{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,18]],"date-time":"2026-08-18T01:37:15Z","timestamp":1787017035865,"version":"build-2736575974"},"reference-count":17,"publisher":"BMJ","issue":"5","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"published-print":{"date-parts":[[1994,5,1]]},"DOI":"10.1136\/jnnp.57.5.635","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T17:20:59Z","timestamp":1226337659000},"page":"635-637","source":"Crossref","is-referenced-by-count":17,"title":["Idiopathic AA amyloidosis manifested by autonomic neuropathy, vestibulocochleopathy, and lattice corneal dystrophy."],"prefix":"10.1136","volume":"57","author":[{"given":"I","family":"Tsunoda","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Awano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"H","family":"Kayama","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T","family":"Tsukamoto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S","family":"Ueno","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T","family":"Fujiwara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"M","family":"Watanabe","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T","family":"Yamamoto","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"432","article-title":"Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation","volume":"79","author":"Meretoja, J.; Teppo, L.","year":"1971","unstructured":"Meretoja J, Teppo L. Histopathological findings of familial amyloidosis with cranial neuropathy as principal manifestation. Acta Pathol Microbiol Scand[A] 1971;79: 432-40.","journal-title":"Acta Pathol Microbiol Scand[A]"},{"key":"ref_2","first-page":"314","article-title":"Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms","volume-title":"Clin Res 1969","volume":"1","author":"Meretoja, J.","unstructured":"Meretoja J. Familial systemic paramyloidosis with lattice dystrophy of the cornea, progressive cranial neuropathy, skin changes and various internal symptoms. Ann Clin Res 1969;1:314-24."},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"546","DOI":"10.1016\/S0002-9394(14)74728-2","article-title":"An immunohistochemical study of gelsolin immunoreactivity in corneal amyloidosis","volume":"113","author":"Loeffler, K.U.; Edward, D.P.; Tso, M.O.M.","year":"1992","unstructured":"Loeffler KU, Edward DP, Tso MOM. An immunohistochemical study of gelsolin immunoreactivity in corneal amyloidosis. Am J7 Ophthalmol 1992;113:546-54.","journal-title":"Am J7 Ophthalmol"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"1865","DOI":"10.1084\/jem.172.6.1865","article-title":"Mutation in gelsolin gene in Finnish hereditary amyloidosis","volume":"172","author":"Levy, E.; Haltia, M.; Fernandez-Madrid, I.","year":"1990","unstructured":"Levy E, Haltia M, Fernandez-Madrid I, et al. Mutation in gelsolin gene in Finnish hereditary amyloidosis. J Exp Med 1990;172:1865-7.","journal-title":"J Exp Med"},{"key":"ref_5","doi-asserted-by":"crossref","first-page":"75","DOI":"10.1016\/0014-5793(90)80510-P","article-title":"Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene","volume":"276","author":"Maury, C.P.J.; Kere, J.; Tolvanen, R.; de la Chapelle, A.","year":"1990","unstructured":"Maury CPJ, Kere J, Tolvanen R, de la Chapelle A. Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene. FEBS Lett 1990;276:75-7.","journal-title":"FEBS Lett"},{"key":"ref_6","first-page":"274","article-title":"Potassium permanganate reaction in amyloidosis. A histologic method to assist in differentiating forms of this disease","volume":"36","author":"Wright, JR, Calkins; E, Humphrey; R.L.","year":"1977","unstructured":"Wright JR, Calkins E, Humphrey RL. Potassium permanganate reaction in amyloidosis. A histologic method to assist in differentiating forms of this disease. Lab Invest 1977;36:274-8 1.","journal-title":"Lab Invest"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"291","DOI":"10.1016\/0002-9343(80)90369-1","article-title":"AA protein in a case of \"primary\" or \"idiopathic\" amyloidosis","volume":"68","author":"Pras, M.; Zaretzky, J.; Frangione, B.; Franklin, E.C.","year":"1980","unstructured":"Pras M, Zaretzky J, Frangione B, Franklin EC. AA protein in a case of \"primary\" or \"idiopathic\" amyloidosis. Am J Med 1980;68:291-4.","journal-title":"Am J Med"},{"key":"ref_8","first-page":"207","article-title":"Primary amyloidosis","volume":"27","author":"Chambers, R.A.; Medd, W.E.; Spencer, H.","year":"1958","unstructured":"Chambers RA, Medd WE, Spencer H. Primary amyloidosis. QJMed 1958;NS27:207-26.","journal-title":"QJMed"},{"key":"ref_9","first-page":"235","article-title":"and amyloidosis: A new heredo-familial syndrome","volume":"31","author":"Muckle, T.J.; Urticaria, Wells M.; deafness","year":"1962","unstructured":"Muckle TJ, Wells M. Urticaria, deafness, and amyloidosis: A new heredo-familial syndrome. Q J Med 1962; NS31:235-48.","journal-title":"Q J Med"},{"key":"ref_10","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1212\/WNL.19.1.10","article-title":"Inherited predisposition to generalized amyloidosis","volume":"19","author":"Van Allen MW, Frohlich JA, Davis JR","year":"1969","unstructured":"Van Allen MW, Frohlich JA, Davis JR. Inherited predisposition to generalized amyloidosis. Neurology 1969;19: 10-25.","journal-title":"Neurology"},{"key":"ref_11","first-page":"293","article-title":"Familial primary amyloidosis with vitreous opacities and gastrointestinal symptoms. Report of a case","volume":"14","author":"Okayama, M.; Goto, I.; Tanaka, T.; Omae, T.","year":"1974","unstructured":"Okayama M, Goto I, Tanaka T, Omae T. Familial primary amyloidosis with vitreous opacities and gastrointestinal symptoms. Report of a case. Rinsho Shinkeigaku 1974;14:293-9.","journal-title":"Rinsho Shinkeigaku"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1093\/brain\/103.3.473","article-title":"Familial oculoleptomeningeal amyloidosis","volume":"103","author":"Goren, H.; Steinberg, M.C.; Farboody, G.H.","year":"1980","unstructured":"Goren H, Steinberg MC, Farboody GH. Familial oculoleptomeningeal amyloidosis. Brain 1980;103:473-95.","journal-title":"Brain"},{"key":"ref_13","first-page":"1223","article-title":"Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin","volume":"136","author":"Haltia, M.; Ghiso, J.; Prelli, F.","year":"1990","unstructured":"Haltia M, Ghiso J, Prelli F, et al. Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolin. Am J Pathol 1990;136:1223-8.","journal-title":"Am J Pathol"},{"key":"ref_14","doi-asserted-by":"crossref","first-page":"85","DOI":"10.1016\/0014-5793(90)80072-Q","article-title":"Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline","volume":"260","author":"Maury, C.P.J.; Alli, K.; Baumann, M.","year":"1990","unstructured":"Maury CPJ, Alli K, Baumann M. Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline. FEBS Letn 1990;260:85-7.","journal-title":"FEBS Letn"},{"key":"ref_15","article-title":"IV (Leyden: Patuliet, 1745; 209). English translation. In: Classic descriptions of disease","author":"medicina Indorum, Bontius J.De; libr","unstructured":"Bontius J. De medicina Indorum, libr. IV (Leyden: Patuliet, 1745;209). English translation. In: Classic descriptions of disease, 3rd edn, Ralph H Major, ed. Oxford: Blackwell, 1945;605.","edition":"3rd edn"},{"issue":"286","key":"ref_16","volume":"1716","author":"medicae. Ch V, Tulp N.Observationes","unstructured":"Tulp N. Observationes medicae. Ch V. Leyden: Vivie, 1716;286.","journal-title":"Leyden: Vivie"},{"key":"ref_17","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1136\/jnnp.53.2.113","article-title":"Robert Graves and multiple neuritis","volume":"53","author":"Pearce, J.M.S.","year":"1990","unstructured":"Pearce JMS. Robert Graves and multiple neuritis. JT Neurol Neurosurg Psychiatry 1990;53: 113.","journal-title":"JT Neurol Neurosurg Psychiatry"}],"container-title":["Journal of Neurology, Neurosurgery & Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.57.5.635","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2020,9,25]],"date-time":"2020-09-25T22:46:54Z","timestamp":1601074014000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.57.5.635"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1994,5,1]]},"references-count":17,"journal-issue":{"issue":"5","published-print":{"date-parts":[[1994,5,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.57.5.635","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1994,5,1]]}}}