These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


87 related items for PubMed ID: 2263391

  • 41. [Fundus flavimaculatus and subretinal neovascularization--case report].
    Aragão RE, Barreira IM, Holanda Filha JG.
    Arq Bras Oftalmol; 2005; 68(2):263-5. PubMed ID: 15905953
    [Abstract] [Full Text] [Related]

  • 42.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 43.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 44.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 45.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 46.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 47.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 48. [Diagnostic error in X-chromosomal hereditary retinoschisis].
    Grützner P, Schmidtborn F.
    Buch Augenarzt; 1978; 73():139-42. PubMed ID: 568984
    [No Abstract] [Full Text] [Related]

  • 49. Idiopathic preretinal macular gliosis.
    Yagoda AD, Walsh JB, Henkind P.
    Int Ophthalmol Clin; 1981; 21(3):107-18. PubMed ID: 7287340
    [No Abstract] [Full Text] [Related]

  • 50. [Hereditary vitreo-retinal dystrophy (Wagner)].
    Dralands L, Stanescu B, Missotten L.
    Bull Soc Belge Ophtalmol; 1975; (172):716-26. PubMed ID: 1230288
    [No Abstract] [Full Text] [Related]

  • 51. [Visually evoked cortical potentials (VECP) in retinal siderosis with macular involvement].
    Makabe R, Adachi-Usami E, Gavriysky V.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1975; (73):306-10. PubMed ID: 1242936
    [No Abstract] [Full Text] [Related]

  • 52.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 53. Benign familial fleck retina.
    Sabel Aish SF, Dajani B.
    Br J Ophthalmol; 1980 Sep; 64(9):652-9. PubMed ID: 7426586
    [Abstract] [Full Text] [Related]

  • 54. [Chorioretinal macular dystrophy with perfectly spiral aspects].
    Amalric P.
    Bull Soc Ophtalmol Fr; 1977 Sep; 77(8-9):919-21. PubMed ID: 614931
    [No Abstract] [Full Text] [Related]

  • 55. [Hereditary peripheral retinoschisis].
    Lisch W, Ullerich K.
    Klin Monbl Augenheilkd; 1979 Mar; 174(3):351-8. PubMed ID: 480801
    [No Abstract] [Full Text] [Related]

  • 56. A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.
    Sivaprasad S, Kung BT, Robson AG, Black G, Webster AR, Bird A, Egan C.
    Clin Exp Ophthalmol; 2008 Mar; 36(1):92-3. PubMed ID: 18290960
    [No Abstract] [Full Text] [Related]

  • 57. [Diagnosis of elevated macular lesions with the slit-lamp microscope (author's transl)].
    Otaki S.
    Nippon Ganka Gakkai Zasshi; 1980 Aug; 84(8):898-911. PubMed ID: 7211604
    [No Abstract] [Full Text] [Related]

  • 58. [Recurrent spontaneous macular hemorrhage].
    Uhlmann S, Nestler A, Wiedemann P.
    Ophthalmologe; 2001 Nov; 98(11):1110-1. PubMed ID: 11729747
    [No Abstract] [Full Text] [Related]

  • 59. [Dominant chorioretinal dystrophy].
    Babel J, Cabernard E, Kräuchi H, Klein D, Korol S, Schafroth P.
    Klin Monbl Augenheilkd; 1980 Apr; 176(4):600. PubMed ID: 7421038
    [Abstract] [Full Text] [Related]

  • 60. North Carolina Macular Dystrophy.
    Tsang SH, Sharma T.
    Adv Exp Med Biol; 2018 Apr; 1085():109-110. PubMed ID: 30578494
    [Abstract] [Full Text] [Related]


    Page: [Previous] [Next] [New Search]
    of 5.