Detalhe da pesquisa
1.
Functional Changes of Retinal Ganglion Cells and Visual Pathways in Patients with Chronic Leber's Hereditary Optic Neuropathy during One Year of Follow-up.
Ophthalmology
; 126(7): 1033-1044, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30822445
2.
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
3.
Natural History of Conversion of Leber's Hereditary Optic Neuropathy: A Prospective Case Series.
Ophthalmology
; 124(6): 843-850, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28196731
4.
Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy.
Brain
; 137(Pt 2): 335-53, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24369379
5.
Multifocal VEP provide electrophysiological evidence of predominant dysfunction of the optic nerve fibers derived from the central retina in Leber's hereditary optic neuropathy.
Graefes Arch Clin Exp Ophthalmol
; 253(9): 1591-600, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-25773998
6.
MOG-IgG positive optic neuritis after SARS-CoV-2 infection.
Eur J Ophthalmol
; 33(5): NP87-NP90, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-36317310
7.
Post-COVID simultaneous onset of Graves' disease and ocular myasthenia gravis in a patient with a complex ocular motility impairment.
Eur J Ophthalmol
; 33(3): NP49-NP51, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35167395
8.
Childhood-Onset Leber Hereditary Optic Neuropathy-Clinical and Prognostic Insights.
Am J Ophthalmol
; 249: 99-107, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36543315
9.
Parsing the differences in affected with LHON: genetic versus environmental triggers of disease conversion.
Brain
; 139(Pt 3): e17, 2016 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-26657166
10.
Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age.
Ophthalmology
; 118(10): 2076-80, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21621262
11.
OPA1 mutations associated with dominant optic atrophy influence optic nerve head size.
Ophthalmology
; 117(8): 1547-53, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20417568
12.
Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome.
Sci Rep
; 10(1): 10398, 2020 Jun 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-32576919
13.
Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome.
Sci Rep
; 10(1): 4785, 2020 03 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-32179840
14.
Idebenone treatment in patients with OPA1-mutant dominant optic atrophy.
Brain
; 136(Pt 2): e231, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23388408
15.
The Tadpole Pupil: Case Series With Review of the Literature and New Considerations.
Front Neurol
; 10: 846, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31481920
16.
Male prevalence of acquired color vision defects in asymptomatic carriers of Leber's hereditary optic neuropathy.
Invest Ophthalmol Vis Sci
; 48(5): 2362-70, 2007 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-17460303
17.
Idebenone treatment in Leber's hereditary optic neuropathy.
Brain
; 134(Pt 9): e188, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21810891
18.
The Photopic Negative Response: An Objective Measure of Retinal Ganglion Cell Function in Patients With Leber's Hereditary Optic Neuropathy.
Invest Ophthalmol Vis Sci
; 58(6): BIO300-BIO306, 2017 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29049835
19.
Leber's hereditary optic neuropathy with childhood onset.
Invest Ophthalmol Vis Sci
; 47(12): 5303-9, 2006 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-17122117
20.
Chromatic and luminance contrast sensitivities in asymptomatic carriers from a large Brazilian pedigree of 11778 Leber hereditary optic neuropathy.
Invest Ophthalmol Vis Sci
; 46(12): 4809-14, 2005 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-16303983