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Results 1 - 10 of 12 for Brugada syndrome 1
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  1. Brugada syndrome 
    ... Testing Registry: Brugada syndrome Genetic Testing Registry: Brugada syndrome 1 Brugada syndrome National Organization for Rare Disorders (NORD) ClinicalTrials. ...
    https://medlineplus.gov/genetics/condition/brugada-syndrome - Genetics
  2. SCN5A gene 
    ... SCN5A gene have been identified in people with Brugada syndrome, which is a heart condition characterized by an ... populations. Researchers have since determined that SUNDS and Brugada syndrome are the same disorder.Some SCN5A gene mutations ...
    https://medlineplus.gov/genetics/gene/scn5a - Genetics
  3. Progressive familial heart block 
    ... is the prevailing phenotype in carriers of a Brugada syndrome SCN5A mutation. J Cardiovasc Electrophysiol. 2006 Mar;17( ... CR. Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J Clin ...
    https://medlineplus.gov/.../progressive-familial-heart-block - Genetics
  4. Romano-Ward syndrome 
    ... on PubMed Vincent GM. The Long QT and Brugada syndromes: causes of unexpected syncope and sudden cardiac death ...
    https://medlineplus.gov/genetics/condition/romano-ward-syndrome - Genetics
  5. CACNA1C gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition Variants in the ...
    https://medlineplus.gov/genetics/gene/cacna1c - Genetics
  6. HCN4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/hcn4 - Genetics
  7. TRPM4 gene 
    ... This Health Condition MedlinePlus Genetics provides information about Brugada syndrome More About This Health Condition calcium-activated non- ...
    https://medlineplus.gov/genetics/gene/trpm4 - Genetics
  8. KCNH2 gene 
    ... Guerchicoff A, Bianchi F, Giustetto C, Schimpf R, Brugada P, Antzelevitch C. Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation. 2004 Jan 6;109(1):30-5. doi: 10.1161/01.CIR.0000109482. ...
    https://medlineplus.gov/genetics/gene/kcnh2 - Genetics
  9. KCNQ1 gene 
    ... Enfante E, Brugada P, Sachse F, Sanguinetti MC, Brugada R. De novo KCNQ1 mutation responsible for atrial fibrillation and short QT syndrome in utero. Cardiovasc Res. 2005 Dec 1;68(3):433-40. doi: 10.1016/j. ...
    https://medlineplus.gov/genetics/gene/kcnq1 - Genetics
  10. Jervell and Lange-Nielsen syndrome 
    ... Nakano Y, Shimizu W. Genetics of long-QT syndrome. J Hum Genet. 2016 Jan;61(1):51-5. doi: 10.1038/jhg.2015.74. Epub 2015 Jun 25. Citation on PubMed Priori SG, Wilde AA, Horie M, Cho Y, Behr ER, Berul C, Blom N, Brugada J, Chiang CE, Huikuri H, Kannankeril P, Krahn ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
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