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Journal Abstract Search

249 related items for PubMed ID: 4020040

  • 1. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    Vallat M, Fritsch D, Van Coppenolle F, Detre J, Moze M, Rabourdin F.
    J Fr Ophtalmol; 1985; 8(4):301-7. PubMed ID: 4020040
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  • 2. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    De la Chapelle AC, Manouvrier S, Dubos JP, Farriaux JP.
    Pediatrie; 1988; 43(4):305-7. PubMed ID: 3419872
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  • 4. The Stickler syndrome: case reports and literature review.
    Bowling EL, Brown MD, Trundle TV.
    Optometry; 2000 Mar; 71(3):177-82. PubMed ID: 10970261
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  • 6. Stickler's syndrome. A report of a family.
    Hill JC, Nelson MM.
    S Afr Med J; 1989 Mar 04; 75(5):238-41. PubMed ID: 2928863
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  • 7. Ocular and systemic manifestations of Stickler's syndrome: a preliminary report.
    Weingeist TA, Hermsen V, Hanson JW, Bumsted RM, Weinstein SL, Olin WH.
    Birth Defects Orig Artic Ser; 1982 Mar 04; 18(6):539-60. PubMed ID: 7171774
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  • 8. The Stickler syndrome (hereditary arthroophthalmopathy).
    Herrmann J, France TD, Spranger JW, Opitz JM, Wiffler C.
    Birth Defects Orig Artic Ser; 1975 Mar 04; 11(2):76-103. PubMed ID: 776247
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  • 12. Osteochondritis dissecans of the knee in an adult with Stickler syndrome.
    Trepman E.
    Orthop Rev; 1993 Mar 04; 22(3):371-6. PubMed ID: 8474775
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  • 14. Stickler's syndrome: a study of 12 families.
    Spallone A.
    Br J Ophthalmol; 1987 Jul 04; 71(7):504-9. PubMed ID: 3651362
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  • 15. [Hereditary progressive arthro-ophthalmopathy (Stickler syndrome)].
    Bernd L, Niethard FU, Schiltenwolf M.
    Z Orthop Ihre Grenzgeb; 1989 Jul 04; 127(3):358-61. PubMed ID: 2750264
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  • 16. [Hereditary progressive arthroophthalmopathy (Stickler syndrome)].
    Neuhäuser G.
    Hippokrates; 1976 Feb 04; 47(1):66-7. PubMed ID: 955946
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  • 18. Vitreous veils and radial lattice in Marshall syndrome.
    Brubaker JW, Mohney BG, Pulido JS, Babovic-Vuksanovic D.
    Ophthalmic Genet; 2008 Dec 04; 29(4):184-5. PubMed ID: 19005991
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  • 20. Congenital scalp defects and vitreoretinal degeneration: redefining the Knobloch syndrome.
    Seaver LH, Joffe L, Spark RP, Smith BL, Hoyme HE.
    Am J Med Genet; 1993 Apr 15; 46(2):203-8. PubMed ID: 8484411
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