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Journal Abstract Search
301 related items for PubMed ID: 6027427
1. Pigmentary degeneration of the retina: early diagnosis and natural history. Sunga RN, Sloan LL. Invest Ophthalmol; 1967 Jun; 6(3):309-25. PubMed ID: 6027427 [No Abstract] [Full Text] [Related]
2. [Pseudoretinopathia pigmentosa following measles]. Jünemann G, Damaske E. Med Klin; 1968 Oct 18; 63(42):1687-90. PubMed ID: 5725567 [No Abstract] [Full Text] [Related]
4. [Electrophysiological study on the retinitis pigmentosa]. Imaizumi K. Nippon Ganka Gakkai Zasshi; 1969 Nov 18; 73(11):2347-496. PubMed ID: 5391946 [No Abstract] [Full Text] [Related]
5. Primary retinal pigmentary degeneration. Adams A, Aspinall P, Hayreh SS. Trans Ophthalmol Soc U K (1962); 1972 Nov 18; 92():233-49. PubMed ID: 4515514 [No Abstract] [Full Text] [Related]
8. Long-term follow-up of retinitis pigmentosa patients with multifocal electroretinography. Nagy D, Schönfisch B, Zrenner E, Jägle H. Invest Ophthalmol Vis Sci; 2008 Oct 18; 49(10):4664-71. PubMed ID: 18566474 [Abstract] [Full Text] [Related]
9. Detection of heterozygotes in families with X-linked pigmentary retinopathy by measurement of retinal rhodopsin concentration. Bird AC, Hyman V. Trans Ophthalmol Soc U K (1962); 1972 Oct 18; 92():221-9. PubMed ID: 4515512 [No Abstract] [Full Text] [Related]
10. [Pigmentary degeneration in symmetrical sectors of the retina]. Pasco M. Arch Ophtalmol Rev Gen Ophtalmol; 1970 Oct 18; 30(6-7):481-6. PubMed ID: 4247457 [No Abstract] [Full Text] [Related]
11. BILATERAL SYMMETRICAL SECTORAL PIGMENTARY LESION OF THE RETINA. GRAHAM MV. Br J Ophthalmol; 1963 Nov 18; 47(11):682-6. PubMed ID: 14211669 [No Abstract] [Full Text] [Related]
13. [Results of clinical examinations after transplantation of human placenta in patients with pigmentary degeneration of the retina]. Setogawa T, Suyama T, Watanabe T. Nihon Ganka Kiyo; 1967 Nov 18; 18(11):1110-20. PubMed ID: 5627288 [No Abstract] [Full Text] [Related]
14. [Mechanical phosphene as an index of the functional state of the retina and its diagnostic significance]. Pivovarov NN, Prokof'ev VN. Vestn Oftalmol; 1974 Nov 18; 0(4):34-8. PubMed ID: 4410089 [No Abstract] [Full Text] [Related]
18. 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 18; 111(10):1910-6. PubMed ID: 15465556 [Abstract] [Full Text] [Related]
19. Yearly rates of rod and cone functional loss in retinitis pigmentosa and cone-rod dystrophy. Birch DG, Anderson JL, Fish GE. Ophthalmology; 1999 Feb 18; 106(2):258-68. PubMed ID: 9951474 [Abstract] [Full Text] [Related]
20. [Familial electrophysiological observation in pigmentary degeneration of the retina with or without consanguinity]. Shoji U. Nippon Ganka Gakkai Zasshi; 1968 Aug 18; 72(8):1218-31. PubMed ID: 5751038 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]