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Journal of the Neurological Sciences
Volume 211, Issue 1
, Pages 93-97
, 15 July 2003
Axonal Guillain–Barré syndrome associated with axonal Charcot–Marie–Tooth disease
References
- . Molecular pathogenesis of hereditary motor, sensory and autonomic neuropathies. Curr. Opin. Neurol. 2001;14:621–627
- . Assessment of current diagnostic criteria for Guillain–Barré syndrome. Ann. Neurol. 1990;27(Suppl.):S21–S24
- . The inflammatory lesion in idiopathic polyneuritis: its role in pathogenesis. Medicine. 1969;48:173–215
-
An acute axonal form of Guillain–Barré polyneuropathy.
Brain. 1986;109:1115–1126
- Acute motor axonal neuropathy: a frequent cause of acute flaccid paralysis in China. Ann. Neurol. 1993;33:333–342
- Pathology of the motor–sensory axonal Guillain–Barré syndrome. Ann. Neurol. 1996;39:17–28
- Early nodal change in the acute motor axonal neuropathy pattern of the Guillain–Barré syndrome. J. Neurocytol. 1996;25:33–51
- Immune attack on the Schwann cell surface in acute inflammatory demyelinating polyneuropathy. Ann. Neurol. 1996;39:625–635
- Acute motor axonal neuropathy: an antibody-mediated attack on axolemma. Ann. Neurol. 1996;40:635–644
- . 2nd Workshop of the European CMT Consortium: 53rd ENMC International Workshop on Classification and Diagnostic Guidelines for Charcot–Marie–Tooth type 2 (CMT-HMSN II) and distal hereditary motor neuropathy (distal HMN-spinal CMT). Neuromuscul. Disord. 1998;8:426–431
- . Acute inflammatory neuropathy in Charcot–Marie–Tooth disease. Neurology. 1999;52:859–861
- . Prednisone-responsive hereditary motor and sensory neuropathy. Mayo Clin. Proc. 1982;57:239–246
-
Guillain–Barré syndromes in northern China: relationship to Campylobacter jejuni infection and anti-glycolipid antibodies.
Brain. 1995;118:597–605
- . Miller Fisher syndrome and Haemophilus influenzae infection. Neurology. 2001;57:686–691
- N-Glycolylneuraminic acid-containing GM1 is a new molecule for serum antibody in Guillain–Barré syndrome. Ann. Neurol. 1998;43:829–834
- . Infectious origins of, and molecular mimicry in, Guillain–Barré and Fisher syndromes. Lancet Infect. Dis. 2001;1:29–37
- . Axonal Guillain–Barré syndrome: relation to anti-ganglioside antibodies and Campylobacter jejuni infection in Japan. Ann. Neurol. 2000;48:624–631
- . GM1b is a new member of antigen for serum antibody in Guillain–Barré syndrome. Neurology. 1996;47:237–242
- Motor nerve terminal degeneration provides a potential mechanism for rapid recovery in acute motor axonal neuropathy after Campylobacter infection. Neurology. 1997;48:717–724
- IgG anti-GM1 antibody is associated with reversible conduction failure and axonal degeneration in Guillain–Barré syndrome. Ann. Neurol. 1998;44:202–208
- . Rapid resolution of nerve conduction blocks after plasamapheresis in Guillain–Barré syndrome associated with anti-GM1b IgG antibody. J. Neurol. 2001;248:148–150
- Axonal involvement at the common entrapment sites in Guillain–Barré syndrome with IgG anti-GM1 antibody. Muscle Nerve. 1999;22:840–845
- Haemophilus influenzae has a GM1 ganglioside-like structure and elicits Guillain–Barré syndrome. Neurology. 1999;52:1282–1284
- Haemophilus influenzae infection and Guillain–Barré syndrome. Brain. 2000;123:2171–2178
- . Indicator of rapid clinical recovery in Guillain–Barré syndrome. J. Neurol. Neurosurg. Psychiatry. 2001;70:560–562
PII: S0022-510X(03)00059-5
doi: 10.1016/S0022-510X(03)00059-5
© 2003 Elsevier Science B.V. All rights reserved.
« Previous
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Journal of the Neurological Sciences
Volume 211, Issue 1
, Pages 93-97
, 15 July 2003
