Results 1 to 10 of about 12,239 (244)

The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort study

open access: yesFrontiers 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, Mandrekar Jay
exaly   +3 more sources

Impaired respiratory function in MELAS‐induced pluripotent stem cells with high heteroplasmy levels

open access: yesFEBS 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.
Shinsuke Yuasa   +2 more
exaly   +2 more sources

MELAS syndrome complicated by anti-GFAP autoantibody positivity: a case report and literature review [PDF]

open access: yesBMC Neurology
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]

open access: yesFrontiers in Immunology
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]

open access: yesFrontiers in Neurology
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]

open access: yesFrontiers in Transplantation
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

open access: yesJournal of the Belgian Society of Radiology, 2022
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

A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt‐ND variants

open access: yesAnnals of Clinical and Translational Neurology, 2023
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]

open access: yesKorean Journal of Anesthesiology, 2010
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]

open access: yesAnalytical Approaches to World Music, 2023
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  

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