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Keeping in shape the dogma of mitochondrial DNA maternal inheritance

PLoS genetics, 2015-05, Vol.11 (5), p.e1005179-e1005179

2015

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Mitochondrial Retinopathies

International journal of molecular sciences, 2021-12, Vol.23 (1), p.210

2021

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Proteolytic Cleavage of Opa1 Stimulates Mitochondrial Inner Membrane Fusion and Couples Fusion to Oxidative Phosphorylation

Cell metabolism, 2014-04, Vol.19 (4), p.630-641

2014

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Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease

Movement disorders, 2017-03, Vol.32 (3), p.346-363

2017

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Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy

Nature communications, 2020-08, Vol.11 (1), p.4029-4029, Article 4029

2020

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The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibility

Nature communications, 2017-04, Vol.8 (1), p.15074-15074, Article 15074

2017

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Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis

Frontiers in neurology, 2021-06, Vol.12, p.681326-681326

2021

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Implications of mitochondrial DNA mutations in human induced pluripotent stem cells

Nature reviews. Genetics, 2022-02, Vol.23 (2), p.69

2022

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Melanopsin Retinal Ganglion Cells and Pupil: Clinical Implications for Neuro-Ophthalmology

Frontiers in neurology, 2018-12, Vol.9, p.1047-1047

2018

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OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions

Cell reports (Cambridge), 2017-06, Vol.19 (12), p.2557-2571

2017

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Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson’s Disease Models

Cell reports (Cambridge), 2018-02, Vol.22 (8), p.2066-2079

2018

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Patterns of Retinal Ganglion Cell Damage in Neurodegenerative Disorders: Parvocellular vs Magnocellular Degeneration in Optical Coherence Tomography Studies

Frontiers in neurology, 2017-12, Vol.8, p.710-710

2017

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Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve

Biomolecules (Basel, Switzerland), 2021-03, Vol.11 (4), p.496

2021

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The relevance of migraine in the clinical spectrum of mitochondrial disorders

Scientific reports, 2022-03, Vol.12 (1), p.4222-4222, Article 4222

2022

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Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations

The international journal of biochemistry & cell biology, 2015-06, Vol.63, p.21-24

2015

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Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Nature genetics, 2015-08, Vol.47 (8), p.926-932

2015

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Chromatic pupillometry for evaluating melanopsin retinal ganglion cell function in Alzheimer's disease and other neurodegenerative disorders: a review

Frontiers in psychology, 2024-01, Vol.14, p.1295129-1295129

2024

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Natural History of Leber's Hereditary Optic Neuropathy: Longitudinal Analysis of the Retinal Nerve Fiber Layer by Optical Coherence Tomography

Ophthalmology (Rochester, Minn.), 2010-03, Vol.117 (3), p.623-627

2010

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Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy

Brain (London, England : 1878), 2011-01, Vol.134 (1), p.220-234

2011

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Mouse mtDNA mutant model of Leber hereditary optic neuropathy

Proceedings of the National Academy of Sciences - PNAS, 2012-12, Vol.109 (49), p.20065-20070

2012

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The yin and the yang of molecular decompensation in LHON

Acta ophthalmologica (Oxford, England), 2024-01, Vol.102 (S279)

Carelli, Valerio

2024

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Retinal Ganglion Cells and Circadian Rhythms in Alzheimer's Disease, Parkinson's Disease, and Beyond

Frontiers in neurology, 2017-05, Vol.8, p.162-162

2017

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Editorial: Hereditary Optic Neuropathies: A New Perspective

Frontiers in neurology, 2021-09, Vol.12, p.742484-742484

2021

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OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation

Brain (London, England : 1878), 2015-03, Vol.138 (Pt 3), p.563-576

2015

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Mitochondrial dysfunction as a cause of optic neuropathies

Progress in retinal and eye research, 2004, Vol.23 (1), p.53-89

2004

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Keeping in shape the dogma of mitochondrial DNA maternal inheritance

Mitochondrial Retinopathies

Proteolytic Cleavage of Opa1 Stimulates Mitochondrial Inner Membrane Fusion and Couples Fusion to Oxidative Phosphorylation

Mitochondrial DNA and primary mitochondrial dysfunction in Parkinson's disease

Inhibition of autophagy curtails visual loss in a model of autosomal dominant optic atrophy

The glutamate/cystine xCT antiporter antagonizes glutamine metabolism and reduces nutrient flexibility

Dominant Optic Atrophy (DOA): Modeling the Kaleidoscopic Roles of OPA1 in Mitochondrial Homeostasis

Implications of mitochondrial DNA mutations in human induced pluripotent stem cells

Melanopsin Retinal Ganglion Cells and Pupil: Clinical Implications for Neuro-Ophthalmology

OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions

Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson’s Disease Models

Patterns of Retinal Ganglion Cell Damage in Neurodegenerative Disorders: Parvocellular vs Magnocellular Degeneration in Optical Coherence Tomography Studies

Molecular Mechanisms behind Inherited Neurodegeneration of the Optic Nerve

The relevance of migraine in the clinical spectrum of mitochondrial disorders

Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Chromatic pupillometry for evaluating melanopsin retinal ganglion cell function in Alzheimer's disease and other neurodegenerative disorders: a review

Natural History of Leber's Hereditary Optic Neuropathy: Longitudinal Analysis of the Retinal Nerve Fiber Layer by Optical Coherence Tomography

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy

Mouse mtDNA mutant model of Leber hereditary optic neuropathy

The yin and the yang of molecular decompensation in LHON

Retinal Ganglion Cells and Circadian Rhythms in Alzheimer's Disease, Parkinson's Disease, and Beyond

Editorial: Hereditary Optic Neuropathies: A New Perspective

OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation

Mitochondrial dysfunction as a cause of optic neuropathies

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