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Journal Abstract Search

262 related items for PubMed ID: 14977063

  • 1. Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy.
    Giliberto F, Ferreiro V, Dalamon V, Szijan I.
    Neurol Res; 2004 Jan; 26(1):83-7. PubMed ID: 14977063
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  • 2. [Central nervous system involvements in Duchenne/Becker muscular dystrophy].
    Kumagai T, Miura K, Ohki T, Matsumoto A, Miyazaki S, Nakamura M, Ochi N, Takahashi O.
    No To Hattatsu; 2001 Nov; 33(6):480-6. PubMed ID: 11725514
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  • 3. MLPA based detection of mutations in the dystrophin gene of 180 Polish families with Duchenne/Becker muscular dystrophy.
    Zimowski JG, Massalska D, Holding M, Jadczak S, Fidziańska E, Lusakowska A, Kostera-Pruszczyk A, Kamińska A, Zaremba J.
    Neurol Neurochir Pol; 2014 Nov; 48(6):416-22. PubMed ID: 25482253
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  • 5. Proximal dystrophin gene deletions and protein alterations in becker muscular dystrophy.
    Novaković I, Bojić D, Todorović S, Apostolski S, Luković L, Stefanović D, Milasin J.
    Ann N Y Acad Sci; 2005 Jun; 1048():406-10. PubMed ID: 16154963
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  • 6. Duchenne and Becker muscular dystrophy: a molecular and immunohistochemical approach.
    Freund AA, Scola RH, Arndt RC, Lorenzoni PJ, Kay CK, Werneck LC.
    Arq Neuropsiquiatr; 2007 Mar; 65(1):73-6. PubMed ID: 17420831
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  • 7. Dystrophin quantification and clinical correlations in Becker muscular dystrophy: implications for clinical trials.
    Anthony K, Cirak S, Torelli S, Tasca G, Feng L, Arechavala-Gomeza V, Armaroli A, Guglieri M, Straathof CS, Verschuuren JJ, Aartsma-Rus A, Helderman-van den Enden P, Bushby K, Straub V, Sewry C, Ferlini A, Ricci E, Morgan JE, Muntoni F.
    Brain; 2011 Dec; 134(Pt 12):3547-59. PubMed ID: 22102647
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  • 9. Distribution of dystrophin gene deletions in a Chinese population.
    Li Y, Liu Z, OuYang S, Zhu Y, Wang L, Wu J.
    J Int Med Res; 2016 Feb; 44(1):99-108. PubMed ID: 26786758
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  • 11. Re-evaluation of reading frame-shift hypothesis in Duchenne and Becker muscular dystrophy.
    Pandey GS, Kesari A, Mukherjee M, Mittal RD, Mittal B.
    Neurol India; 2003 Sep; 51(3):367-9. PubMed ID: 14652441
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  • 12. Loss of Dp140 dystrophin isoform and intellectual impairment in Duchenne dystrophy.
    Felisari G, Martinelli Boneschi F, Bardoni A, Sironi M, Comi GP, Robotti M, Turconi AC, Lai M, Corrao G, Bresolin N.
    Neurology; 2000 Aug 22; 55(4):559-64. PubMed ID: 10953192
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  • 15. Severe cognitive impairment in DMD: obvious clinical indication for Dp71 isoform point mutation screening.
    Moizard MP, Toutain A, Fournier D, Berret F, Raynaud M, Billard C, Andres C, Moraine C.
    Eur J Hum Genet; 2000 Jul 22; 8(7):552-6. PubMed ID: 10909857
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  • 18. Becker muscular dystrophy in Indian patients: analysis of dystrophin gene deletion patterns.
    Dastur RS, Gaitonde PS, Khadilkar SV, Nadkarni JJ.
    Neurol India; 2008 Jul 22; 56(3):374-8. PubMed ID: 18974567
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  • 19. Deletion mutations in the dystrophin gene of Saudi patients with Duchenne and Becker muscular dystrophy.
    Al-Jumah M, Majumdar R, Al-Rajeh S, Chaves-Carballo E, Salih MM, Awada A, Al-Shahwan S, Al-Uthaim S.
    Saudi Med J; 2002 Dec 22; 23(12):1478-82. PubMed ID: 12518196
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  • 20. Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.
    Rani AQ, Sasongko TH, Sulong S, Bunyan D, Salmi AR, Zilfalil BA, Matsuo M, Zabidi-Hussin ZA.
    J Neurogenet; 2013 Jun 22; 27(1-2):11-5. PubMed ID: 23438214
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