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PUBMED FOR HANDHELDS

Journal Abstract Search


130 related items for PubMed ID: 1724729

  • 1. [A rare case of adult-onset Becker muscular dystrophy diagnosed by dystrophin staining].
    Ujike H, Tomita J, Kuroda S, Otsuki S, Arahata K.
    No To Shinkei; 1991 Oct; 43(10):975-9. PubMed ID: 1724729
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  • 3. [A 54-year-old man with progressive proximal muscle atrophy and gynecomastia].
    Anno M, Gotoh K, Hirasawa E, Mori H, Nakajima Y, Mizuno Y.
    No To Shinkei; 1995 Jan; 47(1):87-96. PubMed ID: 7669408
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  • 4. 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; 28(5):634-9. PubMed ID: 2260849
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  • 6. [Complete deficiency of adhalin (50 kDa DAG) in skeletal muscle of malignant limb-girdle muscular dystrophy].
    Kawai H, Inui T, Mitsui T, Campbell KP, Shimizu T, Matsumura K.
    Rinsho Shinkeigaku; 1995 Feb; 35(2):184-9. PubMed ID: 7781237
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  • 8. Left ventricular function in adults with muscular dystrophies: genotype-phenotype correlations.
    Martins E, Silva-Cardoso J, Silveira F, Nadais G, Gonçalves FR.
    Rev Port Cardiol; 2005 Jan; 24(1):23-35. PubMed ID: 15773664
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  • 10. [A case of Down syndrome complicated with Becker muscular dystrophy].
    Sakai K, Kojima S, Matsumura T, Takagi A, Arahata K.
    Rinsho Shinkeigaku; 1993 Nov; 33(11):1201-3. PubMed ID: 8124883
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  • 16. [A manifesting carrier of Duchenne muscular dystrophy presenting mosaic distribution of dystrophin negative and positive muscle fibers].
    Kikumoto O, Yoshinaga J, Sasaki T, Ideshita H, Hikiji A, Arahata K.
    Rinsho Shinkeigaku; 1990 Jan; 30(1):107-9. PubMed ID: 2184962
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  • 17. [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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  • 18. The frequency of patients with dystrophin abnormalities in a limb-girdle patient population.
    Arikawa E, Hoffman EP, Kaido M, Nonaka I, Sugita H, Arahata K.
    Neurology; 1991 Sep; 41(9):1491-6. PubMed ID: 1842672
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  • 19. A case of Becker muscular dystrophy resulting from the skipping of four contiguous exons (71-74) of the dystrophin gene during mRNA maturation.
    Patria SY, Alimsardjono H, Nishio H, Takeshima Y, Nakamura H, Matsuo M.
    Proc Assoc Am Physicians; 1996 Jul; 108(4):308-14. PubMed ID: 8863344
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  • 20. [Limb-girdle syndrome. A study of 46 cases].
    Ferrer X, Larrivière M, Coquet M, Ellie E, Lagueny A, Julien J.
    Rev Neurol (Paris); 1993 Jul; 149(12):788-93. PubMed ID: 7997739
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