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Journal Abstract Search

137 related items for PubMed ID: 973820

  • 1. Autosomal recessive retinitis pigmentosa and Coats disease: a presumed familial incidence.
    Lanier JD, McCrary JA, Justice J.
    Arch Ophthalmol; 1976 Oct; 94(10):1737-42. PubMed ID: 973820
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  • 2. [Familial occurrence of Coats' syndrome combined with retinopathia pigmentosa].
    Schmidt D, Faulborn J.
    Klin Monbl Augenheilkd; 1972 Feb; 160(2):158-63. PubMed ID: 5018064
    [No Abstract] [Full Text] [Related]

  • 3. Autosomal dominant retinitis pigmentosa and Coats'-like disease.
    Spallone A, Carlevaro G, Ridling P.
    Int Ophthalmol; 1985 Sep; 8(3):147-51. PubMed ID: 4066158
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  • 4. [Pigmentary retinopathy and Coats' vasculopathy].
    Munteanu C.
    Oftalmologia; 1990 Sep; 34(2):135-42. PubMed ID: 2101044
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  • 5. [Coats' disease and familial retinal arteriolar tortuosity].
    Imai M, Iijima H.
    Nippon Ganka Gakkai Zasshi; 1990 Nov; 94(11):1091-6. PubMed ID: 2075874
    [Abstract] [Full Text] [Related]

  • 6. Autosomal inheritance of "senile" retinitis pigmentosa. A report of a family with consanguinity.
    Bonneau D, Kaplan J, Girard G, Dufier JL.
    Clin Genet; 1992 Oct; 42(4):199-200. PubMed ID: 1424244
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  • 10. Autosomal recessive cerebellar hypoplasia and tapeto-retinal degeneration: a new syndrome.
    Dooley JM, LaRoche GR, Tremblay F, Riding M.
    Pediatr Neurol; 1992 Oct; 8(3):232-4. PubMed ID: 1622524
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  • 11. Autosomal dominantly inherited retinitis pigmentosa with a severe clinical course.
    Satheesh P, Chacko A, Rajan GV.
    J Assoc Physicians India; 1993 Nov; 41(11):756. PubMed ID: 8005942
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  • 13. Clinical spectrum, genetic associations and management outcomes of Coats-like exudative retinal vasculopathy in autosomal recessive retinitis pigmentosa.
    Magliyah M, Alshamrani AA, Schatz P, Taskintuna I, Alzahrani Y, Nowilaty SR.
    Ophthalmic Genet; 2021 Apr; 42(2):178-185. PubMed ID: 33441055
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  • 14. Usher syndrome in four hard-of-hearing siblings.
    Davenport SL, O'Nuallain S, Omenn GS, Wilkus RJ.
    Pediatrics; 1978 Oct; 62(4):578-83. PubMed ID: 714590
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  • 15. [Coats syndrome in retinitis pigmentosa. Clinical aspects and therapeutic possibilities].
    Schatanek S, Krastel H, Rohrschneider K, Kruse FE, Alexandridis E.
    Ophthalmologe; 1994 Jun; 91(3):329-32. PubMed ID: 8086749
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  • 17. A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation.
    Ayala-Ramirez R, Graue-Wiechers F, Robredo V, Amato-Almanza M, Horta-Diez I, Zenteno JC.
    Mol Vis; 2006 Dec 04; 12():1483-9. PubMed ID: 17167404
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  • 19. Coats'-type retinitis pigmentosa: first reported case of presumed vertical transmission.
    Perrier M, Gauthier D, Sébag M, Marcil G.
    Can J Ophthalmol; 2004 Dec 04; 39(7):782-4. PubMed ID: 15696771
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  • 20. Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.
    Lam BL, Judisch GF.
    Am J Ophthalmol; 1991 Apr 15; 111(4):454-6. PubMed ID: 2012147
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