These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

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
    [Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 7.