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 *

159 related articles for article (PubMed ID: 30371189)

  • 1. Sex-Dependent Phenotypic Variability of an SCN5A Mutation: Brugada Syndrome and Sick Sinus Syndrome.
    Aizawa Y; Fujisawa T; Katsumata Y; Kohsaka S; Kunitomi A; Ohno S; Sonoda K; Hayashi H; Hojo R; Fukamizu S; Nagase S; Ito S; Nakajima K; Nishiyama T; Kimura T; Kurita Y; Furukawa Y; Takatsuki S; Ogawa S; Nakazato Y; Sumiyoshi M; Kosaki K; Horie M; Fukuda K
    J Am Heart Assoc; 2018 Sep; 7(18):e009387. PubMed ID: 30371189
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sodium channelopathy underlying familial sick sinus syndrome with early onset and predominantly male characteristics.
    Abe K; Machida T; Sumitomo N; Yamamoto H; Ohkubo K; Watanabe I; Makiyama T; Fukae S; Kohno M; Harrell DT; Ishikawa T; Tsuji Y; Nogami A; Watabe T; Oginosawa Y; Abe H; Maemura K; Motomura H; Makita N
    Circ Arrhythm Electrophysiol; 2014 Jun; 7(3):511-7. PubMed ID: 24762805
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Dual phenotypic transmission in Brugada syndrome.
    Hermida JS; Arnalsteen-Dassonvalle E; Kubala M; Mathiron A; Traulle S; Anbazhagan K; Hermida A; Rochette J
    Arch Cardiovasc Dis; 2013; 106(6-7):366-72. PubMed ID: 23810369
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. A study of the SCN5A gene in a cohort of 76 patients with Brugada syndrome.
    García-Molina E; Lacunza J; Ruiz-Espejo F; Sabater M; García-Alberola A; Gimeno JR; Cañizares F; García A; Martínez P; Valdés M; Tovar I
    Clin Genet; 2013 Jun; 83(6):530-8. PubMed ID: 22984773
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Familial Brugada Syndrome Associated With a Complete Deletion of the SCN5A and SCN10A Genes.
    Trujillo-Quintero JP; Gutiérrez-Agulló M; Ochoa JP; Martínez-Martínez JG; de Uña D; García-Fernández A
    Rev Esp Cardiol (Engl Ed); 2019 Feb; 72(2):176-178. PubMed ID: 29650450
    [No Abstract]   [Full Text] [Related]  

  • 8. SCN5A-L256del and L1621F exhibit loss-of-function properties related to autosomal recessive congenital cardiac disorders presenting as sick sinus syndrome, dilated cardiomyopathy, and sudden cardiac death.
    Shi J; Pan X; Wang Z; Yi M; Xie S; Zhang X; Tao D; Yang Y; Liu Y
    Gene; 2024 Mar; 898():148093. PubMed ID: 38123004
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
    Monasky MM; Micaglio E; Vicedomini G; Locati ET; Ciconte G; Giannelli L; Giordano F; Crisà S; Vecchi M; Borrelli V; Ghiroldi A; D'Imperio S; Di Resta C; Benedetti S; Ferrari M; Santinelli V; Anastasia L; Pappone C
    Europace; 2019 Oct; 21(10):1550-1558. PubMed ID: 31292628
    [TBL] [Abstract][Full Text] [Related]  

  • 10. MOG1 rescues defective trafficking of Na(v)1.5 mutations in Brugada syndrome and sick sinus syndrome.
    Chakrabarti S; Wu X; Yang Z; Wu L; Yong SL; Zhang C; Hu K; Wang QK; Chen Q
    Circ Arrhythm Electrophysiol; 2013 Apr; 6(2):392-401. PubMed ID: 23420830
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel SCN5A mutation demonstrating a variety of clinical phenotypes in familial sick sinus syndrome.
    Nakajima S; Makiyama T; Hanazawa K; Kaitani K; Amano M; Hayama Y; Onishi N; Tamaki Y; Miyake M; Tamura T; Kondo H; Motooka M; Izumi C; Nakagawa Y; Horie M
    Intern Med; 2013; 52(16):1805-8. PubMed ID: 23955615
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Variants in the SCN5A Promoter Associated With Various Arrhythmia Phenotypes.
    Yagihara N; Watanabe H; Barnett P; Duboscq-Bidot L; Thomas AC; Yang P; Ohno S; Hasegawa K; Kuwano R; Chatel S; Redon R; Schott JJ; Probst V; Koopmann TT; Bezzina CR; Wilde AA; Nakano Y; Aiba T; Miyamoto Y; Kamakura S; Darbar D; Donahue BS; Shigemizu D; Tanaka T; Tsunoda T; Suda M; Sato A; Minamino T; Endo N; Shimizu W; Horie M; Roden DM; Makita N
    J Am Heart Assoc; 2016 Sep; 5(9):. PubMed ID: 27625342
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Novel
    Monasky MM; Micaglio E; Ciconte G; Rivolta I; Borrelli V; Ghiroldi A; D'Imperio S; Binda A; Melgari D; Benedetti S; Mitrovic P; Anastasia L; Mecarocci V; Ćalović Ž; Casari G; Pappone C
    Int J Mol Sci; 2021 Apr; 22(9):. PubMed ID: 33946750
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Copy number variations of SCN5A in Brugada syndrome.
    Sonoda K; Ohno S; Ozawa J; Hayano M; Hattori T; Kobori A; Yahata M; Aburadani I; Watanabe S; Matsumoto Y; Makiyama T; Horie M
    Heart Rhythm; 2018 Aug; 15(8):1179-1188. PubMed ID: 29574140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical Spectrum of
    Villarreal-Molina T; García-Ordóñez GP; Reyes-Quintero ÁE; Domínguez-Pérez M; Jacobo-Albavera L; Nava S; Carnevale A; Medeiros-Domingo A; Iturralde P
    Genes (Basel); 2021 Dec; 13(1):. PubMed ID: 35052356
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Sinus node disease in subjects with type 1 ECG pattern of Brugada syndrome.
    Letsas KP; Korantzopoulos P; Efremidis M; Weber R; Lioni L; Bakosis G; Vassilikos VP; Deftereos S; Sideris A; Arentz T
    J Cardiol; 2013 Mar; 61(3):227-31. PubMed ID: 23403368
    [TBL] [Abstract][Full Text] [Related]  

  • 19. An R1632C variant in the SCN5A gene causing Brugada syndrome.
    García-Molina E; Sabater-Molina M; Muñoz C; Ruiz-Espejo F; Gimeno JR
    Mol Med Rep; 2016 Jun; 13(6):4677-80. PubMed ID: 27082542
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Sick sinus syndrome with HCN4 mutations shows early onset and frequent association with atrial fibrillation and left ventricular noncompaction.
    Ishikawa T; Ohno S; Murakami T; Yoshida K; Mishima H; Fukuoka T; Kimoto H; Sakamoto R; Ohkusa T; Aiba T; Nogami A; Sumitomo N; Shimizu W; Yoshiura KI; Horigome H; Horie M; Makita N
    Heart Rhythm; 2017 May; 14(5):717-724. PubMed ID: 28104484
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.