메뉴 건너뛰기




Volumn 8, Issue 8, 2013, Pages

Quantitative Muscle MRI as an Assessment Tool for Monitoring Disease Progression in LGMD2I: A Multicentre Longitudinal Study

Author keywords

[No Author keywords available]

Indexed keywords

FUKUTIN RELATED PROTEIN;

EID: 84881527343     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0070993     Document Type: Article
Times cited : (153)

References (23)
  • 1
    • 2342590096 scopus 로고    scopus 로고
    • FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. J Med Genet
    • Walter MC, Petersen JA, Stucka R, Fischer D, Schröder R, et al. (2004) FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. J Med Genet. 41: e50.
    • (2004) , vol.41
    • Walter, M.C.1    Petersen, J.A.2    Stucka, R.3    Fischer, D.4    Schröder, R.5
  • 2
    • 18244375299 scopus 로고    scopus 로고
    • Mutations in the fukutin related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum Mol Genet
    • Brockington M, Yuva Y, Prandini P, Brown SC, Torelli S, et al. (2001) Mutations in the fukutin related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum Mol Genet. 10: 2851-2859.
    • (2001) , vol.10 , pp. 2851-2859
    • Brockington, M.1    Yuva, Y.2    Prandini, P.3    Brown, S.C.4    Torelli, S.5
  • 3
    • 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, Eagle M, Bushby K, et al. (2009) Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population. Brain 132: 3175-86.
    • (2009) Brain , vol.132 , pp. 3175-3186
    • Norwood, F.L.1    Harling, C.2    Chinnery, P.F.3    Eagle, M.4    Bushby, K.5
  • 4
  • 5
    • 0037211475 scopus 로고    scopus 로고
    • The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12-14, 2002
    • Bushby K, Beckmann JS, (2003) The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12-14, 2002. Neuromuscul Disord 13: 80-90.
    • (2003) Neuromuscul Disord , vol.13 , pp. 80-90
    • Bushby, K.1    Beckmann, J.S.2
  • 6
    • 0028835527 scopus 로고
    • Diagnostic criteria for limb girdle muscular dystrophies:report of the ENMC workshop on limb girdle muscular dystrophies
    • Bushby K, Beckmann J, (1995) Diagnostic criteria for limb girdle muscular dystrophies:report of the ENMC workshop on limb girdle muscular dystrophies. Neuromuscul Disord 5: 71-74.
    • (1995) Neuromuscul Disord , vol.5 , pp. 71-74
    • Bushby, K.1    Beckmann, J.2
  • 7
    • 0037461314 scopus 로고    scopus 로고
    • The Limb Girdle Muscular Dystrophies. Genetic and phenotypic definition of a disputed entity
    • Wicklund M, Hilton-Jones D, (2003) The Limb Girdle Muscular Dystrophies. Genetic and phenotypic definition of a disputed entity. Neurology 60: 1230-31.
    • (2003) Neurology , vol.60 , pp. 1230-1231
    • Wicklund, M.1    Hilton-Jones, D.2
  • 8
    • 26944484790 scopus 로고    scopus 로고
    • Muscle imaging in clinical practice: diagnostic value of muscle magnetic imaging in inherited neuromuscular disorders
    • Mercuri E, Jungbluth H, Muntoni F, (2005) Muscle imaging in clinical practice: diagnostic value of muscle magnetic imaging in inherited neuromuscular disorders. Curr Opin Neurol 18: 126-37.
    • (2005) Curr Opin Neurol , vol.18 , pp. 126-137
    • Mercuri, E.1    Jungbluth, H.2    Muntoni, F.3
  • 10
    • 0031439460 scopus 로고    scopus 로고
    • Correlative MR Imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy
    • Lodi R, Muntoni F, Taylor J, Kumar S, Sewry CA, et al. (1997) Correlative MR Imaging and 31P-MR spectroscopy study in sarcoglycan deficient limb girdle muscular dystrophy. Neuromuscul Disord 7: 505-511.
    • (1997) Neuromuscul Disord , vol.7 , pp. 505-511
    • Lodi, R.1    Muntoni, F.2    Taylor, J.3    Kumar, S.4    Sewry, C.A.5
  • 11
    • 0023162758 scopus 로고
    • 31P Nuclear magnetic resonance studies in Duchenne Muscular dystrophy: age related metabolic changes
    • Younkin D, Berman P, Sladky J, Chee C, Bank W, et al. (1987) 31P Nuclear magnetic resonance studies in Duchenne Muscular dystrophy: age related metabolic changes. Neurology 37: 165-9.
    • (1987) Neurology , vol.37 , pp. 165-169
    • Younkin, D.1    Berman, P.2    Sladky, J.3    Chee, C.4    Bank, W.5
  • 12
    • 33845887997 scopus 로고    scopus 로고
    • MRI for the demonstration of subclinical muscle involvement in muscular dystrophy
    • Sookhoo S, MacKinnon, Bushby K, Chinnery PF, Birchall D, (2007) MRI for the demonstration of subclinical muscle involvement in muscular dystrophy. Clinical Radiology 62: 160-5.
    • (2007) Clinical Radiology , vol.62 , pp. 160-165
    • Sookhoo, S.1    MacKinnon2    Bushby, K.3    Chinnery, P.F.4    Birchall, D.5
  • 13
    • 0021132985 scopus 로고
    • Simple proton spectroscopic imaging
    • Dixon W, (1984) Simple proton spectroscopic imaging. Radiology 153: 189-194.
    • (1984) Radiology , vol.153 , pp. 189-194
    • Dixon, W.1
  • 15
    • 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: 458-61.
    • (2009) Neuromuscul Disord , vol.19 , pp. 458-461
    • Mazzone, E.S.1    Messina, S.2    Vasco, G.3    Main, M.4    Eagle, M.5
  • 16
    • 0026031194 scopus 로고
    • The timed "Up & Go": a test of basic functional mobility for frail elderly persons
    • Podsiadlo D, Richardson S, (1991) The timed "Up & Go": a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc 39: 142-148.
    • (1991) J Am Geriatr Soc , vol.39 , pp. 142-148
    • Podsiadlo, D.1    Richardson, S.2
  • 17
    • 84969393566 scopus 로고    scopus 로고
    • Use of the 6 min walk test as an endpoint in clinical trials for neuromuscular diseases; Neuromuscul Disord
    • Florence JM, van der Ploeg A, Clemens PR, Escolar DM, Laforet P, et al. (2008) Use of the 6 min walk test as an endpoint in clinical trials for neuromuscular diseases; Neuromuscul Disord. 18: 738-739.
    • (2008) , vol.18 , pp. 738-739
    • Florence, J.M.1    van der Ploeg, A.2    Clemens, P.R.3    Escolar, D.M.4    Laforet, P.5
  • 18
    • 0036644465 scopus 로고    scopus 로고
    • ATS statement: guidelines for the six-minute walk test
    • ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories
    • ATS Committee on Proficiency Standards for Clinical Pulmonary Function Laboratories (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
  • 19
    • 0030662535 scopus 로고    scopus 로고
    • Two-point Dixon technique for water-fat signal decomposition with B0 inhomogeneity correction
    • Coombs BD, Szumowski J, Coshow W, (1997) Two-point Dixon technique for water-fat signal decomposition with B0 inhomogeneity correction. Magn Reson Med 38: 884-889.
    • (1997) Magn Reson Med , vol.38 , pp. 884-889
    • Coombs, B.D.1    Szumowski, J.2    Coshow, W.3
  • 20
    • 0025831477 scopus 로고
    • Three-point Dixon technique for true water/fat decomposition with B0 inhomogeneity correction
    • Glover GH, Schneider E, (1991) Three-point Dixon technique for true water/fat decomposition with B0 inhomogeneity correction. Magn Reson Med 18: 371-383.
    • (1991) Magn Reson Med , vol.18 , pp. 371-383
    • Glover, G.H.1    Schneider, E.2
  • 22
    • 0036787899 scopus 로고    scopus 로고
    • Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p(RSMD1)
    • Mercuri E, Talim B, Moghadaszadeh B, Petit N, Brockington M, et al. (2002) Clinical and imaging findings in six cases of congenital muscular dystrophy with rigid spine syndrome linked to chromosome 1p(RSMD1). Neuromuscul Disord 12: 631-638.
    • (2002) Neuromuscul Disord , vol.12 , pp. 631-638
    • Mercuri, E.1    Talim, B.2    Moghadaszadeh, B.3    Petit, N.4    Brockington, M.5
  • 23
    • 84908219488 scopus 로고
    • Statistical methods for assessing agreement between two methods of clinical measurement
    • Bland JM, Altman DG, (1986) Statistical methods for assessing agreement between two methods of clinical measurement. Lancet 327: 307-310.
    • (1986) Lancet , vol.327 , pp. 307-310
    • Bland, J.M.1    Altman, D.G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.