-
1
-
-
0026697329
-
Epilepsy and anomalies of neuronal migration: MRI and clinical aspects
-
Brodtkorb E, Nilsen G, Smevik O, Rinck PA. Epilepsy and anomalies of neuronal migration: MRI and clinical aspects. Acta Neurol Scand 1992;86:24-32.
-
(1992)
Acta Neurol Scand
, vol.86
, pp. 24-32
-
-
Brodtkorb, E.1
Nilsen, G.2
Smevik, O.3
Rinck, P.A.4
-
2
-
-
0028913884
-
When do brain abnormalities in cerebral palsy occur? An MRI study
-
Sugimoto T, Woo M, Nishida N, et al. When do brain abnormalities in cerebral palsy occur? An MRI study. Dev Med Child Neurol 1995;37:285-292.
-
(1995)
Dev Med Child Neurol
, vol.37
, pp. 285-292
-
-
Sugimoto, T.1
Woo, M.2
Nishida, N.3
-
3
-
-
0027989908
-
Surgical pathology of epilepsy: A review
-
Jay V, Becker LE. Surgical pathology of epilepsy: a review. Pediatr Pathol 1994;14:731-750.
-
(1994)
Pediatr Pathol
, vol.14
, pp. 731-750
-
-
Jay, V.1
Becker, L.E.2
-
5
-
-
0025718486
-
Focal neuronal migration disorders and intractable partial epilepsy: A study of 30 patients
-
Palmini A, Andermann F, Olivier A, et al. Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patients. Ann Neurol 1991;30:741-749.
-
(1991)
Ann Neurol
, vol.30
, pp. 741-749
-
-
Palmini, A.1
Andermann, F.2
Olivier, A.3
-
6
-
-
16944367121
-
Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): Evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22
-
des Portes V, Pinard JM, Smadja D, et al. Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22. J Med Genet 1997;34:177-183.
-
(1997)
J Med Genet
, vol.34
, pp. 177-183
-
-
Des Portes, V.1
Pinard, J.M.2
Smadja, D.3
-
7
-
-
0027473939
-
Congenital bilateral perisylvian syndrome: Study of 31 patients
-
Kuzniecky RI, Andermann F, Guerrini R. Congenital bilateral perisylvian syndrome: study of 31 patients. Lancet 1993;341: 608-612.
-
(1993)
Lancet
, vol.341
, pp. 608-612
-
-
Kuzniecky, R.I.1
Andermann, F.2
Guerrini, R.3
-
8
-
-
0029996736
-
A classification scheme for malformations of cortical development
-
Barkovich AJ, Kuzniecky RI, Dobyns WB, Jackson GD, Becker LE, Evrard P. A classification scheme for malformations of cortical development. Neuropediatrics 1996;27:59-63.
-
(1996)
Neuropediatrics
, vol.27
, pp. 59-63
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Dobyns, W.B.3
Jackson, G.D.4
Becker, L.E.5
Evrard, P.6
-
9
-
-
0023122493
-
Disorders of neuronal migration
-
Barth PG. Disorders of neuronal migration. Can J Neurol Sci 1987;14:1-16.
-
(1987)
Can J Neurol Sci
, vol.14
, pp. 1-16
-
-
Barth, P.G.1
-
10
-
-
0028303886
-
Magnetic resonance imaging in developmental disorders of the cerebral cortex
-
Kuzniecky RI. Magnetic resonance imaging in developmental disorders of the cerebral cortex. Epilepsia 1994;35:S44-S5.
-
(1994)
Epilepsia
, vol.35
-
-
Kuzniecky, R.I.1
-
11
-
-
0029000061
-
Lissencephaly and other malformations of cortical development: 1995 update
-
Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics 1995;26:132-147.
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
12
-
-
0028795670
-
Posterior agyria-pachygyria with polymicrogyria: Evidence for an inherited neuronal migration disorder
-
Ferrie CD, Jackson GD, Giannakodimos S, Panayiotopoulos CP. Posterior agyria-pachygyria with polymicrogyria: evidence for an inherited neuronal migration disorder. Neurology 1995;45:150-153.
-
(1995)
Neurology
, vol.45
, pp. 150-153
-
-
Ferrie, C.D.1
Jackson, G.D.2
Giannakodimos, S.3
Panayiotopoulos, C.P.4
-
13
-
-
0025293627
-
Unilateral megaloencephaly: Correlation of MR imaging and pathologic characteristics
-
Barkovich AJ, Chuang SH. Unilateral megaloencephaly: correlation of MR imaging and pathologic characteristics. AJNR Am J Neuroradiol 1990;11:523-531.
-
(1990)
AJNR Am J Neuroradiol
, vol.11
, pp. 523-531
-
-
Barkovich, A.J.1
Chuang, S.H.2
-
14
-
-
0025333174
-
Unusual MRI appearance of diffuse subcortical heterotopia or "double cortex" in two children
-
Livingston J, Aicardi J. Unusual MRI appearance of diffuse subcortical heterotopia or "double cortex" in two children. J Neurol Neurosurg Psychiatry 1990;33:617-620.
-
(1990)
J Neurol Neurosurg Psychiatry
, vol.33
, pp. 617-620
-
-
Livingston, J.1
Aicardi, J.2
-
15
-
-
0027380669
-
Epilepsia partialis continua due to cortical dysplasia
-
Kuzniecky RI, Powers R. Epilepsia partialis continua due to cortical dysplasia. J Child Neurol 1993;8:386-388.
-
(1993)
J Child Neurol
, vol.8
, pp. 386-388
-
-
Kuzniecky, R.I.1
Powers, R.2
-
16
-
-
0029040779
-
Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy - Clinical, EEG and neuroimaging features in 100 adult patients
-
Raymond AA, Fish DR, Sisodiya SM, Alsanjari N, Stevens JM, Shorvon SD. Abnormalities of gyration, heterotopias, tuberous sclerosis, focal cortical dysplasia, microdysgenesis, dysembryoplastic neuroepithelial tumour and dysgenesis of the archicortex in epilepsy - clinical, EEG and neuroimaging features in 100 adult patients. Brain 1995;118:629-660.
-
(1995)
Brain
, vol.118
, pp. 629-660
-
-
Raymond, A.A.1
Fish, D.R.2
Sisodiya, S.M.3
Alsanjari, N.4
Stevens, J.M.5
Shorvon, S.D.6
-
17
-
-
0026341812
-
Neuronal migration disorders: A contribution of modern neuroimaging to the etiologic diagnosis of epilepsy
-
Palmini A, Andermann F, Olivier A, et al. Neuronal migration disorders: a contribution of modern neuroimaging to the etiologic diagnosis of epilepsy. Can J Neurol Sci 1991;18:580-587.
-
(1991)
Can J Neurol Sci
, vol.18
, pp. 580-587
-
-
Palmini, A.1
Andermann, F.2
Olivier, A.3
-
18
-
-
0028000657
-
The place of neuronal migration abnormalities in child neurology - Review article
-
Aicardi J. The place of neuronal migration abnormalities in child neurology - review article. Can J Neurol Sci 1994;21: 185-193.
-
(1994)
Can J Neurol Sci
, vol.21
, pp. 185-193
-
-
Aicardi, J.1
-
19
-
-
0002835703
-
-
Reston, VA: American College of Radiology
-
American College of Radiology. Index for radiological diagnoses. 4th ed. Reston, VA: American College of Radiology, 1992.
-
(1992)
Index for Radiological Diagnoses. 4th Ed.
-
-
-
21
-
-
0026071721
-
Cortical dysplasia in temporal lobe epilepsy: Magnetic resonance imaging correlations
-
Kuzniecky RI, Garcia JH, Faught E, Morawetz RB. Cortical dysplasia in temporal lobe epilepsy: magnetic resonance imaging correlations. Ann Neurol 1991;29:293-298.
-
(1991)
Ann Neurol
, vol.29
, pp. 293-298
-
-
Kuzniecky, R.I.1
Garcia, J.H.2
Faught, E.3
Morawetz, R.B.4
-
22
-
-
0003103609
-
The neuropathology of human symptomatic epilepsy
-
Engel JJ, ed. New York: Raven Press
-
Vinters HV, Armstrong DL, Babb TL, et al. The neuropathology of human symptomatic epilepsy. In: Engel JJ, ed. Surgical treatment of the epilepsies. 2nd ed. New York: Raven Press, 1993:593-608.
-
(1993)
Surgical Treatment of the Epilepsies. 2nd Ed.
, pp. 593-608
-
-
Vinters, H.V.1
Armstrong, D.L.2
Babb, T.L.3
-
23
-
-
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;49:1148-1153.
-
(1997)
Neurology
, vol.49
, pp. 1148-1153
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Bollen, A.W.3
Grant, P.E.4
-
24
-
-
0030027091
-
Periventricular heterotopia: An X-linked dominant epilepsy locus causing aberrant cerebral cortical development
-
Eksioglu YZ, Scheffer IE, Cardenas P, et al. Periventricular heterotopia: an X-linked dominant epilepsy locus 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
-
25
-
-
10144257864
-
X-linked malformations of neuronal migration
-
Dobyns WB, Andermann E, Andermann F, et al. X-linked malformations of neuronal migration. Neurology 1996;47:331-339.
-
(1996)
Neurology
, vol.47
, pp. 331-339
-
-
Dobyns, W.B.1
Andermann, E.2
Andermann, F.3
-
26
-
-
0020047406
-
Growth patterns in the lateral wall of the mouse telencephalon: I. Autoradiographic studies of the histogenesis of the isocortex and adjacent area
-
Smart IHM, Smart M. Growth patterns in the lateral wall of the mouse telencephalon: I. Autoradiographic studies of the histogenesis of the isocortex and adjacent area. J Anat 1982; 134:273-298.
-
(1982)
J Anat
, vol.134
, pp. 273-298
-
-
Smart, I.H.M.1
Smart, M.2
-
27
-
-
17444444915
-
A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome
-
des Portes V, Pinard JM, Billuart P, et al. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 1998;92:51-61.
-
(1998)
Cell
, vol.92
, pp. 51-61
-
-
Des Portes, V.1
Pinard, J.M.2
Billuart, P.3
-
28
-
-
0032498306
-
Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein
-
Gleeson JG, Allen KM, Fox JW, et al. Doublecortin, 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.M.2
Fox, J.W.3
-
29
-
-
0031829069
-
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects
-
Sossey-Alaoui K, Hartung AJ, Guerrini R, et al. Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects. Hum Mol Genet 1998;7:1327-1332.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1327-1332
-
-
Sossey-Alaoui, K.1
Hartung, A.J.2
Guerrini, R.3
-
30
-
-
7844223263
-
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation
-
Pilz DT, Matsumoto N, Minnerath SR, et al. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation. Hum Mol Genet 1998;7: 2029-2037.
-
(1998)
Hum Mol Genet
, vol.7
, pp. 2029-2037
-
-
Pilz, D.T.1
Matsumoto, N.2
Minnerath, S.R.3
-
31
-
-
0023893655
-
Focal cortical myoclonus and rolandic cortical dysplasia: Clarification by magnetic resonance imaging
-
Kuzniecky RI, Berkovic SF, Andermann F, Melanson D, Olivier A, Robitaille Y. Focal cortical myoclonus and Rolandic cortical dysplasia: clarification by magnetic resonance imaging. Ann Neurol 1988;23:317-325.
-
(1988)
Ann Neurol
, vol.23
, pp. 317-325
-
-
Kuzniecky, R.I.1
Berkovic, S.F.2
Andermann, F.3
Melanson, D.4
Olivier, A.5
Robitaille, Y.6
-
32
-
-
0031942864
-
Temporal lobe malformations and epilepsy: Dual pathology and bilateral hippocampal abnormalities
-
Ho SS, Kuzniecky RI, Gilliam F, Faught E, Morawetz R. Temporal lobe malformations and epilepsy: dual pathology and bilateral hippocampal abnormalities. Neurology 1998;50:748-754.
-
(1998)
Neurology
, vol.50
, pp. 748-754
-
-
Ho, S.S.1
Kuzniecky, R.I.2
Gilliam, F.3
Faught, E.4
Morawetz, R.5
-
33
-
-
17744415149
-
Periventricular nodular heterotopia and intractable temporal lobe epilepsy: Poor outcome after temporal lobe resection
-
Li LM, Dubeau F, Andermann F, et al. Periventricular nodular heterotopia and intractable temporal lobe epilepsy: poor outcome after temporal lobe resection. Ann Neurol 1997;41: 662-668.
-
(1997)
Ann Neurol
, vol.41
, pp. 662-668
-
-
Li, L.M.1
Dubeau, F.2
Andermann, F.3
-
34
-
-
0001929609
-
Neuronal proliferation, migration, organization and myelination
-
Volpe JJ, ed. Philadelphia: WB Saunders
-
Volpe JJ. Neuronal proliferation, migration, organization and myelination. In: Volpe JJ, ed. Neurology of the newborn. 3rd ed. Philadelphia: WB Saunders, 1995:43-92.
-
(1995)
Neurology of the Newborn. 3rd Ed.
, pp. 43-92
-
-
Volpe, J.J.1
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