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author = "Schalla, S."
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Found 3 documents, displaying page 1 of 1
Multivessel myocardial infarction
Author(s) :
Bekkers, S.C.A.M.
,
Lemmert, M.E.
,
Schalla, S.
,
Snoep, R.
,
Crijns, H.J.G.M.
,
Gorgels, A.P
Description :
Repository :
Europe PubMed Central
Language(s) :
English
Exercise related ventricular arrhythmias are related to cardiac fibrosis in hypertrophic cardiomyopathy mutation carriers
Author(s) :
van Rijsingen, I. A. W.
,
Bekkers, S. C. A. M.
,
Schalla, S.
,
Hermans-van Ast, J. F.
,
Snoep, G.
,
Alzand, B. S. N.
Description :
Repository :
Europe PubMed Central
Language(s) :
English
Hypertrophic cardiomyopathy family with double-heterozygous mutations; does disease severity suggest doubleheterozygosity?
Author(s) :
van Rijsingen, I.A.W.
,
Hermans-van Ast, J.F.
,
Arens, Y.H.J.M.
,
Schalla, S.M.
,
de Die-Smulders, C.E.M.
,
van den Wijngaard, A.
Description :
Background. With the improvement in genetic testing over time, double-heterozygous mutations are more often found by coincidence in families with hypertrophic cardiomyopathy (HCM). Double heterozygosity can be a cause of the wellknown clinical diversity within HCM families.
Repository :
Europe PubMed Central
Language(s) :
English
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Found 3 documents, displaying page 1 of 1