{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,26]],"date-time":"2026-01-26T19:38:49Z","timestamp":1769456329996,"version":"3.49.0"},"reference-count":14,"publisher":"Springer Science and Business Media LLC","issue":"10","license":[{"start":{"date-parts":[[2004,10,1]],"date-time":"2004-10-01T00:00:00Z","timestamp":1096588800000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["J Neurol"],"published-print":{"date-parts":[[2004,10]]},"DOI":"10.1007\/s00415-004-0562-5","type":"journal-article","created":{"date-parts":[[2004,10,20]],"date-time":"2004-10-20T07:03:17Z","timestamp":1098255797000},"page":"1285-1287","source":"Crossref","is-referenced-by-count":14,"title":["Complicated hereditary spastic paraplegia with thin corpus callosum: Variation of phenotypic expression over time"],"prefix":"10.1007","volume":"251","author":[{"given":"Anne-D\ufffdrte","family":"Sperfeld","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Jan","family":"Kassubek","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Andrew H.","family":"Crosby","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Beate","family":"Winner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Albert C.","family":"Ludolph","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Ingo","family":"Uttner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C. Oliver","family":"Hanemann","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"CR1","doi-asserted-by":"crossref","first-page":"262","DOI":"10.1212\/WNL.62.2.262","volume":"62","author":"Casali","year":"2004","unstructured":"Casali C, Valente EM, Bertini E, et al. (2004) Clinical and genetic studies in hereditary spastic paraplegia with thin corpus callosum. Neurology 62:262?268","journal-title":"Neurology"},{"key":"CR2","doi-asserted-by":"crossref","first-page":"943","DOI":"10.1001\/archneur.56.8.943","volume":"56","author":"Coutinho","year":"1999","unstructured":"Coutinho P, Barros J, Zemmouri R, et al. (1999) Clinical heterogeneity of autosomal recessive spastic paraplegias. Arch Neurol 56:943?949","journal-title":"Arch Neurol"},{"key":"CR3","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1002\/ana.77777","volume":"54","author":"Dupre","year":"2003","unstructured":"Dupre N, Howard HC, Mathieu J, et al. (2003) Hereditary motor and sensory neuropathy with agenesis of the corpus callosum. Ann Neurol 54:9?18","journal-title":"Ann Neurol"},{"key":"CR4","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1016\/S0303-8467(96)00596-3","volume":"99","author":"Farah","year":"1997","unstructured":"Farah S, Sabry MA, Al-Shubaili AFK, et al. (1997) Hereditary spastic paraparesis with distal muscle wasting, microcephaly, mental retardation, arachnodactyly and tremors: new entity? Clin Neurol Neurosurg 99:66?70","journal-title":"Clin Neurol Neurosurg"},{"key":"CR5","doi-asserted-by":"crossref","first-page":"669","DOI":"10.1002\/ana.10258","volume":"51","author":"Fink","year":"2002","unstructured":"Fink JK (2002) Hereditary spastic paraplegia: the pace quickens. Ann Neurol 51:669?672","journal-title":"Ann Neurol"},{"key":"CR6","doi-asserted-by":"crossref","first-page":"1045","DOI":"10.1001\/archneur.60.8.1045","volume":"60","author":"Fink","year":"2003","unstructured":"Fink JK (2003) The Hereditary Spastic Paraplegias. Arch Neurol 60:1045?1049","journal-title":"Arch Neurol"},{"key":"CR7","unstructured":"Harding AE (1990) The hereditary ataxias and paraplegias. In: Emery AEH, Rimoin DL (eds) Principles and Practice of Medical Genetics. London: Churchill Livingstone, pp 383?396"},{"key":"CR8","first-page":"1","volume":"234","author":"Kantarci","year":"2003","unstructured":"Kantarci M, Ertas U, Alper F, et al. (2003) Gorlin?s syndrome with a thin copus callosum and a third ventricular cyst. Diagn Neuroradiol 234:1?5","journal-title":"Diagn Neuroradiol"},{"key":"CR9","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1016\/0022-510X(95)00349-7","volume":"137","author":"Kobayashi","year":"1996","unstructured":"Kobayashi H, Garcia CA, Alfonso G, et al. (1996) Molecular genetics of familial spastic paraplegia: a multitude of responsible genes. J Neurol Sci 137:131?138","journal-title":"J Neurol Sci"},{"key":"CR10","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1136\/jnnp.69.2.150","volume":"69","author":"McDermott","year":"2000","unstructured":"McDermott CJ, White K, Bushby K, et al. (2000) Hereditary spastic paraparesis: a review of new developments. J Neurol Neurosurg Psychiatry 69:150?160","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"CR11","doi-asserted-by":"crossref","first-page":"35","DOI":"10.1016\/0022-510X(95)00028-Z","volume":"131","author":"Nakamura","year":"1995","unstructured":"Nakamura A, Izumi K, Umehara F, et al. (1995) Familial spastic paraplegia with mental impairment and thin corpus callosum. J Neurol Sci 131:35?42","journal-title":"J Neurol Sci"},{"key":"CR12","doi-asserted-by":"crossref","first-page":"347","DOI":"10.1038\/ng937","volume":"31","author":"Patel","year":"2002","unstructured":"Patel H, Cross H, Proukakis C, et al. (2002) SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia. Nature Genetics 31:347?348","journal-title":"Nature Genetics"},{"key":"CR13","doi-asserted-by":"crossref","first-page":"1147","DOI":"10.1086\/379522","volume":"73","author":"Simpson","year":"2003","unstructured":"Simpson MA, Cross H, Proukakis C, et al. (2003) Maspardin is mutated in MAST syndrome, a complicated form of hereditary spastic paraplegia associated with dementia. Am J Hum Genet 73:1147?1156","journal-title":"Am J Hum Genet"},{"key":"CR14","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1001\/archneur.61.1.117","volume":"61","author":"Winner","year":"2004","unstructured":"Winner B, Uyanik G, Gross C, et al. (2004) Clinical progression and genetic analysis in hereditary spastic paraplegia with thin corpus callosum in spastic gait gene 11 (SPG11). Arch Neurol 61:117?121","journal-title":"Arch Neurol"}],"container-title":["Journal of Neurology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-004-0562-5.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s00415-004-0562-5\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-004-0562-5","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,28]],"date-time":"2019-05-28T15:03:51Z","timestamp":1559055831000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s00415-004-0562-5"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2004,10]]},"references-count":14,"journal-issue":{"issue":"10","published-print":{"date-parts":[[2004,10]]}},"alternative-id":["562"],"URL":"https:\/\/doi.org\/10.1007\/s00415-004-0562-5","relation":{},"ISSN":["0340-5354","1432-1459"],"issn-type":[{"value":"0340-5354","type":"print"},{"value":"1432-1459","type":"electronic"}],"subject":[],"published":{"date-parts":[[2004,10]]}}}