The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort study
ObjectiveMitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) is a severe multisystemic disease, although some have a milder phenotype.
Jay Mandrekar, Mandrekar Jay
exaly +3 more sources
Impaired respiratory function in MELAS‐induced pluripotent stem cells with high heteroplasmy levels
Mitochondrial diseases are heterogeneous disorders, caused by mitochondrial dysfunction. Mitochondria are not regulated solely by nuclear genomic DNA but by mitochondrial DNA.
Shinsuke Yuasa +2 more
exaly +2 more sources
MELAS syndrome complicated by anti-GFAP autoantibody positivity: a case report and literature review [PDF]
Background 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
Migratory vasodilatation of cerebral arteries in MELAS episodes: a case report and literature review [PDF]
Mitochondrial 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
Dynamic reconfiguration and transition of whole-brain networks in patients with MELAS revealed by a hidden Markov model [PDF]
ObjectivesMitochondrial 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
Case Report: Simultaneous pancreas–kidney transplantation in MELAS: first reported case with 5-year follow-up [PDF]
BackgroundMitochondrial 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
Microhemorrhages in MELAS Lesions: A Case Report
Introduction: Microhemorrhages have not been described in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome (MELAS) on magnetic resonance imaging (MRI).
Evelien Martens +2 more
doaj +1 more source
Objective To explore the clinical characteristics of mitochondrial encephalomyopathy, lactic acidosis, and stroke‐like episodes (MELAS) caused by mitochondrial DNA‐encoded complex I subunit (mt‐ND) variants.
Wei Wang +16 more
doaj +1 more source
Total intravenous anesthesia with propofol and remifentanil in a patient with MELAS syndrome -A case report- [PDF]
A 23-year-old woman with MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) underwent a laparoscopy-assisted appendectomy. MELAS syndrome is a multisystemic disease caused by mitochondrial dysfunction.
Jin Suk Park +6 more
doaj +1 more source
Neo-Riemannian Theory and the Melakarta [PDF]
Utilizing a Neo-Riemannian lens and pitch-class set analysis, this article investigates the Melakarta—a South Indian classification system for ragas. There are two main goals.
John King
doaj

