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 *

220 related articles for article (PubMed ID: 35004896)

  • 1. The Mechanism of Ajmaline and Thus Brugada Syndrome: Not Only the Sodium Channel!
    Monasky MM; Micaglio E; D'Imperio S; Pappone C
    Front Cardiovasc Med; 2021; 8():782596. PubMed ID: 35004896
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Value of the sodium-channel blocker challenge in Brugada syndrome.
    Therasse D; Sacher F; Babuty D; Mabo P; Mansourati J; Kyndt F; Redon R; Schott JJ; Barc J; Probst V; Gourraud JB
    Int J Cardiol; 2017 Oct; 245():178-180. PubMed ID: 28784436
    [TBL] [Abstract][Full Text] [Related]  

  • 4. High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
    Hasdemir C; Payzin S; Kocabas U; Sahin H; Yildirim N; Alp A; Aydin M; Pfeiffer R; Burashnikov E; Wu Y; Antzelevitch C
    Heart Rhythm; 2015 Jul; 12(7):1584-94. PubMed ID: 25998140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A cellular model of Brugada syndrome with SCN10A variants using human-induced pluripotent stem cell-derived cardiomyocytes.
    El-Battrawy I; Albers S; Cyganek L; Zhao Z; Lan H; Li X; Xu Q; Kleinsorge M; Huang M; Liao Z; Zhong R; Rudic B; Müller J; Dinkel H; Lang S; Diecke S; Zimmermann WH; Utikal J; Wieland T; Borggrefe M; Zhou X; Akin I
    Europace; 2019 Sep; 21(9):1410-1421. PubMed ID: 31106349
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Diagnostic Yield of Brugada Syndrome After Sudden Death With Normal Autopsy.
    Papadakis M; Papatheodorou E; Mellor G; Raju H; Bastiaenen R; Wijeyeratne Y; Wasim S; Ensam B; Finocchiaro G; Gray B; Malhotra A; D'Silva A; Edwards N; Cole D; Attard V; Batchvarov VN; Tome-Esteban M; Homfray T; Sheppard MN; Sharma S; Behr ER
    J Am Coll Cardiol; 2018 Mar; 71(11):1204-1214. PubMed ID: 29544603
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Brugada Syndrome: Warning of a Systemic Condition?
    D'Imperio S; Monasky MM; Micaglio E; Ciconte G; Anastasia L; Pappone C
    Front Cardiovasc Med; 2021; 8():771349. PubMed ID: 34722688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Predicting cardiac electrical response to sodium-channel blockade and Brugada syndrome using polygenic risk scores.
    Tadros R; Tan HL; ; El Mathari S; Kors JA; Postema PG; Lahrouchi N; Beekman L; Radivojkov-Blagojevic M; Amin AS; Meitinger T; Tanck MW; Wilde AA; Bezzina CR
    Eur Heart J; 2019 Oct; 40(37):3097-3107. PubMed ID: 31504448
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ajmaline blocks I
    Miller DC; Harmer SC; Poliandri A; Nobles M; Edwards EC; Ware JS; Sharp TV; McKay TR; Dunkel L; Lambiase PD; Tinker A
    Stem Cell Res; 2017 Dec; 25():233-244. PubMed ID: 29172153
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A balanced translocation disrupting SCN5A in a family with Brugada syndrome and sudden cardiac death.
    Yeates L; Ingles J; Gray B; Singarayar S; Sy RW; Semsarian C; Bagnall RD
    Heart Rhythm; 2019 Feb; 16(2):231-238. PubMed ID: 30170230
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.
    Hu D; Barajas-Martínez H; Medeiros-Domingo A; Crotti L; Veltmann C; Schimpf R; Urrutia J; Alday A; Casis O; Pfeiffer R; Burashnikov E; Caceres G; Tester DJ; Wolpert C; Borggrefe M; Schwartz P; Ackerman MJ; Antzelevitch C
    Heart Rhythm; 2012 May; 9(5):760-9. PubMed ID: 22155597
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brugada syndrome disease phenotype explained in apparently benign sodium channel mutations.
    Hoshi M; Du XX; Shinlapawittayatorn K; Liu H; Chai S; Wan X; Ficker E; Deschênes I
    Circ Cardiovasc Genet; 2014 Apr; 7(2):123-31. PubMed ID: 24573164
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Single-cell transcriptomics trajectory and molecular convergence of clinically relevant mutations in Brugada syndrome.
    Tambi R; Abdel Hameid R; Bankapur A; Nassir N; Begum G; Alsheikh-Ali A; Uddin M; Berdiev BK
    Am J Physiol Heart Circ Physiol; 2021 May; 320(5):H1935-H1948. PubMed ID: 33797273
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Disease-targeted sequencing of ion channel genes identifies de novo mutations in patients with non-familial Brugada syndrome.
    Juang JM; Lu TP; Lai LC; Ho CC; Liu YB; Tsai CT; Lin LY; Yu CC; Chen WJ; Chiang FT; Yeh SF; Lai LP; Chuang EY; Lin JL
    Sci Rep; 2014 Oct; 4():6733. PubMed ID: 25339316
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations.
    Hong K; Brugada J; Oliva A; Berruezo-Sanchez A; Potenza D; Pollevick GD; Guerchicoff A; Matsuo K; Burashnikov E; Dumaine R; Towbin JA; Nesterenko V; Brugada P; Antzelevitch C; Brugada R
    Circulation; 2004 Nov; 110(19):3023-7. PubMed ID: 15520322
    [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. SCN5A gene variants and arrhythmic risk in Brugada syndrome: An updated systematic review and meta-analysis.
    Doundoulakis I; Pannone L; Chiotis S; Della Rocca DG; Sorgente A; Tsioufis P; Del Monte A; Vetta G; Piperis C; Overeinder I; Bala G; Almorad A; Ströker E; Sieira J; La Meir M; Brugada P; Tsiachris D; Sarkozy A; Chierchia GB; de Asmundis C
    Heart Rhythm; 2024 Apr; ():. PubMed ID: 38614189
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Ventricular arrhythmia during ajmaline challenge for the Brugada syndrome.
    Dobbels B; De Cleen D; Ector J
    Europace; 2016 Oct; 18(10):1501-1506. PubMed ID: 26941343
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutations in SCN10A are responsible for a large fraction of cases of Brugada syndrome.
    Hu D; Barajas-Martínez H; Pfeiffer R; Dezi F; Pfeiffer J; Buch T; Betzenhauser MJ; Belardinelli L; Kahlig KM; Rajamani S; DeAntonio HJ; Myerburg RJ; Ito H; Deshmukh P; Marieb M; Nam GB; Bhatia A; Hasdemir C; Haïssaguerre M; Veltmann C; Schimpf R; Borggrefe M; Viskin S; Antzelevitch C
    J Am Coll Cardiol; 2014 Jul; 64(1):66-79. PubMed ID: 24998131
    [TBL] [Abstract][Full Text] [Related]  

  • 20. T-Peak to T-End Interval for Prediction of Positive Response to Ajmaline Challenge Test in Suspected Brugada Syndrome Patients.
    Thapanasuta M; Chokesuwattanaskul R; Leelapatana P; Rungpradubvong V; Prechawat S
    Med Sci (Basel); 2022 Dec; 10(4):. PubMed ID: 36548004
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.