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Journal Abstract Search

295 related items for PubMed ID: 6568938

  • 1. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

  • 2. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy.
    Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP.
    Ann Neurol; 1996 Apr; 39(4):507-20. PubMed ID: 8619529
    [Abstract] [Full Text] [Related]

  • 3. [A family of autosomal dominant facio-limb-girdle muscular dystrophy].
    Takao S, Kira J, Kohtake N, Yoshimura T, Goto I.
    Fukuoka Igaku Zasshi; 1996 Dec; 87(12):278-82. PubMed ID: 9011111
    [Abstract] [Full Text] [Related]

  • 4. Differential diagnosis of scapuloperoneal syndrome.
    Milanov I, Ishpekova B.
    Electromyogr Clin Neurophysiol; 1997 Mar; 37(2):73-8. PubMed ID: 9098670
    [Abstract] [Full Text] [Related]

  • 5. [Congenital facioscapulohumeral muscular dystrophy associated with tongue atrophy and sensorineural hearing disturbance].
    Shimizu T, Miyamoto K, Hayashi H, Nagashima T, Hirose K, Tanabe H.
    Rinsho Shinkeigaku; 1991 Apr; 31(4):433-8. PubMed ID: 1914330
    [Abstract] [Full Text] [Related]

  • 6. [2 families with benign myopathy predominantly on the limb girdle with dominant autosomal heredity].
    Serratrice G, Pellissier JF.
    Rev Neurol (Paris); 1988 Apr; 144(1):43-6. PubMed ID: 3347807
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  • 10. Scapuloperoneal muscular atrophy: Davidenkow's syndrome. Family report.
    Milanov I, Georgiev D, Krushkov C.
    Electromyogr Clin Neurophysiol; 1996 Apr; 36(5):259-63. PubMed ID: 8877316
    [Abstract] [Full Text] [Related]

  • 11. Distal muscular dystrophy with autosomal recessive inheritance.
    Scoppetta C, Vaccario ML, Casali C, Di Trapani G, Mennuni G.
    Muscle Nerve; 1984 Apr; 7(6):478-81. PubMed ID: 6543900
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  • 12. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
    Kishibayashi J, Sunohara N, Saito Y.
    Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
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  • 14. Emery-Dreifuss syndrome.
    Petty RK, Thomas PK, Landon DN.
    J Neurol; 1986 Apr; 233(2):108-14. PubMed ID: 3701378
    [Abstract] [Full Text] [Related]

  • 15. Emery-Dreifuss muscular dystrophy.
    Rowland LP, Fetell M, Olarte M, Hays A, Singh N, Wanat FE.
    Ann Neurol; 1979 Feb; 5(2):111-7. PubMed ID: 426473
    [Abstract] [Full Text] [Related]

  • 16. Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
    Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F.
    Ann Neurol; 2000 Aug; 48(2):170-80. PubMed ID: 10939567
    [Abstract] [Full Text] [Related]

  • 17. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.
    Hopkins LC, Jackson JA, Elsas LJ.
    Ann Neurol; 1981 Sep; 10(3):230-7. PubMed ID: 7294729
    [Abstract] [Full Text] [Related]

  • 18. Electrophysiologic evaluation of Emery-Dreifuss muscular dystrophy. A single fiber and quantitative EMG study.
    Cruz Martínez A, Du Theil LA.
    Electromyogr Clin Neurophysiol; 1989 Mar; 29(2):99-103. PubMed ID: 2707147
    [Abstract] [Full Text] [Related]

  • 19. Emery-Dreifuss syndrome: genetic and clinical varieties.
    Rudenskaya GE, Ginter EK, Petrin AN, Djomina NA.
    Am J Med Genet; 1994 Apr 15; 50(3):228-33. PubMed ID: 8042665
    [Abstract] [Full Text] [Related]

  • 20. Selective muscle involvement on magnetic resonance imaging in autosomal dominant Emery-Dreifuss muscular dystrophy.
    Mercuri E, Counsell S, Allsop J, Jungbluth H, Kinali M, Bonne G, Schwartz K, Bydder G, Dubowitz V, Muntoni F.
    Neuropediatrics; 2002 Feb 15; 33(1):10-4. PubMed ID: 11930270
    [Abstract] [Full Text] [Related]

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