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Volumn 67, Issue 4, 2003, Pages 427-428

Hereditary vocal cord palsy

Author keywords

Hereditary; Stridor; Vocal cord palsy

Indexed keywords

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; GENETIC DISORDER; HUMAN; LABORATORY TEST; MALE; PRIORITY JOURNAL; STRIDOR; TRACHEOSTOMY; TREATMENT OUTCOME; VOCAL CORD PARALYSIS;

EID: 0037377407     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(02)00398-1     Document Type: Article
Times cited : (5)

References (8)
  • 1
    • 0032557735 scopus 로고
    • Familial laryngeal paralysis
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    • (1988) Am. J. Med. Genet. , vol.77 , Issue.4 , pp. 277-280
    • Manligod, J.M.1    Smith, R.J.2
  • 3
    • 0032764295 scopus 로고    scopus 로고
    • Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy
    • Donaghy M., Kennet R. Varying occurrence of vocal cord paralysis in a family with autosomal dominant hereditary motor and sensory neuropathy. J. Neurol. 246:(7):1999;552-555.
    • (1999) J. Neurol. , vol.246 , Issue.7 , pp. 552-555
    • Donaghy, M.1    Kennet, R.2
  • 4
    • 0024509068 scopus 로고
    • Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: A dominant form of spinal muscular atrophy?
    • Boltshauser E., Lang W., Spillman T., Hof E. Hereditary distal muscular atrophy with vocal cord paralysis and sensorineural hearing loss: a dominant form of spinal muscular atrophy? J. Med. Genet. 26:1989;105-108.
    • (1989) J. Med. Genet. , vol.26 , pp. 105-108
    • Boltshauser, E.1    Lang, W.2    Spillman, T.3    Hof, E.4
  • 5
    • 0034883912 scopus 로고    scopus 로고
    • Localisation of the gene for familial laryngeal abductor paralysis to chromosome 6q16
    • Manaligod J.M., Skaggs, Smith R.J. Localisation of the gene for familial laryngeal abductor paralysis to chromosome 6q16. Arch. Otolaryngol. Head Neck Surg. 127:(8):2001;913-917.
    • (2001) Arch. Otolaryngol. Head Neck Surg. , vol.127 , Issue.8 , pp. 913-917
    • Manaligod, J.M.1    Skaggs2    Smith, R.J.3
  • 6
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot-Marie-tooth disease
    • Skre H. Genetic and clinical aspects of Charcot-Marie-tooth disease. Clin. Genet. 6:1974;98-118.
    • (1974) Clin. Genet. , vol.6 , pp. 98-118
    • Skre, H.1
  • 7
    • 0025054153 scopus 로고
    • Familial congenital laryngeal abductor paralysis: Different expressions in a family with one male and three females affected
    • Schinzel A., Hof E., Dangel P., Robinson W. Familial congenital laryngeal abductor paralysis: different expressions in a family with one male and three females affected. J. Med. Genet. 27:(11):1990;715-716.
    • (1990) J. Med. Genet. , vol.27 , Issue.11 , pp. 715-716
    • Schinzel, A.1    Hof, E.2    Dangel, P.3    Robinson, W.4
  • 8
    • 0018119341 scopus 로고
    • Autosomal dominantly inherited adductor laryngeal paralysis - A new syndrome with suggestion of linkage to HLA
    • Mace M., Williamson E., Morgan D. Autosomal dominantly inherited adductor laryngeal paralysis - a new syndrome with suggestion of linkage to HLA. Clin. Genet. 14:1978;265-270.
    • (1978) Clin. Genet. , vol.14 , pp. 265-270
    • Mace, M.1    Williamson, E.2    Morgan, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.