Results 11 to 20 of about 14,508 (226)

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   +3 more sources

Late-onset mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes with chronic intestinal pseudo-obstruction: a case-based review [PDF]

open access: yesFrontiers in Molecular Biosciences
BackgroundMitochondrial Encephalomyopathy Lactic Acidosis and Stroke-like episodes (MELAS) is rare in people over 40 years of age, and gastrointestinal complications of MELAS are also rare, especially Chronic Intestinal Pseudo-Obstruction (CIPO).Case ...
Lin Zhang   +5 more
doaj   +2 more sources

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.
Benjamin C Cox   +2 more
exaly   +3 more sources

Pterostichus melas subsp. melas melas (Creutzer 1799

open access: yes, 2016
Published as part of Hoess, René, 2016, Interessante Neufunde von Laufkäfern (Coleoptera: Carabidae) aus der Schweiz, pp.
Hoess, René
openaire   +3 more sources

Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes – a case report [PDF]

open access: yesBMC 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   +3 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

Cardiopulmonary Exercise Testing (CPET) Guided Sub-Anaerobic Threshold Rehabilitation in MELAS Syndrome: A Case Report. [PDF]

open access: yesKaohsiung J Med Sci
The Kaohsiung Journal of Medical Sciences, EarlyView.
Tsai YL, Cheng KY, Lu YS, Lin KL.
europepmc   +2 more sources

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

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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