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Journal Abstract Search

113 related items for PubMed ID: 1177401

  • 1. [Tapeto-retinal degeneration combined with incomplete general albinism (author's transl)].
    Ivandić T.
    Klin Monbl Augenheilkd; 1975 May; 166(5):698-703. PubMed ID: 1177401
    [Abstract] [Full Text] [Related]

  • 2. [Degenerative ocular retinal albinism in a girl ten years old (author's transl)].
    Franceschetti A, Fiore C, Korol S, Klein D.
    Klin Monbl Augenheilkd; 1978 Apr; 172(4):484-7. PubMed ID: 651216
    [Abstract] [Full Text] [Related]

  • 3. [Bietti's crystalline fundus dystrophy (author's transl)].
    François J, de Laey JJ.
    Klin Monbl Augenheilkd; 1977 Mar; 170(3):353-62. PubMed ID: 864981
    [Abstract] [Full Text] [Related]

  • 4. [Pigment dispersion in a family with albinism (author's transl)].
    Stefani FH.
    Klin Monbl Augenheilkd; 1975 Dec; 167(6):904-6. PubMed ID: 1226031
    [Abstract] [Full Text] [Related]

  • 5. A family pedigree with corneal dystrophy, tapetoretinal degeneration and albinism.
    Pinckers A, Otto AJ, Van den Heuvel JE.
    Acta Ophthalmol (Copenh); 1973 Dec; 51(4):445-60. PubMed ID: 4543597
    [No Abstract] [Full Text] [Related]

  • 6. Fundus albipunctatus associated with compound heterozygous mutations in RPE65.
    Schatz P, Preising M, Lorenz B, Sander B, Larsen M, Rosenberg T.
    Ophthalmology; 2011 May; 118(5):888-94. PubMed ID: 21211845
    [Abstract] [Full Text] [Related]

  • 7. [Macroreticular and butterfly shaped dystrophies of the retinal pigment epithelium (author's transl)].
    Girard P, Setbon G, Forest A, Coscas G.
    J Fr Ophtalmol; 1980 May; 3(2):101-8. PubMed ID: 7381177
    [Abstract] [Full Text] [Related]

  • 8. Sex-linked chorioretinal heredodegenerations.
    François J.
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):99-116. PubMed ID: 4950918
    [Abstract] [Full Text] [Related]

  • 9. A new form of albinism.
    Bergsma DR, Kaiser-Kupfer M.
    Am J Ophthalmol; 1974 Jun; 77(6):837-44. PubMed ID: 4833873
    [No Abstract] [Full Text] [Related]

  • 10. [Crigler-Najjar syndrome associated with tapeto-retinic degeneration (author's transl)].
    Maggiore G, Prandi MA, Gelmi C.
    Arch Fr Pediatr; 1981 Oct; 38(8):599-600. PubMed ID: 7316672
    [No Abstract] [Full Text] [Related]

  • 11. [A fundus flavimaculatus associated with preretinal new vessels (author's transl)].
    Coscas G, Gaudric A, Barthelemy F.
    J Fr Ophtalmol; 1980 Feb 20; 3(1):27-31. PubMed ID: 6154728
    [Abstract] [Full Text] [Related]

  • 12. Choroideremia (progressive chorioretinal degeneration).
    Francois J.
    Int Ophthalmol Clin; 1968 Feb 20; 8(4):949-64. PubMed ID: 5741530
    [No Abstract] [Full Text] [Related]

  • 13. [Different manifestations of tapetoretinal degeneration in the same family (author's transl)].
    Fiore C.
    J Fr Ophtalmol; 1981 Feb 20; 4(5):431-40. PubMed ID: 7310068
    [Abstract] [Full Text] [Related]

  • 14. Hereditary macular dystrophy. A clinical and genetic study of two specific forms.
    Pearce WG.
    Can J Ophthalmol; 1975 Jul 20; 10(3):319-25. PubMed ID: 1148903
    [Abstract] [Full Text] [Related]

  • 15. [Histology of retinopathia pigmentosa cum et sine pigmento (author's transl)].
    Eichholtz W.
    Klin Monbl Augenheilkd; 1974 Apr 20; 164(4):467-75. PubMed ID: 4843831
    [No Abstract] [Full Text] [Related]

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  • 18. Phenotypic marker for early disease detection in dominant late-onset retinal degeneration.
    Jacobson SG, Cideciyan AV, Wright E, Wright AF.
    Invest Ophthalmol Vis Sci; 2001 Jul 20; 42(8):1882-90. PubMed ID: 11431457
    [Abstract] [Full Text] [Related]

  • 19. Macular degeneration of undetermined type: probable autosomal recessive inheritance.
    Goldberg MF, Nissim J.
    Birth Defects Orig Artic Ser; 1971 Mar 20; 7(3):193-5. PubMed ID: 5173142
    [No Abstract] [Full Text] [Related]

  • 20. [Fundus flavimaculatus. Clinical, functional and genetic study].
    Babel J.
    Arch Ophtalmol Rev Gen Ophtalmol; 1972 Feb 20; 32(2):109-21. PubMed ID: 4262401
    [No Abstract] [Full Text] [Related]

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