메뉴 건너뛰기




Volumn 17, Issue 7, 2010, Pages 874-878

Correlation between muscle atrophy on MRI and manual strength testing in hereditary neuropathies

Author keywords

Charcot Marie Tooth; Hereditary motor neuropathy; MRI; Neuropathy

Indexed keywords

ADULT; AGED; ARTICLE; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE SEVERITY; DYNAMOMETRY; FEMALE; FUNCTIONAL ASSESSMENT; HEREDITARY MOTOR NEUROPATHY; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; IMAGE ANALYSIS; INTERMETHOD COMPARISON; MALE; MOTOR NEUROPATHY; MUSCLE ATROPHY; MUSCLE DENERVATION; MUSCLE STRENGTH; MUSCLE WEAKNESS; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL;

EID: 77952554447     PISSN: 09675868     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jocn.2009.11.006     Document Type: Article
Times cited : (18)

References (19)
  • 1
    • 0037005365 scopus 로고    scopus 로고
    • Clinical features and molecular genetics of hereditary peripheral neuropathies
    • Kuhlenbäumer G., Young P., Hünermund G., et al. Clinical features and molecular genetics of hereditary peripheral neuropathies. J Neurol 249 (2002) 1629-1650
    • (2002) J Neurol , vol.249 , pp. 1629-1650
    • Kuhlenbäumer, G.1    Young, P.2    Hünermund, G.3
  • 2
    • 0014301249 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy I. Neurologic, genetic and electrophysiologic findings in hereditary polyneuropathies
    • Dyck P.J., and Lambert E.H. Lower motor and primary sensory neuron diseases with peroneal muscular atrophy I. Neurologic, genetic and electrophysiologic findings in hereditary polyneuropathies. Arch Neurol 18 (1968) 603-618
    • (1968) Arch Neurol , vol.18 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 3
    • 0001140122 scopus 로고
    • Inherited neuronal atrophy and degeneration predominantly of lower motor neurons
    • Dyck P., and Thomas P. (Eds), W.B. Saunders, Philadelphia
    • Harding A. Inherited neuronal atrophy and degeneration predominantly of lower motor neurons. In: Dyck P., and Thomas P. (Eds). Peripheral neuropathy. 3rd ed. vol. 2 (1993), W.B. Saunders, Philadelphia 1051-1063
    • (1993) Peripheral neuropathy. 3rd ed. , vol.2 , pp. 1051-1063
    • Harding, A.1
  • 4
    • 0018942439 scopus 로고
    • The clinical features of hereditary motor and sensory neuropathy types I and II
    • Harding A.E., and Thomas P.K. The clinical features of hereditary motor and sensory neuropathy types I and II. Brain 103 (1980) 259-280
    • (1980) Brain , vol.103 , pp. 259-280
    • Harding, A.E.1    Thomas, P.K.2
  • 5
    • 5444229769 scopus 로고    scopus 로고
    • Molecular genetics of distal hereditary motor neuropathies
    • Irobi J., De Jonghe P., and Timmerman V. Molecular genetics of distal hereditary motor neuropathies. Hum Mol Gen 13 (2004) 195-202
    • (2004) Hum Mol Gen , vol.13 , pp. 195-202
    • Irobi, J.1    De Jonghe, P.2    Timmerman, V.3
  • 6
    • 0038067742 scopus 로고    scopus 로고
    • Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V
    • Antonellis A., Ellsworth R.E., Sambuughin N., et al. Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V. Am J Hum Genet 72 (2003) 1293-1299
    • (2003) Am J Hum Genet , vol.72 , pp. 1293-1299
    • Antonellis, A.1    Ellsworth, R.E.2    Sambuughin, N.3
  • 7
    • 14844291447 scopus 로고    scopus 로고
    • Characterization of genetically defined types of Charcot-Marie-Tooth neuropathies by using magnetic resonance neurography
    • Ellagala D.B., Monteith S.J., Haynor D., et al. Characterization of genetically defined types of Charcot-Marie-Tooth neuropathies by using magnetic resonance neurography. J Neurosurg 102 (2005) 242-245
    • (2005) J Neurosurg , vol.102 , pp. 242-245
    • Ellagala, D.B.1    Monteith, S.J.2    Haynor, D.3
  • 8
    • 0031290336 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease and related peripheral neuropathies
    • De Jonghe P., Timmerman V., Nelis E., et al. Charcot-Marie-Tooth disease and related peripheral neuropathies. J Peripher Nerv Syst 2 (1997) 370-387
    • (1997) J Peripher Nerv Syst , vol.2 , pp. 370-387
    • De Jonghe, P.1    Timmerman, V.2    Nelis, E.3
  • 9
    • 0036157054 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation
    • Boerkoel C.F., Takashima H., Garcia C.A., et al. Charcot-Marie-Tooth disease and related neuropathies: mutation distribution and genotype-phenotype correlation. Ann Neurol 51 (2002) 190-201
    • (2002) Ann Neurol , vol.51 , pp. 190-201
    • Boerkoel, C.F.1    Takashima, H.2    Garcia, C.A.3
  • 10
    • 0030985749 scopus 로고    scopus 로고
    • The phenotypic manifestations of chromosome 17p11.2 duplication
    • Thomas P.K., Marques Jr. W., and Davis M.B. The phenotypic manifestations of chromosome 17p11.2 duplication. Brain 120 (1997) 465-478
    • (1997) Brain , vol.120 , pp. 465-478
    • Thomas, P.K.1    Marques Jr., W.2    Davis, M.B.3
  • 11
    • 24944456834 scopus 로고    scopus 로고
    • Manual muscle testing: does it meet the standards of an adequate screening test?
    • Bohannon R.W. Manual muscle testing: does it meet the standards of an adequate screening test?. Clin Rehabil 19 (2005) 662-667
    • (2005) Clin Rehabil , vol.19 , pp. 662-667
    • Bohannon, R.W.1
  • 12
    • 0024511985 scopus 로고
    • Relationship of manual muscle testing to objective strength measurements
    • Aitkens S., Lord J., Bernauer E., et al. Relationship of manual muscle testing to objective strength measurements. Muscle Nerve 12 (1989) 173-177
    • (1989) Muscle Nerve , vol.12 , pp. 173-177
    • Aitkens, S.1    Lord, J.2    Bernauer, E.3
  • 13
    • 34147185885 scopus 로고    scopus 로고
    • On the reliability and validity of manual muscle testing: a literature review
    • Cuthbert S.C., and Goodheart Jr. G.J. On the reliability and validity of manual muscle testing: a literature review. Chiropr Osteopat 15 (2007) 4
    • (2007) Chiropr Osteopat , vol.15 , pp. 4
    • Cuthbert, S.C.1    Goodheart Jr., G.J.2
  • 14
    • 0029588693 scopus 로고
    • Patterns of muscle atrophy in the lower limbs in patients with Charcot-Marie-Tooth disease as measured by magnetic resonance imaging
    • Stilwell G., Kilcoyne R.F., and Sherman J.L. Patterns of muscle atrophy in the lower limbs in patients with Charcot-Marie-Tooth disease as measured by magnetic resonance imaging. J Foot Ankle Surg 34 (1995) 583-586
    • (1995) J Foot Ankle Surg , vol.34 , pp. 583-586
    • Stilwell, G.1    Kilcoyne, R.F.2    Sherman, J.L.3
  • 15
    • 0031968663 scopus 로고    scopus 로고
    • MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths
    • Bono F., Gambardella A., Oliveri R.L., et al. MRI of skeletal muscles in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. Eur Neurol 39 (1998) 191-192
    • (1998) Eur Neurol , vol.39 , pp. 191-192
    • Bono, F.1    Gambardella, A.2    Oliveri, R.L.3
  • 16
    • 31544441021 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles
    • Gallardo E., Garcia A., Combarros O., et al. Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles. Brain 129 (2006) 426-437
    • (2006) Brain , vol.129 , pp. 426-437
    • Gallardo, E.1    Garcia, A.2    Combarros, O.3
  • 17
    • 34248218542 scopus 로고    scopus 로고
    • A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36
    • Gopinath S., Blair I.P., Kennerson M.L., et al. A novel locus for distal motor neuron degeneration maps to chromosome 7q34-q36. Hum Genet 121 (2007) 559-564
    • (2007) Hum Genet , vol.121 , pp. 559-564
    • Gopinath, S.1    Blair, I.P.2    Kennerson, M.L.3
  • 18
    • 0030919339 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases
    • Birouk N., Gouider R., Le Guern E., et al. Charcot-Marie-Tooth disease type 1A with 17p11.2 duplication. Clinical and electrophysiological phenotype study and factors influencing disease severity in 119 cases. Brain 120 (1997) 813-823
    • (1997) Brain , vol.120 , pp. 813-823
    • Birouk, N.1    Gouider, R.2    Le Guern, E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.