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Ultrastructural diagnosis of mitochondrial encephalomyopathies revisited
K. Kyriacou
, C. Mikellidou
, A. Hadjianastasiou
, L. Middleton
, A. Panousopoulos
,
T. Kyriakides
Medical School
Cyprus Institute for Neurology and Genetics
Research output
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Article
›
peer-review
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Keyphrases
Mitochondrial Encephalomyopathy
100%
Electron Microscopy
80%
Histology
40%
Muscle Biopsy
20%
Histochemistry
20%
Accurate Diagnosis
20%
Clinical Phenotype
20%
Morphological Method
20%
Heterogeneous Groups
20%
Biochemical Assay
20%
Pediatric Patients
20%
Multisystem Disease
20%
Laboratory Data
20%
Essential Diagnostics
20%
Adult Case
20%
Morphological Diagnosis
20%
Mitochondrial Enzymes
20%
Mitochondrial DNA
20%
Coordinated Approach
20%
Diagnostic Information
20%
Enzyme Histochemistry
20%
Mutation Analysis
20%
Medicine and Dentistry
Mitochondrial Encephalomyopathy
100%
Electron Microscopy
80%
Morphology
40%
Disease
20%
Muscle Biopsy
20%
Diagnosis
20%
Mitochondrial DNA
20%
Pediatrics Patient
20%
Enzyme Histochemistry
20%
Mitochondrial Enzyme
20%
Histochemistry
20%
Biochemistry, Genetics and Molecular Biology
Electron Microscopy
100%
Morphology
50%
Enzyme
50%
Mitochondrial DNA
25%
Neuroscience
Electron Microscopy
100%
Histochemistry
50%
Mitochondrial DNA
25%
Mitochondrial Enzyme
25%