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Journal Abstract Search

167 related items for PubMed ID: 16935506

  • 1. Severe fascioscapulohumeral muscular dystrophy presenting with Coats' disease and mental retardation.
    Bindoff LA, Mjellem N, Sommerfelt K, Krossnes BK, Roberts F, Krohn J, Tranheim RS, Haggerty ID.
    Neuromuscul Disord; 2006 Oct; 16(9-10):559-63. PubMed ID: 16935506
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  • 2. Severe phenotype in infantile facioscapulohumeral muscular dystrophy.
    Klinge L, Eagle M, Haggerty ID, Roberts CE, Straub V, Bushby KM.
    Neuromuscul Disord; 2006 Oct; 16(9-10):553-8. PubMed ID: 16934468
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  • 3. Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy.
    Osborne RJ, Welle S, Venance SL, Thornton CA, Tawil R.
    Neurology; 2007 Feb 20; 68(8):569-77. PubMed ID: 17151338
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  • 4. Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4.
    Deak KL, Lemmers RJ, Stajich JM, Klooster R, Tawil R, Frants RR, Speer MC, van der Maarel SM, Gilbert JR.
    Neurology; 2007 Feb 20; 68(8):578-82. PubMed ID: 17229919
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  • 5. Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
    Trevisan CP, Pastorello E, Tomelleri G, Vercelli L, Bruno C, Scapolan S, Siciliano G, Comacchio F.
    Eur J Neurol; 2008 Dec 20; 15(12):1353-8. PubMed ID: 19049553
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  • 6. Facioscapulohumeral muscular dystrophy with severe mental retardation and epilepsy.
    Saito Y, Miyashita S, Yokoyama A, Komaki H, Seki A, Maegaki Y, Ohno K.
    Brain Dev; 2007 May 20; 29(4):231-3. PubMed ID: 17010549
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  • 7. New POMT2 mutations causing congenital muscular dystrophy: identification of a founder mutation.
    Yanagisawa A, Bouchet C, Van den Bergh PY, Cuisset JM, Viollet L, Leturcq F, Romero NB, Quijano-Roy S, Fardeau M, Seta N, Guicheney P.
    Neurology; 2007 Sep 18; 69(12):1254-60. PubMed ID: 17634419
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  • 15. Myopathy with skeletal asymmetry and hemidiaphragm elevation is caused by myotubularin mutations.
    Grogan PM, Tanner SM, Ørstavik KH, Knudsen GP, Saperstein DS, Vogel H, Barohn RJ, Herbelin LL, McVey AL, Katz JS.
    Neurology; 2005 May 10; 64(9):1638-40. PubMed ID: 15883335
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  • 16. A case of fascioscapulohumeral muscular dystrophy misdiagnosed as Becker's muscular dystrophy for 20 years.
    Ramos VF, Thaisetthawatkul P.
    Age Ageing; 2012 Mar 10; 41(2):273-4. PubMed ID: 21795275
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  • 17. Bilateral Coats' response in a female patient leads to diagnosis of facioscapulohumeral muscular dystrophy.
    Bass SJ, Sherman J, Giovinazzo V.
    Optometry; 2011 Feb 10; 82(2):72-6. PubMed ID: 21130700
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  • 18. Infantile facioscapulohumeral muscular dystrophy revisited: Expansion of clinical phenotypes in patients with a very short EcoRI fragment.
    Chen TH, Lai YH, Lee PL, Hsu JH, Goto K, Hayashi YK, Nishino I, Lin CW, Shih HH, Huang CC, Liang WC, Wang WF, Jong YJ.
    Neuromuscul Disord; 2013 Apr 10; 23(4):298-305. PubMed ID: 23434070
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  • 19. Coats' disease and muscular dystrophy.
    Small RG.
    Trans Am Acad Ophthalmol Otolaryngol; 1968 Apr 10; 72(2):225-31. PubMed ID: 5659903
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