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Journal Abstract Search

379 related items for PubMed ID: 18079309

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  • 3. Autosomal dominant nemaline myopathy with intranuclear rods due to mutation of the skeletal muscle ACTA1 gene: clinical and pathological variability within a kindred.
    Hutchinson DO, Charlton A, Laing NG, Ilkovski B, North KN.
    Neuromuscul Disord; 2006 Feb; 16(2):113-21. PubMed ID: 16427282
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  • 4. Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).
    Tajsharghi H, Ohlsson M, Lindberg C, Oldfors A.
    Arch Neurol; 2007 Sep; 64(9):1334-8. PubMed ID: 17846275
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  • 7. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
    Botelho CH, Carod-Artal FJ, Kalil RK.
    Rev Neurol; 2007 Sep; 32(4):309-14. PubMed ID: 11333383
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  • 9. [Nemaline rod myopathy treated with L-tyrosine to relieve symptoms in a neonate].
    Sahin S, Oncel MY, Bidev D, Okur N, Talim B, Oguz SS.
    Arch Argent Pediatr; 2019 Aug 01; 117(4):e382-e386. PubMed ID: 31339280
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  • 10. Nemaline myopathy caused by mutations in the nebulin gene may present as a distal myopathy.
    Lehtokari VL, Pelin K, Herczegfalvi A, Karcagi V, Pouget J, Franques J, Pellissier JF, Figarella-Branger D, von der Hagen M, Huebner A, Schoser B, Lochmüller H, Wallgren-Pettersson C.
    Neuromuscul Disord; 2011 Aug 01; 21(8):556-62. PubMed ID: 21724397
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  • 12. Heterogeneity of nemaline myopathy cases with skeletal muscle alpha-actin gene mutations.
    Agrawal PB, Strickland CD, Midgett C, Morales A, Newburger DE, Poulos MA, Tomczak KK, Ryan MM, Iannaccone ST, Crawford TO, Laing NG, Beggs AH.
    Ann Neurol; 2004 Jul 01; 56(1):86-96. PubMed ID: 15236405
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  • 13. Intranuclear nemaline rod myopathy.
    Kaimaktchiev V, Goebel H, Laing N, Narus M, Weeks D, Nixon R.
    Muscle Nerve; 2006 Sep 01; 34(3):369-72. PubMed ID: 16477620
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  • 18. [Severe infantile nemaline myopathy].
    Miike T.
    Ryoikibetsu Shokogun Shirizu; 2001 Sep 01; (35):398-401. PubMed ID: 11555968
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