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43. 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; 32(8):1643-51. PubMed ID: 22277927 [TBL] [Abstract][Full Text] [Related]
44. Retinal pigment hypertrophy and chorioretinal dystrophy. De Laey JJ; Leys A; Van Hyfte R Bull Soc Belge Ophtalmol; 1987; 223 Pt 2():67-73. PubMed ID: 3502795 [No Abstract] [Full Text] [Related]
45. Occipital porencephaly in a child with gyrate atrophy of the choroid and retina. Rigante D; Savastano MC; Leone A; Falsini B; Baldascino A; La Torraca I; Lepore D; De Nisco A; Sacco E; Minnella AM J AAPOS; 2010 Oct; 14(5):462-4. PubMed ID: 21035079 [TBL] [Abstract][Full Text] [Related]
46. [The clinical characteristics of different types of peripheral retinal degeneration and their relationship to retinal breaks and detachment]. Franchuk AA Oftalmol Zh; 1989; (8):451-4. PubMed ID: 2636341 [TBL] [Abstract][Full Text] [Related]
47. To lump or to split? Traboulsi EI Ophthalmic Paediatr Genet; 1993 Dec; 14(4):141-2. PubMed ID: 8015784 [No Abstract] [Full Text] [Related]
48. [Changes in the ciliary body and peripheral fundus in chorioretinal degeneration (author's transl)]. Watanabe S; Takase K Nippon Ganka Gakkai Zasshi; 1981 Oct; 85(10):1655-61. PubMed ID: 7337092 [No Abstract] [Full Text] [Related]
49. New insights into genetic eye disease. Wright AF Trends Genet; 1992 Mar; 8(3):85-91. PubMed ID: 1579993 [TBL] [Abstract][Full Text] [Related]
50. DIDANOSINE RETINAL TOXICITY. Haug SJ; Wong RW; Day S; Choudhry N; Sneed S; Prasad P; Read S; McDonald RH; Agarwal A; Davis J; Sarraf D Retina; 2016 Dec; 36 Suppl 1():S159-S167. PubMed ID: 28005674 [TBL] [Abstract][Full Text] [Related]
52. [Electroretinographic study of hereditary vitreo-retinal degeneration]. Dehon P; Comhaire-Poutchinian Y; Watillon M Bull Soc Belge Ophtalmol; 1977; (176):58-81. PubMed ID: 614088 [No Abstract] [Full Text] [Related]
53. Posterior cystoid retinal degeneration in central serous chorioretinopathy. Piccolino FC; De La Longrais RR; Manea M; Cicinelli S Retina; 2008; 28(7):1008-12. PubMed ID: 18698305 [TBL] [Abstract][Full Text] [Related]
54. The Wagner syndrome versus hereditary arthroophthalmopathy. Maumenee IH; Stoll HU; Mets MB Trans Am Ophthalmol Soc; 1982; 80():349-65. PubMed ID: 7182967 [No Abstract] [Full Text] [Related]
55. The role of molecular genetics in the prenatal diagnosis of retinal dystrophies. Evans K; Gregory CY; Fryer A; Whittaker J; Duvall-Young J; Bird AC; Jay MR; Bhattacharya SS Eye (Lond); 1995; 9 ( Pt 1)():24-8. PubMed ID: 7713246 [TBL] [Abstract][Full Text] [Related]
56. [Hereditary peripheral chorioretinal dysplasia]. Vallat M; Bernard JA; Detré J; Van Coppenolle F; Gillibert A Bull Soc Ophtalmol Fr; 1986 Nov; 86(11):1325-6. PubMed ID: 3581350 [No Abstract] [Full Text] [Related]
57. [Hereditary factors in the pathogenesis of retinal detachment. Eugenic counseling]. Longhena L Minerva Med; 1972 Dec; 63(86):4680-3. PubMed ID: 4539344 [No Abstract] [Full Text] [Related]
58. [Chorioretinal degeneration and primary familial microcephaly]. Saudax E; Raspiller A; Tridon P; George JL; Hachet E Bull Mem Soc Fr Ophtalmol; 1986; 97():247-52. PubMed ID: 3790810 [No Abstract] [Full Text] [Related]
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60. [Subacute chorioretinal dystrophy of the arciform type. A new anatomo-clinical entity?]. Amalric P Bull Soc Ophtalmol Fr; 1980; 80(6-7):501-3. PubMed ID: 7408094 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]