BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 30672637)

  • 21. Imipramine for incessant ventricular arrhythmias in 2 unrelated patients with Andersen-Tawil syndrome.
    Bigelow AM; Khalifa MM; Clark JM
    Heart Rhythm; 2015 Jul; 12(7):1654-7. PubMed ID: 25814423
    [No Abstract]   [Full Text] [Related]  

  • 22. Electrocardiographic features in Andersen-Tawil syndrome patients with KCNJ2 mutations: characteristic T-U-wave patterns predict the KCNJ2 genotype.
    Zhang L; Benson DW; Tristani-Firouzi M; Ptacek LJ; Tawil R; Schwartz PJ; George AL; Horie M; Andelfinger G; Snow GL; Fu YH; Ackerman MJ; Vincent GM
    Circulation; 2005 May; 111(21):2720-6. PubMed ID: 15911703
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel FBN1 mutations are responsible for cardiovascular manifestations of Marfan syndrome.
    Wang J; Yan Y; Chen J; Gong L; Zhang Y; Yuan M; Cui B; Wang Y
    Mol Biol Rep; 2016 Nov; 43(11):1227-1232. PubMed ID: 27558095
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Cellular basis for electrocardiographic and arrhythmic manifestations of Andersen-Tawil syndrome (LQT7).
    Tsuboi M; Antzelevitch C
    Heart Rhythm; 2006 Mar; 3(3):328-35. PubMed ID: 16500306
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Andersen-Tawil syndrome with early fixed myopathy.
    Lefter S; Hardiman O; Costigan D; Lynch B; McConville J; Hand CK; Ryan AM
    J Clin Neuromuscul Dis; 2014 Dec; 16(2):79-82. PubMed ID: 25415519
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome.
    Cecchi A; Ogawa N; Martinez HR; Carlson A; Fan Y; Penny DJ; Guo DC; Eisenberg S; Safi H; Estrera A; Lewis RA; Meyers D; Milewicz DM
    Am J Med Genet A; 2013 Sep; 161A(9):2305-10. PubMed ID: 23897642
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Andersen-Tawil Syndrome: A Comprehensive Review.
    Pérez-Riera AR; Barbosa-Barros R; Samesina N; Pastore CA; Scanavacca M; Daminello-Raimundo R; de Abreu LC; Nikus K; Brugada P
    Cardiol Rev; 2021 Jul-Aug 01; 29(4):165-177. PubMed ID: 32947483
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Three Novel Mutations in FBN1 and TGFBR2 in Patients with the Syndromic Form of Thoracic Aortic Aneurysms and Dissections.
    Cao Y; Tan H; Li Z; Linpeng S; Long X; Liang D; Wu L
    Int Heart J; 2018 Sep; 59(5):1059-1068. PubMed ID: 30101859
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotype-phenotype correlations of KCNJ2 mutations in Japanese patients with Andersen-Tawil syndrome.
    Haruna Y; Kobori A; Makiyama T; Yoshida H; Akao M; Doi T; Tsuji K; Ono S; Nishio Y; Shimizu W; Inoue T; Murakami T; Tsuboi N; Yamanouchi H; Ushinohama H; Nakamura Y; Yoshinaga M; Horigome H; Aizawa Y; Kita T; Horie M
    Hum Mutat; 2007 Feb; 28(2):208. PubMed ID: 17221872
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Pathogenic FBN1 variants in familial thoracic aortic aneurysms and dissections.
    Regalado ES; Guo DC; Santos-Cortez RL; Hostetler E; Bensend TA; Pannu H; Estrera A; Safi H; Mitchell AL; Evans JP; Leal SM; Bamshad M; Shendure J; Nickerson DA; ; Milewicz DM
    Clin Genet; 2016 Jun; 89(6):719-23. PubMed ID: 26621581
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Long-term implications of emergency versus elective proximal aortic surgery in patients with Marfan syndrome in the Genetically Triggered Thoracic Aortic Aneurysms and Cardiovascular Conditions Consortium Registry.
    Song HK; Kindem M; Bavaria JE; Dietz HC; Milewicz DM; Devereux RB; Eagle KA; Maslen CL; Kroner BL; Pyeritz RE; Holmes KW; Weinsaft JW; Menashe V; Ravekes W; LeMaire SA;
    J Thorac Cardiovasc Surg; 2012 Feb; 143(2):282-6. PubMed ID: 22104675
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Reversible Dilated Cardiomyopathy Caused by a High Burden of Ventricular Arrhythmias in Andersen-Tawil Syndrome.
    Rezazadeh S; Guo J; Duff HJ; Ferrier RA; Gerull B
    Can J Cardiol; 2016 Dec; 32(12):1576.e15-1576.e18. PubMed ID: 27789106
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Molecular genetic diagnostics of the cause of ventricular arrhythmias in children].
    Brøndberg AK; Bjerre JV; Nielsen JC; Jensen HK
    Ugeskr Laeger; 2015 Sep; 177(38):V04150366. PubMed ID: 26376421
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Andersen-Tawil syndrome: report of 3 novel mutations and high risk of symptomatic cardiac involvement.
    Kostera-Pruszczyk A; Potulska-Chromik A; Pruszczyk P; Bieganowska K; Miszczak-Knecht M; Bienias P; Szczałuba K; Lee HY; Quinn E; Ploski R; Kaminska A; Ptáček LJ
    Muscle Nerve; 2015 Feb; 51(2):192-6. PubMed ID: 24861851
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome.
    Lu CW; Lin JH; Rajawat YS; Jerng H; Rami TG; Sanchez X; DeFreitas G; Carabello B; DeMayo F; Kearney DL; Miller G; Li H; Pfaffinger PJ; Bowles NE; Khoury DS; Towbin JA
    J Med Genet; 2006 Aug; 43(8):653-9. PubMed ID: 16571646
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Identification and functional characterisation of a novel KCNJ2 mutation, Val302del, causing Andersen-Tawil syndrome.
    Ördög B; Hategan L; Kovács M; Seprényi G; Kohajda Z; Nagy I; Hegedűs Z; Környei L; Jost N; Katona M; Szekeres M; Forster T; Papp JG; Varró A; Sepp R
    Can J Physiol Pharmacol; 2015 Jul; 93(7):569-75. PubMed ID: 26103554
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Phenotypic Variability of Andersen-Tawil Syndrome Due to Allelic Mutation c.652C>T in the
    Onore ME; Picillo E; D'Ambrosio P; Morra S; Nigro V; Politano L
    Biomolecules; 2024 Apr; 14(4):. PubMed ID: 38672523
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Vanishing Weakness and Persistent Cardiac Dysrhythmia: Are We Dealing with Andersen Tawil Syndrome?
    Jhansi Rani P; Yashodhara P; Sundarachary NV; Veeramma U; Elahi SM; Amalakanti S; Lalitha A
    Indian J Pediatr; 2015 Jul; 82(7):642-4. PubMed ID: 25616308
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Mutations of KCNJ2 gene associated with Andersen-Tawil syndrome in Korean families.
    Choi BO; Kim J; Suh BC; Yu JS; Sunwoo IN; Kim SJ; Kim GH; Chung KW
    J Hum Genet; 2007; 52(3):280-283. PubMed ID: 17211524
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Hybrid treatment for thoracoabdominal aortic aneurysms in patients with Marfan syndrome.
    Taurino M; Ficarelli R; Rizzo L; Stella N; Persiani F; Capuano F
    Ann Vasc Surg; 2015 Apr; 29(3):595.e5-9. PubMed ID: 25596402
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.