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 *

142 related articles for article (PubMed ID: 27698745)

  • 1. Concomitant presentation of Anderson-Tawil syndrome and myasthenia gravis in an adult patient: A case report.
    Fan R; Ji R; Zou W; Wang G; Wang H; Penney DJ; Luo JJ; Fan Y
    Exp Ther Med; 2016 Oct; 12(4):2435-2438. PubMed ID: 27698745
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Andersen-Tawil Syndrome With Novel Mutation in
    Yim J; Kim KB; Kim M; Lee GD; Kim M
    Front Pediatr; 2021; 9():790075. PubMed ID: 35174115
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. [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]  

  • 5. Thyrotoxic Periodic Paralysis With Features of Andersen-Tawil Syndrome: A Case Report and Literature Review.
    Iskander B; Malik BH; Cancarevic I
    Cureus; 2020 May; 12(5):e8169. PubMed ID: 32432016
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Ventricular tachyarrhythmias in a patient with Andersen-Tawil syndrome.
    Pyo JY; Joh DH; Park JS; Lee SJ; Lee H; Kim W; Joung B
    Korean Circ J; 2013 Jan; 43(1):62-5. PubMed ID: 23407770
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Andersen-Tawil syndrome: clinical and molecular aspects.
    Nguyen HL; Pieper GH; Wilders R
    Int J Cardiol; 2013 Dec; 170(1):1-16. PubMed ID: 24383070
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. Hypokalemic periodic paralysis, facial dysmorphism and ventricular arrhythmia (clinical triad of Andersen-Tawil syndrome).
    Thakkar M; Biswas TK; Desle HB
    J Assoc Physicians India; 2012 Nov; 60():56-8. PubMed ID: 23767205
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.