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Journal Abstract Search

180 related items for PubMed ID: 31495190

  • 1. [Multiorgan manifestations in myotonic dystrophy type 1].
    Varga D, Pál E.
    Orv Hetil; 2019 Sep; 160(37):1447-1454. PubMed ID: 31495190
    [Abstract] [Full Text] [Related]

  • 2. The myotonic dystrophies.
    Thornton C.
    Semin Neurol; 1999 Sep; 19(1):25-33. PubMed ID: 10711986
    [Abstract] [Full Text] [Related]

  • 3. The heart and cardiac pacing in Steinert disease.
    Nigro G, Papa AA, Politano L.
    Acta Myol; 2012 Oct; 31(2):110-6. PubMed ID: 23097601
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  • 5. [Cardiac, respiratory and sleep disorders in patients with myotonic dystrophy].
    Banach M, Rakowicz M, Antczak J, Rola R, Witkowski G, Waliniowska E.
    Przegl Lek; 2009 Oct; 66(12):1065-8. PubMed ID: 20514907
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  • 8. [Ocular findings in patients with Steinert myotonic dystrophy].
    Markowska E, Zalewska R, Mariak Z, Wojnar M.
    Przegl Lek; 2006 Oct; 63(8):662-3. PubMed ID: 17441379
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  • 10. Differential susceptibility of muscles to myotonia and force impairment in a mouse model of myotonic dystrophy.
    Moyer M, Berger DS, Ladd AN, Van Lunteren E.
    Muscle Nerve; 2011 Jun; 43(6):818-27. PubMed ID: 21404300
    [Abstract] [Full Text] [Related]

  • 11. [Dystrophia myotonica (Steinert disease)--a frequently misdiagnosed disease].
    Kuhn E, Lehmann-Horn F, Rüdel R.
    Nervenarzt; 1990 Jun; 61(6):323-31. PubMed ID: 2198475
    [Abstract] [Full Text] [Related]

  • 12. Myotonic dystrophy with no trinucleotide repeat expansion.
    Thornton CA, Griggs RC, Moxley RT.
    Ann Neurol; 1994 Mar; 35(3):269-72. PubMed ID: 8122879
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  • 14. Mice deficient in Six5 develop cataracts: implications for myotonic dystrophy.
    Klesert TR, Cho DH, Clark JI, Maylie J, Adelman J, Snider L, Yuen EC, Soriano P, Tapscott SJ.
    Nat Genet; 2000 May; 25(1):105-9. PubMed ID: 10802667
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  • 16. Correlation between distribution of muscle weakness, electrophysiological findings and CTG expansion in myotonic dystrophy.
    Khoshbakht R, Soltanzadeh A, Zamani B, Abdi S, Gharagozli K, Kahrizi K, Khoshbakht R, Nafissi S.
    J Clin Neurosci; 2014 Jul; 21(7):1123-6. PubMed ID: 24417793
    [Abstract] [Full Text] [Related]

  • 17. Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?
    Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H.
    Neuromuscul Disord; 1997 Jun; 7(4):217-28. PubMed ID: 9196902
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  • 19. Sporadic Myotonic Dystrophy Type 2 in a Japanese Patient.
    Miyashita K, Ii Y, Matsuyama H, Niwa A, Kawana Y, Shibata S, Minami N, Nishino I, Tomimoto H.
    Intern Med; 2023 Oct 15; 62(20):3027-3031. PubMed ID: 36792202
    [Abstract] [Full Text] [Related]

  • 20. [Cataract in a young patient].
    Mayer C, Cordeiro SA, Khoramnia R.
    Ophthalmologe; 2011 Oct 15; 108(10):976-9. PubMed ID: 21698448
    [Abstract] [Full Text] [Related]

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