MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
about
When should MELAS (Mitochondrial myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like episodes) be the diagnosis?Psoriasis, bulbar involvement, and diarrhea in late myoclonic epilepsy with ragged-red fibers-syndrome due to the m.8344A > G tRNA (Lys) mutation.Leukoencephalopathies in mitochondrial disorders: clinical and MRI findings.Mitochondrial deficiency in Cockayne syndrome.Cognitive dysfunction in mitochondrial disorders.Mitochondrial epilepsy in pediatric and adult patients.Seizure semiology and EEG findings in mitochondrial diseases.When should MERRF (myoclonus epilepsy associated with ragged-red fibers) be the diagnosis?Protecting the mitochondrial powerhouse.MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis.Mitochondrial dysfunction and myoclonic epilepsy: cause or effect or both?
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MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年学术文章
@wuu
2011年学术文章
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2011年学术文章
@zh-cn
2011年学术文章
@zh-hans
2011年学术文章
@zh-my
2011年学术文章
@zh-sg
2011年學術文章
@yue
2011年學術文章
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name
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@en
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@nl
type
label
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@en
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@nl
prefLabel
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@en
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@nl
P2093
P1433
P1476
MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients.
@en
P2093
Carlos E Silvado
Cláudia S Kamoi Kay
Lineu C Werneck
Paulo José Lorenzoni
Raquel C Arndt
Rosana H Scola
P304
P356
10.1016/J.MITO.2011.01.003
P577
2011-02-15T00:00:00Z