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Journal Abstract Search
148 related items for PubMed ID: 4543597
21. Clinical and electrophysiological observations on genetic carriers of retinitis pigmentosa in a family (pedigree Tt) showing sex-linked inheritance. Imaizumi K, Takahashi R, Tazawa Y, Yamada K, Mita K. Adv Exp Med Biol; 1972; 24(0):301-7. PubMed ID: 4671885 [No Abstract] [Full Text] [Related]
22. Pigment epithelial pattern dystrophy. Four different manifestations in a family. de Jong PT, Delleman JW. Arch Ophthalmol; 1982 Sep; 100(9):1416-21. PubMed ID: 7115165 [Abstract] [Full Text] [Related]
24. [Juvenile macular degeneration]. François J. Verh K Acad Geneeskd Belg; 1977 Jun; 39(1):29-63. PubMed ID: 930299 [No Abstract] [Full Text] [Related]
25. [Differential diagnosis of early onset tapetoretinal degenerations using retinal functional diagnosis]. Schneider T, Zrenner E. Fortschr Ophthalmol; 1987 Jun; 84(3):292-7. PubMed ID: 3623382 [No Abstract] [Full Text] [Related]
26. [Atypical hereditary chorioretinal degeneration (author's transl)]. Wildberger H, Niemeyer G. Albrecht Von Graefes Arch Klin Exp Ophthalmol; 1974 Mar 22; 190(1):1-11. PubMed ID: 4547921 [No Abstract] [Full Text] [Related]
27. The characterization of retinal phenotype in a family with C1QTNF5-related late-onset retinal degeneration. Vincent A, Munier FL, Vandenhoven CC, Wright T, Westall CA, Héon E. Retina; 2012 Sep 22; 32(8):1643-51. PubMed ID: 22277927 [Abstract] [Full Text] [Related]
29. Electro-oculography in Best's macular dystrophy. Cross HE, Bard L. Am J Ophthalmol; 1974 Jan 22; 77(1):46-50. PubMed ID: 4824173 [No Abstract] [Full Text] [Related]
30. [Electrophysiological study on the retinitis pigmentosa]. Imaizumi K. Nippon Ganka Gakkai Zasshi; 1969 Nov 22; 73(11):2347-496. PubMed ID: 5391946 [No Abstract] [Full Text] [Related]
31. [Fundus flavimaculatus. Clinical, functional and genetic study]. Babel J. Arch Ophtalmol Rev Gen Ophtalmol; 1972 Feb 22; 32(2):109-21. PubMed ID: 4262401 [No Abstract] [Full Text] [Related]
32. Butterfly-shaped pigment dystrophy of the fovea. Deutman AF, van Blommestein JD, Henkes HE, Waardenburg PJ, Solleveld-van Driest E. Arch Ophthalmol; 1970 May 22; 83(5):558-69. PubMed ID: 5442145 [No Abstract] [Full Text] [Related]
33. X-linked recessive fundus dystrophies and their carrier states. Bird AC, Blach RK. Trans Ophthalmol Soc U K (1962); 1970 May 22; 90():127-38. PubMed ID: 5283398 [No Abstract] [Full Text] [Related]
34. Recovery of the human early receptor potential during dark adaptation in hereditary retinal disease. Berson EL, Goldstein EB. Vision Res; 1970 Mar 22; 10(3):219-26. PubMed ID: 5311448 [No Abstract] [Full Text] [Related]
35. Variable expression of albinism within a single kindred. Castronuovo S, Simon JW, Kandel GL, Morier A, Wolf B, Witkop CJ, Jenkins PL. Am J Ophthalmol; 1991 Apr 15; 111(4):419-26. PubMed ID: 1901453 [Abstract] [Full Text] [Related]
36. The cone degenerations. Krill AE, Deutman AF, Fishman M. Doc Ophthalmol; 1973 Apr 16; 35(1):1-80. PubMed ID: 4573331 [No Abstract] [Full Text] [Related]
37. New findings in posterior amorphous corneal dystrophy. Dunn SP, Krachmer JH, Ching SS. Arch Ophthalmol; 1984 Feb 16; 102(2):236-9. PubMed ID: 6607727 [Abstract] [Full Text] [Related]
38. Electrophysiologic and fluorescein studies in vitelliform macular degeneration. Schwartz LJ, Metz HS, Woodward F. Arch Ophthalmol; 1972 Jun 16; 87(6):636-41. PubMed ID: 5032733 [No Abstract] [Full Text] [Related]
39. Temporal aspects of the electroretinogram in sector retinitis pigmentosa. Berson EL, Howard J. Arch Ophthalmol; 1971 Dec 16; 86(6):653-65. PubMed ID: 5128159 [No Abstract] [Full Text] [Related]
40. Posterior polymorphous corneal dystrophy of Schlichting. A clinical study on four families. Hansen TE. Acta Ophthalmol (Copenh); 1983 Jun 16; 61(3):454-60. PubMed ID: 6605017 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]