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Journal Abstract Search

214 related items for PubMed ID: 19005991

  • 21.
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  • 22. [Familial exudative Criswick-Schepens vitreoretinopathy].
    Chynoranský M, Gerinec A, Streicher T.
    Cesk Oftalmol; 1989 Sep; 45(5):334-40. PubMed ID: 2805106
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  • 23.
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  • 24. The pseudo-posterior limiting layer syndrome: a vitreoretinal heredodegeneration with autosomal dominant transmission.
    Rossier J, Eisner G.
    Graefes Arch Clin Exp Ophthalmol; 1994 Jan; 232(1):16-24. PubMed ID: 8119597
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  • 26. Acquired cutis laxa type II (Marshall syndrome) in a 3-month-old boy.
    Sindhuja T, Arunachalam N, Gupta V, Agarwal S, Gomathy S.
    Pediatr Dermatol; 2022 Mar; 39(2):312-313. PubMed ID: 34929762
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  • 28. Clinical features of type 2 Stickler syndrome.
    Poulson AV, Hooymans JM, Richards AJ, Bearcroft P, Murthy R, Baguley DM, Scott JD, Snead MP.
    J Med Genet; 2004 Aug; 41(8):e107. PubMed ID: 15286167
    [No Abstract] [Full Text] [Related]

  • 29. Acquired Nonpigmented Vitreous Cyst Associated With Lattice Degeneration.
    Lu J, Mai G, Liu R, Luo Y, Lu L.
    Ophthalmic Surg Lasers Imaging Retina; 2017 Oct 01; 48(10):856-858. PubMed ID: 29020432
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  • 30. 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 Oct 01; 18(6):539-60. PubMed ID: 7171774
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  • 31.
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  • 32.
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  • 33. Proton relaxation times of the vitreous body in hereditary vitreoretinal dystrophy.
    Ettl A, Fischer-Klein C, Chemelli A, Daxer A, Felber S.
    Ophthalmologica; 1994 Oct 01; 208(4):195-7. PubMed ID: 7970545
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  • 34. The Wagner-Stickler syndrome.
    Liberfarb RM, Hirose T.
    Birth Defects Orig Artic Ser; 1982 Oct 01; 18(6):525-38. PubMed ID: 7171772
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  • 35.
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  • 36. [Stickler syndrome. Apropos of a case].
    Ziegler G, Gastaud P, Euller-Ziegler L, De Galleani B.
    Rev Rhum Mal Osteoartic; 1988 Dec 01; 55(12):1009-10. PubMed ID: 3238297
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  • 37.
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  • 38. Audiovestibular phenotype associated with a COL11A1 mutation in Marshall syndrome.
    Griffith AJ, Gebarski SS, Shepard NT, Kileny PR.
    Arch Otolaryngol Head Neck Surg; 2000 Jul 01; 126(7):891-4. PubMed ID: 10889003
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  • 39. [Stickler's syndrome or hereditary progressive arthro-ophthalmopathy].
    De la Chapelle AC, Manouvrier S, Dubos JP, Farriaux JP.
    Pediatrie; 1988 Jul 01; 43(4):305-7. PubMed ID: 3419872
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  • 40. Congenital keratoglobus with blue sclera in two siblings with overlapping Marshall/Stickler phenotype.
    Imamoglu S, Kaya V, Imamoglu EY, Gok K.
    Indian J Ophthalmol; 2016 Nov 01; 64(11):856-859. PubMed ID: 27958215
    [Abstract] [Full Text] [Related]

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