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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

164 related items for PubMed ID: 5306791

  • 1.
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  • 2. [Achromatopsia congenita combined with sectoral pigment-degeneration of the retina].
    Thaler A, Heilig P, Slezak H.
    Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1972; 183(4):310-6. PubMed ID: 4537008
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  • 3. [Electroretinographic and electroencephalographic studies in Stargardt's disease].
    François J, De Rouck A.
    Klin Monbl Augenheilkd; 1965 Dec; 147(5):654-62. PubMed ID: 5869305
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  • 4. The functional syndromes.
    François J.
    Ophthalmologica; 1974 Dec; 169(1-3):234-9. PubMed ID: 4547324
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  • 9. Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene.
    Bessant DA, Holder GE, Fitzke FW, Payne AM, Bhattacharya SS, Bird AC.
    Arch Ophthalmol; 2003 Jun; 121(6):793-802. PubMed ID: 12796249
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  • 14. Visual functions in pericentral and central pigmentary retinopathy.
    François J, De Rouck A, Cambie E, De Laey JJ.
    Ophthalmologica; 1972 Jun; 165(1):38-61. PubMed ID: 4538423
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  • 15. [Electrophysiological study on the retinitis pigmentosa].
    Imaizumi K.
    Nippon Ganka Gakkai Zasshi; 1969 Nov; 73(11):2347-496. PubMed ID: 5391946
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  • 19. Unilateral retinitis pigmentosa sine pigmento.
    Pearlman JT, Saxton J, Hoffman G.
    Br J Ophthalmol; 1976 May; 60(5):354-60. PubMed ID: 952804
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  • 20. Cosegregation of X-linked retinitis pigmentosa and hemophilia A.
    Rabinowitz YS, Ladda RL, Sassani JW, Eyster ME.
    Am J Ophthalmol; 1988 Jan 15; 105(1):46-56. PubMed ID: 3337193
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