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131 related items for PubMed ID: 3428076
1. Goldmann-Favre syndrome in a four-year-old-girl. Izumi K, Matsuhashi M. Doc Ophthalmol; 1987 Jun; 66(3):219-26. PubMed ID: 3428076 [Abstract] [Full Text] [Related]
2. Clinical features of Goldmann-Favre syndrome. Ikäheimo K, Tuppurainen K, Mäntyjärvi M. Acta Ophthalmol Scand; 1999 Aug; 77(4):459-61. PubMed ID: 10463423 [Abstract] [Full Text] [Related]
5. Diagnostic features of the Favre-Goldmann syndrome. Fishman GA, Jampol LM, Goldberg MF. Br J Ophthalmol; 1976 May; 60(5):345-53. PubMed ID: 1085161 [Abstract] [Full Text] [Related]
6. Histopathology of Goldmann-Favre syndrome obtained by full-thickness eye-wall biopsy. Peyman GA, Fishman GA, Sanders DR, Vlchek J. Ann Ophthalmol; 1977 Apr; 9(4):479-84. PubMed ID: 301373 [Abstract] [Full Text] [Related]
7. [Multimodal imaging in Goldmann-Favre syndrome]. Valler D, Ulbig M, Lohmann CP, Maier M. Ophthalmologe; 2018 Oct; 115(10):878-882. PubMed ID: 29234872 [Abstract] [Full Text] [Related]
8. Optical coherence tomography in the study of the Goldmann-Favre syndrome. Theodossiadis PG, Koutsandrea C, Kollia AC, Theodossiadis GP. Am J Ophthalmol; 2000 Apr; 129(4):542-4. PubMed ID: 10764872 [Abstract] [Full Text] [Related]
9. Relatively enhanced S cone function in the Goldmann-Favre syndrome. Jacobson SG, Román AJ, Román MI, Gass JD, Parker JA. Am J Ophthalmol; 1991 Apr 15; 111(4):446-53. PubMed ID: 2012146 [Abstract] [Full Text] [Related]
10. [Clinical features of Goldmann-Favre vitreoretinal degeneration]. Herrador-Montiel Á, Sánchez-Vicente JL, Arias-Alcalá M. Arch Soc Esp Oftalmol; 2012 Aug 15; 87(8):260-2. PubMed ID: 22794174 [Abstract] [Full Text] [Related]
11. Familial retinoschisis in female patients. Shimazaki J, Matsuhashi M. Doc Ophthalmol; 1987 Mar 15; 65(3):393-400. PubMed ID: 3678011 [Abstract] [Full Text] [Related]
12. Juvenile X-linked retinoschisis from XLRS1 Arg213Trp mutation with preservation of the electroretinogram scotopic b-wave. Sieving PA, Bingham EL, Kemp J, Richards J, Hiriyanna K. Am J Ophthalmol; 1999 Aug 15; 128(2):179-84. PubMed ID: 10458173 [Abstract] [Full Text] [Related]
13. Autosomal dominant vitreoretinochoroidopathy with normal electrooculogram in a German family. Kellner U, Jandeck C, Kraus H, Foerster MH. Graefes Arch Clin Exp Ophthalmol; 1998 Feb 15; 236(2):109-14. PubMed ID: 9498121 [Abstract] [Full Text] [Related]
14. [Idiopathic juvenile retinoschisis of young people]. Salvanet-Bouccara A, Galaup A. J Fr Ophtalmol; 1983 Feb 15; 6(5):487-93. PubMed ID: 6685154 [Abstract] [Full Text] [Related]
15. Autosomal juvenile retinoschisis without foveal retinoschisis. Yamaguchi K, Hara S. Br J Ophthalmol; 1989 Jun 15; 73(6):470-3. PubMed ID: 2751982 [Abstract] [Full Text] [Related]
16. Clinical features in affected males with X-linked retinoschisis. George ND, Yates JR, Moore AT. Arch Ophthalmol; 1996 Mar 15; 114(3):274-80. PubMed ID: 8600886 [Abstract] [Full Text] [Related]
17. A phenotype-genotype correlation study of X-linked retinoschisis. Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE. Ophthalmology; 2013 Jul 15; 120(7):1454-64. PubMed ID: 23453514 [Abstract] [Full Text] [Related]
18. Juvenile vitreoretinal degeneration and retinal detachment. Saari KM. Acta Ophthalmol Suppl (1985); 1985 Jul 15; 173():35-8. PubMed ID: 3002098 [Abstract] [Full Text] [Related]