The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort study
Frontiers in Neurology, 2023 ObjectiveMitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a severe multisystemic disease, although some have a milder phenotype.
Jay Mandrekar +2 more
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Pterostichus melas subsp. melas melas (Creutzer 1799
, 2016 Published as part of Hoess, René, 2016, Interessante Neufunde von Laufkäfern (Coleoptera: Carabidae) aus der Schweiz, pp.
Hoess, René
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Impaired respiratory function in MELAS‐induced pluripotent stem cells with high heteroplasmy levels
FEBS Open Bio, 2015 Mitochondrial diseases are heterogeneous disorders, caused by mitochondrial dysfunction. Mitochondria are not regulated solely by nuclear genomic DNA but by mitochondrial DNA.
Masaki Kodaira +2 more
exaly +2 more sources
MELAS syndrome complicated by anti-GFAP autoantibody positivity: a case report and literature review [PDF]
BMC NeurologyBackground Autoimmune abnormalities have been reported in mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, but anti-glial fibrillary acidic protein (GFAP) antibody positivity in both serum and cerebrospinal ...
Jun Shu +5 more
doaj +2 more sources
Dynamic reconfiguration and transition of whole-brain networks in patients with MELAS revealed by a hidden Markov model [PDF]
Frontiers in NeurologyObjectivesMitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) is a rare maternally inherited disease. The neuropathologic mechanisms and neural network alterations underlying stroke-like episodes (SLEs), a recurrent ...
Qingyun Yu +11 more
doaj +2 more sources
Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes – a case report [PDF]
BMC Neurology, 2019 Background Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) is a mitochondrial cytopathy caused by mutations in mitochondrial DNA. Clinical manifestation is typically before the age of 40. Case presentation We present the
Tim Sinnecker +10 more
doaj +2 more sources
Migratory vasodilatation of cerebral arteries in MELAS episodes: a case report and literature review [PDF]
Frontiers in ImmunologyMitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) is the commonest inherited mitochondrial disorder. Dilation of the major cerebral arteries is seldom mentioned in MELAS because magnetic resonance angiography (MRA ...
Ying Luo +13 more
doaj +2 more sources
Case Report: Simultaneous pancreas–kidney transplantation in MELAS: first reported case with 5-year follow-up [PDF]
Frontiers in TransplantationBackgroundMitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes (MELAS) is a rare mitochondrial DNA disorder that, in severe cases, can result in insulin-dependent diabetes and end-stage renal disease (ESRD).
Vera Nilsén +4 more
doaj +2 more sources
Retinal multimodal-imaging and functional tests in a mitochondrial disease with focal and segmental glomerulosclerosis [PDF]
International Journal of OphthalmologyThe phenotypes of the adenine-to-guanine transition at position 3243 of mitochondrial DNA (m.3243A>G) are highly variable, with different symptoms observed in different patients.
Xiao-Hong Liu, Xi Shen, Yi-Sheng Zhong
doaj +2 more sources
, 2018 Published as part of Yunakov, Nikolai, Nazarenko, Vitalij, Filimonov, Rostislav & Volovnik, Semyon, 2018, A survey of the weevils of Ukraine (Coleoptera: Curculionoidea), pp.
Yunakov, Nikolai +3 more
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