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Titlebook: Diagnosis and Management of Mitochondrial Disorders; Michelangelo Mancuso,Thomas Klopstock Book 2019 Springer Nature Switzerland AG 2019 M

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Mattia Algeri M.D.,Franco Locatelli M.D.s associated with mitochondrial cytopathies corresponds to an increasing number of clinical and neuroimaging phenotypes. This chapter describes the main imaging findings of mitochondrial cytopathies in children, providing a rational approach to their differential diagnosis based on multimodal imaging analysis and clinical evaluation.
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Maria Reichenbach,Robert S. Cohenvivo [2]. Mutations in . are one of the most common causes of mitochondrial disease and responsible for a wide range of phenotypes. Mutations in . are rare. Disease caused by mutations in Twinkle gives a similar spectrum of disease to those caused by POLG and we will discuss them together where this is appropriate.
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