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PUBMED FOR HANDHELDS

Journal Abstract Search

295 related items for PubMed ID: 6568938

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  • 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
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  • 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
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  • 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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  • 7. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug; 20(2):240-8. PubMed ID: 3752967
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  • 9. Distal muscular dystrophy. Case reports.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1997 Aug; 37(4):201-5. PubMed ID: 9208214
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  • 10. Scapuloperoneal muscular atrophy: Davidenkow's syndrome. Family report.
    Milanov I, Georgiev D, Krushkov C.
    Electromyogr Clin Neurophysiol; 1996 Aug; 36(5):259-63. PubMed ID: 8877316
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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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  • 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
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  • 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
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  • 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
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