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Volumn 127, Issue 3, 2001, Pages 322-324

Familial bilateral vocal cord paralysis and Charcot-Marie-Tooth disease type II-C

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CENTRAL NERVOUS SYSTEM MALFORMATION; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; LARYNX SURGERY; MALE; PEDIATRICS; PHYSICAL EXAMINATION; VOCAL CORD PARALYSIS;

EID: 0035098295     PISSN: 08864470     EISSN: None     Source Type: Journal    
DOI: 10.1001/archotol.127.3.322     Document Type: Article
Times cited : (12)

References (15)
  • 1
    • 0002896804 scopus 로고
    • Sur une forme particulière d'atrophie musculaire progressive souvent familiale debutant par les pieds et les jambes et atteignant plus tard les mains
    • (1886) Rev Med , vol.6 , pp. 97-138
    • Charcot, J.-M.1    Marie, P.2
  • 4
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot Marie-Tooth's disease
    • (1974) Clin Genet , vol.6 , pp. 98-118
    • Skre, H.1
  • 5
    • 0014301249 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, I: Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies
    • (1968) Arch Neurol , vol.18 , pp. 603-618
    • Dyck, P.J.1    Lambert, E.H.2
  • 6
    • 0014301112 scopus 로고
    • Lower motor and primary sensory neuron diseases with peroneal muscular atrophy, II: Neurologic, genetic, and electrophysiologic findings in various neuronal degenerations
    • (1968) Arch Neurol , vol.18 , pp. 619-625
    • Dyck, P.J.1    Lambert, E.H.2
  • 7
  • 10
    • 0000954887 scopus 로고
    • Congenital laryngeal-abductor paralsysis due to nucleus ambiguus dysgenesis in three brothers
    • (1976) N Engl J Med , vol.271 , pp. 593-597
    • Plott, D.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.