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Journal Abstract Search

208 related items for PubMed ID: 6633560

  • 1. Severe childhood muscular dystrophy affecting both sexes and frequent in Tunisia.
    Ben Hamida M, Fardeau M, Attia N.
    Muscle Nerve; 1983 Sep; 6(7):469-80. PubMed ID: 6633560
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  • 2. [Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
    Ben Hamida M, Attia N, Chabouni H, Fardeau M.
    Rev Neurol (Paris); 1983 Sep; 139(4):289-97. PubMed ID: 6612142
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  • 4. Becker-type muscular dystrophy.
    Bradley WG, Jones MZ, Mussini JM, Fawcett PR.
    Muscle Nerve; 1978 Sep; 1(2):111-32. PubMed ID: 571527
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  • 5. Novel mutations in three patients with LGMD2C with phenotypic differences.
    Vermeer S, Verrips A, Willemsen MA, ter Laak HJ, Ginjaar IB, Hamel BC.
    Pediatr Neurol; 2004 Apr; 30(4):291-4. PubMed ID: 15087111
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  • 6. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
    Nakamura A, Yoshida K, Ikeda S.
    Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
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  • 7. 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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  • 9. Distal muscular dystrophy of the Miyoshi type.
    Yildiz H, Emre U, Coskun O, Ergün U, Atasoy HT, Inan LE.
    Clin Neuropathol; 2003 Feb; 22(4):204-8. PubMed ID: 12908758
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  • 11. Becker and Duchenne muscular dystrophy: a comparative morphological study.
    Dennett X, Shield LK, Clingan LJ, Woolley DA.
    Aust Paediatr J; 1988 Feb; 24 Suppl 1():15-20. PubMed ID: 3202735
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  • 12. [A female infant of mitochondrial myopathy with findings of active necrosis and regeneration of muscle fibers].
    Nagaura T, Sumi K, Nonaka I.
    Rinsho Shinkeigaku; 1990 Apr; 30(4):432-8. PubMed ID: 2387114
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  • 13. [Estimation of the probability of heterozygosity in Duchenne-type progressive muscular dystrophy].
    Guízar Vázquez J, Navarrete Cadena C, Rico R, Mora G, Zavala C.
    Bol Med Hosp Infant Mex; 1981 Apr; 38(1):23-33. PubMed ID: 7284070
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  • 14. [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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