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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 34843968

  • 1. An overview of heart rhythm disorders and management in myotonic dystrophy type 1.
    Gossios TD, Providencia R, Creta A, Segal OR, Nikolenko N, Turner C, Lopes LR, Wahbi K, Savvatis K.
    Heart Rhythm; 2022 Mar; 19(3):497-504. PubMed ID: 34843968
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. [The electrotherapy of the arrhythmias in 3 cases of myotonic dystrophy (Steinert's disease)].
    Gardini A, Zagami N, Marchini A, Morandi F, Bianchetti F, Curnis A, Politi A.
    Cardiologia; 1996 Dec; 41(12):1209-14. PubMed ID: 9064216
    [Abstract] [Full Text] [Related]

  • 8. Long-term arrhythmia follow-up of patients with myotonic dystrophy.
    Benhayon D, Lugo R, Patel R, Carballeira L, Elman L, Cooper JM.
    J Cardiovasc Electrophysiol; 2015 Mar; 26(3):305-10. PubMed ID: 25546341
    [Abstract] [Full Text] [Related]

  • 9. A 10-year follow-up of a patient affected by myotonic dystrophy type 1 with implantable cardioverter-defibrillator implanted for secondary prevention.
    De Ambroggi G, Ali H, Cappato R, Sansone VA, De Ambroggi L.
    J Cardiovasc Med (Hagerstown); 2020 Feb; 21(2):150-152. PubMed ID: 31490228
    [No Abstract] [Full Text] [Related]

  • 10. Severe cardiac arrhythmias in young patients with myotonic dystrophy type 1.
    Bassez G, Lazarus A, Desguerre I, Varin J, Laforêt P, Bécane HM, Meune C, Arne-Bes MC, Ounnoughene Z, Radvanyi H, Eymard B, Duboc D.
    Neurology; 2004 Nov 23; 63(10):1939-41. PubMed ID: 15557517
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. The heart and cardiac pacing in Steinert disease.
    Nigro G, Papa AA, Politano L.
    Acta Myol; 2012 Oct 23; 31(2):110-6. PubMed ID: 23097601
    [Abstract] [Full Text] [Related]

  • 15. Cardiac Conduction Disorders as Markers of Cardiac Events in Myotonic Dystrophy Type 1.
    Itoh H, Hisamatsu T, Tamura T, Segawa K, Takahashi T, Takada H, Kuru S, Wada C, Suzuki M, Suwazono S, Sasaki S, Okumura K, Horie M, Takahashi MP, Matumura T.
    J Am Heart Assoc; 2020 Sep 23; 9(17):e015709. PubMed ID: 32812471
    [Abstract] [Full Text] [Related]

  • 16. 2022 HRS expert consensus statement on evaluation and management of arrhythmic risk in neuromuscular disorders.
    Groh WJ, Bhakta D, Tomaselli GF, Aleong RG, Teixeira RA, Amato A, Asirvatham SJ, Cha YM, Corrado D, Duboc D, Goldberger ZD, Horie M, Hornyak JE, Jefferies JL, Kääb S, Kalman JM, Kertesz NJ, Lakdawala NK, Lambiase PD, Lubitz SA, McMillan HJ, McNally EM, Milone M, Namboodiri N, Nazarian S, Patton KK, Russo V, Sacher F, Santangeli P, Shen WK, Sobral Filho DC, Stambler BS, Stöllberger C, Wahbi K, Wehrens XHT, Weiner MM, Wheeler MT, Zeppenfeld K.
    Heart Rhythm; 2022 Oct 23; 19(10):e61-e120. PubMed ID: 35500790
    [Abstract] [Full Text] [Related]

  • 17. Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.
    Wahbi K, Babuty D, Probst V, Wissocque L, Labombarda F, Porcher R, Bécane HM, Lazarus A, Béhin A, Laforêt P, Stojkovic T, Clementy N, Dussauge AP, Gourraud JB, Pereon Y, Lacour A, Chapon F, Milliez P, Klug D, Eymard B, Duboc D.
    Eur Heart J; 2017 Mar 07; 38(10):751-758. PubMed ID: 27941019
    [Abstract] [Full Text] [Related]

  • 18. Idiopathic ventricular fibrillation and the V1764fsX1786 frameshift mutation of the SCN5A gene in a myotonic dystrophy type 1 patient.
    Shimoyama T, Hayashi H, Suzuki F, Nishiyama Y, Miyamoto Y, Aiba T, Shimizu W, Kimura K.
    J Clin Neurosci; 2020 Apr 07; 74():242-244. PubMed ID: 32063450
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 10.