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Brugada syndrome 4
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- ... on PubMed Shimizu W. Acquired forms of the Brugada syndrome. J Electrocardiol. 2005 Oct;38(4 Suppl):22-5. doi: 10.1016/j.jelectrocard.2005.06.005. Citation on PubMed Vatta M, Dumaine R, Varghese G, Richard TA, Shimizu W, Aihara N, Nademanee K, Brugada R, Brugada J, Veerakul G, Li H, Bowles ...
- ... 014. Citation on PubMed Juang JM, Huang SK. Brugada syndrome--an under-recognized electrical disease in patients with sudden cardiac death. Cardiology. 2004;101(4):157-69. doi: 10.1159/000076693. Epub 2004 ...
- ... 98. doi: 10.1016/s0002-9343(00)00715-4. Citation on PubMed Vincent GM. The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death ...
- ... on PubMed Hong K, Bjerregaard P, Gussak I, Brugada R. Short QT syndrome and atrial fibrillation caused by mutation in KCNH2. J Cardiovasc Electrophysiol. 2005 Apr;16(4):394-6. doi: 10.1046/j.1540-8167. ...
- ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition calcium-activated non-selective cation channel 1 hTRPM4 long transient receptor potential channel 4 LTrpC4 melastatin-4 transient receptor potential cation channel, ...
- ... This Health Condition MedlinePlus Genetics provides information about Brugada ... cation channel 4 hyperpolarization activated cyclic nucleotide-gated potassium channel 4 ...
- ... Giustetto C, Gaita F, Schimpf R. Short QT syndrome. Genotype-phenotype correlations. J Electrocardiol. 2005 Oct;38(4 Suppl):75-80. doi: 10.1016/j.jelectrocard.2005.06.009. Citation on PubMed or Free article on PubMed Central Brugada R, Hong K, Cordeiro JM, Dumaine R. Short ...
- ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ... 10.1002/ajmg.a.40657. Epub 2018 Dec 4. Citation on PubMed Fukuyama ... M. Long QT syndrome type 8: novel CACNA1C mutations causing QT prolongation ...
- ... causing mutations in the Jervell and Lange-Nielsen syndrome. Cardiovasc Res. 2001 Sep;51(4):670-80. doi: 10.1016/s0008-6363(01) ... mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome. Mol Genet Metab. 2002 Apr;75(4):308-16. doi: 10.1016/S1096-7192(02) ...
- ... mutations in KvLQT1 cause Jervell and Lange-Nielsen syndrome. Mol Genet Metab. 2002 Apr;75(4):308-16. doi: 10.1016/S1096-7192(02)00007-0. Citation on PubMed