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Movement Disorders and Inherited Metabolic Disorders - Recognition, Understanding, Improving Outcomes (Mixed media product, New Ed)
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Movement Disorders and Inherited Metabolic Disorders - Recognition, Understanding, Improving Outcomes (Mixed media product, New Ed)
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Inherited metabolic movement disorders are a significant and
rapidly evolving field of study, linking two subspecialty areas of
childhood-onset movement disorders and inborn errors of metabolism.
Increasing the chance of early recognition of inherited metabolic
movement disorders can have significant therapeutic implications
for patients. Containing information on new disorders of
post-translational modification and autophagy and their
identification and treatment, there is thorough coverage of
disorders of amino acids, energy metabolism, and lysosomal storage,
amongst others. This key resource explores future directions in the
field including next-generation genetic sequencing and novel
therapeutic approaches such as deep brain stimulation.
Supplementary videos are available on Cambridge Core, accessible
via the code printed inside the cover. This essential text bridges
the gap in communication between experts in genetic-metabolic
medicine and movement disorder neurology. With an emphasis on
treatable conditions that should not be missed, this volume guides
you through various disorders from a clinical, biochemical and
genetic perspective.
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