Chiara La Morgia
Chiara La Morgia
IRCCS Istituto delle Scienze Neurologiche di Bologna
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OPA1 mutations induce mitochondrial DNA instability and optic atrophy ‘plus’ phenotypes
P Amati-Bonneau, ML Valentino, P Reynier, ME Gallardo, B Bornstein, ...
Brain 131 (2), 338-351, 2008
Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA–haplogroup background
G Hudson, V Carelli, L Spruijt, M Gerards, C Mowbray, A Achilli, A Pyle, ...
The American Journal of Human Genetics 81 (2), 228-233, 2007
Melanopsin retinal ganglion cell loss in A lzheimer disease
C La Morgia, FN Ross‐Cisneros, Y Koronyo, J Hannibal, R Gallassi, ...
Annals of neurology 79 (1), 90-109, 2016
Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders
V Carelli, C La Morgia, ML Valentino, P Barboni, FN Ross-Cisneros, ...
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1787 (5), 518-528, 2009
Idebenone treatment in Leber's hereditary optic neuropathy
V Carelli, C La Morgia, ML Valentino, G Rizzo, M Carbonelli, AM De Negri, ...
Brain 134 (9), e188-e188, 2011
Melanopsin retinal ganglion cells are resistant to neurodegeneration in mitochondrial optic neuropathies
C La Morgia, FN Ross-Cisneros, AA Sadun, J Hannibal, A Munarini, ...
Brain 133 (8), 2426-2438, 2010
Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder
AJ Abrams, RB Hufnagel, A Rebelo, C Zanna, N Patel, MA Gonzalez, ...
Nature genetics 47 (8), 926-932, 2015
Syndromic parkinsonism and dementia associated with OPA1 missense mutations
V Carelli, O Musumeci, L Caporali, C Zanna, C La Morgia, V Del Dotto, ...
Annals of neurology 78 (1), 21-38, 2015
Leber’s hereditary optic neuropathy
AA Sadun, CL Morgia, V Carelli
Current treatment options in neurology 13 (1), 109-117, 2011
Leber’s hereditary optic neuropathy with childhood onset
P Barboni, G Savini, ML Valentino, C La Morgia, C Bellusci, AM De Negri, ...
Investigative ophthalmology & visual science 47 (12), 5303-5309, 2006
International consensus statement on the clinical and therapeutic management of Leber hereditary optic neuropathy
V Carelli, M Carbonelli, F Irenaeus, A Kawasaki, T Klopstock, WA Lagrèze, ...
Journal of Neuro-Ophthalmology 37 (4), 371-381, 2017
Loss of temporal retinal nerve fibers in Parkinson disease: a mitochondrial pattern?
C La Morgia, P Barboni, G Rizzo, M Carbonelli, G Savini, C Scaglione, ...
European Journal of Neurology 20 (1), 198-201, 2013
A neurodegenerative perspective on mitochondrial optic neuropathies
P Yu-Wai-Man, M Votruba, F Burté, C La Morgia, P Barboni, V Carelli
Acta neuropathologica 132 (6), 789-806, 2016
M itochondrial DNA and primary mitochondrial dysfunction in P arkinson's disease
MP Giannoccaro, C La Morgia, G Rizzo, V Carelli
Movement Disorders 32 (3), 346-363, 2017
The optic nerve: a “mito-window” on mitochondrial neurodegeneration
A Maresca, C La Morgia, L Caporali, ML Valentino, V Carelli
Molecular and Cellular Neuroscience 55, 62-76, 2013
Artificial intelligence to detect papilledema from ocular fundus photographs
D Milea, RP Najjar, Z Jiang, D Ting, C Vasseneix, X Xu, M Aghsaei Fard, ...
New England Journal of Medicine 382 (18), 1687-1695, 2020
Cigarette toxicity triggers Leber’s hereditary optic neuropathy by affecting mtDNA copy number, oxidative phosphorylation and ROS detoxification pathways
L Giordano, S Deceglie, P d'Adamo, ML Valentino, C La Morgia, ...
Cell death & disease 6 (12), e2021-e2021, 2015
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber’s hereditary optic neuropathy
A Achilli, L Iommarini, A Olivieri, M Pala, B Hooshiar Kashani, P Reynier, ...
Public Library of Science 7 (8), e42242, 2012
Melanopsin-expressing retinal ganglion cells: implications for human diseases
C La Morgia, FN Ross-Cisneros, J Hannibal, P Montagna, AA Sadun, ...
Vision research 51 (2), 296-302, 2011
Augmentation of restless legs syndrome with long‐term tramadol treatment
R Vetrugno, C La Morgia, R D'Angelo, D Loi, F Provini, G Plazzi, ...
Movement Disorders: Official Journal of the Movement Disorder Society 22 (3 …, 2007
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