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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

107 related items for PubMed ID: 1908258

  • 21.
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  • 22. 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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  • 23. Epilepsy, speech delay, and mental retardation in facioscapulohumeral muscular dystrophy.
    Grosso S, Mostardini R, Di Bartolo RM, Balestri P, Verrotti A.
    Eur J Paediatr Neurol; 2011 Sep; 15(5):456-60. PubMed ID: 21763164
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  • 25. Progressive myoclonic epilepsy, nerve deafness and spinal muscular atrophy.
    Lance JW, Evans WA.
    Clin Exp Neurol; 1984 Sep; 20():141-51. PubMed ID: 6439445
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  • 27. Retinal vascular abnormalities in facioscapulohumeral muscular dystrophy. A general association with genetic and therapeutic implications.
    Fitzsimons RB, Gurwin EB, Bird AC.
    Brain; 1987 Jun; 110 ( Pt 3)():631-48. PubMed ID: 3580827
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  • 28. Ocular manifestations of congenital muscular dystrophy (Fukuyama type).
    Chijiiwa T, Nishimura M, Inomata H, Yamana T, Narazaki O, Kurokawa T.
    Ann Ophthalmol; 1983 Oct; 15(10):921-3, 926-8. PubMed ID: 6651132
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  • 30. [The study of deafness in patients with facioscapulohumeral dystrophy].
    Sánchez-Alcón MD, Pérez Garrigues H, Vílchez J, Casanova B, Morera C.
    Acta Otorrinolaringol Esp; 1994 Oct; 45(2):79-82. PubMed ID: 8086213
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  • 34. Absence of hearing impairment in adult onset facioscapulohumeral muscular dystrophy.
    Rogers MT, Zhao F, Harper PS, Stephens D.
    Neuromuscul Disord; 2002 May; 12(4):358-65. PubMed ID: 12062253
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  • 35. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy?
    Boltshauser E, Lang W, Spillmann T, Hof E.
    J Med Genet; 1989 Feb; 26(2):105-8. PubMed ID: 2918537
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  • 38. [A family with facioscapulohumeral muscular dystrophy and hereditary long QT syndrome].
    Kimura T, Moriwaki T, Sawada J, Naka T, Hazama T, Nakata T.
    Rinsho Shinkeigaku; 1997 Aug; 37(8):690-2. PubMed ID: 9404145
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