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Augenveränderungen bei MELAS-Syndrom
Klinische Monatsblätter für Augenheilkunde, 1990The present paper reports on the clinical findings of a 34-year-old male patient with MELAS syndrome. MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis and strokelike episodes) belongs to a group of syndromes called mitochondrial encephalomyopathies that are characterized by changes of the mitochondrial respiratory chain and the ...
M. Küchle +3 more
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Statins Provoking MELAS Syndrome
European Neurology, 2007<i>Background:</i> Statins inhibit the production of 2,3-dimethoxy,5-methyl,6-polyisoprene parabenzoquinone also known as ubiquinone or coenzyme Q10 (CoQ10), which is required for mitochondrial electron transport. Idiopathic or primary CoQ10 deficiencies have been known to cause mitochondrial encephalomyopathy.
Joseph E. Thomas +2 more
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Immunonutrition for the acute treatment of MELAS syndrome.
Endocrinología Diabetes y Nutrición, 2021MELAS syndrome (Mitochondrial Encephalopathy, Lactic Acidosis and Stroke-like episodes) is one of the most frequent mitochondrial pathologies. Its diagnosis is based on the classic triad of symptoms its acronym stands for and the presence of ragged red ...
E. Pérez-Cruz +2 more
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Black Toenail Sign in MELAS Syndrome
Pediatric Neurology, 2017Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome is a mitochondrial disorder often causing progressive brain injury that is not confined to large arterial territories. Severe insults ultimately lead to gyral necrosis affecting the cortex and juxtacortical white matter; the neuroimaging correlate is partial ...
Matthew T, Whitehead +4 more
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Journal of neuroradiology = Journal de neuroradiologie, 2021
Major cerebral vessels have been proposed as a target of defective mitochondrial metabolism in patients with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome (MELAS).
L. Gramegna +7 more
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Major cerebral vessels have been proposed as a target of defective mitochondrial metabolism in patients with mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes syndrome (MELAS).
L. Gramegna +7 more
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MELAS: A Mitochondrial Encephalomyopathy Syndrome
Journal of Neuroscience Nursing, 1995MELAS, a syndrome characterized by Myopathy, Encephalopathy, Lactic Acidosis and Stroke-like episodes, is one of a group of diseases known as mitochondrial encephalopathies. These genetically-transmitted diseases result in metabolic abnormalities associated with mitochondrial dysfunction, which contribute to neuronal destruction.
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Sensorineural hearing loss in MELAS syndrome
The Journal of Laryngology & Otology, 1997AbstractA case of sensorineural hearing loss (SNHL) in MELAS syndrome, a variety of mitochondrial cytopathy, is presented. Mitochondrial cytopathies have gone almost unreported in the otolaryngology literature, despite evidence from a recent review that about 60 per cent of such patients suffer from SNHL (Gold and Rapin, 1994). The same review revealed
P D, Warrick, P, Wardrop, D W, Sim
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In the heart of MELAS syndrome
International Journal of Cardiology, 2016no ...
Finsterer, Josef, Zarrouk-Mahjoub, Sinda
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MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report
Annals of Internal Medicine, 2020MELAS Syndrome and MIDD Unmasked by Metformin Use: A Case Report Background: Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) is a syndrome caused by genetic defects in mitochondrial DNA.
Na Hyun Kim +2 more
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Neurology, 1988
Severe prolonged migrainous symptoms and prolonged partial status epilepticus are characteristic features of the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes). Maternal transmission previously found in myoclonus epilepsy and ragged-red fibers (MERRF), another mitochondrial disease, is suggested in this ...
Montagna, P +7 more
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Severe prolonged migrainous symptoms and prolonged partial status epilepticus are characteristic features of the MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes). Maternal transmission previously found in myoclonus epilepsy and ragged-red fibers (MERRF), another mitochondrial disease, is suggested in this ...
Montagna, P +7 more
openaire +2 more sources