Skip Navigation

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (224)
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by BROWN, W. F.
Right arrow Articles by FEASBY, T. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by BROWN, W. F.
Right arrow Articles by FEASBY, T. E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Brain, Vol. 107, No. 1, 219-239, 1984
© 1984 Oxford University Press


research-article

CONDUCTION BLOCK AND DENERVATION IN GUILLAIN-BARRÉ POLYNEUROPATHY

W. F. BROWN and T. E. FEASBY

From the Department of Clinical Neurological Sciences, University Hospital London, Ontario, Canada N6A 5A5

Correspondence to: Reprint requests to: Dr W. F. Brown, Department of Clinical Neurological Sciences, University Hospital, PO Box 5339, Station A, London, Ontario N6A 5A5.

The two main electrophysiological abnormalities seen in the first two weeks of the acute Guillain-Barré syndrome (GBS) were conduction block and, in some patients, low maximum M response amplitudes. In this study period, maximum motor and sensory conduction velocities were often in the normal range and temporal dispersion was relatively less common. The conduction block was generalized in its distribution in some peripheral nerves, while in others the block was predominantly proximal or distal in location. Conduction abnormalities in excess of those proximal or distal to it were frequent at common sites of entrapment. Very low M response amplitudes early in the course of the disease correlated well with the subsequent development and frequency of denervation in the muscle(s) and unfavourable clinical recovery. We conclude that conduction block is the main cause of the acute paralysis and sensory loss in the GBS. Axonal degeneration contributes variably to the acute disorder, but is the main cause of lasting disability.

Received January 13, 1983. Revised July 5, 1983.
Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
NeurologyHome page
K. Kaida, M. Sonoo, G. Ogawa, K. Kamakura, M. Ueda-Sada, M. Arita, K. Motoyoshi, and S. Kusunoki
GM1/GalNAc-GD1a complex: A target for pure motor Guillain-Barre syndrome
Neurology, November 18, 2008; 71(21): 1683 - 1690.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
H. C. Lehmann, P. H. H. Lopez, G. Zhang, T. Ngyuen, J. Zhang, B. C. Kieseier, S. Mori, and K. A. Sheikh
Passive Immunization with Anti-Ganglioside Antibodies Directly Inhibits Axon Regeneration in an Animal Model
J. Neurosci., January 3, 2007; 27(1): 27 - 34.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
J. T. H. Van Asseldonk, L. H. Van den Berg, G. H. Wieneke, J. H. J. Wokke, and H. Franssen
Criteria for conduction block based on computer simulation studies of nerve conduction with human data obtained in the forearm segment of the median nerve.
Brain, September 1, 2006; 129(Pt 9): 2447 - 2460.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
A Ghosh, M Busby, R Kennett, K Mills, and M Donaghy
A practical definition of conduction block in IvIg responsive multifocal motor neuropathy
J. Neurol. Neurosurg. Psychiatry, September 1, 2005; 76(9): 1264 - 1268.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
A Ghosh, A Virgincar, R Kennett, M Busby, and M Donaghy
The effect of treatment upon temporal dispersion in IvIg responsive multifocal motor neuropathy
J. Neurol. Neurosurg. Psychiatry, September 1, 2005; 76(9): 1269 - 1272.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
J. T. H. Van Asseldonk, L. H. Van den Berg, S. Kalmijn, J. H. J. Wokke, and H. Franssen
Criteria for demyelination based on the maximum slowing due to axonal degeneration, determined after warming in water at 37{degrees}C: diagnostic yield in chronic inflammatory demyelinating polyneuropathy
Brain, April 1, 2005; 128(4): 880 - 891.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
J-P Lefaucheur, N A Gregson, I Gray, F von Raison, M Bertocchi, and A Creange
A variant of multifocal motor neuropathy with acute, generalised presentation and persistent conduction blocks
J. Neurol. Neurosurg. Psychiatry, November 1, 2003; 74(11): 1555 - 1561.
[Abstract] [Full Text] [PDF]


Home page
NeurologyHome page
M. Capasso, C. M. Caporale, F. Pomilio, P. Gandolfi, A. Lugaresi, and A. Uncini
Acute motor conduction block neuropathy Another Guillain-Barre syndrome variant
Neurology, September 9, 2003; 61(5): 617 - 622.
[Abstract] [Full Text] [PDF]


Home page
BrainHome page
C.-L. Pan, T.-J. Tseng, Y.-H. Lin, M.-C. Chiang, W.-M. Lin, and S.-T. Hsieh
Cutaneous innervation in Guillain-Barre syndrome: pathology and clinical correlations
Brain, February 1, 2003; 126(2): 386 - 397.
[Abstract] [Full Text] [PDF]


Home page
Postgrad. Med. J.Home page
U. Seneviratne
Guillain-Barre syndrome
Postgrad. Med. J., December 1, 2000; 76(902): 774 - 782.
[Abstract] [Full Text]


Home page
NeurologyHome page
J. Berciano, A. Garcia, J. Figols, R. Munoz, M. T. Berciano, and M. Lafarga
Perineurium contributes to axonal damage in acute inflammatory demyelinating polyneuropathy
Neurology, August 22, 2000; 55(4): 552 - 559.
[Abstract] [Full Text] [PDF]


Home page
NEJMHome page
A. H. Ropper, D. P. Cros, and D. E. Palmer-Toy
Case 39-1999- A 74-Year-Old Woman with Acute, Progressive Paralysis after Diarrhea for One Week
N. Engl. J. Med., December 23, 1999; 341(26): 1996 - 2003.
[Full Text] [PDF]


Home page
Arch NeurolHome page
J. C. Wohrle, K. Spengos, W. Steinke, H. H. Goebel, and M. Hennerici
Alcohol-Related Acute Axonal Polyneuropathy: A Differential Diagnosis of Guillain-Barre Syndrome
Arch Neurol, October 1, 1998; 55(10): 1329 - 1334.
[Abstract] [Full Text] [PDF]


Home page
J. Neurol. Neurosurg. PsychiatryHome page
R.-K. Lyu, L.-M. Tang, S.-Y. Cheng, W.-C. Hsu, and S.-T. Chen
Guillain-Barre syndrome in Taiwan: a clinical study of 167 patients
J. Neurol. Neurosurg. Psychiatry, October 1, 1997; 63(4): 494 - 500.
[Abstract] [Full Text] [PDF]


Home page
J Child NeurolHome page
H. R. Jones JR
Topical Review: Childhood Guillain-Barre Syndrome: Clinical Presentation, Diagnosis, and Therapy
J Child Neurol, January 1, 1996; 11(1): 4 - 12.
[Abstract] [PDF]


Home page
Arch NeurolHome page
E. Tan, D. J. Lynn, A. A. Amato, J. T. Kissel, K. W. Rammohan, Z. Sahenk, J. R. Warmolts, C. E. Jackson, R. J. Barohn, and J. R. Mendell
Immunosuppressive Treatment of Motor Neuron Syndromes: Attempts to Distinguish a Treatable Disorder
Arch Neurol, February 1, 1994; 51(2): 194 - 200.
[Abstract] [PDF]


Home page
Arch NeurolHome page
A. H. Ropper, E. F. M. Wijdicks, and B. T. Shahani
Electrodiagnostic Abnormalities in 113 Consecutive Patients With Guillain-Barre Syndrome
Arch Neurol, August 1, 1990; 47(8): 881 - 887.
[Abstract] [PDF]


Home page
Arch NeurolHome page
J. M. Shefner and D. M. Dawson
The Use of Sensory Action Potentials in the Diagnosis of Peripheral Nerve Disease
Arch Neurol, March 1, 1990; 47(3): 341 - 348.
[Abstract] [PDF]


Home page
Arch NeurolHome page
G. Gruener, E. P. Bosch, R. G. Strauss, M. Klugman, and J. Kimura
Prediction of Early Beneficial Response to Plasma Exchange in Guillain-Barre Syndrome
Arch Neurol, March 1, 1987; 44(3): 295 - 298.
[Abstract] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.