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KVLQT1, the rhythm of imprinting.
Mannens M, Wilde A. Mannens M, et al. Nat Genet. 1997 Feb;15(2):113-5. doi: 10.1038/ng0297-113. Nat Genet. 1997. PMID: 9020829 No abstract available.
A dominant negative isoform of the long QT syndrome 1 gene product.
Demolombe S, Baró I, Péréon Y, Bliek J, Mohammad-Panah R, Pollard H, Morid S, Mannens M, Wilde A, Barhanin J, Charpentier F, Escande D. Demolombe S, et al. J Biol Chem. 1998 Mar 20;273(12):6837-43. doi: 10.1074/jbc.273.12.6837. J Biol Chem. 1998. PMID: 9506986 Free article.
Genotype-phenotype relationship in Brugada syndrome: electrocardiographic features differentiate SCN5A-related patients from non-SCN5A-related patients.
Smits JP, Eckardt L, Probst V, Bezzina CR, Schott JJ, Remme CA, Haverkamp W, Breithardt G, Escande D, Schulze-Bahr E, LeMarec H, Wilde AA. Smits JP, et al. Among authors: wilde aa. J Am Coll Cardiol. 2002 Jul 17;40(2):350-6. doi: 10.1016/s0735-1097(02)01962-9. J Am Coll Cardiol. 2002. PMID: 12106943 Free article.
Proposed diagnostic criteria for the Brugada syndrome.
Wilde AA, Antzelevitch C, Borggrefe M, Brugada J, Brugada R, Brugada P, Corrado D, Hauer RN, Kass RS, Nademanee K, Priori SG, Towbin JA; Study Group on the Molecular Basis of Arrhythmias of the European Society of Cardiology. Wilde AA, et al. Eur Heart J. 2002 Nov;23(21):1648-54. doi: 10.1053/euhj.2002.3382. Eur Heart J. 2002. PMID: 12448445 Review. No abstract available.
906 results