These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
5. New phenotype of familial dilated cardiomyopathy and conduction disorders. Oropeza ES; Cadena CN Am Heart J; 2003 Feb; 145(2):317-23. PubMed ID: 12595850 [TBL] [Abstract][Full Text] [Related]
6. Progressive cardiac conduction defect is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation. Probst V; Allouis M; Sacher F; Pattier S; Babuty D; Mabo P; Mansourati J; Victor J; Nguyen JM; Schott JJ; Boisseau P; Escande D; Le Marec H J Cardiovasc Electrophysiol; 2006 Mar; 17(3):270-5. PubMed ID: 16643399 [TBL] [Abstract][Full Text] [Related]
7. Rare forms of preexcitation: a case study and brief overview of familial forms of preexcitation. Koneru JN; Wood MA; Ellenbogen KA Circ Arrhythm Electrophysiol; 2012 Aug; 5(4):e82-7. PubMed ID: 22895604 [No Abstract] [Full Text] [Related]
8. Images in cardiovascular medicine. Hereditary hypertrophic nonobstructive cardiomyopathy seen on delayed hyperenhancement magnetic resonance imaging. Steen H; Ehlermann P; Merten C; Schnabel P; Lutz M; Giannitsis E; Katus HA Circulation; 2006 Mar; 113(11):e458-9. PubMed ID: 16549643 [No Abstract] [Full Text] [Related]