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Volumn 70, Issue 4, 2011, Pages 662-665

Prevalence of congenital myopathies in a representative pediatric united states population

Author keywords

[No Author keywords available]

Indexed keywords

RYANODINE RECEPTOR 1; RYANODINE RECEPTOR;

EID: 84855404652     PISSN: 03645134     EISSN: 15318249     Source Type: Journal    
DOI: 10.1002/ana.22510     Document Type: Article
Times cited : (121)

References (10)
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    • Emery, A.E.1
  • 3
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    • The prevalence of inherited neuromuscular disease in Northern Ireland
    • DOI 10.1016/0960-8966(94)00017-4
    • Hughes MI, Hicks EM, Nevin NC, Patterson VH. The prevalence of inherited neuromuscular disease in Northern Ireland. Neuromuscul Disord 1996;6:69-73. (Pubitemid 26016503)
    • (1996) Neuromuscular Disorders , vol.6 , Issue.1 , pp. 69-73
    • Hughes, M.I.1    Hicks, E.M.2    Nevin, N.C.3    Patterson, V.H.4
  • 4
    • 0033989832 scopus 로고    scopus 로고
    • Neuromuscular disorders in childhood: A descriptive epidemiological study from western Sweden
    • DOI 10.1016/S0960-8966(99)00055-3, PII S0960896699000553
    • Darin N, Tulinius M. Neuromuscular disorders in childhood: A descriptive epidemiological study from western Sweden. Neuromuscul Disord 2000;10:1-9. (Pubitemid 30006857)
    • (2000) Neuromuscular Disorders , vol.10 , Issue.1 , pp. 1-9
    • Darin, N.1    Tulinius, M.2
  • 5
    • 70350690312 scopus 로고    scopus 로고
    • Prevalence of genetic muscle disease in Northern England: In-depth analysis of a muscle clinic population
    • Norwood FL, Harling C, Chinnery PF, et al., Prevalence of genetic muscle disease in Northern England: In-depth analysis of a muscle clinic population. Brain 2009;132(Pt 11):3175-3186.
    • (2009) Brain , vol.132 , Issue.PART 11 , pp. 3175-3186
    • Norwood, F.L.1    Harling, C.2    Chinnery, P.F.3
  • 6
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    • US Census Bureau
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    • CDC
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    • (2007)
  • 8
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    • Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion
    • Clarke NF, Waddell LB, Cooper ST, et al., Recessive mutations in RYR1 are a common cause of congenital fiber type disproportion. Hum Mutat 31:E1544-E1550.
    • Hum Mutat , vol.31
    • Clarke, N.F.1    Waddell, L.B.2    Cooper, S.T.3
  • 9
    • 78249290502 scopus 로고    scopus 로고
    • RYR1 mutations are a common cause of congenital myopathies with central nuclei
    • Wilmshurst JM, Lillis S, Zhou H, et al., RYR1 mutations are a common cause of congenital myopathies with central nuclei. Ann Neurol 2010;68:717-726.
    • (2010) Ann Neurol , vol.68 , pp. 717-726
    • Wilmshurst, J.M.1    Lillis, S.2    Zhou, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.