Cargando…

Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?

Detalles Bibliográficos
Autores principales:	Amore, Giulia, Vacchiano, Veria, La Morgia, Chiara, Valentino, Maria L., Caporali, Leonardo, Fiorini, Claudio, Ormanbekova, Danara, Salvi, Fabrizio, Bartoletti-Stella, Anna, Capellari, Sabina, Liguori, Rocco, Carelli, Valerio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer Berlin Heidelberg 2022
Materias:	Letter to the Editors
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813087/ https://www.ncbi.nlm.nih.gov/pubmed/36066624 http://dx.doi.org/10.1007/s00415-022-11355-w

Ejemplares similares

Frequency of Parkinson’s Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study
por: Vacchiano, Veria, et al.
Publicado: (2022)

The Italian reappraisal of the most frequent genetic defects in hereditary optic neuropathies and the global top 10
por: Fiorini, Claudio, et al.
Publicado: (2023)

Secondary Post-Geniculate Involvement in Leber’s Hereditary Optic Neuropathy
por: Rizzo, Giovanni, et al.
Publicado: (2012)

Longitudinal Study of Optic Disk Perfusion and Retinal Structure in Leber's Hereditary Optic Neuropathy
por: Calzetti, Giacomo, et al.
Publicado: (2022)

Plasma and CSF Neurofilament Light Chain in Amyotrophic Lateral Sclerosis: A Cross-Sectional and Longitudinal Study
por: Vacchiano, Veria, et al.
Publicado: (2021)

Leber's Hereditary Optic Neuropathy: A Report on Novel mtDNA Pathogenic Variants
por: Peverelli, Lorenzo, et al.
Publicado: (2021)

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy
por: Caporali, Leonardo, et al.
Publicado: (2018)

Rare Primary Mitochondrial DNA Mutations and Probable Synergistic Variants in Leber’s Hereditary Optic Neuropathy
por: Achilli, Alessandro, et al.
Publicado: (2012)

Pathological mitophagy disrupts mitochondrial homeostasis in Leber’s hereditary optic neuropathy
por: Danese, Alberto, et al.
Publicado: (2022)

Therapeutic Options in Hereditary Optic Neuropathies
por: Amore, Giulia, et al.
Publicado: (2020)

Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy
por: Hudson, Gavin, et al.
Publicado: (2010)

Changes in Choroidal Thickness follow the RNFL Changes in Leber’s Hereditary Optic Neuropathy
por: Borrelli, Enrico, et al.
Publicado: (2016)

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber’s hereditary optic neuropathy
por: Giordano, Carla, et al.
Publicado: (2014)

Grand Rounds: Could Occupational Exposure to n-Hexane and Other Solvents Precipitate Visual Failure in Leber Hereditary Optic Neuropathy?
por: Carelli, Valerio, et al.
Publicado: (2007)

Amyloid-Beta Co-Pathology Is a Major Determinant of the Elevated Plasma GFAP Values in Amyotrophic Lateral Sclerosis
por: Mastrangelo, Andrea, et al.
Publicado: (2023)

Gene Therapies for the Treatment of Leber Hereditary Optic Neuropathy
por: Sahel, José-Alain, et al.
Publicado: (2021)

Natural history of patients with Leber hereditary optic neuropathy—results from the REALITY study
por: Yu-Wai-Man, Patrick, et al.
Publicado: (2021)

Leber hereditary optic neuropathy: current perspectives
por: Meyerson, Cherise, et al.
Publicado: (2015)

Leber’s hereditary optic neuropathy - Case report
por: Iorga, Raluca Eugenia, et al.
Publicado: (2018)

Leber’s Hereditary Optic Neuropathy – Case Discussion
por: Culea, Cristina, et al.
Publicado: (2019)

Arterial sheathing in Leber hereditary optic neuropathy
por: Zhou, Henry W., et al.
Publicado: (2022)

Clinical Overview of Leber Hereditary Optic Neuropathy
por: Stramkauskaitė, Almina, et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy and Hypertrophic Cardiomyopathy
por: Hey, Thomas Morris, et al.
Publicado: (2022)

Developments in the Treatment of Leber Hereditary Optic Neuropathy
por: Chen, Benson S., et al.
Publicado: (2022)

Impaired complex I repair causes recessive Leber’s hereditary optic neuropathy
por: Stenton, Sarah L., et al.
Publicado: (2021)

Targeted sequencing panels in Italian ALS patients support different etiologies in the ALS/FTD continuum
por: Bartoletti-Stella, Anna, et al.
Publicado: (2021)

Editorial: Hereditary Optic Neuropathies: A New Perspective
por: Carelli, Valerio, et al.
Publicado: (2021)

Medical Management of Hereditary Optic Neuropathies
por: La Morgia, Chiara, et al.
Publicado: (2014)

A Second Case With the V374A KCND3 Pathogenic Variant in an Italian Patient With Early-Onset Spinocerebellar Ataxia
por: Palombo, Flavia, et al.
Publicado: (2022)

Leber’s Hereditary Optic Neuropathy: The Mitochondrial Connection Revisited
por: Abu-Amero, Khaled K.
Publicado: (2011)

Gene–environment interactions in Leber hereditary optic neuropathy
por: Kirkman, Matthew Anthony, et al.
Publicado: (2009)

Leber’s hereditary optic neuropathy is multiorgan not mono-organ
por: Finsterer, Josef, et al.
Publicado: (2016)

The Progress of Gene Therapy for Leber's Optic Hereditary Neuropathy
por: Zhang, Yong, et al.
Publicado: (2018)

Leber hereditary optic neuropathy: bridging the translational gap
por: Jurkute, Neringa, et al.
Publicado: (2017)

Leber’s Hereditary Optic Neuropathy – Reply Letter to the Editor
por: Manole, Cristina, et al.
Publicado: (2020)

Leber Hereditary Optic Neuropathy: Review of Treatment and Management
por: Hage, Rabih, et al.
Publicado: (2021)

Exploiting hiPSCs in Leber's Hereditary Optic Neuropathy (LHON): Present Achievements and Future Perspectives
por: Peron, Camille, et al.
Publicado: (2021)

DNAJC30 defect: a frequent cause of recessive Leber hereditary optic neuropathy and Leigh syndrome
por: Stenton, Sarah L., et al.
Publicado: (2022)

Long-Term Follow-Up After Unilateral Intravitreal Gene Therapy for Leber Hereditary Optic Neuropathy: The RESTORE Study
por: Biousse, Valérie, et al.
Publicado: (2021)

Diagnostic and Prognostic Value of Conventional Brain MRI in the Clinical Work-Up of Patients with Amyotrophic Lateral Sclerosis
por: Rizzo, Giovanni, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_o9o4vlifuhmogs4k5ijg7tm8pm