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British Journal of Sports Medicine
Volumn 36, Issue 6, 2002, Pages 465-466
Flail arms in a parachutist: An unusual presentation of hereditary neuropathy with liability to pressure palsies
Author keywords

[No Author keywords available]
Indexed keywords

ADULT; ARTICLE; CASE REPORT; DISEASE PREDISPOSITION; DISEASE SEVERITY; FEMALE; FLAIL ARM SYNDROME; HUMAN; JUMPING; MOTOR NERVE CONDUCTION; MUSCLE WEAKNESS; NEUROPATHY; PARACHUTIST; PARALYSIS; RISK ASSESSMENT;
EID: 0036901495     PISSN: 03063674     EISSN: None     Source Type: Journal    
DOI: 10.1136/bjsm.36.6.465     Document Type: Article
Times cited : (4)
References (7)
  • 1
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    • Diseases of the spinal cord
    • Lamsback W, Navrozov M, eds. New York: McGraw-Hill
    • Adams R, Victor M. Diseases of the spinal cord. In: Lamsback W, Navrozov M, eds. Principles of Neurology. 5th Ed. New York: McGraw-Hill, 1993:1078-116.
    • (1993) Principles of Neurology. 5th Ed. , pp. 1078-1116
    • Adams, R.1    Victor, M.2
  • 2
    • 0033594507 scopus 로고    scopus 로고
    • Spectrum of clinical and electrophysiological features in HNPP patients with the 17p11.2 deletion
    • Mouton P, Tardieu S, Gouider R, et al. Spectrum of clinical and electrophysiological features in HNPP patients with the 17p11.2 deletion. Neurology 1999;52:1440-6.
    • (1999) Neurology , vol.52 , pp. 1440-1446
    • Mouton, P.1    Tardieu, S.2    Gouider, R.3
  • 3
    • 0032706596 scopus 로고    scopus 로고
    • Charcot-Marie-Tooth disease and related neuropathies: Molecular basis for distinction and diagnosis
    • Pareyson D. Charcot-Marie-Tooth disease and related neuropathies: Molecular basis for distinction and diagnosis. Muscle Nerve 1999;22:1498-509.
    • (1999) Muscle Nerve , vol.22 , pp. 1498-1509
    • Pareyson, D.1
  • 4
    • 0034017935 scopus 로고    scopus 로고
    • Hereditary neuropathy with liability to pressure palsies: Two cases with a reciprocal translocation t(16;17)(q12;11.2) interrupting the PMP22 gene
    • Nodal M, Valiente A, Domenech A, et al. Hereditary neuropathy with liability to pressure palsies: Two cases with a reciprocal translocation t(16;17)(q12;11.2) interrupting the PMP22 gene [letter]. J Med Genet 2000;37:396-8.
    • (2000) J Med Genet , vol.37 , pp. 396-398
    • Nodal, M.1    Valiente, A.2    Domenech, A.3
  • 5
    • 0034083234 scopus 로고    scopus 로고
    • Fulminant case of hereditary neuropathy with liability to pressure palsy
    • Crum B, Sorenson E, Abad G, et al. Fulminant case of hereditary neuropathy with liability to pressure palsy. Muscle Nerve 2000;23:979-83.
    • (2000) Muscle Nerve , vol.23 , pp. 979-983
    • Crum, B.1    Sorenson, E.2    Abad, G.3
  • 6
    • 2642704986 scopus 로고    scopus 로고
    • Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene
    • Stogbauer F, Young P, Kerschensteiner M, et al. Recurrent brachial plexus palsies as the only clinical expression of hereditary neuropathy with liability to pressure palsies associated with a de novo deletion of the peripheral myelin protein-22 gene. Muscle Nerve 1998;21:1199-201.
    • (1998) Muscle Nerve , vol.21 , pp. 1199-1201
    • Stogbauer, F.1    Young, P.2    Kerschensteiner, M.3
  • 7
    • 0023302336 scopus 로고
    • Parachuting injuries: A study of 110,000 sports jumps
    • Ellitsgard N. Parachuting injuries: A study of 110,000 sports jumps. Br J Sports Med 1987;21:13-17.
    • (1987) Br J Sports Med , vol.21 , pp. 13-17
    • Ellitsgard, N.1

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.