Camille Peron
Overview
Explore the profile of Camille Peron including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
120
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Recent Articles
1.
Fasano C, Cavaliere A, Tiranti V, Peron C
STAR Protoc
. 2024 Jul;
5(3):103127.
PMID: 39012842
Here, we present a protocol describing the quantification of oxygen consumption rate (OCR) and maximal respiration rate (MRR) in living induced pluripotent stem cell (iPSC)-derived neurons using the Seahorse analyzer....
2.
Peron C, Cavaliere A, Fasano C, Iannielli A, Spagnolo M, Legati A, et al.
Stem Cell Res
. 2024 Mar;
77:103406.
PMID: 38552355
Leber hereditary optic neuropathy (LHON) is one of the most common mitochondrial illness, causing retinal ganglion cell degeneration and central vision loss. It stems from point mutations in mitochondrial DNA...
3.
Aleo S, Del Dotto V, Romagnoli M, Fiorini C, Capirossi G, Peron C, et al.
Cell Rep Med
. 2024 Jan;
5(2):101383.
PMID: 38272025
Idebenone, the only approved treatment for Leber hereditary optic neuropathy (LHON), promotes recovery of visual function in up to 50% of patients, but we can neither predict nor understand the...
4.
Gautier C, Huynh M, Peron C, Pol J
Med Sci (Paris)
. 2023 Nov;
39(10):793-795.
PMID: 37943143
No abstract available.
5.
Zanuttigh E, Rusha E, Peron C, Brunetti D, Zorzi G, Pertek A, et al.
Stem Cell Res
. 2023 Sep;
72:103197.
PMID: 37689041
Mitochondrial membrane Protein-Associated Neurodegeneration (MPAN) is a lethal neurodegenerative disorder caused by mutations in the human gene C19orf12. The molecular mechanisms underlying the disorder are still unclear, and no established...
6.
Danese A, Patergnani S, Maresca A, Peron C, Raimondi A, Caporali L, et al.
Cell Rep
. 2022 Jul;
40(3):111124.
PMID: 35858578
Leber's hereditary optic neuropathy (LHON), a disease associated with a mitochondrial DNA mutation, is characterized by blindness due to degeneration of retinal ganglion cells (RGCs) and their axons, which form...
7.
Palombo F, Peron C, Caporali L, Iannielli A, Maresca A, Di Meo I, et al.
Stem Cell Reports
. 2021 Jul;
16(8):1953-1967.
PMID: 34329598
The generation of inducible pluripotent stem cells (iPSCs) is a revolutionary technique allowing production of pluripotent patient-specific cell lines used for disease modeling, drug screening, and cell therapy. Integrity of...
8.
Peron C, Maresca A, Cavaliere A, Iannielli A, Broccoli V, Carelli V, et al.
Front Neurol
. 2021 Jun;
12:648916.
PMID: 34168607
More than 30 years after discovering Leber's hereditary optic neuropathy (LHON) as the first maternally inherited disease associated with homoplasmic mtDNA mutations, we still struggle to achieve effective therapies. LHON...
9.
Carinci M, Testa B, Bordi M, Milletti G, Bonora M, Antonucci L, et al.
EMBO J
. 2021 May;
40(10):e103563.
PMID: 33932238
The early secretory pathway and autophagy are two essential and evolutionarily conserved endomembrane processes that are finely interlinked. Although growing evidence suggests that intracellular trafficking is important for autophagosome biogenesis,...
10.
Legati A, Zanetti N, Nasca A, Peron C, Lamperti C, Lamantea E, et al.
J Mol Diagn
. 2021 Mar;
23(6):732-741.
PMID: 33781964
Mitochondria harbor multiple copies of a maternally inherited nonnuclear genome. Point mutations, deletions, or depletion of the mitochondrial DNA (mtDNA) are associated with various human diseases. mtDNA defects are currently...