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Transthyretin amyloidosis: a phenocopy of hypertrophic cardiomyopathy.

Autor: Vermeer, Alexa M. C.^1,2 (AUTHOR) a.m.vermeer@amc.uva.nl, Janssen, Anneloes¹ (AUTHOR), Boorsma, Peter C.¹ (AUTHOR), Mannens, Marcel M. A. M.¹ (AUTHOR), Wilde, Arthur A. M.^2,3 (AUTHOR), Christiaans, Imke¹ (AUTHOR)

Publikováno v: Amyloid. 2017, Vol. 24 Issue 2, p87-91. 5p.

Quality of Life in Young Adult Patients with a Cardiogenetic Condition Receiving an ICD for Primary Prevention of Sudden Cardiac Death.

Autor: VERKERK, AGNES J.¹, VERMEER, ALEXA M.², SMETS, ELLEN M.³, DEKKER, LUKAS R.⁴, WILDE, ARTHUR A.¹, VAN LANGEN, IRENE M.⁵, CHRISTIAANS, IMKE², NIEUWKERK, PYTHIA T.³

Publikováno v: Pacing & Clinical Electrophysiology. Jul2015, Vol. 38 Issue 7, p870-877. 8p.

Human genetics of cardiomyopathies

Autor: Vermeer, Alexa M. C., Wilde, Arthur A. M., Christiaans, Imke, Rickert-Sperling, Silke, Kelly, Robert G., Driscoll, D. J.

Publikováno v: Congenital heart diseases: the broken heart; clinical features, human genetics and molecular pathways, 675-686
STARTPAGE=675;ENDPAGE=686;TITLE=Congenital heart diseases: the broken heart; clinical features, human genetics and molecular pathways
Congenital Heart Diseases: The Broken Heart, 675-686
ISSUE=1;STARTPAGE=675;ENDPAGE=686;TITLE=Congenital Heart Diseases
Congenital Heart Diseases: The Broken Heart ISBN: 9783709118825

Over the past few decades, there has been notable progress in knowledge and implication of genetics in cardiomyopathies. Twenty-five years ago we started to recognize the genes; nowadays dozens ‑of genes associated with cardiomyopathies have been d

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4ac6cbf6b58a6e2d0d3eddf6f32e36c
https://pure.amc.nl/en/publications/human-genetics-of-cardiomyopathies(81ca527b-bfd0-447c-b326-d84e8440e829).html