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Volumn 43, Issue 4, 2006, Pages 236-238

Bilateral corneal perforation in an infant with congenital alacrima

Author keywords

[No Author keywords available]

Indexed keywords

HYALURONIC ACID; OFLOXACIN;

EID: 33746995941     PISSN: 01913913     EISSN: None     Source Type: Journal    
DOI: 10.3928/01913913-20060701-06     Document Type: Article
Times cited : (5)

References (8)
  • 2
    • 0036942791 scopus 로고    scopus 로고
    • Familial dysautonomia in review: Diagnosis and treatment of ocular manifestations
    • Josaitis CA, Matisoff M. Familial dysautonomia in review: diagnosis and treatment of ocular manifestations. Adv Exp Med Biol 2002;506:71-80.
    • (2002) Adv Exp Med Biol , vol.506 , pp. 71-80
    • Josaitis, C.A.1    Matisoff, M.2
  • 3
    • 0021738204 scopus 로고
    • Congenital sensory neuropathies: Diagnostic distinction from familial dysautonomia
    • Axelrod FB, Pearson J. Congenital sensory neuropathies: diagnostic distinction from familial dysautonomia. Am J Dis Child 1984;138:947-954.
    • (1984) Am J Dis Child , vol.138 , pp. 947-954
    • Axelrod, F.B.1    Pearson, J.2
  • 4
    • 0017280620 scopus 로고
    • A case of new dysautonomia-like disorder found in Japan: I. Clinical and metabolic studies
    • Suzuki T, Higa S, Hayashi A, Nakagawa T, Fujii K. A case of new dysautonomia-like disorder found in Japan: I. Clinical and metabolic studies. Eur Neurol 1976;14:146-160.
    • (1976) Eur Neurol , vol.14 , pp. 146-160
    • Suzuki, T.1    Higa, S.2    Hayashi, A.3    Nakagawa, T.4    Fujii, K.5
  • 5
    • 0035097484 scopus 로고    scopus 로고
    • Familial dysautonomia is caused by mutations of the IKAP gene
    • Anderson SL, Coli R, Daly IW, et al. Familial dysautonomia is caused by mutations of the IKAP gene. Am J Hum Genet 2001;68:753-758.
    • (2001) Am J Hum Genet , vol.68 , pp. 753-758
    • Anderson, S.L.1    Coli, R.2    Daly, I.W.3
  • 6
    • 0041329911 scopus 로고    scopus 로고
    • Identification of the first non-Jewish mutation in familial dysautonomia
    • Leyne M, Mull J, Gill SP, et al. Identification of the first non-Jewish mutation in familial dysautonomia. Am J Med Genet 2003;118A:305-308.
    • (2003) Am J Med Genet , vol.118 A , pp. 305-308
    • Leyne, M.1    Mull, J.2    Gill, S.P.3
  • 7
    • 0023051095 scopus 로고
    • Congenital absence of the lacrimal gland
    • Keith GC, Boldt DW. Congenital absence of the lacrimal gland. Am J Ophthalmol 1986;102:800-801.
    • (1986) Am J Ophthalmol , vol.102 , pp. 800-801
    • Keith, G.C.1    Boldt, D.W.2
  • 8
    • 0006823449 scopus 로고
    • Congenital deformities
    • Duke-Elder SS, ed. London: Kimpton
    • Duke-Elder SS. Congenital deformities. In: Duke-Elder SS, ed. System of Ophthalmology, vol. 3, part 2. London: Kimpton; 1963:913-916.
    • (1963) System of Ophthalmology , vol.3 , Issue.PART 2 , pp. 913-916
    • Duke-Elder, S.S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.