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American Journal of Ophthalmology
Volumn 137, Issue 1, 2004, Pages 181-183
Two patients with severe corneal disease in KID syndrome
Author keywords

[No Author keywords available]
Indexed keywords

ANTIBIOTIC AGENT; CONNEXIN 26; CORTICOSTEROID; EYE DROPS; PROTEIN; PROTEIN GJB2; UNCLASSIFIED DRUG;
EID: 0346099253     PISSN: 00029394     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9394(03)00739-6     Document Type: Article
Times cited : (31)
References (7)
  • 1
    • 0019462223 scopus 로고
    • The keratitis, ichthyosis, and deafness (KID) syndrome
    • Skinner B.A., Greist M.C., Norins A. The keratitis, ichthyosis, and deafness (KID) syndrome. Arch Dermatol. 117:1981;285-289.
    • (1981) Arch Dermatol , vol.117 , pp. 285-289
    • Skinner, B.A.1    Greist, M.C.2    Norins, A.3
  • 2
    • 0030001734 scopus 로고    scopus 로고
    • Keratitis, ichthyosis, and deafness (KID syndrome): Review of the literature and proposal of a new terminology
    • Caceres-Rois H., Tamayo-Sanchez L., Duran-Mckinster C., et al. Keratitis, ichthyosis, and deafness (KID syndrome) review of the literature and proposal of a new terminology . Pediatr Dermatol. 13:1996;105-113.
    • (1996) Pediatr Dermatol , vol.13 , pp. 105-113
    • Caceres-Rois, H.1    Tamayo-Sanchez, L.2    Duran-Mckinster, C.3
  • 3
    • 0016243112 scopus 로고
    • Corneal leucomas in ichthyosis
    • Milot J., Sheridan S. Corneal leucomas in ichthyosis. J Pediat Ophthalmol. 11:1974;209-212.
    • (1974) J Pediat Ophthalmol , vol.11 , pp. 209-212
    • Milot, J.1    Sheridan, S.2
  • 4
    • 0346451138 scopus 로고    scopus 로고
    • Limbal stem cell deficiency associated with KID syndrome, about a case
    • Gicquel J.J., Lami M.C., Catier A., et al. Limbal stem cell deficiency associated with KID syndrome, about a case. J Fr Opthalmol. 19:2002;513-516.
    • (2002) J Fr Opthalmol , vol.19 , pp. 513-516
    • Gicquel, J.J.1    Lami, M.C.2    Catier, A.3
  • 5
    • 0037565175 scopus 로고    scopus 로고
    • Novel mutation in GJB2 encoding connexin 26 in Japanese patients diagnosed with keratitis-ichthyosis-deafness syndrome
    • Yotsumoto S., Hashiguchi T., Chen X., et al. Novel mutation in GJB2 encoding connexin 26 in Japanese patients diagnosed with keratitis-ichthyosis- deafness syndrome. Br J Dermatol. 148:2003;649-653.
    • (2003) Br J Dermatol , vol.148 , pp. 649-653
    • Yotsumoto, S.1    Hashiguchi, T.2    Chen, X.3
  • 6
    • 18344395853 scopus 로고    scopus 로고
    • Missense mutation in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis-deafness syndrome
    • Richard G., Rouan F., Willoughby C., et al. Missense mutation in GJB2 encoding connexin-26 cause the ectodermal dysplasia keratitis-ichthyosis- deafness syndrome. J Am Hum Genet. 70:2002;1341-1348.
    • (2002) J Am Hum Genet , vol.70 , pp. 1341-1348
    • Richard, G.1    Rouan, F.2    Willoughby, C.3
  • 7
    • 0033002783 scopus 로고    scopus 로고
    • Genetic disease and gene knockouts reveal diverse connexin function
    • White T.W., Paul D. Genetic disease and gene knockouts reveal diverse connexin function. Annu Rev Physiol. 61:1999;283-310.
    • (1999) Annu Rev Physiol , vol.61 , pp. 283-310
    • White, T.W.1    Paul, D.2

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.