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Volumn 36, Issue 8, 1996, Pages 469-475

Differential diagnosis of limb girdle syndromes

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CONTROLLED STUDY; ELECTROMYOGRAM; HUMAN; LIMB GIRDLE MUSCULAR DYSTROPHY; MAJOR CLINICAL STUDY; SPINAL MUSCULAR ATROPHY;

EID: 0029777732     PISSN: 0301150X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (25)
  • 2
    • 0020606260 scopus 로고
    • Severe childhood muscular dystrophy affecing both sexes and frequent in Tunisia
    • BEN HAMIDA, M., FARDEAU, M. and ATTIA, N.: Severe childhood muscular dystrophy affecing both sexes and frequent in Tunisia. Muscle Nerve, 6: 496-480, 1983.
    • (1983) Muscle Nerve , vol.6 , pp. 496-1480
    • Ben Hamida, M.1    Fardeau, M.2    Attia, N.3
  • 3
    • 0017259099 scopus 로고
    • Benign myopathy with autosomal dominant inheritance: A report of three pedigrees
    • BETHLEM, J. and VAN WIJNGAARDEN, G.: Benign myopathy with autosomal dominant inheritance: a report of three pedigrees. Brain, 99: 91-100, 1976.
    • (1976) Brain , vol.99 , pp. 91-100
    • Bethlem, J.1    Van Wijngaarden, G.2
  • 4
    • 0011290733 scopus 로고
    • The limb-girdle syndrome
    • Vinken, P. J., Bruyn, G.W. (eds.), Amsterdam: North Holland
    • BRADLEY, W.G.: The limb-girdle syndrome. In: Vinken, P. J., Bruyn, G.W. (eds.), Handbook of clinical neurology. Vol. 40. Amsterdam: North Holland, 433-469, 1979.
    • (1979) Handbook of Clinical Neurology. , vol.40 , pp. 433-469
    • Bradley, W.G.1
  • 5
    • 10544221103 scopus 로고
    • Electrodiagnostic features of Charcot-Marie-Tooth disease
    • CHRISTIE, B.G.B.: Electrodiagnostic features of Charcot-Marie-Tooth disease. Proc. Roy. Soc. Med., 54: 321-324, 1961.
    • (1961) Proc. Roy. Soc. Med. , vol.54 , pp. 321-324
    • Christie, B.G.B.1
  • 6
    • 0022497685 scopus 로고
    • Adult onset autosomal dominant limb-girdle muscular dystrophy
    • CHUTKOW, J.G., HEFFNER, R.R., KRAMER, A.A. and EDWARDS, J.M.: Adult onset autosomal dominant limb-girdle muscular dystrophy. Ann. Neurol., 20: 240-248, 1986.
    • (1986) Ann. Neurol. , vol.20 , pp. 240-248
    • Chutkow, J.G.1    Heffner, R.R.2    Kramer, A.A.3    Edwards, J.M.4
  • 7
    • 0015788562 scopus 로고
    • Histopathologie des unités motrices dans les maladies neuromusculaires
    • COERS, C. and TELERMAN-TOPPET, N.: Histopathologie des unités motrices dans les maladies neuromusculaires. Ann. Anatol. Pathol., 18: 235-250, 1973.
    • (1973) Ann. Anatol. Pathol. , vol.18 , pp. 235-250
    • Coers, C.1    Telerman-Toppet, N.2
  • 8
    • 0019188802 scopus 로고
    • Clinical features and classification of the muscular dystrophies
    • GARDNER-MEDWIN, D.: Clinical features and classification of the muscular dystrophies. Br. Med. Bull., 36: 109, 1980.
    • (1980) Br. Med. Bull. , vol.36 , pp. 109
    • Gardner-Medwin, D.1
  • 9
    • 0023856168 scopus 로고
    • Clinical and genetic investigation in autosomal dominant limb-girdle dystrophy
    • GILCHRIST, J.M., PERICAK-VANCE, M. A., SILVERMAN, L. and ROSES, A.D.: Clinical and genetic investigation in autosomal dominant limb-girdle dystrophy. Neurology, 38: 5-9, 1988.
    • (1988) Neurology , vol.38 , pp. 5-9
    • Gilchrist, J.M.1    Pericak-Vance, M.A.2    Silverman, L.3    Roses, A.D.4
  • 10
    • 0026764256 scopus 로고
    • Dystrophinopathy in isolated cases of myopathy in females
    • HOFFMAN, E. P., ARAHTA, K., MINETTI, C. et al.: Dystrophinopathy in isolated cases of myopathy in females. Neurology, 42: 967-975, 1992.
    • (1992) Neurology , vol.42 , pp. 967-975
    • Hoffman, E.P.1    Arahta, K.2    Minetti, C.3
  • 11
    • 0017569986 scopus 로고
    • Chronic-spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy
    • KAZAKOV, V.M., KOVALENKO, T.M., SKOROMETZ, A.A. and MIKHAILOV, E.P.: Chronic-spinal muscular atrophy simulating facioscapulohumeral type and limb-girdle type of muscular dystrophy. Eur. Neurol., 16: 90-98, 1977.
    • (1977) Eur. Neurol. , vol.16 , pp. 90-98
    • Kazakov, V.M.1    Kovalenko, T.M.2    Skorometz, A.A.3    Mikhailov, E.P.4
  • 12
    • 0000089061 scopus 로고
    • Heredofamilial proximal spinal muscular atrophy simulating muscular dystrophy
    • KUGELBERG, E. and WELANDER, L.: Heredofamilial proximal spinal muscular atrophy simulating muscular dystrophy. Arch. Neurol. Psychiat. (Chic.), 75: 500-509, 1956.
    • (1956) Arch. Neurol. Psychiat. (Chic.) , vol.75 , pp. 500-509
    • Kugelberg, E.1    Welander, L.2
  • 13
    • 0027102414 scopus 로고
    • A large inbred Palestinian family with two forms of muscular dystrophy
    • MAHJNEH, I., VANELLI, G., BUSHBY, K. and MARCONI, G.: A large inbred Palestinian family with two forms of muscular dystrophy. Neuromusc. Dis., 2: 277-283, 1992.
    • (1992) Neuromusc. Dis. , vol.2 , pp. 277-283
    • Mahjneh, I.1    Vanelli, G.2    Bushby, K.3    Marconi, G.4
  • 14
    • 0025876630 scopus 로고
    • Limb-girdle muscular dystrophy with autosomal dominant inheritance
    • MARCONI, G.P., PIZZI, A., ARIMONDI, C.G. and VANELLI, B.: Limb-girdle muscular dystrophy with autosomal dominant inheritance. Acta Neurol. Scand., 38: 234-238, 1991.
    • (1991) Acta Neurol. Scand. , vol.38 , pp. 234-238
    • Marconi, G.P.1    Pizzi, A.2    Arimondi, C.G.3    Vanelli, B.4
  • 15
    • 0014598411 scopus 로고
    • Chronic spinal muscular atrophy in adults. Part 1. The Kugelberg-Welander syndrome
    • MEADOWS, J.C., MARSDEN, C.D. and HARRIMAN, D.G.F.: Chronic spinal muscular atrophy in adults. Part 1. The Kugelberg-Welander syndrome. J. Neurol. Sci., 9: 527-550, 1969.
    • (1969) J. Neurol. Sci. , vol.9 , pp. 527-550
    • Meadows, J.C.1    Marsden, C.D.2    Harriman, D.G.F.3
  • 17
    • 17644431425 scopus 로고
    • Progressive muskeldystrophie, VIII Haufigkeit, Klinik und Genetik der Typen I und II
    • MOSER VON, H., WIESMANN, U., RICHTERICH, R. and ROSSI, E.: Progressive muskeldystrophie, VIII Haufigkeit, Klinik und Genetik der Typen I und II. Schweis. Med. Wochenschr., 96: 169-205, 1966.
    • (1966) Schweis. Med. Wochenschr. , vol.96 , pp. 169-205
    • Von Moser, H.1    Wiesmann, U.2    Richterich, R.3    Rossi, E.4
  • 18
    • 0024510023 scopus 로고
    • Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin DNA probes
    • NORMAN, A., THOMAS, N., COACKLEY, J. and HARPER, P.: Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin DNA probes. Lancet, I: 466-468, 1989.
    • (1989) Lancet , vol.1 , pp. 466-468
    • Norman, A.1    Thomas, N.2    Coackley, J.3    Harper, P.4
  • 19
    • 0025753198 scopus 로고
    • Limb-girdle syndrome: A genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies
    • PASSOS-BUENO, M.R., VAINZOF, M., PAVANELLO, R. C., PAVANELLO-FILHO, I., LIMA, M. and SATS, M.: Limb-girdle syndrome: a genetic study of 22 large Brazilian families comparison with X-linked Duchenne and Becker dystrophies. J. Neurol. Sci., 103: 65-75, 1991.
    • (1991) J. Neurol. Sci. , vol.103 , pp. 65-75
    • Passos-Bueno, M.R.1    Vainzof, M.2    Pavanello, R.C.3    Pavanello-Filho, I.4    Lima, M.5    Sats, M.6
  • 20
    • 0026356242 scopus 로고
    • Benign muscular dystrophy with autosomal dominant inheritance
    • SOMER, H., LAULAMAA, V., PALJARVI, L. et al.: Benign muscular dystrophy with autosomal dominant inheritance. Neuromusc. Dis., 1: 267-274, 1991.
    • (1991) Neuromusc. Dis. , vol.1 , pp. 267-274
    • Somer, H.1    Laulamaa, V.2    Paljarvi, L.3
  • 21
    • 0020519420 scopus 로고
    • Quadriceps myopathy: A variant of the limb-girdle dystrophy syndrome
    • SWASH, M. and HEATHFIELD, K. W. G.: Quadriceps myopathy: a variant of the limb-girdle dystrophy syndrome. J. Neurol. Neurosurg. Psychiat., 46: 355-357, 1983.
    • (1983) J. Neurol. Neurosurg. Psychiat. , vol.46 , pp. 355-357
    • Swash, M.1    Heathfield, K.W.G.2
  • 23
    • 0000042975 scopus 로고
    • On classification, natural history and treatment of the myopathies
    • WALTON, J.N. and NATTRASS, F.J.: On classification, natural history and treatment of the myopathies. Brain, 77: 169, 1954.
    • (1954) Brain , vol.77 , pp. 169
    • Walton, J.N.1    Nattrass, F.J.2
  • 24
    • 10544227162 scopus 로고
    • Two cases of myopathy limited to the quadriceps
    • WALTON, J.N.: Two cases of myopathy limited to the quadriceps. J. Neurol. Neurosurg. Psychiat., 19: 106-108, 1956.
    • (1956) J. Neurol. Neurosurg. Psychiat. , vol.19 , pp. 106-108
    • Walton, J.N.1
  • 25
    • 0344222928 scopus 로고
    • Heriditary proximal spinal muscular atrophy - A clinical entity simulating muscular dystrophy
    • WOHLFART, G., FEX, G. and ELIASSON, S.: Heriditary proximal spinal muscular atrophy - a clinical entity simulating muscular dystrophy. Acta Psychiat. Scand., 30: 395-406, 1955.
    • (1955) Acta Psychiat. Scand. , vol.30 , pp. 395-406
    • Wohlfart, G.1    Fex, G.2    Eliasson, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.