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Journal Abstract Search

226 related items for PubMed ID: 11517491

  • 1. [Two adult cases of nemaline myopathy presenting different clinical symptoms and CT findings].
    Tajima Y, Yoshida A, Ura S.
    No To Shinkei; 2001 Jul; 53(7):653-8. PubMed ID: 11517491
    [Abstract] [Full Text] [Related]

  • 2. [A 34-year-old woman with delayed motor milestones, high arched palate, and proximal muscle weakness].
    Yamamoto T, Kitada T, Hirasawa E, Mori H, Mizuno Y.
    No To Shinkei; 1996 Jul; 48(7):677-84. PubMed ID: 8753005
    [Abstract] [Full Text] [Related]

  • 3. [Two cases of nemaline myopathy diagnosed after episodes of respiratory failure].
    Kudou M, Kobayashi Y, Yamashita K, Kita H, Yasuba H, Hamada K.
    Nihon Kokyuki Gakkai Zasshi; 2006 Jun; 44(6):474-8. PubMed ID: 16841721
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  • 4. [An adulthood progressive case of congenital nemaline myopathy showing rimmed vacuoles in muscle biopsy and diffuse neurogenic changes on electromyography].
    Ikezoe K, Murai H, Kawajiri M, Ohyagi Y, Kira J.
    Rinsho Shinkeigaku; 2004 Jul; 44(7):450-3. PubMed ID: 15384708
    [Abstract] [Full Text] [Related]

  • 5. Clinical, histological and radiological responses to methylprednisolone in HIV-associated rod myopathy.
    Silva AMS, Mendonça RH, Moreno CAM, Estephan EP, Helito PVP, Carvalho MS, Zanoteli E.
    Neuromuscul Disord; 2017 Aug; 27(8):756-759. PubMed ID: 28606402
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  • 6. [A 22-year-old man with long-standing weakness and atrophy predominantly in the lower extremities].
    Mori H, Sato K, Hirasawa E, Kondo T, Mizuno Y.
    No To Shinkei; 1996 Aug; 48(8):763-71. PubMed ID: 8797213
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  • 10. [Nemaline congenital myopathy:clinical features and histopathological findings in nine patients].
    Botelho CH, Carod-Artal FJ, Kalil RK.
    Rev Neurol; 1996 Aug; 32(4):309-14. PubMed ID: 11333383
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  • 11. [Adult-onset nemaline myopathy with distal muscle atrophy--case report].
    Niwa F, Shiga K, Kimura M, Yamaguchi T, Kondo M, Nakagawa M.
    Brain Nerve; 2009 Jun; 61(6):695-9. PubMed ID: 19526838
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  • 12. [A comparative study of the clinical and histological characteristics between classic nemaline myopathy and that associated with the human immunodeficiency virus].
    Miró O, Masanés F, Pedrol E, García-Carrasco M, Mallolas J, Casademont J, Grau JM.
    Med Clin (Barc); 1995 Oct 21; 105(13):500-3. PubMed ID: 7494440
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  • 14. Adult-onset nemaline myopathy: a case report and review of the literature.
    Gyure KA, Prayson RA, Estes ML.
    Arch Pathol Lab Med; 1997 Nov 21; 121(11):1210-3. PubMed ID: 9372751
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  • 15. [Sibling cases of severe infantile form of nemaline myopathy with ACTA1-gene mutation].
    Sudo A, Hayashi Y, Sano H, Kawamura N, Nishino I, Nonaka I.
    No To Hattatsu; 2013 Nov 21; 45(6):452-6. PubMed ID: 24313005
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  • 16. Idiopathic adult-onset nemaline myopathy presenting with isolated respiratory failure.
    Whitaker J, Love S, Williams AP, Plummeridge M.
    Muscle Nerve; 2009 Mar 21; 39(3):406-8. PubMed ID: 19208402
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  • 17. [Two cases of sporadic late onset nemaline myopathy effectively treated with immunotherapy].
    Mizuno Y, Mori-Yoshimura M, Okamoto T, Oya Y, Nishino I, Murata M.
    Rinsho Shinkeigaku; 2016 Sep 29; 56(9):605-11. PubMed ID: 27580764
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  • 18. 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 29; 64(9):1334-8. PubMed ID: 17846275
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  • 20. Histopathologic progression and a novel mutation in a child with nemaline myopathy.
    Ladha S, Coons S, Johnsen S, Sambuughin N, Bien-Wilner R, Sivakumar K.
    J Child Neurol; 2008 Jul 29; 23(7):813-7. PubMed ID: 18487519
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