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Volumn 18, Issue 8, 2004, Pages 863-864

A case of familial trichomegaly in association with oculocutaneous albinism type 1 [15]

Author keywords

[No Author keywords available]

Indexed keywords

PIGMENT;

EID: 4444323483     PISSN: 0950222X     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.eye.6701326     Document Type: Letter
Times cited : (13)

References (11)
  • 1
    • 4444307338 scopus 로고
    • Abnormes Langenwachstum der Wimpern bei Ueberfunction der Nebennieren
    • Reitter. Abnormes Langenwachstum der Wimpern bei Ueberfunction der Nebennieren. Klin Mbl Augenheilk 1926; 76: 726.
    • (1926) Klin. Mbl. Augenheilk , vol.76 , pp. 726
    • Reitter, A.1
  • 2
    • 4444301966 scopus 로고
    • Abnormes Langenwachstum der Wimpern
    • Bab W. Abnormes Langenwachstum der Wimpern. Klin Mbl Augenheilk 1931; 87: 804.
    • (1931) Klin. Mbl. Augenheilk , vol.87 , pp. 804
    • Bab, W.1
  • 3
    • 4444334710 scopus 로고
    • Trichomegaly or movie lashes
    • Gray H. Trichomegaly or movie lashes. Stanford Med Bull 1944; 2: 157-158.
    • (1944) Stanford Med. Bull. , vol.2 , pp. 157-158
    • Gray, H.1
  • 4
    • 4444250365 scopus 로고
    • Disorders of the eyelashes and eyebrows
    • Albert DM, Jacobiec FA (eds) WB Saunders Co: Philadelphia, PA
    • Rubin PAD. Disorders of the eyelashes and eyebrows. In: Albert DM, Jacobiec FA (eds) Principles and practice of Ophthalmology. WB Saunders Co: Philadelphia, PA, 1994, P 1852.
    • (1994) Principles and Practice of Ophthalmology , pp. 1852
    • Rubin, P.A.D.1
  • 5
    • 0023521159 scopus 로고
    • Hypertrichosis of the eyelashes in acquired immunodeficiency syndrome
    • Casanova JM, Puig T, Rubio M. Hypertrichosis of the eyelashes in acquired immunodeficiency syndrome. Arch Dermatol 1987; 123: 1599-1601.
    • (1987) Arch. Dermatol. , vol.123 , pp. 1599-1601
    • Casanova, J.M.1    Puig, T.2    Rubio, M.3
  • 6
    • 0000914496 scopus 로고
    • Congenital trichomegaly with associated pigmentary degeneration of the retina, dwarfism, and mental retardation
    • Oliver GL, McFarlane DC. Congenital trichomegaly with associated pigmentary degeneration of the retina, dwarfism, and mental retardation. Arch Ophthalmol 1965; 74: 169-171.
    • (1965) Arch. Ophthalmol. , vol.74 , pp. 169-171
    • Oliver, G.L.1    McFarlane, D.C.2
  • 7
    • 0344410719 scopus 로고
    • de Lange syndrome (Brachmann-de Lange syndrome)
    • Gorlin RJ, (ed) Oxford University Press: New York, NY
    • Gorlin RJ, Cohen MM, Levin LS. de Lange syndrome (Brachmann-de Lange syndrome). In: Gorlin RJ, (ed) Syndromes of the Head and Neck. Oxford University Press: New York, NY, 1990, pp. 300-304.
    • (1990) Syndromes of the Head and Neck , pp. 300-304
    • Gorlin, R.J.1    Cohen, M.M.2    Levin, L.S.3
  • 8
    • 0015303080 scopus 로고
    • Trichomegaly, cataract, and hereditary spherocytosis in two siblings
    • Goldstein JH, Hutt AE. Trichomegaly, cataract, and hereditary spherocytosis in two siblings. Am J Ophthalmol 1972; 73: 333-335.
    • (1972) Am. J. Ophthalmol. , vol.73 , pp. 333-335
    • Goldstein, J.H.1    Hutt, A.E.2
  • 9
    • 0024383996 scopus 로고
    • Cone-rod congenital amaurosis associated with congenital hypertrichosis: An autosomal recessive condition
    • Jalili IK. Cone-rod congenital amaurosis associated with congenital hypertrichosis: an autosomal recessive condition. J Med Genet 1989; 26: 504-510.
    • (1989) J. Med. Genet. , vol.26 , pp. 504-510
    • Jalili, I.K.1
  • 10
    • 0032798812 scopus 로고    scopus 로고
    • Dermatologic manifestations of Hermansky-Pudlak syndrome in patients with and without a 16-base pair duplication in the HPS1 gene
    • Toro J, Turner M, Gahl WA. Dermatologic manifestations of Hermansky-Pudlak syndrome in patients with and without a 16-base pair duplication in the HPS1 gene. Arch Dermatol 1999; 135: 774-780.
    • (1999) Arch. Dermatol. , vol.135 , pp. 774-780
    • Toro, J.1    Turner, M.2    Gahl, W.A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.