Polycranial neuropathy and sensory ataxia with IgG anti-GD1a antibody as a variant of Guillain-Barré syndrome

Journal of Clinical Neuroscience

Volumn 20, Issue 3, 2013, Pages 473-475

  Kim, Sun Young ^a   Kim, Jong Kuk ^b   Suh, Chung Kyu ^c  

^a University of Ulsan College of Medicine   (South Korea)

^b Dong A University College of Medicine   (South Korea)

^c Kyungpook National University School of Medicine   (South Korea)

Author keywords

Ataxia; Cranial nerve disease; Facial palsy; GD1a ganglioside; Guillain Barr syndrome

Indexed keywords

GANGLIOSIDE GD 1A ANTIBODY; IMMUNOGLOBULIN G; UNCLASSIFIED DRUG;

ADULT; ARTICLE; ATAXIA; CASE REPORT; DIARRHEA; DYSPHAGIA; FEMALE; GAIT DISORDER; GUILLAIN BARRE SYNDROME; HUMAN; HUMAN TISSUE; NEUROLOGIC EXAMINATION; POLYCRANIAL NEUROPATHY; POLYNEUROPATHY; PRIORITY JOURNAL; SENSORY ATAXIA; SENSORY DYSFUNCTION; SLURRED SPEECH; TREATMENT RESPONSE; VIBRATION SENSE;

ATAXIA; AUTOANTIBODIES; AUTOANTIGENS; CRANIAL NERVE DISEASES; ENZYME-LINKED IMMUNOSORBENT ASSAY; FEMALE; GANGLIOSIDES; GUILLAIN-BARRE SYNDROME; HUMANS; IMMUNOGLOBULIN G; MIDDLE AGED;

EID: 84875213128     PISSN: 09675868     EISSN: 15322653     Source Type: Journal    
DOI: 10.1016/j.jocn.2012.02.035     Document Type: Article

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