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Journal Abstract Search
177 related items for PubMed ID: 21108168
1. [Case report on OCT findings in a patient with hereditary optic neuropathy and a patient with autosomal dominant optic atrophy]. Schild AM, Fricke J, Liakopoulos S. Klin Monbl Augenheilkd; 2011 Jun; 228(6):565-8. PubMed ID: 21108168 [Abstract] [Full Text] [Related]
2. Reduction of inner retinal thickness in patients with autosomal dominant optic atrophy associated with OPA1 mutations. Ito Y, Nakamura M, Yamakoshi T, Lin J, Yatsuya H, Terasaki H. Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4079-86. PubMed ID: 17724190 [Abstract] [Full Text] [Related]
4. Optical Coherence Tomography of the Retinal Ganglion Cell Complex in Leber's Hereditary Optic Neuropathy and Dominant Optic Atrophy. Asanad S, Tian JJ, Frousiakis S, Jiang JP, Kogachi K, Felix CM, Fatemeh D, Irvine AG, Ter-Zakarian A, Falavarjani KG, Barboni P, Karanjia R, Sadun AA. Curr Eye Res; 2019 Jun; 44(6):638-644. PubMed ID: 30649972 [Abstract] [Full Text] [Related]
5. Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry. Cesareo M, Ciuffoletti E, Martucci A, Sebastiani J, Sorge RP, Lamantea E, Garavaglia B, Ricci F, Cusumano A, Nucci C, Brancati F. PLoS One; 2017 Jun; 12(3):e0174560. PubMed ID: 28358911 [Abstract] [Full Text] [Related]
8. Visual system involvement in patients with Friedreich's ataxia. Fortuna F, Barboni P, Liguori R, Valentino ML, Savini G, Gellera C, Mariotti C, Rizzo G, Tonon C, Manners D, Lodi R, Sadun AA, Carelli V. Brain; 2009 Jan; 132(Pt 1):116-23. PubMed ID: 18931386 [Abstract] [Full Text] [Related]
9. Macular thickness changes in a patient with Leber's hereditary optic neuropathy. Mizoguchi A, Hashimoto Y, Shinmei Y, Nozaki M, Ishijima K, Tagawa Y, Ishida S. BMC Ophthalmol; 2015 Mar 18; 15():27. PubMed ID: 25885098 [Abstract] [Full Text] [Related]
11. [Hereditary Optic Neuropathies]. Rüther K. Klin Monbl Augenheilkd; 2018 Jun 18; 235(6):747-763. PubMed ID: 29490390 [Abstract] [Full Text] [Related]
12. Reduction of oscillatory potentials and photopic negative response in patients with autosomal dominant optic atrophy with OPA1 mutations. Miyata K, Nakamura M, Kondo M, Lin J, Ueno S, Miyake Y, Terasaki H. Invest Ophthalmol Vis Sci; 2007 Feb 18; 48(2):820-4. PubMed ID: 17251483 [Abstract] [Full Text] [Related]
13. Leber's hereditary optic neuropathy with childhood onset. Barboni P, Savini G, Valentino ML, La Morgia C, Bellusci C, De Negri AM, Sadun F, Carta A, Carbonelli M, Sadun AA, Carelli V. Invest Ophthalmol Vis Sci; 2006 Dec 18; 47(12):5303-9. PubMed ID: 17122117 [Abstract] [Full Text] [Related]
14. Retinal vessel diameters decrease with macular ganglion cell layer thickness in autosomal dominant optic atrophy and in healthy subjects. Rönnbäck C, Grønskov K, Larsen M. Acta Ophthalmol; 2014 Nov 18; 92(7):670-4. PubMed ID: 24612963 [Abstract] [Full Text] [Related]
15. [Retinal atrophy using optical coherence tomography (OCT) in 15 patients with multiple sclerosis and comparison with healthy subjects]. Jeanjean L, Castelnovo G, Carlander B, Villain M, Mura F, Dupeyron G, Labauge P. Rev Neurol (Paris); 2008 Nov 18; 164(11):927-34. PubMed ID: 18808761 [Abstract] [Full Text] [Related]
16. [Applications of optical coherence tomography (OCT) in neuro-ophthalmology]. Kernstock C, Friebe K, Tonagel F. Klin Monbl Augenheilkd; 2013 Nov 18; 230(11):1097-105. PubMed ID: 24065512 [Abstract] [Full Text] [Related]