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Journal Abstract Search

111 related items for PubMed ID: 1822805

  • 1. Benign muscular dystrophy with autosomal dominant inheritance.
    Somer H, Laulumaa V, Paljärvi L, Partanen J, Lamminen A, Pihko H, Sariola H, Haltia M.
    Neuromuscul Disord; 1991; 1(4):267-73. PubMed ID: 1822805
    [Abstract] [Full Text] [Related]

  • 2. A Danish family with limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Nielsen JF, Jakobsen J.
    Neuromuscul Disord; 1994 Mar; 4(2):139-42. PubMed ID: 8012194
    [Abstract] [Full Text] [Related]

  • 3. Limb girdle muscular dystrophy with autosomal dominant inheritance.
    Marconi G, Pizzi A, Arimondi CG, Vannelli B.
    Acta Neurol Scand; 1991 Apr; 83(4):234-8. PubMed ID: 2048397
    [Abstract] [Full Text] [Related]

  • 4. [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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  • 7. Benign congenital muscular dystrophy with autosomal dominant heredity: problems of classification.
    Schmalbruch H, Kamieniecka Z, Fuglsang-Frederiksen A, Trojaborg W.
    J Neurol; 1987 Apr; 234(3):146-51. PubMed ID: 3585421
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  • 8. [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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  • 9. Autosomal-dominant distal myopathy with a myotilin S55F mutation: sorting out the phenotype.
    Berciano J, Gallardo E, Domínguez-Perles R, Gallardo E, García A, García-Barredo R, Combarros O, Infante J, Illa I.
    J Neurol Neurosurg Psychiatry; 2008 Feb; 79(2):205-8. PubMed ID: 17698502
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  • 10. A newly recognized autosomal dominant limb girdle muscular dystrophy with cardiac involvement.
    van der Kooi AJ, Ledderhof TM, de Voogt WG, Res CJ, Bouwsma G, Troost D, Busch HF, Becker AE, de Visser M.
    Ann Neurol; 1996 May; 39(5):636-42. PubMed ID: 8619549
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  • 11. A distinct phenotype of distal myopathy in a large Finnish family.
    Mahjneh I, Haravuori H, Paetau A, Anderson LV, Saarinen A, Udd B, Somer H.
    Neurology; 2003 Jul 08; 61(1):87-92. PubMed ID: 12847162
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  • 12. Merosin-positive congenital muscular dystrophy: a large inbred family.
    Mahjneh I, Bushby K, Anderson L, Muntoni F, Tolvanen-Mahjneh H, Bashir R, Pizzi A, Brockington M, Marconi G.
    Neuropediatrics; 1999 Feb 08; 30(1):22-8. PubMed ID: 10222457
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  • 13. Emery-dreifuss humeroperoneal muscular dystrophy: an x-linked myopathy with unusual contractures and bradycardia.
    Hopkins LC, Jackson JA, Elsas LJ.
    Ann Neurol; 1981 Sep 08; 10(3):230-7. PubMed ID: 7294729
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  • 14. Distal muscular dystrophy. Case reports.
    Ishpekova B, Milanov I.
    Electromyogr Clin Neurophysiol; 1997 Sep 08; 37(4):201-5. PubMed ID: 9208214
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  • 15. Benign muscular dystrophy with contractures: a new syndrome?
    Bailey RO, Dentinger MP, Toms ME, Hans MB.
    Acta Neurol Scand; 1986 Apr 08; 73(4):439-43. PubMed ID: 3727920
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  • 16. Emery-Dreifuss muscular dystrophy with autosomal dominant transmission.
    Miller RG, Layzer RB, Mellenthin MA, Golabi M, Francoz RA, Mall JC.
    Neurology; 1985 Aug 08; 35(8):1230-3. PubMed ID: 4022362
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  • 17. Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophy.
    Udd B, Rapola J, Nokelainen P, Arikawa E, Somer H.
    J Neurol Sci; 1992 Dec 08; 113(2):214-21. PubMed ID: 1487757
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  • 18. Quadriceps myopathy: forme fruste of Becker muscular dystrophy.
    Sunohara N, Arahata K, Hoffman EP, Yamada H, Nishimiya J, Arikawa E, Kaido M, Nonaka I, Sugita H.
    Ann Neurol; 1990 Nov 08; 28(5):634-9. PubMed ID: 2260849
    [Abstract] [Full Text] [Related]

  • 19. [Early-onset benign autosomal dominant limb-girdle myopathy with contractures (Bethlem myopathy) in a Japanese family].
    Sasabe F, Takase Y, Fukusako T, Yamamoto K, Morimatsu M.
    Rinsho Shinkeigaku; 1992 Feb 08; 32(2):138-42. PubMed ID: 1611771
    [Abstract] [Full Text] [Related]

  • 20. Scapuloperoneal myopathy.
    Todman DH, Cooke RA.
    Clin Exp Neurol; 1984 Feb 08; 20():169-74. PubMed ID: 6568938
    [Abstract] [Full Text] [Related]

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