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“Unmasked Brugada pattern by ajmaline challenge in patients with myotonic dystrophy type 1.”, Ann Noninvasive Electrocardiol, vol. 20, no. 1, pp. 28-36, 2015.
, “Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.”, Heart Rhythm, vol. 11, no. 8, pp. 1393-400, 2014.
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