Detalhe da pesquisa
1.
Recessive MECR pathogenic variants cause an LHON-like optic neuropathy.
J Med Genet
; 61(1): 93-101, 2023 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-37734847
2.
Peripapillary hyperreflective ovoid mass-like structures (PHOMS) in patients with acute Leber's hereditary optic neuropathy.
Graefes Arch Clin Exp Ophthalmol
; 262(1): 261-265, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37584789
3.
PREVALENCE AND MORPHOLOGIC BIOMARKERS OF METAMORPHOPSIA IN EYES WITH "RESOLVED" CHRONIC CENTRAL SEROUS CHORIORETINOPATHY.
Retina
; 43(9): 1563-1572, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37229754
4.
The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10.
Brain
; 146(9): e67-e70, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36913248
5.
Recurrence of Visual Loss in Recessive Leber Hereditary Optic Neuropathy: New Paradigm.
J Neuroophthalmol
; 2024 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38381526
6.
Wolfram Syndrome: Only a Neurodegenerative Disease or Also a Maculopathy?
J Neuroophthalmol
; 2023 Aug 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37581949
7.
Peripapillary vessel density changes in Leber's hereditary optic neuropathy: a new biomarker.
Clin Exp Ophthalmol
; 46(9): 1055-1062, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29790285
8.
NUTRITIONAL SUPPLEMENTATION IN AGE-RELATED MACULAR DEGENERATION.
Retina
; 36(6): 1119-25, 2016 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26579787
9.
Combined Optic Atrophy and Rod-Cone Dystrophy Expands the RTN4IP1 (Optic Atrophy 10) Phenotype.
J Neuroophthalmol
; 41(3): e290-e292, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33136666
10.
Prospective evaluation of morphological and functional changes after repeated intravitreal dexamethasone implant (Ozurdex®) for retinal vein occlusion.
Ophthalmic Res
; 53(4): 207-16, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25896233
11.
Changes in macular function after ozurdex for retinal vein occlusion.
Optom Vis Sci
; 91(7): 760-8, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24927143
12.
Fluorescein angiography and spectral-domain optical coherence tomography for monitoring anti-VEGF therapy in myopic choroidal neovascularization.
Ophthalmic Res
; 52(1): 25-31, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24861045
13.
Cardiac Wolframinopathies: A Case Report of Myocarditis and a Literature Review of Cardiac Involvement in Wolfram Syndrome 1.
J Clin Med
; 13(6)2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38542026
14.
Sectorial Ganglion Cell Complex Thickness as Biomarker of Vision Outcome in Patients With Dominant Optic Atrophy.
Invest Ophthalmol Vis Sci
; 65(1): 24, 2024 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-38193759
15.
AFG3L2 and ACO2-Linked Dominant Optic Atrophy: Genotype-Phenotype Characterization Compared to OPA1 Patients.
Am J Ophthalmol
; 262: 114-124, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38278202
16.
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy.
Cell Rep Med
; 5(2): 101383, 2024 Feb 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38272025
17.
Repeated intravitreal dexamethasone implant (Ozurdex®) for retinal vein occlusion.
Ophthalmologica
; 229(1): 21-5, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23006995
18.
Visual Outcomes and Optical Coherence Tomography Biomarkers of Vision Improvement in Patients With Leber Hereditary Optic Neuropathy Treated With Idebenone.
Am J Ophthalmol
; 247: 35-41, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36375592
19.
Choroidal vascularity index in hereditary optic neuropathies.
Eye (Lond)
; 37(13): 2679-2684, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-36747110
20.
Capturing the Transition From Intermediate to Neovascular AMD: Longitudinal Inner Retinal Thinning and Factors Associated With Neuronal Loss.
Invest Ophthalmol Vis Sci
; 64(4): 21, 2023 04 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37074695