{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,13]],"date-time":"2026-03-13T01:31:09Z","timestamp":1773365469975,"version":"3.50.1"},"reference-count":23,"publisher":"Springer Science and Business Media LLC","issue":"3","license":[{"start":{"date-parts":[[1989,3,1]],"date-time":"1989-03-01T00:00:00Z","timestamp":604713600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/www.springer.com\/tdm"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Pediatr Radiol"],"published-print":{"date-parts":[[1989,3]]},"DOI":"10.1007\/bf02388642","type":"journal-article","created":{"date-parts":[[2006,4,10]],"date-time":"2006-04-10T04:39:27Z","timestamp":1144643967000},"page":"145-150","source":"Crossref","is-referenced-by-count":61,"title":["Septo-optic-dysplasia-schizencephaly"],"prefix":"10.1007","volume":"19","author":[{"given":"K. C. K.","family":"Kuban","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rita Littlewood","family":"Teele","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"Wallman","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"BF02388642_CR1","first-page":"61","volume":"69","author":"DL Reeves","year":"1941","unstructured":"Reeves DL (1941) Congenital absence of the septum pellucidum. A case diagnosed encephalographically and associated with congenital amaurosis. Bull John Hopkins Hosp 69: 61","journal-title":"Bull John Hopkins Hosp"},{"key":"BF02388642_CR2","first-page":"267","volume":"77","author":"G DeMorsier","year":"1956","unstructured":"DeMorsier G (1956) Etudes sur les Dysraphies Cranio-Encephaliques III. Agenesie du Septum Lucidum avec Malformation du Tractus Optique. La Dysplacic Septo-optique. Schweiz Arch Neurol Psychiat 77: 267","journal-title":"Schweiz Arch Neurol Psychiat"},{"key":"BF02388642_CR3","first-page":"425","volume":"79","author":"TE Acers","year":"1981","unstructured":"Acers TE (1981) Optic nerve hypoplasia: septo-optic-pituitary dysplasia syndrome. Trans Am Ophthalmol Soc 79: 425","journal-title":"Trans Am Ophthalmol Soc"},{"key":"BF02388642_CR4","doi-asserted-by":"crossref","first-page":"319","DOI":"10.1055\/s-2008-1059664","volume":"12","author":"J Aicardi","year":"1981","unstructured":"Aicardi J, Goutieres F (1981) The syndrome of absence of the septum pellucidum with porencephalies and other developmental defects. Neuropediatrics 12: 319","journal-title":"Neuropediatrics"},{"key":"BF02388642_CR5","first-page":"249","volume":"139","author":"G Costin","year":"1985","unstructured":"Costin G, Morphree AL (1985) Hypothalamic-pituitary function in children with optic nerve hypoplasia. AJDC 139: 249","journal-title":"AJDC"},{"key":"BF02388642_CR6","doi-asserted-by":"crossref","first-page":"893","DOI":"10.1016\/S0140-6736(70)91717-4","volume":"I","author":"WF Hoyt","year":"1970","unstructured":"Hoyt WF, Kaplan SL, Grumbach MM, Glaser JS (1970) Septo-optic dysplasia and pituitary dwarfism. Lancet I: 893","journal-title":"Lancet"},{"key":"BF02388642_CR7","doi-asserted-by":"crossref","first-page":"1157","DOI":"10.2214\/ajr.133.6.1157","volume":"133","author":"C Manelfe","year":"1979","unstructured":"Manelfe C, Rochiccioli P (1979) CT of septo-optic dysplasia. AJR 133: 1157","journal-title":"AJR"},{"key":"BF02388642_CR8","doi-asserted-by":"crossref","first-page":"311","DOI":"10.1111\/j.1469-8749.1984.tb04447.x","volume":"26","author":"D Margalith","year":"1984","unstructured":"Margalith D, Jan JE, McCormick AQ, Tze WJ, Lapointe J (1984) Clinical spectum of congenital optic nerve hypoplasia: review of 51 patients. Dev Med Child Neurol 26: 311","journal-title":"Dev Med Child Neurol"},{"key":"BF02388642_CR9","first-page":"361","volume":"139","author":"D Margalith","year":"1985","unstructured":"Margalith D, Tze WJ, Jan JE (1985) Congenital optic nerve hypoplasia with hypothalamic-pituitary dysplasia: a review of 16 cases. AJDC 139: 361","journal-title":"AJDC"},{"key":"BF02388642_CR10","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1001\/archneur.1985.04210090033010","volume":"42","author":"SA Morgan","year":"1985","unstructured":"Morgan SA, Emsellem HA, Sandler JR (1985) Absence of the septum pellucidum overlapping clinical syndromes. Arch Neurol 42: 769","journal-title":"Arch Neurol"},{"key":"BF02388642_CR11","first-page":"175","volume":"129","author":"H Patel","year":"1975","unstructured":"Patel H, Tze WH, Crichton JU, McCormick AQ, Robinson GC, Dolman CL (1975) Optic nerve hypoplasia with hypoplasia with hypopituitarism. ADJC 129: 175","journal-title":"ADJC"},{"key":"BF02388642_CR12","first-page":"552","volume":"24","author":"L Aubert","year":"1963","unstructured":"Aubert L, Detolle P, Armand P, Reboul O, Faure J, Bruno M (1963) Panhypopituitarisme avec tetanie et agenesie du septum lucidum. Annales D'Endocrinologie 24: 552","journal-title":"Annales D'Endocrinologie"},{"key":"BF02388642_CR13","volume-title":"Agenesis septi pellucidi, cavum septi Pellucidi, Cavum Vergae, and Cavum Veli Interpositi: Hamdbook of clinical neurology, vol 30, chapter 13","author":"GW Bruyn","year":"1977","unstructured":"Bruyn GW (1977) Agenesis septi pellucidi, cavum septi Pellucidi, Cavum Vergae, and Cavum Veli Interpositi: Hamdbook of clinical neurology, vol 30, chapter 13. North-Holland Publishing, Amsterdam"},{"key":"BF02388642_CR14","doi-asserted-by":"crossref","first-page":"391","DOI":"10.1111\/j.1469-8749.1984.tb04459.x","volume":"26","author":"P Griffiths","year":"1984","unstructured":"Griffiths P, Hunt S (1984) Specific spatial defect in a child with septo-optic dysplasia. Dev Med Child Neurol 26: 391","journal-title":"Dev Med Child Neurol"},{"key":"BF02388642_CR15","doi-asserted-by":"crossref","first-page":"960","DOI":"10.1016\/0002-9394(70)92475-X","volume":"70","author":"C Ellenberger","year":"1970","unstructured":"Ellenberger C, Runyan TE (1970) Holoprosencephaly with hypoplasia of the optic nerves, dwarfism, and agenesis of the septum pelluicidum. Am J Ophthalmol 70: 960","journal-title":"Am J Ophthalmol"},{"key":"BF02388642_CR16","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1002\/cne.901320103","volume":"132","author":"P Rakic","year":"1968","unstructured":"Rakic P, Yakovlev PI (1968) Development of the corpus callosum and cavum septi in man. J Comp Neurol 132: 45","journal-title":"J Comp Neurol"},{"key":"BF02388642_CR17","doi-asserted-by":"crossref","first-page":"3","DOI":"10.1177\/088307388600100102","volume":"1","author":"RW Leech","year":"1986","unstructured":"Leech RW, Shuman RM (1986) Holoprosencephaly and related midline cerebral anomalies: a review. J Child Neurol 1: 3","journal-title":"J Child Neurol"},{"key":"BF02388642_CR18","doi-asserted-by":"crossref","first-page":"265","DOI":"10.7863\/jum.1985.4.5.265","volume":"4","author":"JL Williams","year":"1985","unstructured":"Williams JL, Faerber EN (1985) Septo-optic dysplasia (de morsier syndrome). J Ultrasound Med 4: 265","journal-title":"J Ultrasound Med"},{"key":"BF02388642_CR19","doi-asserted-by":"crossref","first-page":"997","DOI":"10.1212\/WNL.34.8.997","volume":"34","author":"GM Miller","year":"1984","unstructured":"Miller GM, Stears JC, Guggenheim MA, Wilkening GN (1984) Schizencephaly: a clinical and CT study. Neurology 34: 997","journal-title":"Neurology"},{"key":"BF02388642_CR20","first-page":"89","volume-title":"Human neuroanatomy","author":"RC Truex","year":"1969","unstructured":"Truex RC, Carpenter MB (1969) Human neuroanatomy. Williams and Wilkins, Baltimore, p 89"},{"key":"BF02388642_CR21","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1097\/00005072-194604000-00003","volume":"5","author":"PI Yakovlev","year":"1946","unstructured":"Yakovlev PI, Wadsworth RC (1946) Schizencephalies: a study of the congenital clefts in the cerebral mantle. J Neuropathol Exp Neurol 5: 116, 169","journal-title":"J Neuropathol Exp Neurol"},{"key":"BF02388642_CR22","first-page":"196","volume":"5","author":"MA DiPietro","year":"1984","unstructured":"DiPietro MA, Brody BA, Kuban K, Cole FS (1984) Schizencephaly: rare cerebral malformation demonstrated by sonography. AJNR 5: 196","journal-title":"AJNR"},{"key":"BF02388642_CR23","first-page":"466","volume-title":"Recognizable patterns of human malformation: genetic, embryologic and clinical aspects","author":"DW Smith","year":"1982","unstructured":"Smith DW, Jones KL (1982) Recognizable patterns of human malformation: genetic, embryologic and clinical aspects. Saunders, Philadelphia, p 466"}],"container-title":["Pediatric Radiology"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02388642.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/article\/10.1007\/BF02388642\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"http:\/\/link.springer.com\/content\/pdf\/10.1007\/BF02388642","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,17]],"date-time":"2019-05-17T11:58:40Z","timestamp":1558094320000},"score":1,"resource":{"primary":{"URL":"http:\/\/link.springer.com\/10.1007\/BF02388642"}},"subtitle":["Radiographic and clinical features"],"short-title":[],"issued":{"date-parts":[[1989,3]]},"references-count":23,"journal-issue":{"issue":"3","published-print":{"date-parts":[[1989,3]]}},"alternative-id":["BF02388642"],"URL":"https:\/\/doi.org\/10.1007\/bf02388642","relation":{},"ISSN":["0301-0449","1432-1998"],"issn-type":[{"value":"0301-0449","type":"print"},{"value":"1432-1998","type":"electronic"}],"subject":[],"published":{"date-parts":[[1989,3]]}}}