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 *

144 related articles for article (PubMed ID: 32765855)

  • 1. Lack of association between mitochondrial DNA haplogroups J and T and clinical manifestation in Russian patients with Brugada syndrome.
    Golubenko M; Mikhailov V; Rusinova V; Shestak A; Zaklyazminskaya E
    Biomed Rep; 2020 Sep; 13(3):16. PubMed ID: 32765855
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Mutational analysis of mitochondrial DNA in Brugada syndrome.
    Stocchi L; Polidori E; Potenza L; Rocchi MB; Calcabrini C; Busacca P; Capalbo M; Potenza D; Amati F; Mango R; Romeo F; Novelli G; Stocchi V
    Cardiovasc Pathol; 2016; 25(1):47-54. PubMed ID: 26549652
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene].
    Zakliaz'minskaia EV; Shestak AG; Revishvili ASh; Pronicheva IV; Podoliak DG; Nechaenko MA; Poliakov AV; Dzemeshkevich SL
    Khirurgiia (Mosk); 2013; (2):49-53. PubMed ID: 23503384
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome.
    Zaklyazminskaya E; Shestak A; Podolyak D; Komoliatova V; Makarov L; Novitskaya A; Revishvili A
    Front Pharmacol; 2022; 13():984299. PubMed ID: 36091819
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Doubts of the cardiologist regarding an electrocardiogram presenting QRS V1-V2 complexes with positive terminal wave and ST segment elevation. Consensus Conference promoted by the Italian Cardiology Society].
    Oreto G; Corrado D; Delise P; Fedele F; Gaita F; Gentile F; Giustetto C; Michelucci A; Padeletti L; Priori S
    G Ital Cardiol (Rome); 2010 Nov; 11(11 Suppl 2):3S-22S. PubMed ID: 21361048
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Brugada Syndrome: Clinical Features, Risk Stratification, and Management.
    Malik BR; Ali Rudwan AM; Abdelghani MS; Mohsen M; Khan SHA; Aljefairi N; Mahmoud E; Asaad N; Hayat SA
    Heart Views; 2020; 21(2):88-96. PubMed ID: 33014301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Long-Term Prognosis of Brugada-Type ECG and ECG With Atypical ST-Segment Elevation in the Right Precordial Leads Over 20 Years: Results From the Circulatory Risk in Communities Study (CIRCS).
    Tsuneoka H; Takagi M; Murakoshi N; Yamagishi K; Yokoyama Y; Xu D; Sekiguchi Y; Yamasaki H; Naruse Y; Ito Y; Igarashi M; Kitamura A; Okada T; Tanigawa T; Kuga K; Ohira T; Tada H; Aonuma K; Iso H;
    J Am Heart Assoc; 2016 Aug; 5(8):. PubMed ID: 27503848
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetics of Brugada syndrome.
    Juang JJ; Horie M
    J Arrhythm; 2016 Oct; 32(5):418-425. PubMed ID: 27761167
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Brugada syndrome: A general cardiologist's perspective.
    Polovina MM; Vukicevic M; Banko B; Lip GYH; Potpara TS
    Eur J Intern Med; 2017 Oct; 44():19-27. PubMed ID: 28645806
    [TBL] [Abstract][Full Text] [Related]  

  • 10. The genetic component of Brugada syndrome.
    Nielsen MW; Holst AG; Olesen SP; Olesen MS
    Front Physiol; 2013; 4():179. PubMed ID: 23874304
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Electrocardiographic methods for diagnosis and risk stratification in the Brugada syndrome.
    Naseef A; Behr ER; Batchvarov VN
    J Saudi Heart Assoc; 2015 Apr; 27(2):96-108. PubMed ID: 25870503
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Brugada syndrome.
    Napolitano C; Priori SG
    Orphanet J Rare Dis; 2006 Sep; 1():35. PubMed ID: 16972995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. [Mitochondrial DNA variation in Russian populations of Stavropol krai, Orel and Saratov oblasts].
    Maliarchuk BA; Derenko MV; Grzybowski T; Czarny J; Miscicka-Slivka D; Denisova GA; Kostiunina EA
    Genetika; 2002 Nov; 38(11):1532-8. PubMed ID: 12500679
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel and heteroplasmic mutations in mitochondrial tRNA genes in Brugada syndrome.
    Tafti MF; Khatami M; Rezaei S; Heidari MM; Hadadzadeh M
    Cardiol J; 2018; 25(1):113-119. PubMed ID: 28980288
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Complex Brugada syndrome inheritance in a family harbouring compound SCN5A and CACNA1C mutations.
    Béziau DM; Barc J; O'Hara T; Le Gloan L; Amarouch MY; Solnon A; Pavin D; Lecointe S; Bouillet P; Gourraud JB; Guicheney P; Denjoy I; Redon R; Mabo P; le Marec H; Loussouarn G; Kyndt F; Schott JJ; Probst V; Baró I
    Basic Res Cardiol; 2014; 109(6):446. PubMed ID: 25341504
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum Disorders.
    Chalkia D; Singh LN; Leipzig J; Lvova M; Derbeneva O; Lakatos A; Hadley D; Hakonarson H; Wallace DC
    JAMA Psychiatry; 2017 Nov; 74(11):1161-1168. PubMed ID: 28832883
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel SCN10A variants associated with Brugada syndrome.
    Fukuyama M; Ohno S; Makiyama T; Horie M
    Europace; 2016 Jun; 18(6):905-11. PubMed ID: 25842276
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Brugada syndrome: a fatal disease with complex genetic etiologies - still a long way to go.
    Wu Y; Ai M; Bardeesi ASA; Xu L; Zheng J; Zheng D; Yin K; Wu Q; Zhang L; Huang L; Cheng J
    Forensic Sci Res; 2017; 2(3):115-125. PubMed ID: 30483629
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The Diagnosis, Risk Stratification, and Treatment of Brugada Syndrome.
    Steinfurt J; Biermann J; Bode C; Odening KE
    Dtsch Arztebl Int; 2015 Jun; 112(23):394-401. PubMed ID: 26157012
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.