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 +3 more sources
Late-onset mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes with chronic intestinal pseudo-obstruction: a case-based review [PDF]
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
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
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]
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]
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
Cardiopulmonary Exercise Testing (CPET) Guided Sub-Anaerobic Threshold Rehabilitation in MELAS Syndrome: A Case Report. [PDF]
The Kaohsiung Journal of Medical Sciences, EarlyView.
Tsai YL, Cheng KY, Lu YS, Lin KL.
europepmc +2 more sources
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]
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

