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Lancet, The, ISSN 0140-6736, 2016, Volume 388, Issue 10045, pp. 717 - 727
Summary Guillain-Barré syndrome is the most common and most severe acute paralytic neuropathy, with about 100 000 people developing the disorder every year... 
Internal Medicine | MEDICINE, GENERAL & INTERNAL | CAMPYLOBACTER-JEJUNI INFECTION | GLYCOLIPID ANTIBODIES | REVERSIBLE CONDUCTION FAILURE | RANDOMIZED-TRIAL | GBS | ANTIBODY-MEDIATED NEUROPATHIES | INFLAMMATORY DEMYELINATING POLYRADICULONEUROPATHY | FISHER SYNDROME | PERIPHERAL NEUROPATHIES | HEPATITIS-E | Campylobacter Infections - complications | Influenza Vaccines - administration & dosage | Prognosis | Humans | Muscle Weakness - complications | Electrophysiology | Respiratory Insufficiency - etiology | Plasma Exchange | Respiratory Insufficiency - prevention & control | Guillain-Barre Syndrome - complications | Guillain-Barre Syndrome - epidemiology | Muscle Weakness - etiology | Diagnosis, Differential | Influenza Vaccines - adverse effects | Paralysis - immunology | Treatment Outcome | Clinical Trials as Topic | Guillain-Barre Syndrome - physiopathology | Campylobacter jejuni | Paralysis - complications | Plasmapheresis | Guillain-Barre Syndrome - therapy | Campylobacter Infections - immunology | Guillain-Barre Syndrome - diagnosis | Guillain-Barre Syndrome - immunology | Immunoglobulins, Intravenous - therapeutic use | Axons - pathology | Disease Management | Axons - immunology | Neural Conduction - immunology | Guillain-Barre syndrome | Neuropathology | Medical prognosis | Biomarkers | Infections | Vaccines | Epidemiology
Journal Article
2013, ISBN 0521171857, 184
There are over 600 neuromuscular disorders and the variability of these syndromes can leave clinicians feeling as if they are lost in a maze as they seek to... 
Neuromuscular diseases | Clinical & internal medicine | Case studies | Diagnosis
Book
PLoS ONE, ISSN 1932-6203, 07/2016, Volume 11, Issue 7, p. e0158912
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 88 - 88
Journal Article
PLoS ONE, ISSN 1932-6203, 02/2016, Volume 11, Issue 2, p. e0143837
Journal Article
Orphanet journal of rare diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 73 - 73
Journal Article