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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

378 related articles for article (PubMed ID: 33221895)

  • 1. Brugada syndrome genetics is associated with phenotype severity.
    Ciconte G; Monasky MM; Santinelli V; Micaglio E; Vicedomini G; Anastasia L; Negro G; Borrelli V; Giannelli L; Santini F; de Innocentiis C; Rondine R; Locati ET; Bernardini A; Mazza BC; Mecarocci V; Ćalović Ž; Ghiroldi A; D'Imperio S; Benedetti S; Di Resta C; Rivolta I; Casari G; Petretto E; Pappone C
    Eur Heart J; 2021 Mar; 42(11):1082-1090. PubMed ID: 33221895
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-Phenotype Correlation of
    Yamagata K; Horie M; Aiba T; Ogawa S; Aizawa Y; Ohe T; Yamagishi M; Makita N; Sakurada H; Tanaka T; Shimizu A; Hagiwara N; Kishi R; Nakano Y; Takagi M; Makiyama T; Ohno S; Fukuda K; Watanabe H; Morita H; Hayashi K; Kusano K; Kamakura S; Yasuda S; Ogawa H; Miyamoto Y; Kapplinger JD; Ackerman MJ; Shimizu W
    Circulation; 2017 Jun; 135(23):2255-2270. PubMed ID: 28341781
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
    Rudic B; Schimpf R; Veltmann C; Doesch C; Tülümen E; Schoenberg SO; Borggrefe M; Papavassiliu T
    Europace; 2016 Sep; 18(9):1411-9. PubMed ID: 26511399
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genotype-Phenotype Correlation of
    Milman A; Behr ER; Gray B; Johnson DC; Andorin A; Hochstadt A; Gourraud JB; Maeda S; Takahashi Y; Jm Juang J; Kim SH; Kamakura T; Aiba T; Postema PG; Mizusawa Y; Denjoy I; Giustetto C; Conte G; Huang Z; Sarquella-Brugada G; Mazzanti A; Jespersen CH; Arbelo E; Brugada R; Calo L; Corrado D; Casado-Arroyo R; Allocca G; Takagi M; Delise P; Brugada J; Tfelt-Hansen J; Priori SG; Veltmann C; Yan GX; Brugada P; Gaita F; Leenhardt A; Wilde AAM; Kusano KF; Nam GB; Hirao K; Probst V; Belhassen B
    Circ Genom Precis Med; 2021 Oct; 14(5):e003222. PubMed ID: 34461752
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Non-invasive assessment of the arrhythmogenic substrate in Brugada syndrome using signal-averaged electrocardiogram: clinical implications from a prospective clinical trial.
    Ciconte G; Santinelli V; Vicedomini G; Borrelli V; Monasky MM; Micaglio E; Giannelli L; Negro G; Giordano F; Mecarocci V; Mazza BC; Locati E; Anastasia L; Calovic Z; Pappone C
    Europace; 2019 Dec; 21(12):1900-1910. PubMed ID: 31647530
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Further Insights in the Most Common SCN5A Mutation Causing Overlapping Phenotype of Long QT Syndrome, Brugada Syndrome, and Conduction Defect.
    Veltmann C; Barajas-Martinez H; Wolpert C; Borggrefe M; Schimpf R; Pfeiffer R; Cáceres G; Burashnikov E; Antzelevitch C; Hu D
    J Am Heart Assoc; 2016 Jul; 5(7):. PubMed ID: 27381756
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genotype-phenotype relationship and risk stratification in loss-of-function SCN5A mutation carriers.
    Robyns T; Nuyens D; Vandenberk B; Kuiperi C; Corveleyn A; Breckpot J; Garweg C; Ector J; Willems R
    Ann Noninvasive Electrocardiol; 2018 Sep; 23(5):e12548. PubMed ID: 29709101
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Brugada syndrome proband with compound heterozygote SCN5A mutations identified from a Chinese family in Singapore.
    Tan BY; Yong RY; Barajas-Martinez H; Dumaine R; Chew YX; Wasan PS; Ching CK; Ho KL; Gan LS; Morin N; Chong AP; Yap SH; Neo JL; Yap EP; Moochhala S; Chong DT; Chow W; Seow SC; Hu D; Uttamchandani M; Teo WS
    Europace; 2016 Jun; 18(6):897-904. PubMed ID: 25829473
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical characteristics and electrophysiologic properties of SCN5A variants in fever-induced Brugada syndrome.
    Chen GX; Barajas-Martínez H; Ciconte G; Wu CI; Monasky MM; Xia H; Li B; Capra JA; Guo K; Zhang ZH; Chen X; Yang B; Jiang H; Tse G; Mak CM; Aizawa Y; Gollob MH; Antzelevitch C; Wilde AAM; Pappone C; Hu D
    EBioMedicine; 2023 Jan; 87():104388. PubMed ID: 36516610
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Myotonic dystrophy type 1 mimics and exacerbates Brugada phenotype induced by Nav1.5 sodium channel loss-of-function mutation.
    Pambrun T; Mercier A; Chatelier A; Patri S; Schott JJ; Le Scouarnec S; Chahine M; Degand B; Bois P
    Heart Rhythm; 2014 Aug; 11(8):1393-400. PubMed ID: 24768612
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Impact of clinical and genetic findings on the management of young patients with Brugada syndrome.
    Andorin A; Behr ER; Denjoy I; Crotti L; Dagradi F; Jesel L; Sacher F; Petit B; Mabo P; Maltret A; Wong LC; Degand B; Bertaux G; Maury P; Dulac Y; Delasalle B; Gourraud JB; Babuty D; Blom NA; Schwartz PJ; Wilde AA; Probst V
    Heart Rhythm; 2016 Jun; 13(6):1274-82. PubMed ID: 26921764
    [TBL] [Abstract][Full Text] [Related]  

  • 12. SCN5A mutation status increases the risk of major arrhythmic events in Asian populations with Brugada syndrome: systematic review and meta-analysis.
    Rattanawong P; Chenbhanich J; Mekraksakit P; Vutthikraivit W; Chongsathidkiet P; Limpruttidham N; Prasitlumkum N; Chung EH
    Ann Noninvasive Electrocardiol; 2019 Jan; 24(1):e12589. PubMed ID: 30126015
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional Characterization of Two Novel Mutations in
    Balla C; Conte E; Selvatici R; Marsano RM; Gerbino A; Farnè M; Blunck R; Vitali F; Armaroli A; Brieda A; Liantonio A; De Luca A; Ferlini A; Rapezzi C; Bertini M; Gualandi F; Imbrici P
    Int J Mol Sci; 2021 Jun; 22(12):. PubMed ID: 34204499
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Identification of a SCN5A founder mutation causing sudden death, Brugada syndrome, and conduction blocks in Southern Italy.
    Curcio A; Malovini A; Mazzanti A; Memmi M; Gambelli P; La Rosa F; Bloise R; Indolfi C; Bellazzi R; Napolitano C
    Heart Rhythm; 2021 Oct; 18(10):1698-1706. PubMed ID: 34245912
    [TBL] [Abstract][Full Text] [Related]  

  • 15.
    Wijeyeratne YD; Tanck MW; Mizusawa Y; Batchvarov V; Barc J; Crotti L; Bos JM; Tester DJ; Muir A; Veltmann C; Ohno S; Page SP; Galvin J; Tadros R; Muggenthaler M; Raju H; Denjoy I; Schott JJ; Gourraud JB; Skoric-Milosavljevic D; Nannenberg EA; Redon R; Papadakis M; Kyndt F; Dagradi F; Castelletti S; Torchio M; Meitinger T; Lichtner P; Ishikawa T; Wilde AAM; Takahashi K; Sharma S; Roden DM; Borggrefe MM; McKeown PP; Shimizu W; Horie M; Makita N; Aiba T; Ackerman MJ; Schwartz PJ; Probst V; Bezzina CR; Behr ER
    Circ Genom Precis Med; 2020 Dec; 13(6):e002911. PubMed ID: 33164571
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Role of SCN5A coding and non-coding sequences in Brugada syndrome onset: What's behind the scenes?
    Daimi H; Khelil AH; Neji A; Ben Hamda K; Maaoui S; Aranega A; Be Chibani J; Franco D
    Biomed J; 2019 Aug; 42(4):252-260. PubMed ID: 31627867
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The SCN5A Gene Is a Predictor of Phenotype Severity in Brugada Syndrome: A Comprehensive Literature Review.
    Deica AV; Paduraru LF; Paduraru DN; Andronic O
    Med Princ Pract; 2023; 32(1):1-8. PubMed ID: 36446338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Characterization of the epicardial substrate for catheter ablation of Brugada syndrome.
    Zhang P; Tung R; Zhang Z; Sheng X; Liu Q; Jiang R; Sun Y; Chen S; Yu L; Ye Y; Fu G; Shivkumar K; Jiang C
    Heart Rhythm; 2016 Nov; 13(11):2151-2158. PubMed ID: 27453126
    [TBL] [Abstract][Full Text] [Related]  

  • 19. In silico validation revealed the role of SCN5A mutations and their genotype-phenotype correlations in Brugada syndrome.
    Pham HM; Dang DP; Ta TD; Le TP; Phan DP; Trinh HA; Tran TV; Luong TLA; Nguyen HM; Bui TH; Tran TH; Ta TV; Tran VK
    Mol Genet Genomic Med; 2023 Dec; 11(12):e2263. PubMed ID: 37547970
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Brugada syndrome with SCN5A mutations exhibits more pronounced electrophysiological defects and more severe prognosis: A meta-analysis.
    Chen C; Tan Z; Zhu W; Fu L; Kong Q; Xiong Q; Yu J; Hong K
    Clin Genet; 2020 Jan; 97(1):198-208. PubMed ID: 30963536
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.