Pages that link to "Q48462967"
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The following pages link to Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement (Q48462967):
Displaying 50 items.
- Mitochondrial vasculopathy (Q26745617) (← links)
- Genetics of ischaemic stroke in young adults (Q26775633) (← links)
- When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis? (Q26777744) (← links)
- Mitochondrial encephalomyopathies--fifty years on: the Robert Wartenberg Lecture (Q28657573) (← links)
- The many faces of paediatric mitochondrial disease on neuroimaging (Q31116989) (← links)
- Quantitative cellular level analysis of mitochondrial DNA 3243A > G mutations in individual tissues from the archival temporal bones of a MELAS patient (Q33494096) (← links)
- Mechanism of neurodegeneration of neurons with mitochondrial DNA mutations (Q33742421) (← links)
- Cerebellar ataxia in patients with mitochondrial DNA disease: a molecular clinicopathological study (Q34128925) (← links)
- The neuro-ophthalmology of mitochondrial disease (Q34338783) (← links)
- Friedrich Nietzsche (1844-1900): a classical case of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome? (Q34611405) (← links)
- Synaptic mitochondria in synaptic transmission and organization of vesicle pools in health and disease (Q34689753) (← links)
- Mitochondrial DNA: impacting central and peripheral nervous systems (Q34737643) (← links)
- Sensory neuronopathy in patients harbouring recessive polymerase γ mutations (Q35706479) (← links)
- Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 Mutations. (Q35751411) (← links)
- Microangiopathy in the cerebellum of patients with mitochondrial DNA disease (Q35986703) (← links)
- Mitochondrial dysfunction and mitochondrial DNA mutations in atherosclerotic complications in diabetes (Q35999426) (← links)
- Stroke and Stroke-like Episodes in Muscle Disease (Q36041117) (← links)
- Epilepsy in adults with mitochondrial disease: A cohort study. (Q36533148) (← links)
- Extensive respiratory chain defects in inhibitory interneurones in patients with mitochondrial disease. (Q36634566) (← links)
- Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes (MELAS): A Case Report and Critical Reappraisal of Treatment Options (Q36679929) (← links)
- Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults (Q37225729) (← links)
- Mitochondrial m.3243A > G mutation and carotid artery dissection (Q37253705) (← links)
- Migraine and stroke: current perspectives (Q37282908) (← links)
- The mitochondrial brain: From mitochondrial genome to neurodegeneration (Q37483489) (← links)
- Mitochondrial dysfunction in autism (Q37558748) (← links)
- The genetics and pathology of mitochondrial disease. (Q37560946) (← links)
- The clinical maze of mitochondrial neurology (Q37648911) (← links)
- Pathogenesis and treatment of mitochondrial myopathies: recent advances (Q37840050) (← links)
- Migraine and epilepsy: review of the literature (Q38371291) (← links)
- Review: Central nervous system involvement in mitochondrial disease (Q38861730) (← links)
- Imaging of MELAS. (Q38914260) (← links)
- Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects (Q39536524) (← links)
- The m.3243A>G mtDNA mutation is pathogenic in an in vitro model of the human blood brain barrier (Q39812451) (← links)
- Loss of thymidine kinase 2 alters neuronal bioenergetics and leads to neurodegeneration. (Q39927495) (← links)
- Episodic Aphasia Associated With Cortical Spreading Depression After Subdural Hemorrhage Evacuation (Q41942175) (← links)
- Neuroprotection and acidosis induced by cortical spreading depression (Q42350918) (← links)
- Evidence of reactive oxygen species-mediated damage to mitochondrial DNA in children with typical autism (Q43248182) (← links)
- The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? (Q44261496) (← links)
- The appearance of ADCs in the non-affected areas of the patients with MELAS. (Q46077230) (← links)
- Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study. (Q48201984) (← links)
- A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder (Q48281550) (← links)
- MELAS: A Multigenerational Impact of the MTTL1 A3243G MELAS Mutation. (Q50426007) (← links)
- The impact of pathogenic mitochondrial DNA mutations on substantia nigra neurons. (Q50875675) (← links)
- Primer effect in the detection of mitochondrial DNA point heteroplasmy by automated sequencing. (Q51835622) (← links)
- High frequency of migraine-only patients negative for the 3243 A>G tRNALeu mtDNA mutation in two MELAS families. (Q54418514) (← links)
- Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors. (Q54937614) (← links)
- Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study. (Q55071414) (← links)
- mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease. (Q55482857) (�� links)
- A novel tRNA(Val) mitochondrial DNA mutation causing MELAS (Q80806062) (← links)
- Carotid dissection in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (Q82454694) (← links)