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

255 related items for PubMed ID: 32063450

  • 21. Fuchs' Endothelial Corneal Dystrophy and RNA Foci in Patients With Myotonic Dystrophy.
    Mootha VV, Hansen B, Rong Z, Mammen PP, Zhou Z, Xing C, Gong X.
    Invest Ophthalmol Vis Sci; 2017 Sep 01; 58(11):4579-4585. PubMed ID: 28886202
    [Abstract] [Full Text] [Related]

  • 22. Gain of RNA function in pathological cases: Focus on myotonic dystrophy.
    Klein AF, Gasnier E, Furling D.
    Biochimie; 2011 Nov 01; 93(11):2006-12. PubMed ID: 21763392
    [Abstract] [Full Text] [Related]

  • 23. Myotonic dystrophy: clinical and molecular parallels between myotonic dystrophy type 1 and type 2.
    Ranum LP, Day JW.
    Curr Neurol Neurosci Rep; 2002 Sep 01; 2(5):465-70. PubMed ID: 12169228
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Diastolic heart dysfunction is correlated with CTG repeat length in myotonic dystrophy type 1.
    Park JS, Kim N, Park D.
    Neurol Sci; 2018 Nov 01; 39(11):1935-1943. PubMed ID: 30094526
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. Brugada syndrome: clinical presentation and genotype-correlation with magnetic resonance imaging parameters.
    Rudic B, Schimpf R, Veltmann C, Doesch C, Tülümen E, Schoenberg SO, Borggrefe M, Papavassiliu T.
    Europace; 2016 Sep 01; 18(9):1411-9. PubMed ID: 26511399
    [Abstract] [Full Text] [Related]

  • 32. Reentry in cardiac ventricular epicardial tissue due to SCN5A L812Q gene mutation: a computational study.
    Satish H, Reddy MR.
    Biomed Phys Eng Express; 2022 Apr 14; 8(3):. PubMed ID: 35320795
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case-series report.
    van der Crabben SN, Kowsoleea AIE, Clur SB, Wilde AAM.
    J Cardiovasc Electrophysiol; 2022 Jan 14; 33(1):123-127. PubMed ID: 34674339
    [Abstract] [Full Text] [Related]

  • 36. [From gene to disease; altered RNA processing as a cause of myotonic dystrophy type 1].
    de Die-Smulders CE, Faber CG, Smeets HJ.
    Ned Tijdschr Geneeskd; 2005 Sep 10; 149(37):2043-6. PubMed ID: 16184945
    [Abstract] [Full Text] [Related]

  • 37. Myotonic dystrophy type 2 and related myotonic disorders.
    Meola G, Moxley RT.
    J Neurol; 2004 Oct 10; 251(10):1173-82. PubMed ID: 15503094
    [Abstract] [Full Text] [Related]

  • 38. Correlation between cardiac involvement and CTG trinucleotide repeat length in myotonic dystrophy.
    Melacini P, Villanova C, Menegazzo E, Novelli G, Danieli G, Rizzoli G, Fasoli G, Angelini C, Buja G, Miorelli M.
    J Am Coll Cardiol; 1995 Jan 10; 25(1):239-45. PubMed ID: 7798509
    [Abstract] [Full Text] [Related]

  • 39. Variant CCG and GGC repeats within the CTG expansion dramatically modify mutational dynamics and likely contribute toward unusual symptoms in some myotonic dystrophy type 1 patients.
    Braida C, Stefanatos RK, Adam B, Mahajan N, Smeets HJ, Niel F, Goizet C, Arveiler B, Koenig M, Lagier-Tourenne C, Mandel JL, Faber CG, de Die-Smulders CE, Spaans F, Monckton DG.
    Hum Mol Genet; 2010 Apr 15; 19(8):1399-412. PubMed ID: 20080938
    [Abstract] [Full Text] [Related]

  • 40. Allele length of the DMPK CTG repeat is a predictor of progressive myotonic dystrophy type 1 phenotypes.
    Overend G, Légaré C, Mathieu J, Bouchard L, Gagnon C, Monckton DG.
    Hum Mol Genet; 2019 Jul 01; 28(13):2245-2254. PubMed ID: 31220271
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.