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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

311 related items for PubMed ID: 8720327

  • 21. [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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  • 22. [Symptomatic carriers of dystrophinopathy with chromosome X inactivation bias].
    Lesca G, Demarquay G, Llense S, Streichenberger N, Petiot P, Michel-Calemard L, Récan D, Vial C, Ollagnon-Roman E.
    Rev Neurol (Paris); 2003 Sep; 159(8-9):775-80. PubMed ID: 13679720
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  • 24. Echocardiography in duchenne muscular dystrophy.
    Danilowicz D, Rutkowski M, Myung D, Schively D.
    Muscle Nerve; 1980 Sep; 3(4):298-303. PubMed ID: 7412774
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  • 25. Mosaic expression of dystrophin in carriers of canine X-linked muscular dystrophy.
    Cooper BJ, Gallagher EA, Smith CA, Valentine BA, Winand NJ.
    Lab Invest; 1990 Feb; 62(2):171-8. PubMed ID: 2406503
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  • 27. X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers.
    Wenger SL, Steele MW, Hoffman EP, Barmada MA, Wessel HB.
    Am J Med Genet; 1992 Aug 01; 43(6):1012-5. PubMed ID: 1415326
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  • 29. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP, Pegoraro E, Scacheri P, Burns RG, Taber JW, Weiss L, Spiro A, Blattner P.
    Am J Med Genet; 1996 Jun 28; 63(4):573-80. PubMed ID: 8826437
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  • 30. [Manifesting carriers of Duchenne muscular dystrophy over two generations].
    Itagaki Y, Saida K, Nishitani H, Matsuo M, Nishio H.
    Rinsho Shinkeigaku; 1993 Apr 28; 33(4):377-81. PubMed ID: 8103723
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  • 32. Sequence of cardiac changes in Duchenne muscular dystrophy.
    Heymsfield SB, McNish T, Perkins JV, Felner JM.
    Am Heart J; 1978 Mar 28; 95(3):283-94. PubMed ID: 622971
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  • 35. Cardiac involvement in adults with m.3243A>G MELAS gene mutation.
    Vydt TC, de Coo RF, Soliman OI, Ten Cate FJ, van Geuns RJ, Vletter WB, Schoonderwoerd K, van den Bosch BJ, Smeets HJ, Geleijnse ML.
    Am J Cardiol; 2007 Jan 15; 99(2):264-9. PubMed ID: 17223431
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  • 39. Transgenic overexpression of caveolin-3 in the heart induces a cardiomyopathic phenotype.
    Aravamudan B, Volonte D, Ramani R, Gursoy E, Lisanti MP, London B, Galbiati F.
    Hum Mol Genet; 2003 Nov 01; 12(21):2777-88. PubMed ID: 12966035
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  • 40. Element analysis of skeletal muscle in Duchenne muscular dystrophy using x-ray fluorescence spectrometry.
    Maunder-Sewry CA, Gorodetsky R, Yarom R, Dubowitz V.
    Muscle Nerve; 1980 Nov 01; 3(6):502-8. PubMed ID: 7453715
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