Case report: 5year follow-up of adult late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS)
Author:
Publisher
Elsevier BV
Subject
Endocrinology,Genetics,Molecular Biology
Reference19 articles.
1. A case with late-onset MELAS with hallucination and delusion;Narita;No To Shinkei,2004
2. A case of late-onset MELAS;Kimata;Arch. Neurol.,1998
3. Late-onset mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with bitemporal lesions;Kisanuki;Arch. Neurol.,2006
4. Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation;Bataillard;Neurology,2001
5. Late onset of stroke-like episode associated with a 3256C–>T point mutation of mitochondrial DNA;Jeppesen;J. Neurol. Sci.,2003
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1. The clinical spectrum of MELAS and associated disorders across ages: a retrospective cohort study;Frontiers in Neurology;2023-12-14
2. Clinical Approaches for Mitochondrial Diseases;Cells;2023-10-20
3. Late-onset MELAS syndrome in a 46-year-old man with initial symptom of chest tightness: a case report;European Heart Journal - Case Reports;2023-09-01
4. Droplet digital polymerase chain reaction to measure heteroplasmic m.3243A>G mitochondrial mutations;Laboratory Medicine;2023-07-21
5. l-Arginine in Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes;Neurology;2022-04-15
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