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Journal Abstract Search

554 related items for PubMed ID: 27665240

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  • 3. Comparisons of intellectual capacities between mild and classic adult-onset phenotypes of myotonic dystrophy type 1 (DM1).
    Jean S, Richer L, Laberge L, Mathieu J.
    Orphanet J Rare Dis; 2014 Nov 26; 9():186. PubMed ID: 25424323
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  • 7. [Myotonic dystrophies: clinical presentation, pathogenesis, diagnostics and therapy].
    Finsterer J, Rudnik-Schöneborn S.
    Fortschr Neurol Psychiatr; 2015 Jan 26; 83(1):9-17. PubMed ID: 25602187
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  • 8. Myotonic dystrophies.
    Huang CC, Kuo HC.
    Chang Gung Med J; 2005 Aug 26; 28(8):517-26. PubMed ID: 16265841
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  • 9. Major involvement of trunk muscles in myotonic dystrophy type 1.
    Solbakken G, Ørstavik K, Hagen T, Dietrichs E, Naerland T.
    Acta Neurol Scand; 2016 Dec 26; 134(6):467-473. PubMed ID: 26984572
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  • 11. The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical research.
    Wood L, Cordts I, Atalaia A, Marini-Bettolo C, Maddison P, Phillips M, Roberts M, Rogers M, Hammans S, Straub V, Petty R, Orrell R, Monckton DG, Nikolenko N, Jimenez-Moreno AC, Thompson R, Hilton-Jones D, Turner C, Lochmüller H.
    J Neurol; 2017 May 26; 264(5):979-988. PubMed ID: 28397002
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  • 12. Cognition and adaptive skills in myotonic dystrophy type 1: a study of 55 individuals with congenital and childhood forms.
    Ekström AB, Hakenäs-Plate L, Tulinius M, Wentz E.
    Dev Med Child Neurol; 2009 Dec 26; 51(12):982-90. PubMed ID: 19459914
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  • 14. Scapular dyskinesis in myotonic dystrophy type 1: clinical characteristics and genetic investigations.
    Voermans NC, van der Bilt RC, IJspeert J, Hogrel JY, Jeanpierre M, Behin A, Laforet P, Stojkovic T, van Engelen BG, Padberg GW, Sacconi S, Lemmers RJLF, van der Maarel SM, Eymard B, Bassez G.
    J Neurol; 2019 Dec 26; 266(12):2987-2996. PubMed ID: 31471688
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  • 16. Progressive conduction disturbance in myotonic dystrophy.
    Palazzolo J, Trucco E, Arce M, Riera AR, Femenía F.
    Cardiol J; 2011 Dec 26; 18(3):322-5. PubMed ID: 21660927
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  • 17. Clinical features and genetic spectrum of a multicenter Chinese cohort with myotonic dystrophy type 1.
    Zhong H, Zeng L, Yu X, Ke Q, Dong J, Chen Y, Luo L, Chang X, Guo J, Wang Y, Xiong H, Liu R, Liu C, Wu J, Lin J, Xi J, Zhu W, Tan S, Liu F, Lu J, Zhao C, Luo S.
    Orphanet J Rare Dis; 2024 Mar 07; 19(1):103. PubMed ID: 38454488
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  • 18. Visual function in congenital and childhood myotonic dystrophy type 1.
    Ekström AB, Tulinius M, Sjöström A, Aring E.
    Ophthalmology; 2010 May 07; 117(5):976-82. PubMed ID: 20346513
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  • 19. Variability of multisystemic features in myotonic dystrophy type 1--lessons from Serbian registry.
    Rakocevic-Stojanovic V, Peric S, Basta I, Dobricic V, Ralic V, Kacar A, Peric M, Novakovic I.
    Neurol Res; 2015 Nov 07; 37(11):939-44. PubMed ID: 26184384
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  • 20. Speech characteristics in the congenital and childhood-onset forms of myotonic dystrophy type 1.
    Sjögreen L, Mårtensson Å, Ekström AB.
    Int J Lang Commun Disord; 2018 May 07; 53(3):576-583. PubMed ID: 29327796
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