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Journal Abstract Search

85 related items for PubMed ID: 2740412

  • 1. Adult onset limb-girdle muscular dystrophy with autosomal dominant inheritance.
    Somer H, Laulumaa V, Paljärvi L, Partanen J, Haltia M.
    Prog Clin Biol Res; 1989; 306():69-71. PubMed ID: 2740412
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  • 3. [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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  • 4. Limb-girdle muscular dystrophy: clinical manifestations and detection of preclinical disease.
    Jackson CE, Strehler DA.
    Pediatrics; 1968 Feb; 41(2):495-502. PubMed ID: 5637795
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  • 7. [Two sisters with autosomal recessive muscular dystrophy (Miyoshi) with early involvement of limb girdle muscles].
    Nishida Y, Ishimoto S, Kobayashi T, Goto I, Kuroiwa Y, Mitsuo K, Higashi Y.
    Rinsho Shinkeigaku; 1987 Jun; 27(6):756-9. PubMed ID: 3665270
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  • 11. [Biochemical, histological and clinical findings in carriers of Duchenne-type progressive muscular dystrophy].
    Moser H, Mumenthaler M, Wiesmann U.
    Schweiz Med Wochenschr; 1971 Apr 17; 101(15):537-42. PubMed ID: 5576948
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  • 12. [Limb-girdle syndrome. A study of 46 cases].
    Ferrer X, Larrivière M, Coquet M, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1993 Apr 17; 149(12):788-93. PubMed ID: 7997739
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  • 13. Adult-onset autosomal dominant limb-girdle muscular dystrophy.
    Chutkow JG, Heffner RR, Kramer AA, Edwards JA.
    Ann Neurol; 1986 Aug 17; 20(2):240-8. PubMed ID: 3752967
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  • 15. Muscular dystrophy in Saskatchewan Hutterites.
    Shokeir MH, Rozdilsky B.
    Am J Med Genet; 1985 Nov 17; 22(3):487-93. PubMed ID: 4061485
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  • 17. A new form of autosomal dominant limb-girdle muscular dystrophy (LGMD1G) with progressive fingers and toes flexion limitation maps to chromosome 4p21.
    Starling A, Kok F, Passos-Bueno MR, Vainzof M, Zatz M.
    Eur J Hum Genet; 2004 Dec 17; 12(12):1033-40. PubMed ID: 15367920
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  • 19. Familial adult-onset muscular dystrophy with leukoencephalopathy.
    van Engelen BG, Leyten QH, Bernsen PL, Gabreëls FJ, Barkhof F, Joosten EM, Hamel BC, ter Laak HJ, Ruijs MB, Cruysberg JR.
    Ann Neurol; 1992 Oct 17; 32(4):577-80. PubMed ID: 1456743
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  • 20. Consequences of a novel caveolin-3 mutation in a large German family.
    Fischer D, Schroers A, Blümcke I, Urbach H, Zerres K, Mortier W, Vorgerd M, Schröder R.
    Ann Neurol; 2003 Feb 17; 53(2):233-41. PubMed ID: 12557291
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