-
1
-
-
0035956478
-
Classification system for malformation of cortical development: Update 2001
-
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformation of cortical development: update 2001. Neurology 2001; 57: 2168-78.
-
(2001)
Neurology
, vol.57
, pp. 2168-2178
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Jackson, G.D.3
Guerrini, R.4
Dobyns, W.B.5
-
2
-
-
0031869221
-
Microlissencephaly, a heterogeneous malformation of cortical development
-
Barkovich AJ, Ferrero DM, Barr RM, et al. Microlissencephaly, a heterogeneous malformation of cortical development. Neuropediatrics 1998; 29: 113-9.
-
(1998)
Neuropediatrics
, vol.29
, pp. 113-119
-
-
Barkovich, A.J.1
Ferrero, D.M.2
Barr, R.M.3
-
3
-
-
0027529279
-
Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34
-
Harris RM, Carter NP, Griffiths B, et al. Physical mapping within the tuberous sclerosis linkage group in region 9q32-q34. Genomics 1993; 15: 265-74.
-
(1993)
Genomics
, vol.15
, pp. 265-274
-
-
Harris, R.M.1
Carter, N.P.2
Griffiths, B.3
-
4
-
-
0027770784
-
Identification and characterization of the tuberous sclerosis gene on chromosome 16
-
Consortium ECTS. Identification and characterization of the tuberous sclerosis gene on chromosome 16. Cell 1993; 75: 1305-15.
-
(1993)
Cell
, vol.75
, pp. 1305-1315
-
-
-
5
-
-
0022655376
-
Tuberous sclerosis: A clinicoradiological evaluation of 110 cases with particular reference to atypical presentation
-
Kingsley D, Kendall B, Fitz C. Tuberous sclerosis: a clinicoradiological evaluation of 110 cases with particular reference to atypical presentation. Neuroradiology 1986; 28: 171-90.
-
(1986)
Neuroradiology
, vol.28
, pp. 171-190
-
-
Kingsley, D.1
Kendall, B.2
Fitz, C.3
-
6
-
-
0024361220
-
Neonatal tuberous sclerosis. US, CT, and MR diagnosis of brain and cardiac lesions
-
Christophe C, Bartholome J, Blum D, et al. Neonatal tuberous sclerosis. US, CT, and MR diagnosis of brain and cardiac lesions. Pediatr Radiol 1989; 19 (6-7): 446-8.
-
(1989)
Pediatr Radiol
, vol.19
, Issue.6-7
, pp. 446-448
-
-
Christophe, C.1
Bartholome, J.2
Blum, D.3
-
7
-
-
0003669985
-
-
New York: Raven Press
-
nd ed. New York: Raven Press, 1988.
-
(1988)
nd Ed.
-
-
Gomez, M.1
-
8
-
-
0026538490
-
MR imaging of tuberous sclerosis: Pathogenesis of this phakomatosis, use of gadopentate dimeglumine, and literature review
-
Braffmann B, Bilaniuk L, Naidich T, et al. MR imaging of tuberous sclerosis: pathogenesis of this phakomatosis, use of gadopentate dimeglumine, and literature review. Radiology 1992; 183: 227-38.
-
(1992)
Radiology
, vol.183
, pp. 227-238
-
-
Braffmann, B.1
Bilaniuk, L.2
Naidich, T.3
-
9
-
-
0026583705
-
Formation, maturation and disorders of brain neocortex
-
Barkovich AJ, Gressens P, Evrard P. Formation, maturation and disorders of brain neocortex. Am J Neuroradiol 1992; 13: 423-46.
-
(1992)
Am J Neuroradiol
, vol.13
, pp. 423-446
-
-
Barkovich, A.J.1
Gressens, P.2
Evrard, P.3
-
10
-
-
0030691110
-
Focal transmantle dysplasia: A specific malformation of cortical development
-
Barkovich AJ, Kuzniecky RI, Bollen AW, Grant PE. Focal transmantle dysplasia: a specific malformation of cortical development. Neurology 1997; 49: 1148-52.
-
(1997)
Neurology
, vol.49
, pp. 1148-1152
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Bollen, A.W.3
Grant, P.E.4
-
11
-
-
0025719941
-
Focal neuronal migration, disorders and intractable partial epilepsy: Result of surgical treatment
-
Palmini A, Andermann F, Olivier A, Tampieri D, Robitaille Y. Focal neuronal migration, disorders and intractable partial epilepsy: result of surgical treatment. Ann Neurol 1991; 30: 750-7.
-
(1991)
Ann Neurol
, vol.30
, pp. 750-757
-
-
Palmini, A.1
Andermann, F.2
Olivier, A.3
Tampieri, D.4
Robitaille, Y.5
-
12
-
-
0004289354
-
-
Philadelphia: Lippincott Williams and Wilkins
-
rd ed. Philadelphia: Lippincott Williams and Wilkins, 2000.
-
(2000)
rd Ed.
-
-
Barkovich, A.J.1
-
13
-
-
0025293627
-
Unilateral megalencephaly: Correlation of MR imaging and pathologic characteristics
-
Barkovich AJ, Chuang SH. Unilateral megalencephaly: correlation of MR imaging and pathologic characteristics. Am J Neuroradiol 1990; 11: 523-31.
-
(1990)
Am J Neuroradiol
, vol.11
, pp. 523-531
-
-
Barkovich, A.J.1
Chuang, S.H.2
-
14
-
-
0026065777
-
Epidermal nevus syndrome: A neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures and facial hemiatrophy
-
Paione L, Curatolo P, Rizzo R, et al. Epidermal nevus syndrome: a neurologic variant with hemimegalencephaly, gyral malformation, mental retardation, seizures and facial hemiatrophy. Neurology 1991; 41: 266-71.
-
(1991)
Neurology
, vol.41
, pp. 266-271
-
-
Paione, L.1
Curatolo, P.2
Rizzo, R.3
-
15
-
-
0028041289
-
The radiological features of hemimegalencephaly including three cases associated with proteus syndrome
-
Griffiths PD, Welch R, Gardner-Medwin D, et al. The radiological features of hemimegalencephaly including three cases associated with proteus syndrome. Neuropediatrics 1994; 25: 140-4.
-
(1994)
Neuropediatrics
, vol.25
, pp. 140-144
-
-
Griffiths, P.D.1
Welch, R.2
Gardner-Medwin, D.3
-
18
-
-
0002048550
-
Hemispherectomy techniques. A critical review
-
Tuxhorn I, Holthausen H, Boenigk H eds. London: John Libbey
-
Villemure JG. Hemispherectomy techniques. A critical review. In: Tuxhorn I, Holthausen H, Boenigk H eds. Paediatric epilepsy syndromes and their surgical treatment. London: John Libbey, 1997: 729-38.
-
(1997)
Paediatric Epilepsy Syndromes and their Surgical Treatment
, pp. 729-738
-
-
Villemure, J.G.1
-
19
-
-
0025800608
-
Intracerebral gangliogliomas in patients with partial complex seizures: CT and MR imaging findings
-
Tampieri D, Moundjian H, Melanson D, Ethier R. Intracerebral gangliogliomas in patients with partial complex seizures: CT and MR imaging findings. Am J Neuroradiol 1991; 12: 749-55.
-
(1991)
Am J Neuroradiol
, vol.12
, pp. 749-755
-
-
Tampieri, D.1
Moundjian, H.2
Melanson, D.3
Ethier, R.4
-
20
-
-
0027435090
-
Pleomorphic xanthoastrocytoma, a distinctive astroglial tumor: Neuroradiologic and pathologic features
-
Lipper MH, Eberhard DA. Pleomorphic xanthoastrocytoma, a distinctive astroglial tumor: neuroradiologic and pathologic features. Am J Neuroradiol 1993; 141: 1397-404.
-
(1993)
Am J Neuroradiol
, vol.141
, pp. 1397-1404
-
-
Lipper, M.H.1
Eberhard, D.A.2
-
21
-
-
0035699257
-
Dysembryoplastic neuroepithelial tumors: CT, MR findings and imaging follow-up: A study of 53 cases
-
Stanescu Cosson R, Varlet P, Beuvon F, et al. Dysembryoplastic neuroepithelial tumors: CT, MR findings and imaging follow-up: a study of 53 cases. J Neuroradiol 2001; 28: 230-40.
-
(2001)
J Neuroradiol
, vol.28
, pp. 230-240
-
-
Stanescu Cosson, R.1
Varlet, P.2
Beuvon, F.3
-
22
-
-
0029000061
-
Lissencephaly and other malformations of cortical development
-
Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development. Neuropediatrics 1995; 26: 132-47.
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
23
-
-
0033595252
-
Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly
-
Dobyns WB, Truwit CL, Ross ME, et al. Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly. Neurology 1999; 53: 270-7.
-
(1999)
Neurology
, vol.53
, pp. 270-277
-
-
Dobyns, W.B.1
Truwit, C.L.2
Ross, M.E.3
-
24
-
-
0000757793
-
High-definition magnetic resonance imaging of cortical dysplasias: Micropolygyria versus lissencephaly
-
Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfaner P, eds. Philadelphia: Lippincott-Raven Publisher
-
Raybaud C, Girard N, Canto-Moreira F, et al. High-definition magnetic resonance imaging of cortical dysplasias: micropolygyria versus lissencephaly. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin BG, Pfaner P, eds. Dysplasias of cerebral cortex and epilepsy. Philadelphia: Lippincott-Raven Publisher, 1996: 131-43.
-
(1996)
Dysplasias of Cerebral Cortex and Epilepsy
, pp. 131-143
-
-
Raybaud, C.1
Girard, N.2
Canto-Moreira, F.3
-
25
-
-
0035213853
-
Lissencephaly with cerebellar hypoplasia (LCH). A heterogeneous group of cortical malformations
-
Rosa ME, Swanson K, Dobyns WB. Lissencephaly with cerebellar hypoplasia (LCH). A heterogeneous group of cortical malformations. Neuropediatrics 2001; 32: 256-63.
-
(2001)
Neuropediatrics
, vol.32
, pp. 256-263
-
-
Rosa, M.E.1
Swanson, K.2
Dobyns, W.B.3
-
26
-
-
0032231712
-
Neuroimaging manifestations and classification of congenital muscular dystrophies
-
Barkovich AJ. Neuroimaging manifestations and classification of congenital muscular dystrophies. Am J Neuroradiol 1998; 19: 1389-96.
-
(1998)
Am J Neuroradiol
, vol.19
, pp. 1389-1396
-
-
Barkovich, A.J.1
-
27
-
-
0036135841
-
Neuronal migration, cerebral cortical development and cerebral cortical anomalies
-
Pilz D, Stoodley N, Jeffrey A, Golden J. Neuronal migration, cerebral cortical development and cerebral cortical anomalies. J Neuropathol Exp Neurol 2002; 61: 1-11.
-
(2002)
J Neuropathol Exp Neurol
, vol.61
, pp. 1-11
-
-
Pilz, D.1
Stoodley, N.2
Jeffrey, A.3
Golden, J.4
-
28
-
-
0027180939
-
Development of the cortical dysplasia of type II lissencephaly
-
Squier MV. Development of the cortical dysplasia of type II lissencephaly. Neuropathol Appl Neurobiol 1993; 19: 209-13.
-
(1993)
Neuropathol Appl Neurobiol
, vol.19
, pp. 209-213
-
-
Squier, M.V.1
-
29
-
-
0033984489
-
Morphological characteristics of subcortical heterotopia: MR imaging study
-
Barkovich AJ. Morphological characteristics of subcortical heterotopia: MR imaging study. Am J Neuroradiol 2000; 21: 290-5.
-
(2000)
Am J Neuroradiol
, vol.21
, pp. 290-295
-
-
Barkovich, A.J.1
-
30
-
-
0030027091
-
Periventricular heterotopia: An X-linked dominant epilepsy causing aberrant cerebral cortical development
-
Eksioglu YZ, Scheffer IE, Cardenas P, et al. Periventricular heterotopia: an X-linked dominant epilepsy causing aberrant cerebral cortical development. Neuron 1996; 16: 77-87.
-
(1996)
Neuron
, vol.16
, pp. 77-87
-
-
Eksioglu, Y.Z.1
Scheffer, I.E.2
Cardenas, P.3
-
31
-
-
0030701560
-
Bilateral periventricular nodular heterotopia with mental retardation and with syndactily in boys: A new X-linked mental retardation syndrome
-
Dobyns WB, Guerrini R, Czapans H, Beilman D. Bilateral periventricular nodular heterotopia with mental retardation and with syndactily in boys: a new X-linked mental retardation syndrome. Neurology 1997; 49: 1042-7.
-
(1997)
Neurology
, vol.49
, pp. 1042-1047
-
-
Dobyns, W.B.1
Guerrini, R.2
Czapans, H.3
Beilman, D.4
-
32
-
-
0028024069
-
Band heterotopia: Correlation of outcome with MR imaging parameters
-
Barkovich AJ, Guerrini R, Battaglia G, et al. Band heterotopia: correlation of outcome with MR imaging parameters. Ann Neurol 1994; 36: 609-17.
-
(1994)
Ann Neurol
, vol.36
, pp. 609-617
-
-
Barkovich, A.J.1
Guerrini, R.2
Battaglia, G.3
-
33
-
-
0032498306
-
Double cortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson JG, Allen KA, Fox JW, et al. Double cortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein. Cell 1998; 92: 63-72.
-
(1998)
Cell
, vol.92
, pp. 63-72
-
-
Gleeson, J.G.1
Allen, K.A.2
Fox, J.W.3
-
34
-
-
0028968605
-
Correlation of prenatal events with the development of polymicrogyria
-
Barkovich AJ, Rowley HA, Bollen A. Correlation of prenatal events with the development of polymicrogyria. Am J Neuroradiol 1995; 16: 822-7.
-
(1995)
Am J Neuroradiol
, vol.16
, pp. 822-827
-
-
Barkovich, A.J.1
Rowley, H.A.2
Bollen, A.3
-
35
-
-
0027473939
-
Congenital bilateral perisylvian syndrome: Study of 31 patients. The congenital bilateral perisylvian syndrome multicenter collaborative study
-
Kuzniecky R, Andermann F, Guerrini R. Congenital bilateral perisylvian syndrome: study of 31 patients. The congenital bilateral perisylvian syndrome multicenter collaborative study. Lancet 1993; 341: 608-12.
-
(1993)
Lancet
, vol.341
, pp. 608-612
-
-
Kuzniecky, R.1
Andermann, F.2
Guerrini, R.3
-
36
-
-
0000541397
-
Schizencephalies. A study of the congenital clefts in the cerebral mantle. 1. Clefts with fused lips
-
Yakovlev PI, Wadsworth RC. Schizencephalies. A study of the congenital clefts in the cerebral mantle. 1. Clefts with fused lips. J Neuropathol Exp Neurol 1946; 5: 116-30.
-
(1946)
J Neuropathol Exp Neurol
, vol.5
, pp. 116-130
-
-
Yakovlev, P.I.1
Wadsworth, R.C.2
-
37
-
-
0000541396
-
Schizencephalies. A study of the congenital clefts in the cerebral mantle. 2. Clefts with hydrocephalus and lips separated
-
Yakovlev PI, Wadsworth RC. Schizencephalies. A study of the congenital clefts in the cerebral mantle. 2. Clefts with hydrocephalus and lips separated. J Neuropathol Exp Neurol 1946; 5: 169-206.
-
(1946)
J Neuropathol Exp Neurol
, vol.5
, pp. 169-206
-
-
Yakovlev, P.I.1
Wadsworth, R.C.2
-
39
-
-
0026563229
-
Schizencephaly, correlation of clinical findings with MR characteristics
-
Barkovich AJ, Kjos BO. Schizencephaly, correlation of clinical findings with MR characteristics. Am J Neuroradiol 1992; 13: 85-94.
-
(1992)
Am J Neuroradiol
, vol.13
, pp. 85-94
-
-
Barkovich, A.J.1
Kjos, B.O.2
-
41
-
-
0030065606
-
Germline mutations in the homeobox gene EMX 2 in patients with severe schizencephaly
-
Brunelli S, Faiella A, Capra V, et al. Germline mutations in the homeobox gene EMX 2 in patients with severe schizencephaly. Nat Genet 1996; 12: 94-6.
-
(1996)
Nat Genet
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
-
42
-
-
0030975567
-
Familial schizencephaly associated with EMX2 mutation
-
Granata T, Farina L, Faiella A, et al. Familial schizencephaly associated with EMX2 mutation. Neurology 1997; 48: 1403-6.
-
(1997)
Neurology
, vol.48
, pp. 1403-1406
-
-
Granata, T.1
Farina, L.2
Faiella, A.3
|