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

168 related items for PubMed ID: 20482818

  • 1. Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.
    Winblad S, Jensen C, Månsson JE, Samuelsson L, Lindberg C.
    Behav Brain Funct; 2010 May 19; 6():25. PubMed ID: 20482818
    [Abstract] [Full Text] [Related]

  • 2. Prevalence and correlates of apathy in myotonic dystrophy type 1.
    Gallais B, Montreuil M, Gargiulo M, Eymard B, Gagnon C, Laberge L.
    BMC Neurol; 2015 Aug 22; 15():148. PubMed ID: 26296336
    [Abstract] [Full Text] [Related]

  • 3. A hospital based epidemiological study of genetically determined muscle disease in south western Norway.
    Husebye SA, Rebne CB, Stokland AE, Sanaker PS, Bindoff LA.
    Neuromuscul Disord; 2020 Mar 22; 30(3):181-185. PubMed ID: 32146000
    [Abstract] [Full Text] [Related]

  • 4. Medication adherence in patients with myotonic dystrophy and facioscapulohumeral muscular dystrophy.
    Fitzgerald BP, Conn KM, Smith J, Walker A, Parkhill AL, Hilbert JE, Luebbe EA, Moxley RT.
    J Neurol; 2016 Dec 22; 263(12):2528-2537. PubMed ID: 27734165
    [Abstract] [Full Text] [Related]

  • 5. Muscle pathology in myotonic dystrophy: light and electron microscopic investigation in eighteen patients.
    Nadaj-Pakleza A, Lusakowska A, Sułek-Piątkowska A, Krysa W, Rajkiewicz M, Kwieciński H, Kamińska A.
    Folia Morphol (Warsz); 2011 May 22; 70(2):121-9. PubMed ID: 21630234
    [Abstract] [Full Text] [Related]

  • 6. The brain in myotonic dystrophy 1 and 2: evidence for a predominant white matter disease.
    Minnerop M, Weber B, Schoene-Bake JC, Roeske S, Mirbach S, Anspach C, Schneider-Gold C, Betz RC, Helmstaedter C, Tittgemeyer M, Klockgether T, Kornblum C.
    Brain; 2011 Dec 22; 134(Pt 12):3530-46. PubMed ID: 22131273
    [Abstract] [Full Text] [Related]

  • 7. A Systematic Review and Meta-analysis on the Epidemiology of the Muscular Dystrophies.
    Mah JK, Korngut L, Fiest KM, Dykeman J, Day LJ, Pringsheim T, Jette N.
    Can J Neurol Sci; 2016 Jan 22; 43(1):163-77. PubMed ID: 26786644
    [Abstract] [Full Text] [Related]

  • 8. Regional brain atrophy in gray and white matter is associated with cognitive impairment in Myotonic Dystrophy type 1.
    Labayru G, Diez I, Sepulcre J, Fernández E, Zulaica M, Cortés JM, López de Munain A, Sistiaga A.
    Neuroimage Clin; 2019 Jan 22; 24():102078. PubMed ID: 31795042
    [Abstract] [Full Text] [Related]

  • 9. Shank sign in myotonic dystrophy type-1 (DM-1).
    Pradhan S.
    J Clin Neurosci; 2007 Jan 22; 14(1):27-32. PubMed ID: 17092719
    [Abstract] [Full Text] [Related]

  • 10. Quantification of brain atrophy in patients with myotonic dystrophy and proximal myotonic myopathy: a controlled 3-dimensional magnetic resonance imaging study.
    Kassubek J, Juengling FD, Hoffmann S, Rosenbohm A, Kurt A, Jurkat-Rott K, Steinbach P, Wolf M, Ludolph AC, Lehmann-Horn F, Lerche H, Weber YG.
    Neurosci Lett; 2003 Sep 11; 348(2):73-6. PubMed ID: 12902021
    [Abstract] [Full Text] [Related]

  • 11. Temperament and character in patients with classical myotonic dystrophy type 1 (DM-1).
    Winblad S, Lindberg C, Hansen S.
    Neuromuscul Disord; 2005 Apr 11; 15(4):287-92. PubMed ID: 15792867
    [Abstract] [Full Text] [Related]

  • 12. 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 11; 266(12):2987-2996. PubMed ID: 31471688
    [Abstract] [Full Text] [Related]

  • 13. Affective symptoms and apathy in myotonic dystrophy type 1 a systematic review and meta-analysis.
    van der Velden BG, Okkersen K, Kessels RP, Groenewoud J, van Engelen B, Knoop H, Raaphorst J.
    J Affect Disord; 2019 May 01; 250():260-269. PubMed ID: 30870776
    [Abstract] [Full Text] [Related]

  • 14. MRI in the assessment of muscular pathology: a comparison between limb-girdle muscular dystrophies, hyaline body myopathies and myotonic dystrophies.
    Stramare R, Beltrame V, Dal Borgo R, Gallimberti L, Frigo AC, Pegoraro E, Angelini C, Rubaltelli L, Feltrin GP.
    Radiol Med; 2010 Jun 01; 115(4):585-99. PubMed ID: 20177980
    [Abstract] [Full Text] [Related]

  • 15. Cross-sectional serum metabolomic study of multiple forms of muscular dystrophy.
    Spitali P, Hettne K, Tsonaka R, Sabir E, Seyer A, Hemerik JBA, Goeman JJ, Picillo E, Ergoli M, Politano L, Aartsma-Rus A.
    J Cell Mol Med; 2018 Apr 01; 22(4):2442-2448. PubMed ID: 29441734
    [Abstract] [Full Text] [Related]

  • 16. Aberrantly spliced alpha-dystrobrevin alters alpha-syntrophin binding in myotonic dystrophy type 1.
    Nakamori M, Kimura T, Kubota T, Matsumura T, Sumi H, Fujimura H, Takahashi MP, Sakoda S.
    Neurology; 2008 Feb 26; 70(9):677-85. PubMed ID: 18299519
    [Abstract] [Full Text] [Related]

  • 17. Cortical damage in brains of patients with adult-form of myotonic dystrophy type 1 and no or minimal MRI abnormalities.
    Giorgio A, Dotti MT, Battaglini M, Marino S, Mortilla M, Stromillo ML, Bramanti P, Orrico A, Federico A, De Stefano N.
    J Neurol; 2006 Nov 26; 253(11):1471-7. PubMed ID: 16786209
    [Abstract] [Full Text] [Related]

  • 18. 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
    [Abstract] [Full Text] [Related]

  • 19. Lower limb muscle magnetic resonance imaging in Chinese patients with myotonic dystrophy type 1.
    Song J, Fu J, Ma M, Pang M, Li G, Gao L, Zhang J.
    Neurol Res; 2020 Feb 26; 42(2):170-177. PubMed ID: 31951783
    [Abstract] [Full Text] [Related]

  • 20. Cranial magnetic resonance imaging in genetically proven myotonic dystrophy type 1 and 2.
    Kornblum C, Reul J, Kress W, Grothe C, Amanatidis N, Klockgether T, Schröder R.
    J Neurol; 2004 Jun 26; 251(6):710-4. PubMed ID: 15311347
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.