Early-onset multisystem degeneration with central motor, autonomic and optic nerve disturbances: unusual Riley–Day syndrome or new clinical entity?
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[1] J. Haines,et al. Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis , 1993, Nature Genetics.
[2] G. Diamond,et al. Optic nerve dysfunction in familial dysautonomia. , 1987, American journal of ophthalmology.
[3] J. Rizzo,et al. Optic atrophy in familial dysautonomia. , 1986, American journal of ophthalmology.
[4] J. Pearson,et al. Familial dysautonomia (a brief review). , 1979, Journal of the autonomic nervous system.
[5] J. Pearson,et al. Tyrosine hydroxylase immunoreactivity in familial dysautonomia. , 1979, Science.
[6] A. Aguayo,et al. Peripheral nerve abnormalities in the Riley-Day syndrome. Findings in a sural nerve biopsy. , 1971, Archives of neurology.
[7] Riley Cm,et al. Central autonomic dysfunction with defective lacrimation; report of five cases. , 1949 .
[8] J. Dancis,et al. Familial dysautonomia: diagnosis, pathogenesis and management. , 1974, Advances in pediatrics.