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

PUBMED FOR HANDHELDS

Journal Abstract Search

102 related items for PubMed ID: 7850274

  • 1. Genetic isolate and preserved para-arteriole retinal pigment epithelium.
    Piantanida A, Nucci P, Brancato R.
    Ophthalmic Genet; 1994 Jun; 15(2):95-8. PubMed ID: 7850274
    [Abstract] [Full Text] [Related]

  • 2. Preserved para-arteriolar retinal pigment epithelium retinitis pigmentosa.
    Porta A, Pierrottet C, Aschero M, Orzalesi N.
    Am J Ophthalmol; 1992 Feb 15; 113(2):161-4. PubMed ID: 1550183
    [Abstract] [Full Text] [Related]

  • 3. Autosomal recessive retinitis pigmentosa with preserved para-arteriolar retinal pigment epithelium.
    van den Born LI, van Soest S, van Schooneveld MJ, Riemslag FC, de Jong PT, Bleeker-Wagemakers EM.
    Am J Ophthalmol; 1994 Oct 15; 118(4):430-9. PubMed ID: 7943119
    [Abstract] [Full Text] [Related]

  • 4. Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.
    Heckenlively JR.
    Br J Ophthalmol; 1982 Jan 15; 66(1):26-30. PubMed ID: 7055539
    [Abstract] [Full Text] [Related]

  • 5. Preserved para-arteriole retinal pigment epithelium (PPRPE) in retinitis pigmentosa.
    Heckenlively JR.
    Birth Defects Orig Artic Ser; 1982 Jan 15; 18(6):193-6. PubMed ID: 7171755
    [No Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. CRB1 mutations may result in retinitis pigmentosa without para-arteriolar RPE preservation.
    Lotery AJ, Malik A, Shami SA, Sindhi M, Chohan B, Maqbool C, Moore PA, Denton MJ, Stone EM.
    Ophthalmic Genet; 2001 Sep 15; 22(3):163-9. PubMed ID: 11559858
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. No pigment deposition in a patient with advanced retinitis punctata albescens.
    Fujii M, Hayasaka S.
    Ophthalmologica; 1994 Sep 15; 208(6):339-41. PubMed ID: 7845653
    [Abstract] [Full Text] [Related]

  • 10. Selected pigmented fundus lesions of children.
    Ellis FD.
    J AAPOS; 2005 Aug 15; 9(4):306-14. PubMed ID: 16102478
    [Abstract] [Full Text] [Related]

  • 11. Acute retinal pigment epitheliitis.
    Luttrull JK, Chittum ME.
    Am J Ophthalmol; 1995 Sep 15; 120(3):389-91. PubMed ID: 7661213
    [Abstract] [Full Text] [Related]

  • 12. Retinal fluorescein leakage in retinitis pigmentosa.
    Newsome DA.
    Am J Ophthalmol; 1986 Mar 15; 101(3):354-60. PubMed ID: 3953729
    [Abstract] [Full Text] [Related]

  • 13. Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.
    van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA.
    Genomics; 1994 Aug 15; 22(3):499-504. PubMed ID: 8001962
    [Abstract] [Full Text] [Related]

  • 14. [A case of acute diffuse atrophy of retinal pigment epithelium].
    Yamashita A, Nakagawa Y, Tamai M.
    Nippon Ganka Gakkai Zasshi; 2000 Feb 15; 104(2):114-20. PubMed ID: 10714161
    [Abstract] [Full Text] [Related]

  • 15. Multifocal retinopathy of Great Pyrenees dogs.
    Grahn BH, Sandmeyer LS.
    Can Vet J; 2006 May 15; 47(5):491-2. PubMed ID: 16734379
    [No Abstract] [Full Text] [Related]

  • 16. Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNA(Leu) A to G mutation.
    Smith PR, Bain SC, Good PA, Hattersley AT, Barnett AH, Gibson JM, Dodson PM.
    Ophthalmology; 1999 Jun 15; 106(6):1101-8. PubMed ID: 10366077
    [Abstract] [Full Text] [Related]

  • 17. [Genetic pathology of the retina].
    Grange JD.
    J Genet Hum; 1986 Jan 15; 34(1):45-60. PubMed ID: 3958699
    [No Abstract] [Full Text] [Related]

  • 18. Pathologic findings in the retinal pigment epitheliopathy associated with the amyotrophic lateral sclerosis/parkinsonism-dementia complex of Guam.
    Campbell RJ, Steele JC, Cox TA, Loerzel AJ, Belli M, Belli DD, Kurland LT.
    Ophthalmology; 1993 Jan 15; 100(1):37-42. PubMed ID: 8433825
    [Abstract] [Full Text] [Related]

  • 19. Pigmented paravenous retinochoroidal atrophy. Discordant expression in monozygotic twins.
    Small KW, Anderson WB.
    Arch Ophthalmol; 1991 Oct 15; 109(10):1408-10. PubMed ID: 1929930
    [Abstract] [Full Text] [Related]

  • 20. Concurrent retinitis pigmentosa and pigmented paravenous retinochoroidal atrophy phenotypes in the same patient.
    Ratra D, Chandrasekharan DP, Aruldas P, Ratra V.
    Indian J Ophthalmol; 2016 Oct 15; 64(10):775-777. PubMed ID: 27905344
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 6.