Disease: Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
- "When," "Where," and "How" of SARS-CoV-2 Infection Affects the Human Cardiovascular System: A Narrative Review
- A - 190 Neuropsychological Profile of an Adolescent with Primary Mitochondrial Disorder
- A burning encephalitis: Fluid-attenuated inversion recovery-hyperintense lesions in Anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures in anti-myelin oligodendrocyte glycoprotein-associated encephalitis with seizures-A case rep
- A case of exacerbated encephalopathy with stroke-like episodes and lactic acidosis triggered by metformin in a patient with MELAS
- A Case Report of a Clinically Suspected Diagnosis of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) Syndrome With Cardiac Impairment
- A case report of neuronal intranuclear inclusion disease (NIID) with MELAS-like imaging findings
- A case series of appendicitis and pseudo-appendicitis in a paediatric intensive care unit
- A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt-ND variants
- A patient with MELAS syndrome combined with autoimmune abnormalities: a case report
- Acute noise is harmful on the anti-predator behaviour of commercially important juvenile coral reef fishes
- Adult-onset MELAS syndrome in a 51-year-old woman without typical clinical manifestations: a case report
- Adult-onset mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS): a diagnostic challenge
- Advances in Management of the Stroke Etiology One-Percenters
- Alterations in coenzyme Q(10) status in a cybrid line harboring the 3243A>G mutation of mitochondrial DNA is associated with abnormal mitochondrial bioenergetics and dysregulated mitochondrial biogenesis
- Altered Neurovascular Coupling in Patients With Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS): A Combined Resting-State fMRI and Arterial Spin Labeling Study
- An Aedes-Anopheles Vaccine Candidate Supplemented with BCG Epitopes Against the Aedes and Anopheles Genera to Overcome Hypersensitivity to Mosquito Bites
- An Interesting Case of Wolf-Parkinson-White Syndrome in a Young Patient With Sensorineural Deafness
- Anesthetic Management of a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes Syndrome During Extensive Spinal Surgery With Both Motor Evoked Potentials and Somatosensory Evoked Potentials: A Case Report
- Antigen receptor stimulation induces purifying selection against pathogenic mitochondrial tRNA mutations
- Arginine Supplementation in MELAS Syndrome: What Do We Know about the Mechanisms?
- Assessing the effect of oral glutamine on the MELAS phenotype requires appropriate study designs
- Before Attributing Malnutrition in Melas to Superior Mesenterica Artery Syndrome, all Differentials must be Excluded
- Before blaming metformin as a trigger for stroke-like lesions in MELAS, alternative etiologies must be off the table
- Bilateral cochlear implants in a MELAS patient
- Case report: Late-onset MELAS syndrome with mtDNA 5783G>A mutation diagnosed by urinary sediment genetic testing
- Case report: Late-onset MELAS syndrome with mtDNA 5783G>A mutation diagnosed by urinary sediment genetic testing
- Case report: MELAS and T3271C mitochondrial mutation in an adult woman
- Characteristics and management of mitochondrial stroke-like episodes
- Clinical Reasoning: A 17-Year-Old Girl With Progressive Cognitive Impairment
- Clinical, imaging, and pathological characteristics of 35 cases of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome
- Clinicoradiologic Criteria for the Diagnosis of Stroke-like Episodes in MELAS
- Coating-Free Culture Medium for Establishing and Maintaining Human Induced Pluripotent Stem Cells
- Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an <em>MT-TL1 m.3243A</em>><em>G</em> point mutation: neuroradiological features and their implications for underlying pathogenes
- Commentary: Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes with an MT-TL1 m.3243A>G point mutation: neuroradiological features and their implications for underlying pathogenesis
- Diabetes ketoacidosis and Recurrent Childhood Stroke-like Episodes
- Diffuse posterior leukoencephalopathy in MELAS without stroke-like episodes: A case report
- Distinctive metabolic remodeling in TYMP deficiency beyond mitochondrial dysfunction
- Do not biopsy the MELAS brain
- Editorial for "Altered Neurovascular Coupling in Patients With Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS): A Combined Resting-State fMRI and Arterial Spin Labeling Study"
- Efficient elimination of MELAS-associated m.3243G mutant mitochondrial DNA by an engineered mitoARCUS nuclease
- Elderly onset of MELAS carried an M.3243A >G mutation in a female with deafness and visual deficits: A case report
- Gastrointestinal Complications of Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome Managed By Parenteral Nutrition
- Glutamine metabolism in diseases associated with mitochondrial dysfunction
- Heteroplasmic pathogenic m.12315G>A variant in MT-TL2 presenting with MELAS syndrome and depletion of nitric oxide donors
- Heteroplasmic pathogenic m.12315G>A variant in MT-TL2 presenting with MELAS syndrome and depletion of nitric oxide donors
- Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia
- Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia
- Infraclavicular Catheter in MELAS Syndrome for Analgesic Purposes
- Late-onset MELAS syndrome in a 46-year-old man with initial symptom of chest tightness: a case report
- Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis: A case report
- Late-onset mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes syndrome with mitochondrial DNA 3243A>G mutation masquerading as autoimmune encephalitis: A case report
- Late-onset mitochondrial encephalopathy with lactic acidosis and stroke-like episodes and the role of serial imaging
- Long-term ketogenic diet therapy improves mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS): A case report
- Long-Term Safety of Systemic Ozone Therapy in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS)
- Lysosomal dysfunction and overload of nucleosides in thymidine phosphorylase deficiency of MNGIE
- Magnetic resonance spectroscopy in MELAS syndrome: correlation with CSF and plasma metabolite levels and change after glutamine supplementation
- Melas Syndrome
- MELAS syndrome: Insights into cardiac mechanics
- MELAS-Derived Neurons Functionally Improve by Mitochondrial Transfer from Highly Purified Mesenchymal Stem Cells (REC)
- Metformin adverse event profile: a pharmacovigilance study based on the FDA Adverse Event Reporting System (FAERS) from 2004 to 2022
- Migraine and mitochondrial diseases : Energy deficit in the brain
- Migraine and mitochondrial diseases : Energy deficit in the brain
- Miro1 improves the exogenous engraftment efficiency and therapeutic potential of mitochondria transfer using Wharton's jelly mesenchymal stem cells
- Mitochondrial dysfunction characterized in human induced pluripotent stem cell disease models in MELAS syndrome: A brief summary
- Mitochondrial encephalomyopathy
- Mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS): Special MRI features
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: a case report from Nepal
- Mitochondrial encephalopathy with lactic-acidosis and stroke-like episodes syndrome presenting as progressive supranuclear palsy
- Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation
- Mitochondrial haplotype mutation alleviates respiratory defect of MELAS by restoring taurine modification in tRNA with 3243A > G mutation
- Mitochondrial myopathies diagnosed in adulthood: clinico-genetic spectrum and long-term outcomes
- Mitochondrial myopathy without extraocular muscle involvement: a unique clinicopathologic profile
- Multimodal single-cell analysis of nonrandom heteroplasmy distribution in human retinal mitochondrial disease
- Multiomics analysis reveals serine catabolism as a potential therapeutic target for MELAS
- Negative correlation between organ heteroplasmy, particularly hepatic heteroplasmy, and age at death revealed by post-mortem studies of m.3243A > G cases
- Neovascular Glaucoma in MELAS syndrome
- Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
- Neuropathological hallmarks in autopsied cases with mitochondrial diseases caused by the mitochondrial 3243A>G mutation
- Ocular manifestations of the genetic causes of focal and segmental glomerulosclerosis
- Pathophysiology of myocardial infarction in MELAS
- Primary mitochondrial diseases: The intertwined pathophysiology of bioenergetic dysregulation, oxidative stress and neuroinflammation
- Prolonged misdiagnosis of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes syndrome: A case report
- Refractory Hypotension in a Late-Onset Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Male with m.3243 A>G Mutation: A Case Report
- Refractory Hypotension in a Late-Onset Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) Male with m.3243 A>G Mutation: A Case Report
- Renal manifestations in adults with mitochondrial disease from the mtDNA m.3243A>G pathogenic variant
- Renal manifestations in adults with mitochondrial disease from the mtDNA m.3243A>G pathogenic variant
- Reply: assessing the effect of oral glutamine on the MELAS phenotype requires appropriate study designs
- Seizure phenomenology in MELAS
- T cell activation contributes to purifying selection against the MELAS-associated m.3243A>G pathogenic variant in blood
- T cell activation contributes to purifying selection against the MELAS-associated m.3243A>G pathogenic variant in blood
- The clinical and genetic spectrum of mitochondrial diseases in China: A multicenter retrospective cross-sectional study
- The clinical characteristics of neuronal intranuclear inclusion disease and its relation with inflammation
- The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort study
- The mitochondrial tRNA MT-TW m.5537_5538insT variant presents with significant intra-familial clinical variability
- The Possible Role of COVID-19 in the Triggering of Underlying Mitochondrial Dysfunction in MELAS Syndrome, A Brief Report of three cases
- Therapeutics for Mitochondrial Encephalomyopathy
- Unraveling RNA Conformation Dynamics in Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like Episode Syndrome with Solid-State Nanopores
- Unraveling the Diagnostic Puzzle: Minor Stroke-Like Lesions and Normal Muscle Histopathology in MELAS Syndrome
- Wide diagnostic and genotypic spectrum in patients with suspected mitochondrial disease
- X-linked hypophosphatemia due to a de novo novel splice-site variant in a 7-year-old girl with scaphocephaly, Chiari syndrome type I and syringomyelia