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Journal Abstract Search

124 related items for PubMed ID: 5601357

  • 41. A dominantly inherited syndrome of hyaloideoretinal degeneration, cleft palate and maxillary hypoplasia (Cervenka syndrome).
    Cohen MM, Knobloch WH, Gorlin RJ.
    Birth Defects Orig Artic Ser; 1971 Jun; 7(7):83-6. PubMed ID: 5173248
    [Abstract] [Full Text] [Related]

  • 42. [Cavity structures in the peripheral retina].
    Pau H.
    Doc Ophthalmol; 1976 Oct 15; 41(2):241-56. PubMed ID: 1009817
    [Abstract] [Full Text] [Related]

  • 43. [Heredofamilial aspects of lattice degeneration of the retina].
    Cambiaggi A.
    Boll Ocul; 1969 Jan 15; 48(1):36-45. PubMed ID: 5371693
    [No Abstract] [Full Text] [Related]

  • 44. [Familial exudative Criswick-Schepens vitreoretinopathy].
    Chynoranský M, Gerinec A, Streicher T.
    Cesk Oftalmol; 1989 Sep 15; 45(5):334-40. PubMed ID: 2805106
    [Abstract] [Full Text] [Related]

  • 45. [Use of hydrophilic contact lenses in patients with dystrophic and degenerative changes in the retina, choroid and vitreous body].
    Szymankiewiczowa S.
    Klin Oczna; 1982 Oct 15; 84(10):347-8. PubMed ID: 7182665
    [No Abstract] [Full Text] [Related]

  • 46. [Familial exudative vitreoretinopathy--vitreoretinopathia familiaris exsudative. I. Review of the literature].
    Starzycka M.
    Klin Oczna; 1991 Oct 15; 93(7-8):202-4. PubMed ID: 1762366
    [Abstract] [Full Text] [Related]

  • 47. Familial exudative vitreo-retinopathy.
    Dudgeon J.
    Trans Ophthalmol Soc U K (1962); 1979 Apr 15; 99(1):45-9. PubMed ID: 95062
    [Abstract] [Full Text] [Related]

  • 48. [Heredity in ophthalmology].
    Eremenko NS.
    Oftalmol Zh; 1970 Apr 15; 25(2):127-31. PubMed ID: 4990455
    [No Abstract] [Full Text] [Related]

  • 49. Pathways to photoreceptor cell death in inherited retinal degenerations.
    Pierce EA.
    Bioessays; 2001 Jul 15; 23(7):605-18. PubMed ID: 11462214
    [Abstract] [Full Text] [Related]

  • 50. Goldmann-Favre maculopathy.
    Nasr YG, Cherfan GM, Michels RG, Wilkinson CP.
    Retina; 1990 Jul 15; 10(3):178-80. PubMed ID: 2236941
    [Abstract] [Full Text] [Related]

  • 51. [Idiopathic juvenile retinoschisis of young people].
    Salvanet-Bouccara A, Galaup A.
    J Fr Ophtalmol; 1983 Jul 15; 6(5):487-93. PubMed ID: 6685154
    [Abstract] [Full Text] [Related]

  • 52. [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 Jul 15; 8(4):301-7. PubMed ID: 4020040
    [Abstract] [Full Text] [Related]

  • 53. [Comparative research on behavior of the vitreous body, retina and vitreo-retinal relationships in both eyes of subjects with mono-ocular retinal detachment].
    Cambiaggi A, Sanna G, Nervi I.
    Ann Ottalmol Clin Ocul; 1965 Aug 15; 91(8):679-88. PubMed ID: 5857842
    [No Abstract] [Full Text] [Related]

  • 54. [X-chromosomal recessive retinoschisis].
    Eriksson AW, Forsius H, Vainio-Mattila B.
    Duodecim; 1972 Aug 15; 88(1):43-51. PubMed ID: 5013576
    [No Abstract] [Full Text] [Related]

  • 55. [Value of genetic, functional, electrophysiological and angiographic examination in choroideremia].
    Fouanon C, Ardouin M, Perdriel G, Dary J.
    Bull Soc Ophtalmol Fr; 1971 Aug 15; 71(5-6):541-7. PubMed ID: 5317144
    [No Abstract] [Full Text] [Related]

  • 56. [Retinal antigen expression in diabetic retinopathy and retinal detachment with vitreo-retinal proliferation. Preliminary results].
    Gastaud P, Fredj-Reygrobellet D, Baudouin C, Lapalus P.
    Ophtalmologie; 1988 Aug 15; 2(1):25-8. PubMed ID: 3073341
    [No Abstract] [Full Text] [Related]

  • 57. Autosomal recessive vitreoretinopathy and encephaloceles.
    van Nouhuys E.
    Am J Ophthalmol; 1982 Dec 15; 94(6):820. PubMed ID: 7180923
    [No Abstract] [Full Text] [Related]

  • 58. [Tapeto-retinal degenerations. (Presentation of some cases with unusual clinico-ophthalmoscopic and evolutive characteristics)].
    Manuelli GF, Manfredini U.
    Ann Ottalmol Clin Ocul; 1965 Dec 15; 91(12):1175-88. PubMed ID: 5885273
    [No Abstract] [Full Text] [Related]

  • 59. Human genetics. Deficiencies in sight with the candidate gene approach.
    Dryja TP.
    Nature; 1990 Oct 18; 347(6294):614. PubMed ID: 2215691
    [No Abstract] [Full Text] [Related]

  • 60. [The heterogenicity of falciform folding of the retina and congenital detachment of the retina].
    Warburg M.
    J Genet Hum; 1976 Nov 18; 24 Suppl():55-64. PubMed ID: 799728
    [No Abstract] [Full Text] [Related]

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