{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T23:32:51Z","timestamp":1791329571522,"version":"4.3.1"},"reference-count":46,"publisher":"BMJ","issue":"8","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"published-print":{"date-parts":[[1994,8,1]]},"DOI":"10.1136\/jnnp.57.8.914","type":"journal-article","created":{"date-parts":[[2008,11,10]],"date-time":"2008-11-10T17:20:59Z","timestamp":1226337659000},"page":"914-920","source":"Crossref","is-referenced-by-count":87,"title":["Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant gene."],"prefix":"10.1136","volume":"57","author":[{"given":"J M","family":"Pinard","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"J","family":"Motte","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"C","family":"Chiron","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"R","family":"Brian","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"E","family":"Andermann","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"O","family":"Dulac","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"239","reference":[{"key":"ref_1","first-page":"96","article-title":"Congenital malformations of the brain. In: Contemporary neuroimaging. Pediatric neuroimaging","volume":"1","author":"Barkovich, A.J.","year":"1990","unstructured":"Barkovich AJ (ed.). Congenital malformations of the brain. In: Contemporary neuroimaging. Pediatric neuroimaging. Raven Press: New York, 1990;Vol 1;96-121."},{"key":"ref_2","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1148\/radiology.171.2.2468173","article-title":"Band heterotopias: a newly recognized neuronal migration anomaly","volume":"171","author":"Barkovich, A.J.; Jackson, D.E.; Boyer, R.S.","year":"1989","unstructured":"Barkovich AJ, Jackson DE, Boyer RS. Band heterotopias: a newly recognized neuronal migration anomaly. Radiology 1989;171:455-8.","journal-title":"Radiology"},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"430","DOI":"10.1001\/archneur.1989.00520400090025","article-title":"Generalized cortical dysplasia manifested by diffusely thick cerebral cortex","volume":"46","author":"Marchal, G.; Andermann, F.; Tampieri, D.","year":"1989","unstructured":"Marchal G, Andermann F, Tampieri D, et al. Generalized cortical dysplasia manifested by diffusely thick cerebral cortex. Arch Neurol 1989;46:430-4.","journal-title":"Arch Neurol"},{"key":"ref_4","doi-asserted-by":"crossref","first-page":"617","DOI":"10.1136\/jnnp.53.7.617","article-title":"Unusual MRI appearance of diffuse subcortical heterotopia or \"double cortex\"","volume":"53","author":"Livingston, J.H.; Aicardi, J.","year":"1990","unstructured":"Livingston JH, Aicardi J. Unusual MRI appearance of diffuse subcortical heterotopia or \"double cortex\" in two children. J Neurol Neurosurg Psychiatry 1990;53:617-20.","journal-title":"in two children. J Neurol Neurosurg Psychiatry"},{"key":"ref_5","first-page":"27","article-title":"Dulac 0 (eds.). Malformations du cortex cerebral","author":"Diebler, C.","year":"1990","unstructured":"Diebler C, Dulac 0 (eds.). Malformations du cortex cerebral. In: Neuroradiologie, neuropediatrie, SpringerVerlag: Paris, 1990, 27-33."},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"552","DOI":"10.1016\/S0022-3476(83)80183-8","article-title":"Miller-Dieker syndrome: lissencephaly and monosomy 17p","volume":"102","author":"Dobyns, W.B.; Stratton, R.F.; Parke, J.T.","year":"1983","unstructured":"Dobyns WB, Stratton RF, Parke JT, et al. Miller-Dieker syndrome: lissencephaly and monosomy 17p. J Pediatr 1983;102:552-8.","journal-title":"J Pediatr"},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1007\/BF00696881","article-title":"Lissencephaly and pachygyria. An architectonic and topographical analysis","volume":"31","author":"Stewart, R.M.; Richman, D.P.; Caviness, V.S.","year":"1975","unstructured":"Stewart RM, Richman DP, Caviness VS. Lissencephaly and pachygyria. An architectonic and topographical analysis. Acta Neuropathol (Berl) 1975;31:1-12.","journal-title":"Acta Neuropathol (Berl)"},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"40","DOI":"10.1016\/0022-510X(64)90053-X","article-title":"Forme familiale d'hypertelorisme avec lissencephalie se presentant cliniquement sous forme d'une arrieration mentale avec epilepsie et paraplegie spasmodique","volume":"1","author":"Reznik, M.; Alberca-Serrano, R.","year":"1964","unstructured":"Reznik M, Alberca-Serrano R. Forme familiale d'hypertelorisme avec lissencephalie se presentant cliniquement sous forme d'une arrieration mentale avec epilepsie et paraplegie spasmodique. JNeurol Sci 1964;1:40-58.","journal-title":"JNeurol Sci"},{"key":"ref_9","first-page":"555","article-title":"Turricephalie hereditaire, microcephalie familiale avec lissencephalie. Rapport de ce syndrome malformatif avec les dysraphies cerebromedullaires","volume":"1","author":"Alberca-Serrano, R.; Reznik, M.","year":"1964","unstructured":"Alberca-Serrano R, Reznik M. Turricephalie hereditaire, microcephalie familiale avec lissencephalie. Rapport de ce syndrome malformatif avec les dysraphies cerebromedullaires. 7 Neurol Sci 1964;1:555-77.","journal-title":"7 Neurol Sci"},{"issue":"25","key":"ref_10","first-page":"124","article-title":"Ein Fall von Heterotopie der grauen Substanz in den beiden Hemispharen des Grosshims","volume":"1893","author":"Matell, M.","unstructured":"Matell M. Ein Fall von Heterotopie der grauen Substanz in den beiden Hemispharen des Grosshims. Arch Psychiat Nervenkr 1893;25: 124-36.","journal-title":"Arch Psychiat Nervenkr"},{"key":"ref_11","doi-asserted-by":"crossref","first-page":"1656","DOI":"10.1212\/WNL.41.10.1656","article-title":"Diffuse cortical dysplasia, or the \"double cortex\" syndrome: the clinical and epileptic spectrum in 10 patients","volume":"41","author":"Palmini, A.; Andermann, F.; Aicardi, J.","year":"1991","unstructured":"Palmini A, Andermann F, Aicardi J, et al. Diffuse cortical dysplasia, or the \"double cortex\" syndrome: the clinical and epileptic spectrum in 10 patients. Neurology 1991;41: 1656-62.","journal-title":"Neurology"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"61","DOI":"10.1001\/archneur.1992.00530250065017","article-title":"Double cortex: a neuronal migration anomaly as a possible cause of LennoxGastaut syndrome","volume":"49","author":"Ricci, S.; Cusmai, R.; Fariello, G.","year":"1992","unstructured":"Ricci S, Cusmai R, Fariello G, et al. Double cortex: a neuronal migration anomaly as a possible cause of LennoxGastaut syndrome. Arch Neurol 1992;49:61-4.","journal-title":"Arch Neurol"},{"key":"ref_13","doi-asserted-by":"crossref","first-page":"218","DOI":"10.1055\/s-2008-1071501","article-title":"Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings","volume":"21","author":"Harbord, M.G.; Boyd, S.; Hall-Craggs, M.A.","year":"1990","unstructured":"Harbord MG, Boyd S, Hall-Craggs MA, et al. Ataxia, developmental delay and an extensive neuronal migration abnormality in 2 siblings. Neuropediatrics 1990;21: 218-21.","journal-title":"Neuropediatrics"},{"key":"ref_14","first-page":"224","volume":"178","author":"Weist, W.D.; in Groj, Hallervorden J.Migrationshemmung; und Kleinhirn. Dtsch Z Nervenheilk","year":"1958","unstructured":"Weist WD, Hallervorden J. Migrationshemmung in Groj, und Kleinhirn. Dtsch Z Nervenheilk 1958;178:224-38."},{"key":"ref_15","first-page":"280","article-title":"Friede RL (ed.). Dysplasia of cerebral hemispheric organization. In: Developmental neuropathology","year":"1975","unstructured":"Friede RL (ed.). Dysplasia of cerebral hemispheric organization. In: Developmental neuropathology. New York: Springer-Verlag, 1975:280-313."},{"issue":"155","key":"ref_16","first-page":"1","article-title":"Faktoren bei der Entstehung der normalen und der entwiicklungsgestorten Hirnrinde","volume":"1936","author":"Jacob, H.","unstructured":"Jacob H. Faktoren bei der Entstehung der normalen und der entwiicklungsgestorten Hirnrinde. Z Ges Neurol Psychiat 1936;155:1-39.","journal-title":"Z Ges Neurol Psychiat"},{"issue":"160","key":"ref_17","first-page":"615","article-title":"Genetisch verschiedene Gruppen entwicklungsgestorter Gehirne","volume":"1938","author":"Jacob, H.","unstructured":"Jacob H. Genetisch verschiedene Gruppen entwicklungsgestorter Gehirne. Z Ges Neurol Psychiat 1938;160: 615-48.","journal-title":"Z Ges Neurol Psychiat"},{"key":"ref_18","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1212\/WNL.16.2_Part_1.179","article-title":"Lissencephaly: two cases","volume":"2","author":"Daube, JR, Chou; S.M.","year":"1966","unstructured":"Daube JR, Chou SM. Lissencephaly: two cases. Neurology 1966;2:179-91.","journal-title":"Neurology"},{"key":"ref_19","first-page":"53","article-title":"The lissencephaly syndrome. Birth defects: original articles series 1969; 2","author":"Dieker, H.; Edwards, R.H.; Zurhein, G.","unstructured":"Dieker H, Edwards RH, Zurhein G, et al. The lissencephaly syndrome. Birth defects: original articles series 1969;2:53-64."},{"key":"ref_20","doi-asserted-by":"crossref","first-page":"335","DOI":"10.1002\/path.1700710208","volume":"71","author":"Pachygyria, Crome L.","year":"1956","unstructured":"Crome L. Pachygyria. J Pathol Bacteriol 1956;71:335-52.","journal-title":"J Pathol Bacteriol"},{"key":"ref_21","doi-asserted-by":"crossref","first-page":"841","DOI":"10.1212\/WNL.13.10.841","article-title":"Lissencephaly in 2 siblings","volume":"13","author":"Miller, J.Q.","year":"1963","unstructured":"Miller JQ. Lissencephaly in 2 siblings. Neurology 1963; 13:841-50.","journal-title":"Neurology"},{"key":"ref_22","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1007\/BF00273000","article-title":"New chromosomal syndrome: Miller-Dieker syndrome and monosomy l7p13 Am","volume":"67","author":"Stratton, R.F.; Dobyns, W.B.; Airhart, S.D.; Ledbetter, D.H.","year":"1984","unstructured":"Stratton RF, Dobyns WB, Airhart SD, Ledbetter DH. New chromosomal syndrome: Miller-Dieker syndrome and monosomy l7p13 Am J Hum Genet 1984;67: 193-200.","journal-title":"J Hum Genet"},{"key":"ref_23","first-page":"587","article-title":"Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome","volume":"43","author":"Vantuinen, P.; Dobyns, W.B.; Rich, D.C.","year":"1988","unstructured":"Vantuinen P, Dobyns WB, Rich DC, et al. Molecular detection of microscopic and submicroscopic deletions associated with Miller-Dieker syndrome. Am J Hum Genet 1988;43:587-96.","journal-title":"Am J Hum Genet"},{"key":"ref_24","first-page":"597","article-title":"Detection of submicroscopic deletions in Band 17p 13 in patients with the Miller-Dieker syndrome","volume":"43","author":"Schwartz, C.E.; Johnson, J.P.; Holycross, B.","year":"1988","unstructured":"Schwartz CE, Johnson JP, Holycross B, et al. Detection of submicroscopic deletions in Band 17p 13 in patients with the Miller-Dieker syndrome. Am J Hum Genet 1988; 43:597-604.","journal-title":"Am J Hum Genet"},{"key":"ref_25","doi-asserted-by":"crossref","first-page":"509","DOI":"10.1002\/ajmg.1320180320","article-title":"Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly","volume":"18","author":"Dobyns, W.B.; Stratton, R.F.; Greenberg, F.","year":"1984","unstructured":"Dobyns WB, Stratton RF, Greenberg F. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. Am J Med Genet 1984;18:509-26.","journal-title":"Am J Med Genet"},{"issue":"197-21","key":"ref_26","first-page":"1","article-title":"Letter to the Editor: further comments on the lissencephaly syndromes","volume":"22","author":"Dobyns, W.B.; Gilbert, E.F.; Opitz, J.M.","year":"1985","unstructured":"Dobyns WB, Gilbert EF, Opitz JM. Letter to the Editor: further comments on the lissencephaly syndromes. Am J Med Genet 1985;22:197-21 1.","journal-title":"Am J Med Genet"},{"key":"ref_27","first-page":"11","article-title":"Microdeletions of 17pl3 in Miller-Dieker syndrome and isolated lissencephaly sequence","volume":"49","author":"Ledbetter, D.H.","year":"1991","unstructured":"Ledbetter DH. Microdeletions of 17pl3 in Miller-Dieker syndrome and isolated lissencephaly sequence. Am J Hum Genet 1991;49(supp):11.","journal-title":"Am J Hum Genet"},{"key":"ref_28","first-page":"46","article-title":"Causal heterogeneity in isolated lissencephaly sequence. Am_7 Hum Genet","volume":"49","author":"Dobyns, W.B.; Ledbetter, D.H.","year":"1991","unstructured":"Dobyns WB, Ledbetter DH. Causal heterogeneity in isolated lissencephaly sequence. Am_7 Hum Genet 1991; 49(supp):46."},{"key":"ref_29","first-page":"225","article-title":"Developmental aspects of lissencephaly and the lissencephaly syndromes. Birth Defects: original articles series","volume":"23","author":"Dobyns, W.B.","year":"1987","unstructured":"Dobyns WB. Developmental aspects of lissencephaly and the lissencephaly syndromes. Birth Defects: original articles series 1987;23:225-41."},{"key":"ref_30","doi-asserted-by":"crossref","first-page":"707","DOI":"10.1111\/j.1469-8749.1990.tb08431.x","article-title":"Diagnostic features and clinical signs of 21 patients with lissencephaly type","volume":"32","author":"JF, Dekijk-Van Andel; WF, Arts; PG, Barth; MC, Loonen","year":"1990","unstructured":"Dekijk-Van Andel JF, Arts WF, Barth PG, Loonen MC. Diagnostic features and clinical signs of 21 patients with lissencephaly type I. Dev Med Child Neurol 1990;32: 707-17.","journal-title":"I. Dev Med Child Neurol"},{"key":"ref_31","first-page":"970","article-title":"Hypertelorisme et lissencephalie. Etude d'une forme familiale (Famille Ma...)","volume":"63","author":"Reznik, M.; Alberca, R.S.","year":"1963","unstructured":"Reznik M, Alberca RS. Hypertelorisme et lissencephalie. Etude d'une forme familiale (Famille Ma...). Acta Neurol Belg 1963;63:970-3.","journal-title":"Acta Neurol Belg"},{"key":"ref_32","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1111\/j.1469-8749.1993.tb11645.x","article-title":"Stages and patterns of centrifugal arrest in diffuse neuronal migration disorders","volume":"35","author":"Palmini, A.; Andermann, F.; de Grissac, H.","year":"1993","unstructured":"Palmini A, Andermann F, de Grissac H, et al. Stages and patterns of centrifugal arrest in diffuse neuronal migration disorders. Dev Med Child Neurol 1993;35: 331-9.","journal-title":"Dev Med Child Neurol"},{"key":"ref_33","first-page":"222","article-title":"Vitamine D-resistant ricketts. Analysis of twenty-four pedigrees with hereditary and sporadic cases","volume":"36","author":"Burnett, C.H.; Dent, C.E.; Harper, C.; Warland, B.J.","year":"1964","unstructured":"Burnett CH, Dent CE, Harper C, Warland BJ. Vitamine D-resistant ricketts. Analysis of twenty-four pedigrees with hereditary and sporadic cases. Ani. Med 1964;36: 222-32.","journal-title":"Ani. Med"},{"key":"ref_34","doi-asserted-by":"crossref","first-page":"1073","DOI":"10.1056\/NEJM196411192712101","article-title":"Studies of a family with oral-facial-digital syndrome","volume":"271","author":"Doege, T.C.; Thuline, H.C.; Priest, J.H.","year":"1964","unstructured":"Doege TC, Thuline HC, Priest JH. Studies of a family with oral-facial-digital syndrome. N Engl Med 1964; 271:1073-80.","journal-title":"N Engl Med"},{"key":"ref_35","doi-asserted-by":"crossref","first-page":"582","DOI":"10.1001\/archneur.1989.00520410118036","article-title":"Familial aplasia of the cerebellar vermis: possible X-linked dominant inheritance","volume":"46","author":"Fenichel, G.M.; Phillips, J.A.","year":"1989","unstructured":"Fenichel GM, Phillips JA. Familial aplasia of the cerebellar vermis: possible X-linked dominant inheritance. Arch Neurol 1989;46:582-3.","journal-title":"Arch Neurol"},{"key":"ref_36","article-title":"The gene for incontinentia pigmenti is assigned to Xq 28","author":"Stefani, A.; Abel, L.; Hevertz, S.","year":"1994","unstructured":"Stefani A, Abel L, Hevertz S, et al. The gene for incontinentia pigmenti is assigned to Xq 28. Genoniics 1994 (in press).","journal-title":"Genoniics"},{"key":"ref_37","doi-asserted-by":"crossref","first-page":"176","DOI":"10.7326\/0003-4819-88-2-176","article-title":"Hereditary nephritis: a re-examination of its clinical and genetic features","volume":"88","author":"O'Neill, W.M.; Atkins, C.L.; Bloomer, H.A.","year":"1978","unstructured":"O'Neill WM, Atkins CL, Bloomer HA. Hereditary nephritis: a re-examination of its clinical and genetic features. Ann Intern Med 1978;88:176-82.","journal-title":"Ann Intern Med"},{"key":"ref_38","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1002\/ajmg.1320380203","article-title":"Bibliography on X-linked mental retardation, the fragile-X, and related subjects","volume":"38","author":"Spano, L.V.M.; Opitz, J.M.","year":"1991","unstructured":"Spano LVM, Opitz JM. Bibliography on X-linked mental retardation, the fragile-X, and related subjects. Anm Med Genet 1991;38:173-85.","journal-title":"Anm Med Genet"},{"key":"ref_39","first-page":"461","article-title":"Familial periventricular heterotopia and seizures in 4 generations","volume":"30","author":"Huttenlocher, P.R.; Taravath, S.; Mojtahedi, S.","year":"1991","unstructured":"Huttenlocher PR, Taravath S, Mojtahedi S. Familial periventricular heterotopia and seizures in 4 generations. Ann Neurol 1991;30:461.","journal-title":"Ann Neurol"},{"key":"ref_40","doi-asserted-by":"crossref","first-page":"237","DOI":"10.1016\/0387-7604(93)90073-H","article-title":"Familial periventricular nodular heterotopia","volume":"15","author":"Kamuro, K.; Tenokuchi, Y.","year":"1993","unstructured":"Kamuro K, Tenokuchi Y. Familial periventricular nodular heterotopia. Brain Dev 1993;15:237-41.","journal-title":"Brain Dev"},{"key":"ref_41","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1002\/ana.410140412","article-title":"A progressive syndrome of autism, dementia, ataxia and loss of purposeful hand use in girls. Rett's syndrome: report of 35 cases","volume":"14","author":"Hagberg, B.; Aicardi, J.; Dias, K.","year":"1983","unstructured":"Hagberg B, Aicardi J, Dias K, et al. A progressive syndrome of autism, dementia, ataxia and loss of purposeful hand use in girls. Rett's syndrome: report of 35 cases. Ann Neurol 1983;14:471-9.","journal-title":"Ann Neurol"},{"key":"ref_42","first-page":"1103","article-title":"Le syndrome spasmes en flexion, agenesie calleuse, anomalies chorioretiniennes","volume":"26","author":"Aicardi, J.; Chevrie, J.-J.; Rousselie, F.","year":"1966","unstructured":"Aicardi J, Chevrie J-J, Rousselie F. Le syndrome spasmes en flexion, agenesie calleuse, anomalies chorioretiniennes. Arch Fr Pediatr 1966;26: 1103-20.","journal-title":"Arch Fr Pediatr"},{"key":"ref_43","doi-asserted-by":"crossref","first-page":"382","DOI":"10.1111\/j.1469-8749.1972.tb02604.x","article-title":"The Aicardi syndrome","volume":"14","author":"Denis, J.; Bower, B.D.","year":"1972","unstructured":"Denis J, Bower BD. The Aicardi syndrome. Dev Med Child Neurol 1972;14:382-90.","journal-title":"Dev Med Child Neurol"},{"key":"ref_44","first-page":"6455","article-title":"An endogenous lectin and one of its neuronal glycoprotein ligands are involved in contact guidance","volume-title":"of neuron migration. Proc NatlAcad Sci USA","volume":"87","author":"Lehmann, S.; Kuchler, S.; Theveniau, M.","year":"1990","unstructured":"Lehmann S, Kuchler S, Theveniau M, et al. An endogenous lectin and one of its neuronal glycoprotein ligands are involved in contact guidance of neuron migration. Proc NatlAcad Sci USA 1990;87:6455-9."},{"key":"ref_45","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/0166-2236(90)90044-B","article-title":"Riding the glial monorail: a common mechanism for glial-guided neuronal migration in different regions of the developing mammalian brain","volume":"13","author":"Hatten, M.E.","year":"1990","unstructured":"Hatten ME. Riding the glial monorail: a common mechanism for glial-guided neuronal migration in different regions of the developing mammalian brain. Trends Neurosci 1990;13:179-84.","journal-title":"Trends Neurosci"},{"key":"ref_46","doi-asserted-by":"crossref","first-page":"717","DOI":"10.1038\/364717a0","article-title":"Isolation of a Miller-Dieker lissencephaly gene containing G protein fl-subunit-like repeats","volume":"364","author":"Reiner 0, Carrozzo R, Shen Y","year":"1993","unstructured":"Reiner 0, Carrozzo R, Shen Y, et al. Isolation of a Miller-Dieker lissencephaly gene containing G protein fl-subunit-like repeats. Nature 1993;364:717-21.","journal-title":"Nature"}],"container-title":["Journal of Neurology, Neurosurgery &amp; Psychiatry"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/syndication.highwire.org\/content\/doi\/10.1136\/jnnp.57.8.914","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,2,2]],"date-time":"2025-02-02T11:46:50Z","timestamp":1738496810000},"score":1,"resource":{"primary":{"URL":"https:\/\/jnnp.bmj.com\/lookup\/doi\/10.1136\/jnnp.57.8.914"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[1994,8,1]]},"references-count":46,"journal-issue":{"issue":"8","published-print":{"date-parts":[[1994,8,1]]}},"URL":"https:\/\/doi.org\/10.1136\/jnnp.57.8.914","relation":{},"ISSN":["0022-3050"],"issn-type":[{"value":"0022-3050","type":"print"}],"subject":[],"published":{"date-parts":[[1994,8,1]]}}}