99 related articles for article (PubMed ID: 22785536)
1. Optical coherence tomography findings in a case of cone-rod dystrophy.
Emfietzoglou I; Grigoropoulos V; Nikolaidis P; Theodossiadis G; Rouvas A; Theodossiadis P
Ophthalmic Surg Lasers Imaging; 2010 Dec; 41 Online():e1-3. PubMed ID: 22785536
[TBL] [Abstract][Full Text] [Related]
2. Optical coherence tomography findings in a case of cone-rod dystrophy.
Emfietzoglou I; Grigoropoulos V; Nikolaidis P; Theodossiadis G; Rouvas A; Theodossiadis P
Ophthalmic Surg Lasers Imaging; 2010 Dec; 41 Online():e1-3. PubMed ID: 21117575
[TBL] [Abstract][Full Text] [Related]
3. Outer retina analysis by optical coherence tomography in cone-rod dystrophy patients.
Lima LH; Sallum JM; Spaide RF
Retina; 2013 Oct; 33(9):1877-80. PubMed ID: 23648999
[TBL] [Abstract][Full Text] [Related]
4. Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.
Jacobson SG; Buraczynska M; Milam AH; Chen C; Järvaläinen M; Fujita R; Wu W; Huang Y; Cideciyan AV; Swaroop A
Invest Ophthalmol Vis Sci; 1997 Sep; 38(10):1983-97. PubMed ID: 9331262
[TBL] [Abstract][Full Text] [Related]
5. Retinal fluorescein and indocyanine green angiography and spectral-domain optical coherence tomography findings in acute retinal pigment epitheliitis.
Baillif S; Wolff B; Paoli V; Gastaud P; Mauget-Faÿsse M
Retina; 2011 Jun; 31(6):1156-63. PubMed ID: 21293312
[TBL] [Abstract][Full Text] [Related]
6. Intravitreal injection of autologous bone marrow-derived mononuclear cells for hereditary retinal dystrophy: a phase I trial.
Siqueira RC; Messias A; Voltarelli JC; Scott IU; Jorge R
Retina; 2011 Jun; 31(6):1207-14. PubMed ID: 21293313
[TBL] [Abstract][Full Text] [Related]
7. Spectral-domain optical coherence tomography imaging of the detached macula in rhegmatogenous retinal detachment.
Nakanishi H; Hangai M; Unoki N; Sakamoto A; Tsujikawa A; Kita M; Yoshimura N
Retina; 2009 Feb; 29(2):232-42. PubMed ID: 18997641
[TBL] [Abstract][Full Text] [Related]
8. Rod sensitivity, cone sensitivity, and photoreceptor layer thickness in retinal degenerative diseases.
Birch DG; Wen Y; Locke K; Hood DC
Invest Ophthalmol Vis Sci; 2011 Sep; 52(10):7141-7. PubMed ID: 21810977
[TBL] [Abstract][Full Text] [Related]
9. Rod-cone dystrophy with maculopathy in genetic glutathione synthetase deficiency: a morphologic and electrophysiologic study.
Burstedt MS; Ristoff E; Larsson A; Wachtmeister L
Ophthalmology; 2009 Feb; 116(2):324-31. PubMed ID: 19111905
[TBL] [Abstract][Full Text] [Related]
10. High-resolution optical coherence tomography imaging in KCNV2 retinopathy.
Sergouniotis PI; Holder GE; Robson AG; Michaelides M; Webster AR; Moore AT
Br J Ophthalmol; 2012 Feb; 96(2):213-7. PubMed ID: 21558291
[TBL] [Abstract][Full Text] [Related]
11. Outer retinal tubulation in inherited retinal degenerative disease.
Iriyama A; Aihara Y; Yanagi Y
Retina; 2013; 33(7):1462-5. PubMed ID: 23538577
[TBL] [Abstract][Full Text] [Related]
12. Rod phototransduction in retinitis pigmentosa: estimation and interpretation of parameters derived from the rod a-wave.
Hood DC; Birch DG
Invest Ophthalmol Vis Sci; 1994 Jun; 35(7):2948-61. PubMed ID: 8206712
[TBL] [Abstract][Full Text] [Related]
13. High-resolution retinal imaging of cone-rod dystrophy.
Wolfing JI; Chung M; Carroll J; Roorda A; Williams DR
Ophthalmology; 2006 Jun; 113(6):1019.e1. PubMed ID: 16650474
[TBL] [Abstract][Full Text] [Related]
14. [Retinitis pigmentosa and central serous choroiditis. Retinal imaging and optical coherence tomography views].
Meunier I; Ben Salah S; Arndt C; Hamel C
J Fr Ophtalmol; 2008 Sep; 31(7):735. PubMed ID: 18971860
[No Abstract] [Full Text] [Related]
15. Ocular phenotype of CORD5, an autosomal dominant retinal dystrophy associated with PITPNM3 p.Q626H mutation.
Reinis A; Golovleva I; Köhn L; Sandgren O
Acta Ophthalmol; 2013 May; 91(3):259-66. PubMed ID: 22405330
[TBL] [Abstract][Full Text] [Related]
16. Clinical-ultrastructural study of a retinal dystrophy.
Bunt-Milam AH; Kalina RE; Pagon RA
Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):458-69. PubMed ID: 6682096
[TBL] [Abstract][Full Text] [Related]
17. Optical coherence tomography images of retinitis pigmentosa.
Hamada S; Yoshida K; Chihara E
Ophthalmic Surg Lasers; 2000; 31(3):253-6. PubMed ID: 10847508
[TBL] [Abstract][Full Text] [Related]
18. Outer retinal circular structures in patients with Bietti crystalline retinopathy.
Kojima H; Otani A; Ogino K; Nakagawa S; Makiyama Y; Kurimoto M; Guo C; Yoshimura N
Br J Ophthalmol; 2012 Mar; 96(3):390-3. PubMed ID: 21803923
[TBL] [Abstract][Full Text] [Related]
19. Clinical characteristics of rod and cone photoreceptor dystrophies in patients with mutations in the C8orf37 gene.
van Huet RA; Estrada-Cuzcano A; Banin E; Rotenstreich Y; Hipp S; Kohl S; Hoyng CB; den Hollander AI; Collin RW; Klevering BJ
Invest Ophthalmol Vis Sci; 2013 Jul; 54(7):4683-90. PubMed ID: 23788369
[TBL] [Abstract][Full Text] [Related]
20. Maternal uniparental isodisomy of chromosome 6 reveals a TULP1 mutation as a novel cause of cone dysfunction.
Roosing S; van den Born LI; Hoyng CB; Thiadens AA; de Baere E; Collin RW; Koenekoop RK; Leroy BP; van Moll-Ramirez N; Venselaar H; Riemslag FC; Cremers FP; Klaver CC; den Hollander AI
Ophthalmology; 2013 Jun; 120(6):1239-46. PubMed ID: 23499059
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
