Results 11 to 20 of about 37,493 (266)

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

Screening of effective pharmacological treatments for MELAS syndrome using yeasts, fibroblasts and cybrid models of the disease [PDF]

open access: bronzeBritish Journal of Pharmacology, 2012
Juan Garrido-Maraver   +2 more
exaly   +2 more sources

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  

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

Topological reorganization of brain functional networks in patients with mitochondrial encephalomyopathy with lactic acidosis and stroke‐like episodes

open access: yesNeuroImage: Clinical, 2020
Mitochondrial encephalomyopathy with lactic acidosis and stroke‐like episodes (MELAS) is a rare maternally inherited genetic disease; however, little is known about its underlying brain basis. Furthermore, the topological organization of brain functional
Rong Wang   +7 more
doaj   +1 more source

Clinical Characteristics of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

open access: yesLife, 2021
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome, a maternally inherited mitochondrial disorder, is characterized by its genetic, biochemical and clinical complexity.
Hueng-Chuen Fan   +3 more
doaj   +1 more source

Stroke-like lesions in mitochondrial disease may resemble ischemic stroke

open access: yesJournal of Family Medicine and Primary Care, 2021
The patient is a 73-y-male who was referred after a fall without losing consciousness or secessus. Clinical exam revealed disorientation, ophthalmoparesis, hemianopia to the left, left hemineglect, hypoacusis, quadruparesis, general wasting, generally ...
Josef Finsterer
doaj   +1 more source

Progress in Diagnosing Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes

open access: yesChinese Medical Journal, 2015
Objective: Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a progressive, multisystem affected mitochondrial disease associated with a number of disease-related defective genes.
Ying-Xin Wang, Wei-Dong Le
doaj   +1 more source

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