Precise diagnosis and treatment and pathogenesis of neurogenetic/rare diseases, including:

1. Precise diagnosis and treatment of Wilson's disease and its pathogenesis;

2. Precise diagnosis and treatment of paroxysmal dyskinesia and the neural circuit mechanism;

3. Precise diagnosis, treatment and comprehensive management of hereditary peripheral neuropathy and muscle diseases;

4. Clinical and basic research on hereditary ataxia, Huntington's disease, hereditary spastic paraplegia, hereditary leukoencephalopathy, and mitochondrial diseases;

5. Clinical and basic research on rare diseases such as motor neuron disease, multisystem atrophy, multiple sclerosis, neuromyelitis optica and spectrum diseases, myasthenia gravis, and so on.


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