Cargando…

The relevance of migraine in the clinical spectrum of mitochondrial disorders

Recent scientific evidence suggests a link between migraine and brain energy metabolism. In fact, migraine is frequently observed in mitochondrial disorders. We studied 46 patients affected by mitochondrial disorders, through a headache-focused semi-structured interview, to evaluate the prevalence o...

Descripción completa

Detalles Bibliográficos
Autores principales:	Terrin, Alberto, Bello, Luca, Valentino, Maria Lucia, Caporali, Leonardo, Sorarù, Gianni, Carelli, Valerio, Maggioni, Ferdinando, Zeviani, Massimo, Pegoraro, Elena
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Nature Publishing Group UK 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913605/ https://www.ncbi.nlm.nih.gov/pubmed/35273322 http://dx.doi.org/10.1038/s41598-022-08206-z

Ejemplares similares

Mitochondrial Retinopathies
por: Zeviani, Massimo, et al.
Publicado: (2021)

The optic nerve: A “mito-window” on mitochondrial neurodegeneration
por: Maresca, Alessandra, et al.
Publicado: (2013)

Rapamycin rescues mitochondrial dysfunction in cells carrying the m.8344A > G mutation in the mitochondrial tRNA(Lys)
por: Capristo, Mariantonietta, et al.
Publicado: (2022)

DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?
por: Maresca, Alessandra, et al.
Publicado: (2015)

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

O051. Chronic migraine and onabotulinumtoxinA: a prospective study on patients treated at the Headache Centre of the Padua University and analysis of possible predictors of responsivity
por: Disco, Caterina, et al.
Publicado: (2015)

P050. Migrainous aura: when to worry?
por: Fuccaro, Matteo, et al.
Publicado: (2015)

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)

The relevance of mitochondrial DNA variants fluctuation during reprogramming and neuronal differentiation of human iPSCs
por: Palombo, Flavia, et al.
Publicado: (2021)

Dissecting the multifaceted contribution of the mitochondrial genome to autism spectrum disorder
por: Caporali, Leonardo, et al.
Publicado: (2022)

Co-occurrence of amyotrophic lateral sclerosis and Leber’s hereditary optic neuropathy: is mitochondrial dysfunction a modifier?
por: Amore, Giulia, et al.
Publicado: (2022)

Mitochondrial Neurodegeneration
por: Zeviani, Massimo, et al.
Publicado: (2022)

Functional changes in Becker muscular dystrophy: implications for clinical trials in dystrophinopathies
por: Bello, Luca, et al.
Publicado: (2016)

O002. Did Picasso and De Chirico really suffer from migraine auras?
por: Lisotto, Carlo, et al.
Publicado: (2015)

P051. Olfactory migrainous hallucinations: a typical aura manifestation?
por: Bellamio, Matteo, et al.
Publicado: (2015)

Influence of physiologic hormonal modification and of hormonal treatment in a patient with a history of migraine with aura
por: Maggioni, Ferdinando, et al.
Publicado: (2008)

TYMP Variants Result in Late-Onset Mitochondrial Myopathy With Altered Muscle Mitochondrial DNA Homeostasis
por: Ronchi, Dario, et al.
Publicado: (2020)

Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
por: Manini, Arianna, et al.
Publicado: (2022)

Expanding and validating the biomarkers for mitochondrial diseases
por: Maresca, Alessandra, et al.
Publicado: (2020)

Mitochondrial Structure and Bioenergetics in Normal and Disease Conditions
por: Protasoni, Margherita, et al.
Publicado: (2021)

Keeping in Shape the Dogma of Mitochondrial DNA Maternal Inheritance
por: Carelli, Valerio
Publicado: (2015)

Muscle MRI and functional outcome measures in Becker muscular dystrophy
por: Barp, Andrea, et al.
Publicado: (2017)

Lipomatosis Incidence and Characteristics in an Italian Cohort of Mitochondrial Patients
por: Musumeci, Olimpia, et al.
Publicado: (2019)

TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study
por: Percetti, Marco, et al.
Publicado: (2022)

P049. Migraine influence on female reproductive life and motherhood
por: Fuccaro, Matteo, et al.
Publicado: (2015)

Nuclear gene mutations as the cause of mitochondrial complex III deficiency
por: Fernández-Vizarra, Erika, et al.
Publicado: (2015)

The borderline between cluster headache and migraine: does cluster-migraine exist?
por: Lisotto, C, et al.
Publicado: (2013)

Brain MRS correlates with mitochondrial dysfunction biomarkers in MELAS‐associated mtDNA mutations
por: Gramegna, Laura L., et al.
Publicado: (2021)

OPA1-related auditory neuropathy: site of lesion and outcome of cochlear implantation
por: Santarelli, Rosamaria, et al.
Publicado: (2015)

Subjective Sleep Quality as it Relates to Cognitive and Physical Function in Spinal Muscular Atrophy Patients
por: Wennberg, Alexandra, et al.
Publicado: (2023)

Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performance
por: Fortuna, Andrea, et al.
Publicado: (2022)

Correction to: Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performance
por: Fortuna, Andrea, et al.
Publicado: (2023)

The value of serum creatinine as biomarker of disease progression in spinal and bulbar muscular atrophy (SBMA)
por: Blasi, Lorenzo, et al.
Publicado: (2023)

Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
por: La Morgia, Chiara, et al.
Publicado: (2020)

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

Novel mutations in DNA2 associated with myopathy and mtDNA instability
por: Ronchi, Dario, et al.
Publicado: (2019)

Variation in MAPT is not a contributing factor to the incomplete penetrance in LHON
por: Hudson, Gavin, et al.
Publicado: (2011)

Author Correction: Calcium mishandling in absence of primary mitochondrial dysfunction drives cellular pathology in Wolfram Syndrome
por: La Morgia, Chiara, et al.
Publicado: (2020)

Beyond motor neurons: expanding the clinical spectrum in Kennedy’s disease
por: Manzano, Raquel, et al.
Publicado: (2018)

The comorbidity between migraine and hypothyroidism
por: Lisotto, C, et al.
Publicado: (2013)

Cannot write session to /tmp/vufind_sessions/sess_variocr8q93ucrp5325qk8uog4