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  2. Mitochondrial disease - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_disease

    Mitochondrial disease is a group of disorders ... (apparently affecting between 1 in 30,000 and 1 in 50,000 people [5 ... and stroke-like episodes; Mitochondrial DNA ...

  3. MELAS syndrome - Wikipedia

    en.wikipedia.org/wiki/MELAS_syndrome

    In most cases, people with MELAS inherit an altered mitochondrial gene from their mother. Less commonly, the disorder results from a new mutation in a mitochondrial gene and occurs in people with no family history of MELAS. [citation needed] Although first recognised and described in 1984 the condition occurred well before that date.

  4. MT-TL1 - Wikipedia

    en.wikipedia.org/wiki/MT-TL1

    Mutations in MT-TL1 can result in multiple mitochondrial deficiencies and associated disorders. It is associated with mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes . [5] MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain.

  5. First Participant Dosed in Tisento Therapeutics’ Global Phase ...

    lite.aol.com/tech/story/0022/20250127/9347559.htm

    The study is investigating the impact of once-daily oral zagociguat treatment on fatigue, cognitive impairment, and other key aspects of the rare mitochondrial disease MELAS (Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes). The PRIZM study is centered in multiple ways on what matters to people living with MELAS.

  6. Mitochondrial encephalomyopathy - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial...

    A mitochondrial encephalomyopathy is a form of encephalomyopathy that is associated with a mitochondrial disease. MELAS syndrome Examples include MELAS syndrome and MERRF syndrome. These conditions can sometimes present together. [1] [2] KSS is sometimes included in this category, [3] but it is not included in this category in MeSH.

  7. Mitochondrial myopathy - Wikipedia

    en.wikipedia.org/wiki/Mitochondrial_myopathy

    Mitochondrial myopathy literally means mitochondrial muscle disease, muscle disease caused by mitochondrial dysfunction. The mitochondrion is the primary producer of energy in nearly all cells throughout the body. The exception is mature erythrocytes (red blood cells), so that they do not use up the oxygen that they carry.

  8. MT-TH - Wikipedia

    en.wikipedia.org/wiki/MT-TH

    A small number of people with symptoms of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) have been found to have mutations in the MT-TH gene. MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain.

  9. Excitotoxicity - Wikipedia

    en.wikipedia.org/wiki/Excitotoxicity

    Excitotoxicity may be involved in cancers, spinal cord injury, stroke, traumatic brain injury, hearing loss (through noise overexposure or ototoxicity), and in neurodegenerative diseases of the central nervous system such as multiple sclerosis, Alzheimer's disease, amyotrophic lateral sclerosis (ALS), Parkinson's disease, alcoholism, alcohol ...