Chorea-acanthocytosis with polyclonal antibodies to ganglioside GM1
暂无分享,去创建一个
[1] Keita Ito,et al. Application of Liposome Immune Lysis Assay for Studies on Anti-Ganglioside Antibodies , 1995 .
[2] A. Pestronk,et al. Invited review: motor neuropathies, motor neuron disorders, and antiglycolipid antibodies. , 1991, Muscle & nerve.
[3] G. Legname,et al. Anti‐GM1 IgM antibodies in motor neuron disease and neuropathy , 1990, Neurology.
[4] A. Hays,et al. IgM deposits at nodes of ranvier in a patient with amyotrophic lateral sclerosis, anti‐GM1 antibodies, and multifocal motor conduction block , 1990, Annals of neurology.
[5] G. Sobue,et al. Peripheral nerve involvement in familial chorea-acanthocytosis , 1986, Journal of Neurological Sciences.
[6] Mark J. Brown,et al. Multifocal demyelinating neuropathy with persistent conduction block , 1982, Neurology.
[7] Y. Kuroiwa,et al. Neurogenic muscular atrophy and low density of large myelinated fibres of sural nerve in chorea-acanthocytosis. , 1981, Journal of neurology, neurosurgery, and psychiatry.
[8] E M Critchley,et al. Acanthocytosis and neurological disorder without betalipoproteinemia. , 1968, Archives of neurology.
[9] J W Estes,et al. A new hereditary acanthocytosis syndrome. , 1967, The American journal of medicine.