{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,3]],"date-time":"2025-11-03T09:05:53Z","timestamp":1762160753731},"reference-count":19,"publisher":"Springer Science and Business Media LLC","issue":"1-2","license":[{"start":{"date-parts":[[2009,1,1]],"date-time":"2009-01-01T00:00:00Z","timestamp":1230768000000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Wien Med Wochenschr"],"published-print":{"date-parts":[[2009,1]]},"DOI":"10.1007\/s10354-008-0584-1","type":"journal-article","created":{"date-parts":[[2009,2,18]],"date-time":"2009-02-18T15:44:42Z","timestamp":1234971882000},"page":"62-64","source":"Crossref","is-referenced-by-count":2,"title":["Akute Verhaltensst\u00f6rung bei einem Patienten mit Verdacht auf X-chromosomal heredit\u00e4ren Normaldruckhydrozephalus","Acute behaviour disorder in a patient with X-linked hydrocephalus with normal pressure"],"prefix":"10.1007","volume":"159","author":[{"given":"Horst J.","family":"Koch","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Deyan","family":"Nanev","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kay","family":"Becker","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"584_CR1","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1002\/ajmg.1320310228","volume":"31","author":"ST Ahmad","year":"1988","unstructured":"Ahmad ST, Kamal KN. Autosomal recessive nonsyndromal hydrocephalus. Am J Med Gen, 31: 467\u2013470, 1988","journal-title":"Am J Med Gen"},{"key":"584_CR2","doi-asserted-by":"crossref","first-page":"101","DOI":"10.1016\/S0022-510X(98)00097-5","volume":"158","author":"W Verhagen","year":"1998","unstructured":"Verhagen W, Bartels R, Fransen E, van Camp G, Renier WO, Grotenhuis WA. Familial congenital hydrocephalus and aqueduct stenosis with probably autosomal dominant inheritance and variable expression. J Neurol Sci, 158: 101\u2013105, 1998","journal-title":"J Neurol Sci"},{"key":"584_CR3","doi-asserted-by":"crossref","first-page":"246","DOI":"10.1093\/brain\/72.2.246","volume":"72","author":"DS Bickers","year":"1949","unstructured":"Bickers DS, Adams RD. Hereditary stenosis of the aqueduct of sylvius as a cause of congenital hydrocephalus. Brain, 72: 246\u2013262, 1949","journal-title":"Brain"},{"key":"584_CR4","doi-asserted-by":"crossref","first-page":"443","DOI":"10.1111\/j.1399-0004.1978.tb04143.x","volume":"13","author":"VM Riccardi","year":"1978","unstructured":"Riccardi VM, Marcus ES. Congenital hydrocephalus and cerebellar agenesis. Clin Genet, 13: 443\u2013447, 1978","journal-title":"Clin Genet"},{"key":"584_CR5","doi-asserted-by":"crossref","first-page":"637","DOI":"10.1111\/j.1469-8749.1979.tb01678.x","volume":"21","author":"P Landrieu","year":"1979","unstructured":"Landrieu P, Ninane J, Ferriere G, Lyon G. Aqueductal stenosis in X-linked hydrocephalus: a secondary phenomenon? Dev Med Child Neurol, 21: 637\u2013652, 1979","journal-title":"Dev Med Child Neurol"},{"key":"584_CR6","doi-asserted-by":"crossref","first-page":"252","DOI":"10.1136\/jmg.18.4.252","volume":"18","author":"FM Howard","year":"1981","unstructured":"Howard FM, Till K, Carter CO. A familial study of hydrocephalus resulting from aqueduct stenosis. J Med Gen, 18: 252\u2013255, 1981","journal-title":"J Med Gen"},{"key":"584_CR7","doi-asserted-by":"crossref","first-page":"486","DOI":"10.1136\/adc.36.189.486","volume":"36","author":"JH Edward","year":"1961","unstructured":"Edward JH. The syndrome of sex-linked hydrocephalus. Arch Dis Child, 36: 486\u2013493, 1961","journal-title":"Arch Dis Child"},{"key":"584_CR8","doi-asserted-by":"crossref","first-page":"260","DOI":"10.1212\/WNL.18.3.260","volume":"18","author":"MH Sajid","year":"1968","unstructured":"Sajid MH, Copple PJ. Familial aqueductal stenosis and basilar impression. Neurology, 18: 260\u2013262, 1968","journal-title":"Neurology"},{"key":"584_CR9","doi-asserted-by":"crossref","first-page":"697","DOI":"10.1542\/peds.51.4.697","volume":"51","author":"LB Holmes","year":"1973","unstructured":"Holmes LB, Nash A, ZuRhein GM, Levin M, Opitz JM. X-linked aqueductal stenosis: clinical and neuropathological findings in two families. Pediatrics, 51: 697\u2013704, 1973","journal-title":"Pediatrics"},{"key":"584_CR10","doi-asserted-by":"crossref","first-page":"921","DOI":"10.1002\/ajmg.1320270419","volume":"27","author":"P Willems","year":"1987","unstructured":"Willems P, Brouwer OF, Dijkstra I, Wilmink J. X-linked hydrocephalus. Am J Med Gen, 27: 921\u2013928, 1987","journal-title":"Am J Med Gen"},{"key":"584_CR11","doi-asserted-by":"crossref","first-page":"107","DOI":"10.1002\/ajmg.1320570122","volume":"57","author":"C Schrander-Stumpel","year":"1995","unstructured":"Schrander-Stumpel C, H\u00f6weler C, Jones M, Sommer A, Stevens C, Tinschert S, Israel J, Fryns JP. Spectrum of X-linked hydrocephalus (HSAS), MASA syndrome, and complicated spastic paraplegia (SPG1): clinical review with six additional families. Am J Med Gen, 57: 107\u2013116, 1995","journal-title":"Am J Med Gen"},{"key":"584_CR12","doi-asserted-by":"crossref","first-page":"273","DOI":"10.1159\/000472311","volume":"3","author":"E Fransen","year":"1995","unstructured":"Fransen E, Lemmon V, Camp G, Vits L, Couke P, Willems PJ. CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, hydrocephalus due to mutations in one single gene, L1. Eur Hum Genet, 3: 273\u2013284, 1995","journal-title":"Eur Hum Genet"},{"key":"584_CR13","doi-asserted-by":"crossref","first-page":"402","DOI":"10.1038\/ng0794-402","volume":"7","author":"M Jouet","year":"1994","unstructured":"Jouet M, Rosenthal A, Armstrong G, MacFarlane J, Stevenson R, Paterson J, Metzenberg A, Ionasescu V, Temple K, Kenwrick S. X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene. Nature Genet, 7: 402\u2013407, 1994","journal-title":"Nature Genet"},{"key":"584_CR14","doi-asserted-by":"crossref","first-page":"549","DOI":"10.1136\/jmg.32.7.549","volume":"32","author":"JC Ruiz","year":"1995","unstructured":"Ruiz JC, Cuppens H, Legius E, Fryns JP, Glover T, Marynen P, Cassiman JJ. Mutations in L1-CAM in two families with X-linked complicated spastic paraplegia, MASA syndrome, and HSAS. J Med Gen, 32: 549\u2013552, 1995","journal-title":"J Med Gen"},{"key":"584_CR15","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1002\/(SICI)1096-8628(19960712)64:1<73::AID-AJMG11>3.0.CO;2-P","volume":"64","author":"E Fransen","year":"1996","unstructured":"Fransen E, Vits L, Camp GV, Willems PJ. The clinical spectrum of mutations in L1, a neuronal cell adhesion molecule. Am J Med Gen, 64: 73\u201377, 1996","journal-title":"Am J Med Gen"},{"key":"584_CR16","doi-asserted-by":"crossref","first-page":"487","DOI":"10.1046\/j.1440-1819.2000.00740.x","volume":"54","author":"S Katsuragi","year":"2000","unstructured":"Katsuragi S, Teraoka K, Ikegami K, et al. Late onset X-linked hydrocephalus with normal cerebrospinal fluid pressure. Psychiat Clin Neurosci, 54: 487\u2013492, 2000","journal-title":"Psychiat Clin Neurosci"},{"key":"584_CR17","doi-asserted-by":"crossref","first-page":"586","DOI":"10.1002\/ajmg.1320510458","volume":"51","author":"SS Brooks","year":"1994","unstructured":"Brooks SS, Wisniewski K, Brown WT. New X-linked mental retardation (XLMR) syndrome with distinct facial appearance and growth retardation. Am J Med Gen, 51: 586\u2013590, 1994","journal-title":"Am J Med Gen"},{"key":"584_CR18","doi-asserted-by":"crossref","first-page":"103","DOI":"10.1007\/3-211-31221-8_4","volume-title":"Polypharmazie in der Behandlung psychischer Erkrankungen","author":"F H\u00e4ssler","year":"2006","unstructured":"H\u00e4ssler F. Polypharmazie in der Behandlung von Menschen mit geistiger Behinderung. In: Messer Th, Schmau\u00df M (Hrsg) Polypharmazie in der Behandlung psychischer Erkrankungen. Springer, Wien, pp 103\u2013120, 2006"},{"key":"584_CR19","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1016\/S0140-6736(08)60072-0","volume":"371","author":"P Tyrer","year":"2008","unstructured":"Tyrer P, Oliver-Africano PC, Ahmed Z, Bouras N, Cooray S, Deb S, Murphy D, Hare M, Meade M, Reece B, Kramp K, Bhaumi S, Harley D, Regan A, Thomas D, Rao B, North B, Eliahoo J, Karatela S, Soni A, Crawford M. Risperidone, haloperidole, and placebo in the treatment of aggressive challenging behaviour in patients with intellectual disability: a randomised controlled trial. Lancet, 371: 57\u201363, 2008","journal-title":"Lancet"}],"container-title":["Wiener Medizinische Wochenschrift"],"original-title":[],"language":"de","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10354-008-0584-1.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/s10354-008-0584-1\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/s10354-008-0584-1","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,5,24]],"date-time":"2023-05-24T02:28:50Z","timestamp":1684895330000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/s10354-008-0584-1"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2009,1]]},"references-count":19,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2009,1]]}},"alternative-id":["584"],"URL":"https:\/\/doi.org\/10.1007\/s10354-008-0584-1","relation":{},"ISSN":["0043-5341","1563-258X"],"issn-type":[{"value":"0043-5341","type":"print"},{"value":"1563-258X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2009,1]]}}}