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Mitochondrial vasculopathyWhen should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?Arrhythmias in MELAS syndrome.MELAS syndrome due to the m.3291T > C mutation.Low blood heteroplasmy-rate may cause late-onset MELAS.Skeletal muscle microvasculature in the diagnosis of neuromuscular disease.Unclassified cardiomyopathies in neuromuscular disorders.Assessment of the phenotype genotype variability and correlation in m.3243A > G mutation carriers requires prospective studies.Response to: Letter to the Editor Regarding: The Expanding Phenotype of MELAS Caused by the m.3291 T > C tRNA Mutation E Kelland, C. A. Rupar, Asuri N. Prasad, K. Y. Tay, A. Downie and C. Prasad (1) by Josef Finsterer, MD, PhD [1], Sinda Zarrouk-MahMechanical thrombectomy in a young stroke patient with Duchenne muscular dystrophy.Affection of immune cells by a C10orf2 mutation manifesting as mitochondrial myopathy and transient sensory transverse syndrome.Mitochondrial diseases caused by mtDNA mutations: a mini-review
P2860
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P2860
description
2012 nî lūn-bûn
@nan
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
2012年论文
@zh
2012年论文
@zh-cn
name
Stroke and Stroke-like Episodes in Muscle Disease.
@ast
Stroke and Stroke-like Episodes in Muscle Disease.
@en
type
label
Stroke and Stroke-like Episodes in Muscle Disease.
@ast
Stroke and Stroke-like Episodes in Muscle Disease.
@en
prefLabel
Stroke and Stroke-like Episodes in Muscle Disease.
@ast
Stroke and Stroke-like Episodes in Muscle Disease.
@en
P2860
P1476
Stroke and Stroke-like Episodes in Muscle Disease.
@en
P2093
Josef Finsterer
P2860
P356
10.2174/1874205X01206010026
P577
2012-05-18T00:00:00Z