Increased left ventricular torsion in hypertrophic cardiomyopathy mutation carriers with normal wall thickness

Autor: Götte Marco, Marcus Tim, Germans Tjeerd, Brouwer Wessel P, Rüssel Iris, van Rossum Albert

Publikováno v: Journal of Cardiovascular Magnetic Resonance, Vol 11, Iss Suppl 1, p P201 (2009)

Externí odkaz: https://doaj.org/article/8cc66e73fbf34e4f8698bb5b7d4ba277

The development of familial hypertrophic cardiomyopathy: from mutation to bedside.

Autor: Brouwer, Wessel P.^1,2 w.brouwer@vumc.nl, van Dijk, Sabine J.³, Stienen, Ger J. M.³, van Rossum, Albert C.^1,2, van der Velden, Jolanda³, Germans, Tjeerd¹

Publikováno v: European Journal of Clinical Investigation. May2011, Vol. 41 Issue 5, p568-578. 11p. 2 Black and White Photographs, 1 Diagram, 1 Graph.

Cardiac involvement with amyloidosis:mechanisms of disease, diagnosis and management

Autor: Marcu, Constantin B, Niessen, Hans W, Beek, Aernout M, Brouwer, Wessel P, Robbers, Lourens F, Van Rossum, Albert C

Publikováno v: Marcu, C B, Niessen, H W, Beek, A M, Brouwer, W P, Robbers, L F & Van Rossum, A C 2012, ' Cardiac involvement with amyloidosis : mechanisms of disease, diagnosis and management ', Connecticut medicine, vol. 75, no. 10, pp. 581-90 .

The amyloidoses represent a group of clinical disorders of diverse etiologies that have as a common pathophysiologic denominator the deposition of misfolded protein based amyloid fibrils in the interstitial space of various organs. They are uncommon

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=od_____10172::6c58374e9f0a4866add896c67b0b4e37
https://research.vumc.nl/en/publications/42a16014-28d0-40ad-8482-2f0b95081d14

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