{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2022,3,30]],"date-time":"2022-03-30T00:20:39Z","timestamp":1648599639010},"reference-count":7,"publisher":"BMJ","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"published-print":{"date-parts":[[1989,8,1]]},"DOI":"10.1136\/jnnp.52.8.1013","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T21:16:40Z","timestamp":1226351800000},"page":"1013-1014","source":"Crossref","is-referenced-by-count":0,"title":["CSF oligoclonal IgG bands in a patient with torsion dystonia."],"prefix":"10.1136","volume":"52","author":[{"given":"S J","family":"Wroe","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"P D","family":"Gills","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"R E","family":"Cull","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"141","article-title":"A rapid method for detecting oligoclonal IgG in unconcentrated CSF, by agarose isoelectric focusing, transfer to cellulose nitrate and immunoperoxidase small compound muscle action potential on the left. The left medial plantar sensory action potential (SAP) was absent; the right medial SAP was 0 7 gV ofamplitude (normal values: 0 1-3 5 pV),' with a sensory conducto arms and increasing disability with walking identify this as the syndrome termed dystonia musculorum deformans by Oppenheim and idiopathic generalised dystonia by later authors.4 Absence of ocular dysmobility, spasticity, ataxia, identifiable biostaining","author":"Walker, R.W.H.; Keir, G.; Johnson, M.H.; Thompson, E.J.","year":"1983","unstructured":"Walker RWH, Keir G, Johnson MH, Thompson EJ. A rapid method for detecting oligoclonal IgG in unconcentrated CSF, by agarose isoelectric focusing, transfer to cellulose nitrate and immunoperoxidase small compound muscle action potential on the left. The left medial plantar sensory action potential (SAP) was absent; the right medial SAP was 0 7 gV ofamplitude (normal values: 0 1-3 5 pV),' with a sensory conducto arms and increasing disability with walking identify this as the syndrome termed dystonia musculorum deformans by Oppenheim and idiopathic generalised dystonia by later authors.4 Absence of ocular dysmobility, spasticity, ataxia, identifiable biostaining. J Neuroimmunol 1983:141-8.","journal-title":"J Neuroimmunol"},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"1669","DOI":"10.1093\/clinchem\/33.9.1669","article-title":"Immunoblotting on polyvinyldifluoride improves detection of oligoclonal IgG bands in","volume":"33","author":"Nespolo, A.; Bianchi, G.; Salmaggi, A.; Cerrato, D.","year":"1987","unstructured":"Nespolo A, Bianchi G, Salmaggi A, Cerrato D. Immunoblotting on polyvinyldifluoride improves detection of oligoclonal IgG bands in CSF. Clin Chem 1987;33:1669.","journal-title":"CSF. Clin Chem"},{"key":"ref_3","first-page":"313","article-title":"The anatomical and physiological basis of torsion dystonia. In: tion velocity of42 m\/s (normal values: 36-50 m\/s).' The patient underwent surgery. A curved incision was made superior, posterior, and inferior to the medial malleolus. The neurovascular bundle was isolated just proximal to the tarsal tunnel, which was chemical abnormalities or structural brain Marsden CD","volume-title":"Disorentered by dividing the flexor retinaculum. A defects makes a diagnosis of secondary dysders 2","author":"Rothwell, J.C.; Obeso, J.A.","year":"1987","unstructured":"Rothwell JC, Obeso JA. The anatomical and physiological basis of torsion dystonia. In: tion velocity of42 m\/s (normal values: 36-50 m\/s).' The patient underwent surgery. A curved incision was made superior, posterior, and inferior to the medial malleolus. The neurovascular bundle was isolated just proximal to the tarsal tunnel, which was chemical abnormalities or structural brain Marsden CD, Fahn S, eds. Movement Disorentered by dividing the flexor retinaculum. A defects makes a diagnosis of secondary dysders 2. London: Butterworths, 1987:313-31. calcaneal branch, and the medial and lateral tonia unlikely. The presence of oligoclonal IgG bands in the CSF of patients with idiopathic torsion dystonia has not been reported previously. Kjellin and Stibler found increased cathodal protein fractions on isoelectric focusing of"},{"key":"ref_4","first-page":"332","article-title":"Classification and investigation of dystonia","volume":"2","author":"Fahn, S.; Marsden, C.D.; Caine, D.B.","year":"1987","unstructured":"Fahn S, Marsden CD, Caine DB. Classification and investigation of dystonia. In: Marsden CD, Fahn S, eds. Movement Disorders 2. London: Butterworths, 1987:332-58.","journal-title":"Movement Disorders"},{"key":"ref_5","article-title":"Protein pattern of cerebrospinal fluid in spasmodic torticollis","author":"Kjellin, K.G.; Stibler, H.","year":"1974","unstructured":"Kjellin KG, Stibler H. Protein pattern of cerebrospinal fluid in spasmodic torticollis. J Neurol Neurosurg Psychiatry 1974;37: plantar nerves were dissected free. Within the tarsal tunnel, the posterior tibial nerve showed an eccentric, translucent, rubbery, bean-sized swelling. The epineurium was incised longitudinally, and clear gelatinous material evacuated (fig). As the swelling","journal-title":"J Neurol Neurosurg Psychiatry; 37: plantar nerves were dissected free. Within the tarsal tunnel, the posterior tibial nerve showed an eccentric, translucent, rubbery, bean-sized swelling. The epineurium was incised longitudinally, and clear gelatinous material evacuated (fig"},{"key":"ref_6","first-page":"600","article-title":"Electrophoresis of CSF proteins","author":"Thompson, E.J.; Johnson, M.H.","year":"1982","unstructured":"Thompson EJ, Johnson MH. Electrophoresis of CSF proteins. Br J Hosp Med 1982:600-4.","journal-title":"Br J Hosp Med"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1093\/brain\/110.1.19","article-title":"Encephalitis lethargica. A report of four recent cases","volume":"110","author":"Howard, R.S.; Lees, A.J.","year":"1987","unstructured":"Howard RS, Lees AJ. Encephalitis lethargica. A report of four recent cases. 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