Ulla Wedén, Nanna Dahl Rendtorff, Joakim Klar, Marianne Lodahl, Carina Frykholm
Publikováno v:
Gene. 563:10-16
Linkage to an interval overlapping the DFNA10 locus on chromosome 6q22-23 was found through genome wide linkage analysis in a seven-generation Swedish family segregating postlingual, autosomal dominant nonsyndromic sensorineural hearing impairment. A