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 *

160 related articles for article (PubMed ID: 19223265)

  • 21. Clinical and neurophysiological variability in Andersen-Tawil syndrome.
    Kokubun N; Aoki R; Nagashima T; Komagamine T; Kuroda Y; Horie M; Hirata K
    Muscle Nerve; 2019 Dec; 60(6):752-757. PubMed ID: 31509255
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Lack of any cardiac involvement in a patient with Andersen-Tawil syndrome associated with the c.574A→G mutation in KCNJ2.
    Modoni A; Bianchi ML; Vitulano N; Pagliarani S; Perna F; Sanna T; Rizzo V; Silvestri G
    Cardiology; 2011; 120(4):200-3. PubMed ID: 22286118
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Andersen-Tawil syndrome: deep phenotyping reveals significant cardiac and neuromuscular morbidity.
    Vivekanandam V; Männikkö R; Skorupinska I; Germain L; Gray B; Wedderburn S; Kozyra D; Sud R; James N; Holmes S; Savvatis K; Fialho D; Merve A; Pattni J; Farrugia M; Behr ER; Marini-Bettolo C; Hanna MG; Matthews E
    Brain; 2022 Jun; 145(6):2108-2120. PubMed ID: 34919635
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Sudden cardiac death in Andersen-Tawil syndrome.
    Peters S; Schulze-Bahr E; Etheridge SP; Tristani-Firouzi M
    Europace; 2007 Mar; 9(3):162-6. PubMed ID: 17272325
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mosaic KCNJ2 mutation in Andersen-Tawil syndrome: targeted deep sequencing is useful for the detection of mosaicism.
    Hasegawa K; Ohno S; Kimura H; Itoh H; Makiyama T; Yoshida Y; Horie M
    Clin Genet; 2015 Mar; 87(3):279-83. PubMed ID: 24635491
    [TBL] [Abstract][Full Text] [Related]  

  • 27. KCNJ2 variant of unknown significance reclassified as long QT syndrome causing ventricular fibrillation.
    Obeyesekere MN; Klein GJ; Conacher S; Krahn AD
    Can J Cardiol; 2011; 27(6):870.e11-3. PubMed ID: 21875779
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Andersen-Tawil Syndrome Presenting with Complete Heart Block.
    Suetterlin K; Männikkö R; Flossmann E; Sud R; Fialho D; Vivekanandam V; James N; Gossios TD; Hanna MG; Savvatis K; Matthews E
    J Neuromuscul Dis; 2021; 8(1):151-154. PubMed ID: 33074188
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Intrafamilial phenotypic variability in Andersen-Tawil syndrome: A diagnostic challenge in a potentially treatable condition.
    Ardissone A; Sansone V; Colleoni L; Bernasconi P; Moroni I
    Neuromuscul Disord; 2017 Mar; 27(3):294-297. PubMed ID: 28024840
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Unique post-exercise electrophysiological test results in a new Andersen-Tawil syndrome mutation.
    Díaz-Manera J; Querol L; Clarimón J; Yagüe S; Illa I
    Clin Neurophysiol; 2011 Dec; 122(12):2537-9. PubMed ID: 21640645
    [No Abstract]   [Full Text] [Related]  

  • 31. [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]  

  • 32. Efficacy of flecainide in bidirectional ventricular tachycardia and tachycardia-induced cardiomyopathy with Andersen-Tawil syndrome.
    Ünal Yüksekgönül A; Azak E; Akalın A; Ertuğrul İ; Kılıç E; Utine GE; Karagöz T
    Eur J Med Genet; 2022 Jun; 65(6):104499. PubMed ID: 35429663
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Andersen-Tawil syndrome: definition of a neurocognitive phenotype.
    Yoon G; Quitania L; Kramer JH; Fu YH; Miller BL; Ptácek LJ
    Neurology; 2006 Jun; 66(11):1703-10. PubMed ID: 16769944
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Trafficking-competent and trafficking-defective KCNJ2 mutations in Andersen syndrome.
    Ballester LY; Benson DW; Wong B; Law IH; Mathews KD; Vanoye CG; George AL
    Hum Mutat; 2006 Apr; 27(4):388. PubMed ID: 16541386
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.
    Davies NP; Imbrici P; Fialho D; Herd C; Bilsland LG; Weber A; Mueller R; Hilton-Jones D; Ealing J; Boothman BR; Giunti P; Parsons LM; Thomas M; Manzur AY; Jurkat-Rott K; Lehmann-Horn F; Chinnery PF; Rose M; Kullmann DM; Hanna MG
    Neurology; 2005 Oct; 65(7):1083-9. PubMed ID: 16217063
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Flecainide suppresses bidirectional ventricular tachycardia and reverses tachycardia-induced cardiomyopathy in Andersen-Tawil syndrome.
    Pellizzón OA; Kalaizich L; Ptácek LJ; Tristani-Firouzi M; Gonzalez MD
    J Cardiovasc Electrophysiol; 2008 Jan; 19(1):95-7. PubMed ID: 17655675
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A novel KCNJ2 nonsense mutation, S369X, impedes trafficking and causes a limited form of Andersen-Tawil syndrome.
    Doi T; Makiyama T; Morimoto T; Haruna Y; Tsuji K; Ohno S; Akao M; Takahashi Y; Kimura T; Horie M
    Circ Cardiovasc Genet; 2011 Jun; 4(3):253-60. PubMed ID: 21493816
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Obstetric management of a patient with Andersen-Tawil syndrome: A case report.
    Inagaki M; Tatsumi T; Yomogita H; Hirose A; Kubo T; Sekiguchi M; Miyasaka N
    J Obstet Gynaecol Res; 2021 Jan; 47(1):446-451. PubMed ID: 33205612
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Marked reduction in paralytic attacks in a patient with Andersen-Tawil syndrome switched from acetazolamide to dichlorphenamide.
    Gupta A; Iyadurai S; Roggenbuck J; LoRusso S
    Neuromuscul Disord; 2021 Jul; 31(7):656-659. PubMed ID: 34078557
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.