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Journal Abstract Search

394 related items for PubMed ID: 7557060

  • 1.
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  • 3. [Relations between delayed diagnosis and forms of onset in Duchenne muscular dystrophy].
    Alvarez Leal M, Morales Aguilera A, Pérez Zuno JA, Segura Romero S, Quiroz Góngora MC, Paredes García A.
    Gac Med Mex; 1994; 130(6):459-64. PubMed ID: 7557061
    [Abstract] [Full Text] [Related]

  • 4. Absence of correlation between skewed X inactivation in blood and serum creatine-kinase levels in Duchenne/Becker female carriers.
    Sumita DR, Vainzof M, Campiotto S, Cerqueira AM, Cánovas M, Otto PA, Passos-Bueno MR, Zatz M.
    Am J Med Genet; 1998 Dec 04; 80(4):356-61. PubMed ID: 9856563
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  • 5. Serum myoglobin in muscular dystrophy.
    Kagen LJ, Moussavi S, Miller SL, Tsairis P.
    Muscle Nerve; 1980 Dec 04; 3(3):221-6. PubMed ID: 7374673
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  • 6. Serum CK-MB activity in progressive muscular dystrophy: is it of nosologic value?
    Vainzof M, Zatz M, Otto PA.
    Am J Med Genet; 1985 Sep 04; 22(1):81-7. PubMed ID: 4050853
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  • 7. Serum creatine kinase isoenzymes in Duchenne muscular dystrophy determined by sensitive enzyme immunoassay methods.
    Mokuno K, Riku S, Sugimura K, Takahashi A, Kato K, Osugi S.
    Muscle Nerve; 1987 Jun 04; 10(5):459-63. PubMed ID: 3302699
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  • 8. Valley sign in Becker muscular dystrophy and outliers of Duchenne and Becker muscular dystrophy.
    Pradhan S.
    Neurol India; 2004 Jun 04; 52(2):203-5. PubMed ID: 15269471
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  • 9. Becker and Duchenne muscular dystrophy: a comparative morphological study.
    Dennett X, Shield LK, Clingan LJ, Woolley DA.
    Aust Paediatr J; 1988 Jun 04; 24 Suppl 1():15-20. PubMed ID: 3202735
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  • 11. Comparative analysis between Duchenne and Becker types muscular dystrophy.
    Ishpekova B, Milanov I, Christova LG, Alexandrov AS.
    Electromyogr Clin Neurophysiol; 1999 Jun 04; 39(5):315-8. PubMed ID: 10422002
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  • 12. Investigation on genetic heterogeneity in Duchenne muscular dystrophy.
    Rabbi-Bortolini E, Zatz M.
    Am J Med Genet; 1986 May 04; 24(1):111-7. PubMed ID: 3706399
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  • 13. The muscular dystrophies.
    Seiler J, Bope ET.
    Am Fam Physician; 1986 Jul 04; 34(1):123-8. PubMed ID: 3728255
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  • 14. Creatine kinase activity in normal and Duchenne muscular dystrophy fibroblasts.
    Davis MH, Cappel R, Vester JW, Samaha FJ, Gruenstein E.
    Muscle Nerve; 1982 Jan 04; 5(1):1-6. PubMed ID: 7057800
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  • 15. Studies on the creatine kinase MM isoforms of normal and Duchenne muscular dystrophic patients.
    Zhao X, Bi C, Yang Z.
    Chin Med J (Engl); 1998 Jan 04; 111(1):75-7. PubMed ID: 10322660
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  • 16. Muscle and serum enzymes and isoenzymes in muscular dystrophies.
    Ibrahim GA, Zweber BA, Awad EA.
    Arch Phys Med Rehabil; 1981 Jun 04; 62(6):265-9. PubMed ID: 7235920
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  • 17. [Neonatal screening for duchenne myopathy by serum elevation of creatine phosphokinase activity. 5 years experience].
    Plauchu H, Dellamonica C, Pascal B, Jolivet MJ, Guibaud P, Cotte J, Robert JM.
    J Genet Hum; 1981 Mar 04; 29(1):59-69. PubMed ID: 7334342
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  • 18. Genetic predictors and remodeling of dilated cardiomyopathy in muscular dystrophy.
    Jefferies JL, Eidem BW, Belmont JW, Craigen WJ, Ware SM, Fernbach SD, Neish SR, Smith EO, Towbin JA.
    Circulation; 2005 Nov 01; 112(18):2799-804. PubMed ID: 16246949
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  • 19. Cardiorespiratory function in Duchenne and Becker muscular dystrophy.
    Taşdemir HA, Cil E, Topaloğlu H, Yalaz K, Aysun S, Renda Y, Ozme S.
    Turk J Pediatr; 1996 Nov 01; 38(3):307-14. PubMed ID: 8827899
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  • 20. Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy.
    Zatz M, Rapaport D, Vainzof M, Passos-Bueno MR, Bortolini ER, Pavanello Rde C, Peres CA.
    J Neurol Sci; 1991 Apr 01; 102(2):190-6. PubMed ID: 2072118
    [Abstract] [Full Text] [Related]

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