메뉴 건너뛰기




Volumn 66, Issue 3, 2002, Pages 303-307

Upper airway abnormalities in Canavan disease

Author keywords

Airway obstruction; Canavan; Tracheostomy

Indexed keywords

ARTICLE; ASPIRATION PNEUMONIA; CANAVAN DISEASE; CASE REPORT; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE COURSE; HUMAN; MALE; PHYSICAL EXAMINATION; PRESCHOOL CHILD; PRIORITY JOURNAL; TRACHEOSTOMY; TREATMENT INDICATION; UPPER RESPIRATORY TRACT OBSTRUCTION;

EID: 0037010758     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0165-5876(02)00258-6     Document Type: Article
Times cited : (8)

References (8)
  • 1
    • 0027284253 scopus 로고
    • The inherited leukodystrophies: A clinical overview
    • Aicardi J. The inherited leukodystrophies: a clinical overview. J. Inherit. Metab. Dis. 16:1993;733-743.
    • (1993) J. Inherit. Metab. Dis. , vol.16 , pp. 733-743
    • Aicardi, J.1
  • 3
    • 0023220775 scopus 로고
    • N-acetylaspartic aciduria due to aspartoacylase deficiency - A new etiology of childhood leukodystrophy
    • Hagenfeldt L., Bollgren I., Venizelos N. N-acetylaspartic aciduria due to aspartoacylase deficiency - a new etiology of childhood leukodystrophy. J. Inherit. Metab. Dis. 10:1967;135-141.
    • (1967) J. Inherit. Metab. Dis. , vol.10 , pp. 135-141
    • Hagenfeldt, L.1    Bollgren, I.2    Venizelos, N.3
  • 4
    • 0027362434 scopus 로고
    • Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease
    • Kaul R., Gao G.P., Balamurugan K., Matalon R. Cloning of the human aspartoacylase cDNA and a common missense mutation in Canavan disease. Nat. Genet. 5:1993;118-123.
    • (1993) Nat. Genet. , vol.5 , pp. 118-123
    • Kaul, R.1    Gao, G.P.2    Balamurugan, K.3    Matalon, R.4
  • 5
    • 0033937515 scopus 로고    scopus 로고
    • Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: Four new mutations in the non-Jewish population
    • Sistermans E.A., de Coo R.F., van Beerendonk H.M., Poll-The B.T., Kleijer W.J., van Oost B.A. Mutation detection in the aspartoacylase gene in 17 patients with Canavan disease: four new mutations in the non-Jewish population. Eur. J. Hum. Genet. 8:2000;557-560.
    • (2000) Eur. J. Hum. Genet. , vol.8 , pp. 557-560
    • Sistermans, E.A.1    De Coo, R.F.2    Van Beerendonk, H.M.3    Poll-The, B.T.4    Kleijer, W.J.5    Van Oost, B.A.6
  • 6
    • 0004183059 scopus 로고    scopus 로고
    • Washington DC: American College of Obstetrics and Gynecology
    • Screening for Canavan Disease. Washington DC: American College of Obstetrics and Gynecology, 1998.
    • (1998) Screening for Canavan Disease
  • 7
    • 0033916925 scopus 로고    scopus 로고
    • Gene therapy for Canavan disease?
    • Fink D.J. Gene therapy for Canavan disease? Ann. Neurol. 48:2000;9-10.
    • (2000) Ann. Neurol. , vol.48 , pp. 9-10
    • Fink, D.J.1
  • 8
    • 0031893872 scopus 로고    scopus 로고
    • The clinical course of Canavan disease
    • Traeger E.C., Rapin I. The clinical course of Canavan disease. Pediatr. Neurol. 18:1998;207-212.
    • (1998) Pediatr. Neurol. , vol.18 , pp. 207-212
    • Traeger, E.C.1    Rapin, I.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.