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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

325 related items for PubMed ID: 21288719

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  • 5. Hereditary myosin myopathies.
    Oldfors A.
    Neuromuscul Disord; 2007 May; 17(5):355-67. PubMed ID: 17434305
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  • 6. Symptomatic distal myopathy with cardiomyopathy due to a MYH7 mutation.
    Overeem S, Schelhaas HJ, Blijham PJ, Grootscholten MI, ter Laak HJ, Timmermans J, van den Wijngaard A, Zwarts MJ.
    Neuromuscul Disord; 2007 Jun; 17(6):490-3. PubMed ID: 17383184
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  • 7. Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement.
    Cullup T, Lamont PJ, Cirak S, Damian MS, Wallefeld W, Gooding R, Tan SV, Sheehan J, Muntoni F, Abbs S, Sewry CA, Dubowitz V, Laing NG, Jungbluth H.
    Neuromuscul Disord; 2012 Dec; 22(12):1096-104. PubMed ID: 22784669
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  • 9. Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.
    Uro-Coste E, Arné-Bes MC, Pellissier JF, Richard P, Levade T, Heitz F, Figarella-Branger D, Delisle MB.
    Neuromuscul Disord; 2009 Feb; 19(2):163-6. PubMed ID: 19138847
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  • 12. New phenotype and pathology features in MYH7-related distal myopathy.
    Tasca G, Ricci E, Penttilä S, Monforte M, Giglio V, Ottaviani P, Camastra G, Silvestri G, Udd B.
    Neuromuscul Disord; 2012 Jul; 22(7):640-7. PubMed ID: 22521714
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  • 18. New skeletal myopathy and cardiomyopathy associated with a missense mutation in MYH7.
    Darin N, Tajsharghi H, Ostman-Smith I, Gilljam T, Oldfors A.
    Neurology; 2007 Jun 05; 68(23):2041-2. PubMed ID: 17548557
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  • 19. A novel missense mutation in the MYH7 gene causes an uncharacteristic phenotype of myosin storage myopathy: a case report.
    Mamelona J, Filice L, Oussedik Y, Crapoulet N, Ouellette RJ, Marrero A.
    BMC Med Genet; 2019 May 08; 20(1):78. PubMed ID: 31068177
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