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Journal Abstract Search

121 related items for PubMed ID: 8225518

  • 1. A genetic analysis of retinitis pigmentosa.
    Shanker J, Ramesh A.
    Indian J Ophthalmol; 1993 Apr; 41(1):23-5. PubMed ID: 8225518
    [Abstract] [Full Text] [Related]

  • 2. Retinitis pigmentosa in Spain. The Spanish Multicentric and Multidisciplinary Group for Research into Retinitis Pigmentosa.
    Ayuso C, Garcia-Sandoval B, Najera C, Valverde D, Carballo M, Antiñolo G.
    Clin Genet; 1995 Sep; 48(3):120-2. PubMed ID: 8556816
    [Abstract] [Full Text] [Related]

  • 3. Tapeto-retinal degeneration in four Norwegian counties, II. Diagnostic evaluation of 407 relatives and genetic evaluation of 87 families.
    Grøndahl J.
    Clin Genet; 1986 Jan; 29(1):17-41. PubMed ID: 3948428
    [Abstract] [Full Text] [Related]

  • 4. [Distribution of the frequency of various Mendelian modes of inheritance in families with retinopathia pigmentosa. Results of an evaluation of the RP register of the Munster University Ophthalmology Clinic].
    Gerding H, Busse H.
    Ophthalmologe; 1994 Jun; 91(3):322-8. PubMed ID: 8086748
    [Abstract] [Full Text] [Related]

  • 5. Epidemiology of retinitis pigmentosa in the Valencian community (Spain).
    Nájera C, Millán JM, Beneyto M, Prieto F.
    Genet Epidemiol; 1995 Jun; 12(1):37-46. PubMed ID: 7713399
    [Abstract] [Full Text] [Related]

  • 6. A genetic analysis of retinitis pigmentosa.
    Boughman JA, Fishman GA.
    Br J Ophthalmol; 1983 Jul; 67(7):449-54. PubMed ID: 6860611
    [Abstract] [Full Text] [Related]

  • 7. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Jul; 46(7):2264-70. PubMed ID: 15980210
    [Abstract] [Full Text] [Related]

  • 8. Assessment of clinical variables and counseling needs in patients with retinitis pigmentosa.
    Boughman JA, Caldwell RJ.
    Am J Med Genet; 1982 Jun; 12(2):185-93. PubMed ID: 7102723
    [Abstract] [Full Text] [Related]

  • 9. [Hereditary maculopathy in typical retinitis pigmentosa. Apropos of 40 cases].
    Chachia N, Romdane K, Zaghdane M, Hadj Hamida FB, Khayrallah M, Haddad M.
    Ophtalmologie; 1989 Jun; 3(1):67-8. PubMed ID: 2641075
    [Abstract] [Full Text] [Related]

  • 10. Retinitis pigmentosa genetics: a study in Indian population.
    Vinchurkar MS, Sathye SM, Dikshit M.
    Indian J Ophthalmol; 1996 Jun; 44(2):77-82. PubMed ID: 8916593
    [Abstract] [Full Text] [Related]

  • 11. Comprehensive survey of mutations in RP2 and RPGR in patients affected with distinct retinal dystrophies: genotype-phenotype correlations and impact on genetic counseling.
    Pelletier V, Jambou M, Delphin N, Zinovieva E, Stum M, Gigarel N, Dollfus H, Hamel C, Toutain A, Dufier JL, Roche O, Munnich A, Bonnefont JP, Kaplan J, Rozet JM.
    Hum Mutat; 2007 Jan; 28(1):81-91. PubMed ID: 16969763
    [Abstract] [Full Text] [Related]

  • 12. [Investigations on retinopathia pigmentosa. Statistical analysis of perimetry results (author's transl)].
    Tanino T, Ohba N, Mishima S.
    Klin Monbl Augenheilkd; 1977 Jun; 170(6):808-13. PubMed ID: 894982
    [Abstract] [Full Text] [Related]

  • 13. Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa.
    Danciger M, Blaney J, Gao YQ, Zhao DY, Heckenlively JR, Jacobson SG, Farber DB.
    Genomics; 1995 Nov 01; 30(1):1-7. PubMed ID: 8595886
    [Abstract] [Full Text] [Related]

  • 14. A novel IMPDH1 mutation (Arg231Pro) in a family with a severe form of autosomal dominant retinitis pigmentosa.
    Grover S, Fishman GA, Stone EM.
    Ophthalmology; 2004 Oct 01; 111(10):1910-6. PubMed ID: 15465556
    [Abstract] [Full Text] [Related]

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  • 17. Autosomal dominant retinitis pigmentosa in a five-generation pedigree in People's Republic of China.
    Teng Y, Wang W, Tian H, Wang H, Hu X, Chen Y, Bittles AH.
    Eye (Lond); 2003 Nov 01; 17(9):1036-9. PubMed ID: 14704756
    [No Abstract] [Full Text] [Related]

  • 18. [Genetic heterogeneity of retinitis pigmentosa].
    Krawczyński MR, Pecold K.
    Klin Oczna; 1994 Jan 01; 96(1):24-9. PubMed ID: 8078270
    [Abstract] [Full Text] [Related]

  • 19. Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
    Martinez-Gimeno M, Maseras M, Baiget M, Beneito M, Antiñolo G, Ayuso C, Carballo M.
    Hum Mutat; 2001 Jun 01; 17(6):520. PubMed ID: 11385710
    [Abstract] [Full Text] [Related]

  • 20. Retinitis pigmentosa and renal failure in a patient with mutations in INVS.
    O'Toole JF, Otto EA, Frishberg Y, Hildebrandt F.
    Nephrol Dial Transplant; 2006 Jul 01; 21(7):1989-91. PubMed ID: 16522655
    [Abstract] [Full Text] [Related]

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