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Volumn 9, Issue 10, 2014, Pages

Long term natural history data in ambulant boys with duchenne muscular dystrophy: 36-month changes

(39)  Pane, Marika a   Mazzone, Elena Stacy a   Sivo, Serena a   Sormani, Maria Pia b   Messina, Sonia c   D'Amico, Adele d   Carlesi, Adelina d   Vita, Gianluca c   Fanelli, Lavinia a   Berardinelli, Angela e   Torrente, Yvan f   Lanzillotta, Valentina g   Viggiano, Emanuela h   D'Ambrosio, Paola h   Cavallaro, Filippo c   Frosini, Silvia i   Barp, Andrea j   Bonfiglio, Serena k   Scalise, Roberta a   De Sanctis, Roberto a   more..


Author keywords

[No Author keywords available]

Indexed keywords

DEFLAZACORT; PREDNISONE;

EID: 84907487779     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0108205     Document Type: Article
Times cited : (101)

References (19)
  • 1
    • 84883055833 scopus 로고    scopus 로고
    • The 6-minute walk test and other endpoints in duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study
    • McDonald CM, Henricson EK, Abresch R.T., Florence JM, Eagle M, et al. (2013) The 6-minute walk test and other endpoints in Duchenne muscular dystrophy: Longitudinal natural history observations over 48 weeks from a multicenter study. Muscle Nerve 48: 343-356.
    • (2013) Muscle Nerve , vol.48 , pp. 343-356
    • McDonald, C.M.1    Henricson, E.K.2    Abresch, R.T.3    Florence, J.M.4    Eagle, M.5
  • 2
    • 84879554058 scopus 로고    scopus 로고
    • The cooperative international neuromuscular research group duchenne natural history study - A longitudinal investigation in the era of glucocorticoid therapy: Design of protocol and the methods used
    • McDonald CM, Henricson EK, Abresch R.T., Han JJ, Escolar DM, et al. (2013) The cooperative international neuromuscular research group Duchenne natural history study-a longitudinal investigation in the era of glucocorticoid therapy: design of protocol and the methods used. Muscle Nerve 48: 32-54.
    • (2013) Muscle Nerve , vol.48 , pp. 32-54
    • McDonald, C.M.1    Henricson, E.K.2    Abresch, R.T.3    Han, J.J.4    Escolar, D.M.5
  • 3
    • 84883050768 scopus 로고    scopus 로고
    • The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from a multicenter study
    • McDonald CM, Henricson EK, Abresch R.T., Florence J., Eagle M, et al. (2013) The 6-minute walk test and other clinical endpoints in duchenne muscular dystrophy: Reliability, concurrent validity, and minimal clinically important differences from a multicenter study. Muscle Nerve 48: 343-356.
    • (2013) Muscle Nerve , vol.48 , pp. 343-356
    • McDonald, C.M.1    Henricson, E.K.2    Abresch, R.T.3    Florence, J.4    Eagle, M.5
  • 4
    • 84879551615 scopus 로고    scopus 로고
    • The cooperative international neuromuscular research group duchenne natural history study: Glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures
    • Henricson EK, Abresch RT, Cnaan A, Hu F., Duong T, et al. (2013) The cooperative international neuromuscular research group Duchenne natural history study: glucocorticoid treatment preserves clinically meaningful functional milestones and reduces rate of disease progression as measured by manual muscle testing and other commonly used clinical trial outcome measures. Muscle Nerve 48: 55-67.
    • (2013) Muscle Nerve , vol.48 , pp. 55-67
    • Henricson, E.K.1    Abresch, R.T.2    Cnaan, A.3    Hu, F.4    Duong, T.5
  • 5
    • 84885175848 scopus 로고    scopus 로고
    • Development of the performance of the upper limb module for duchenne muscular dystrophy
    • Mayhew A, Mazzone ES, Eagle M, Duong T., Ash M, et al. (2013) Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy. Dev Med Child Neurol 55: 1038-1045.
    • (2013) Dev Med Child Neurol , vol.55 , pp. 1038-1045
    • Mayhew, A.1    Mazzone, E.S.2    Eagle, M.3    Duong, T.4    Ash, M.5
  • 6
    • 77950210043 scopus 로고    scopus 로고
    • The 6-minute walk test as a new outcome measure in duchenne muscular dystrophy
    • McDonald CM, Henricson EK, Han J.J., Abresch RT, Nicorici A, et al. (2010) The 6-minute walk test as a new outcome measure in Duchenne muscular dystrophy. Muscle Nerve 41: 500-510.
    • (2010) Muscle Nerve , vol.41 , pp. 500-510
    • McDonald, C.M.1    Henricson, E.K.2    Han, J.J.3    Abresch, R.T.4    Nicorici, A.5
  • 7
    • 84860908668 scopus 로고    scopus 로고
    • Percent-predicted 6-minute walk distance in duchenne muscular dystrophy to account for maturational influences
    • Henricson E, Abresch R, Han J.J., Nicorici A., Goude Keller E, et al. (2012) Percent-Predicted 6-Minute Walk Distance in Duchenne Muscular Dystrophy to Account for Maturational Influences. PLoS Curr 4: RRN1297.
    • (2012) PLoS Curr , vol.4 , pp. RRN1297
    • Henricson, E.1    Abresch, R.2    Han, J.J.3    Nicorici, A.4    Goude Keller, E.5
  • 8
    • 77957748915 scopus 로고    scopus 로고
    • North star ambulatory assessment, 6-minute walk test and timed items in ambulant boys with duchenne muscular dystrophy
    • Mazzone ES, Martinelli D, Berardinelli A., Messina S, D'Amico A, et al. (2010) North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophy. Neuromuscul Disord 20: 712-716.
    • (2010) Neuromuscul Disord , vol.20 , pp. 712-716
    • Mazzone, E.S.1    Martinelli, D.2    Berardinelli, A.3    Messina, S.4    D'Amico, A.5
  • 9
    • 80051478879 scopus 로고    scopus 로고
    • Functional changes in duchenne muscular dystrophy: A 12-month longitudinal cohort study
    • Mazzone ES, Vasco G, Sormani M.P., Torrente Y., Berardinelli A, et al. (2011) Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort study. Neurology 77: 250-256.
    • (2011) Neurology , vol.77 , pp. 250-256
    • Mazzone, E.S.1    Vasco, G.2    Sormani, M.P.3    Torrente, Y.4    Berardinelli, A.5
  • 10
    • 67649842377 scopus 로고    scopus 로고
    • Reliability of the north star ambulatory assessment in a multicentric setting
    • Mazzone ES, Messina S, Vasco G., Main M, Eagle M, et al. (2009) Reliability of the North Star Ambulatory Assessment in a multicentric setting. Neuromuscul Disord 19: 458-461.
    • (2009) Neuromuscul Disord , vol.19 , pp. 458-461
    • Mazzone, E.S.1    Messina, S.2    Vasco, G.3    Main, M.4    Eagle, M.5
  • 11
    • 79956006620 scopus 로고    scopus 로고
    • Moving towards meaningful measurement: Rasch analysis of the north star ambulatory assessment in duchenne muscular dystrophy
    • Mayhew A, Cano S, Scott E., Eagle M, Bushby K, et al. (2011) Moving towards meaningful measurement: Rasch analysis of the North Star Ambulatory Assessment in Duchenne muscular dystrophy. Dev Med Child Neurol 53: 535-542.
    • (2011) Dev Med Child Neurol , vol.53 , pp. 535-542
    • Mayhew, A.1    Cano, S.2    Scott, E.3    Eagle, M.4    Bushby, K.5
  • 12
    • 84862004315 scopus 로고    scopus 로고
    • Development of a functional assessment scale for ambulatory boys with duchenne muscular dystrophy
    • Scott E, Eagle M, Mayhew A., Freeman J, Main M, et al. (2011) Development of a Functional Assessment Scale for Ambulatory Boys with Duchenne Muscular Dystrophy. Physiother Res Int.
    • (2011) Physiother Res Int.
    • Scott, E.1    Eagle, M.2    Mayhew, A.3    Freeman, J.4    Main, M.5
  • 13
    • 84872223337 scopus 로고    scopus 로고
    • 24 month longitudinal data in ambulant boys with duchenne muscular dystrophy
    • Mazzone ES, Pane M, Sormani M.P., Scalise R., Berardinelli A, et al. (2013) 24 month longitudinal data in ambulant boys with Duchenne muscular dystrophy. PLoS One 8: e52512.
    • (2013) PLoS One , vol.8 , pp. e52512
    • Mazzone, E.S.1    Pane, M.2    Sormani, M.P.3    Scalise, R.4    Berardinelli, A.5
  • 14
    • 0036644465 scopus 로고    scopus 로고
    • ATS statement: Guidelines for the six-minute walk test
    • - (2002) ATS statement: guidelines for the six-minute walk test. Am J Respir Crit Care Med 166: 111-117.
    • (2002) Am J Respir Crit Care Med , vol.166 , pp. 111-117
  • 15
    • 84897449030 scopus 로고    scopus 로고
    • 6 minute walk test in duchenne MD patients with different mutations: 12 month changes
    • Pane M, Mazzone ES, Sormani M.P., Messina S., Vita GL, et al. (2014) 6 minute walk test in Duchenne MD patients with different mutations: 12 month changes. PLoS One 9: e83400.
    • (2014) PLoS One , vol.9 , pp. e83400
    • Pane, M.1    Mazzone, E.S.2    Sormani, M.P.3    Messina, S.4    Vita, G.L.5
  • 16
    • 84896710462 scopus 로고    scopus 로고
    • Six-minute walk test: Reference values And prediction equation in healthy boys aged 5 to 12 years
    • Goemans N, Klingels K, van den Hauwe M, Boons S, Verstraete L, et al. (2013) Six-minute walk test: reference values and prediction equation in healthy boys aged 5 to 12 years. PLoS One 8: e84120.
    • (2013) PLoS One , vol.8 , pp. e84120
    • Goemans, N.1    Klingels, K.2    Van Den Hauwe, M.3    Boons, S.4    Verstraete, L.5
  • 17
    • 84860908668 scopus 로고    scopus 로고
    • Percent-predicted 6-minute walk distance in duchenne muscular dystrophy to account for maturational influences
    • Henricson E, Abresch R, Han J.J., Nicorici A., Goude Keller E, et al. (2012) Percent-predicted 6-minute walk distance in duchenne muscular dystrophy to account for maturational influences. PLoS Curr 4: RRN1297.
    • (2012) PLoS Curr , vol.4 , pp. RRN1297
    • Henricson, E.1    Abresch, R.2    Han, J.J.3    Nicorici, A.4    Goude Keller, E.5
  • 18
    • 78751634526 scopus 로고    scopus 로고
    • SPP1 genotype is a determinant of disease severity in duchenne muscular dystrophy
    • Pegoraro E, Hoffman EP, Piva L, Gavassini B.F., Cagnin S., et al. (2011) SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy. Neurology 76: 219-226.
    • (2011) Neurology , vol.76 , pp. 219-226
    • Pegoraro, E.1    Hoffman, E.P.2    Piva, L.3    Gavassini, B.F.4    Cagnin, S.5
  • 19
    • 84878390222 scopus 로고    scopus 로고
    • LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy
    • Flanigan KM, Ceco E, Lamar K.M., Kaminoh Y., Dunn DM, et al. (2013) LTBP4 genotype predicts age of ambulatory loss in duchenne muscular dystrophy. Ann Neurol 73: 481-488.
    • (2013) Ann Neurol , vol.73 , pp. 481-488
    • Flanigan, K.M.1    Ceco, E.2    Lamar, K.M.3    Kaminoh, Y.4    Dunn, D.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.