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Volumn 53, Issue 1, 1996, Pages 7-19

Severe hereditary retinal diseases in childhood;Schwerwiegende hereditäre netzhauterkrankungen im kindesalter

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; CHILD; CHROMOSOME ABERRATION; GENETIC DISORDER; GENETICS; HETEROZYGOTE DETECTION; HUMAN; INFANT; NEWBORN; PRESCHOOL CHILD; RETINA DISEASE; REVIEW;

EID: 0029685635     PISSN: 00405930     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (1)

References (13)
  • 2
    • 0029119784 scopus 로고
    • A gene for Leber's congenital amaurosis maps to chromosome 17p
    • Camuzat A., Dollfus H., Rozet J. M., Gerber S., Bonneau D. et al.: A gene for Leber's congenital amaurosis maps to chromosome 17p. Hum. Mol. Gen. 4, 1447-1452, 1995.
    • (1995) Hum. Mol. Gen. , vol.4 , pp. 1447-1452
    • Camuzat, A.1    Dollfus, H.2    Rozet, J.M.3    Gerber, S.4    Bonneau, D.5
  • 3
    • 0029063743 scopus 로고
    • Hereditary disease as a cause of childhood blindness - Regional variation. Result of blind school studies undertaken in countries of Latin America, Asia and Africa
    • Gilbert C., Rahi J., Eckstein M., Foster A.: Hereditary disease as a cause of childhood blindness - regional variation. Result of blind school studies undertaken in countries of Latin America, Asia and Africa. Ophthalmic Genetics 16, 1-10, 1995.
    • (1995) Ophthalmic Genetics , vol.16 , pp. 1-10
    • Gilbert, C.1    Rahi, J.2    Eckstein, M.3    Foster, A.4
  • 5
    • 0027225696 scopus 로고
    • Human forms of neuronal Ceroid-lipofuscinosis (Batten disease). Consensus on diagnostic criteria, Hamburg, 1992
    • Kohlschütter A., Gardiner R. M., Goebel H. H.: Human forms of neuronal Ceroid-lipofuscinosis (Batten disease). Consensus on diagnostic criteria, Hamburg, 1992. J. Inher. Metab. Dis. 16, 241-244, 1993.
    • (1993) J. Inher. Metab. Dis. , vol.16 , pp. 241-244
    • Kohlschütter, A.1    Gardiner, R.M.2    Goebel, H.H.3
  • 7
    • 3743143129 scopus 로고
    • Hereditäre Erblindungsursachen und schwere Sehbehinderungen im Kindes- und frühen Erwachsenenalter
    • Lorenz B.: Hereditäre Erblindungsursachen und schwere Sehbehinderungen im Kindes- und frühen Erwachsenenalter. Zschr. Prakt. Augenheilkd. 9, 356-365, 1988.
    • (1988) Zschr. Prakt. Augenheilkd. , vol.9 , pp. 356-365
    • Lorenz, B.1
  • 9
    • 0028607407 scopus 로고
    • Recent advances in the gene map of inherited eye disorders primary hereditary diseases of the retina, choroid, and vitreous
    • Rosenfeld P. J., McKusick V. A., Amberger J. S., Dryja T. P.: Recent advances in the gene map of inherited eye disorders primary hereditary diseases of the retina, choroid, and vitreous. J. Med. Genet. 31, 903-915, 1994.
    • (1994) J. Med. Genet. , vol.31 , pp. 903-915
    • Rosenfeld, P.J.1    McKusick, V.A.2    Amberger, J.S.3    Dryja, T.P.4
  • 10
    • 0004241956 scopus 로고
    • Blackwell Scientific Publications, London
    • Taylor D.: Pediatric Ophthalmology. Blackwell Scientific Publications, London, 1990.
    • (1990) Pediatric Ophthalmology
    • Taylor, D.1
  • 11
    • 0029031159 scopus 로고
    • Photoaversion in Leber's congenital amaurosis
    • Traboulsi E. I., Maumenee I. H.: Photoaversion in Leber's congenital amaurosis. Ophthalmic Genetics 16, 27-30, 1995.
    • (1995) Ophthalmic Genetics , vol.16 , pp. 27-30
    • Traboulsi, E.I.1    Maumenee, I.H.2
  • 13
    • 0024165923 scopus 로고
    • Blauzapfenmonochromasie, Diagnose, genetische Beratung und optische Hilismittel
    • Zrenner E., Magnussen S., Lorenz B.: Blauzapfenmonochromasie, Diagnose, genetische Beratung und optische Hilismittel. Klin. Mbl. 193, 510-517, 1988.
    • (1988) Klin. Mbl. , vol.193 , pp. 510-517
    • Zrenner, E.1    Magnussen, S.2    Lorenz, B.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.