BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 21640645)

  • 1. 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]  

  • 2. Andersen cardiodysrhythmic periodic paralysis with KCNJ2 mutations: a novel mutation in the pore selectivity filter residue.
    Lim BC; Kim GB; Bae EJ; Noh CI; Hwang H; Kim KJ; Hwang YS; Ko TS; Chae JH
    J Child Neurol; 2010 Apr; 25(4):490-3. PubMed ID: 20382953
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Muscle weakness, palpitations and a small chin: the Andersen-Tawil syndrome.
    Rajakulendran S; Tan SV; Hanna MG
    Pract Neurol; 2010 Aug; 10(4):227-31. PubMed ID: 20647529
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A Kir3.4 mutation causes Andersen-Tawil syndrome by an inhibitory effect on Kir2.1.
    Kokunai Y; Nakata T; Furuta M; Sakata S; Kimura H; Aiba T; Yoshinaga M; Osaki Y; Nakamori M; Itoh H; Sato T; Kubota T; Kadota K; Shindo K; Mochizuki H; Shimizu W; Horie M; Okamura Y; Ohno K; Takahashi MP
    Neurology; 2014 Mar; 82(12):1058-64. PubMed ID: 24574546
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Case report: A Chinese child with Andersen-Tawil syndrome due to a de novo KCNJ2 mutation.
    Liu XL; Huang XJ; Luan XH; Zhou HY; Wang T; Wang JY; Shen JY; Chen SD; Tang HD; Cao L
    J Neurol Sci; 2015 May; 352(1-2):105-6. PubMed ID: 25847018
    [No Abstract]   [Full Text] [Related]  

  • 7. IK1: the long and the short QT of it.
    Gross GJ
    Heart Rhythm; 2006 Mar; 3(3):336-8. PubMed ID: 16500307
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. Biophysical and molecular characterization of a novel de novo KCNJ2 mutation associated with Andersen-Tawil syndrome and catecholaminergic polymorphic ventricular tachycardia mimicry.
    Barajas-Martinez H; Hu D; Ontiveros G; Caceres G; Desai M; Burashnikov E; Scaglione J; Antzelevitch C
    Circ Cardiovasc Genet; 2011 Feb; 4(1):51-7. PubMed ID: 21148745
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Novel de novo mutation in the KCNJ2 gene in a patient with Andersen-Tawil syndrome.
    Kim JB; Chung KW
    Pediatr Neurol; 2009 Dec; 41(6):464-6. PubMed ID: 19931173
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. [QTU pattern in a patient with the Anderson-Tawil syndrome].
    Ciurzyński M; Bienias P; Kostera-Pruszczyk A; Pruszczyk P
    Kardiol Pol; 2010 Mar; 68(3):339-41; discussion 342. PubMed ID: 20411461
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A study supporting possible expression of inward-rectifying potassium channel 2.1 channels in peripheral nerve in a patient with Andersen-Tawil syndrome.
    Shibuya K; Tsuneyama A; Beppu M; Misawa S; Sekiguchi Y; Amino H; Suzuki YI; Suichi T; Nakamura K; Kuwabara S
    Muscle Nerve; 2019 Apr; 59(4):E28-E30. PubMed ID: 30681175
    [No Abstract]   [Full Text] [Related]  

  • 16. Kir 2.1 channelopathies: the Andersen-Tawil syndrome.
    Tristani-Firouzi M; Etheridge SP
    Pflugers Arch; 2010 Jul; 460(2):289-94. PubMed ID: 20306271
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Andersen-Tawil syndrome presenting as premenstrual periodic paralysis.
    Parihar J; Chakraborty P; Kaul B
    Muscle Nerve; 2021 Jan; 63(1):E5-E6. PubMed ID: 33094497
    [No Abstract]   [Full Text] [Related]  

  • 18. Electrophysiological mechanisms of ventricular arrhythmias in relation to Andersen-Tawil syndrome under conditions of reduced IK1: a simulation study.
    Sung RJ; Wu SN; Wu JS; Chang HD; Luo CH
    Am J Physiol Heart Circ Physiol; 2006 Dec; 291(6):H2597-605. PubMed ID: 16877549
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Neurophysiologic characterization of periodic paralysis episode in a patient with Andersen-Tawil syndrome.
    Falcão de Campos C; de Carvalho M
    Clin Neurophysiol; 2018 Mar; 129(3):558-559. PubMed ID: 29353185
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.