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Volumn 11, Issue 11, 2004, Pages 1336-1338

Hereditary neuralgic amyotrophy: A paediatric and familial presentation of Parsonage-Turner syndrome;Névralgie amyotrophiante héréditaire ou forme pédiatrique familiale du syndrome de Parsonage et Turner

Author keywords

Brachial plexus neuropathies; Child; Neuropathie focale h r ditaire; Neuropathies, hereditary motor and sensory; Plexus brachial; Syndrome de Parsonage et Turner

Indexed keywords

CORTICOSTEROID; HEPATITIS B VACCINE; PREDNISOLONE; PYRIDOXINE; THIAMINE;

EID: 7444235516     PISSN: 0929693X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.arcped.2004.06.023     Document Type: Article
Times cited : (6)

References (10)
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    • Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: Two distinct clinical, electrophysiologic, and genetic entities
    • Gouider R., LeGuern E., Emile J., Tardieu S., Cabon F., and Samid M. Hereditary neuralgic amyotrophy and hereditary neuropathy with liability to pressure palsies: two distinct clinical, electrophysiologic, and genetic entities Neurology 44 1994 2250 2252
    • (1994) Neurology , vol.44 , pp. 2250-2252
    • Gouider, R.1    Leguern, E.2    Emile, J.3    Tardieu, S.4    Cabon, F.5    Samid, M.6
  • 3
    • 0034308262 scopus 로고    scopus 로고
    • Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the european CMT Consortium
    • Kuhlenbäumer G., Stögbauer F., Timmerman V., and De Jonghe P. Diagnostic guidelines for hereditary neuralgic amyotrophy or heredofamilial neuritis with brachial plexus predilection. On behalf of the european CMT Consortium Neuromuscul Disord 10 2000 515 517
    • (2000) Neuromuscul Disord , vol.10 , pp. 515-517
    • Kuhlenbäumer, G.1    Stögbauer, F.2    Timmerman, V.3    De Jonghe, P.4
  • 5
  • 6
    • 0034121589 scopus 로고    scopus 로고
    • The natural history of hereditary neuralgic amyotrophy in the Dutch population. Two distinct types?
    • van Alfen N., van Engelen B.G., Reinders J.W., Kremer H., and Gabreëls F.J.M. The natural history of hereditary neuralgic amyotrophy in the Dutch population. Two distinct types? Brain 123 2000 718 723
    • (2000) Brain , vol.123 , pp. 718-723
    • Van Alfen, N.1    Van Engelen, B.G.2    Reinders, J.W.3    Kremer, H.4    Gabreëls, F.J.M.5
  • 7
    • 17844371957 scopus 로고    scopus 로고
    • Mutation analysis of four candidate genes for hereditary neuralgic amyotrophy (HNA)
    • Meuleman J., Kuhlenbäumer G., Audenaert D., Hünermund G., Hor H., and Young P. Mutation analysis of four candidate genes for hereditary neuralgic amyotrophy (HNA) Hum Genet 108 2001 390 393
    • (2001) Hum Genet , vol.108 , pp. 390-393
    • Meuleman, J.1    Kuhlenbäumer, G.2    Audenaert, D.3    Hünermund, G.4    Hor, H.5    Young, P.6
  • 8
    • 0035846539 scopus 로고    scopus 로고
    • Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy
    • Jeannet P.Y., Watts G.D., Bird T.D., and Chance P.F. Craniofacial and cutaneous findings expand the phenotype of hereditary neuralgic amyotrophy Neurology 57 2001 1963 1968
    • (2001) Neurology , vol.57 , pp. 1963-1968
    • Jeannet, P.Y.1    Watts, G.D.2    Bird, T.D.3    Chance, P.F.4
  • 10
    • 0030867316 scopus 로고    scopus 로고
    • Chronic relapsing brachial plexus neuropathy with persistent conduction block
    • Amato A.A., Jackson C.E., Kim J.Y., and Worley K.L. Chronic relapsing brachial plexus neuropathy with persistent conduction block Muscle Nerve 20 1997 1303 1307
    • (1997) Muscle Nerve , vol.20 , pp. 1303-1307
    • Amato, A.A.1    Jackson, C.E.2    Kim, J.Y.3    Worley, K.L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.