-
2
-
-
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
-
3
-
-
0025869079
-
The agyria-pachygyria complex: A spectrum of cortical malformations
-
Aicardi J. The agyria-pachygyria complex: a spectrum of cortical malformations. Brain Dev 1991;13:1-8
-
(1991)
Brain Dev
, vol.13
, pp. 1-8
-
-
Aicardi, J.1
-
4
-
-
0027486966
-
Lissencephaly: A human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13
-
Dobyns W, Reiner O, Carrozzo R, Ledbetter D. Lissencephaly: a human brain malformation associated with deletion of the LIS1 gene located at chromosome 17p13. J Am Med Assoc 1993;270: 2838-2842
-
(1993)
J Am Med Assoc
, vol.270
, pp. 2838-2842
-
-
Dobyns, W.1
Reiner, O.2
Carrozzo, R.3
Ledbetter, D.4
-
5
-
-
0029000061
-
Lissencephaly and other malformations of cortical development
-
Dobyns WB, Truwit CL. Lissencephaly and other malformations of cortical development. Neuropediatrics 1995;26:132-147
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
6
-
-
0028024069
-
Band heterotopia: Correlation of outcome with MR imaging parameters
-
Barkovich AJ, Guerrini R, Battaglia Q, et al. Band heterotopia: correlation of outcome with MR imaging parameters. Ann Neurol 1994;36:609-617
-
(1994)
Ann Neurol
, vol.36
, pp. 609-617
-
-
Barkovich, A.J.1
Guerrini, R.2
Battaglia, Q.3
-
7
-
-
0026055460
-
Diffuse cortical dysplasia, or the "double cortex" syndrome: The clinical and epileptic spectrum in 10 patients
-
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;41:1656-1662
-
(1991)
Neurology
, vol.41
, pp. 1656-1662
-
-
Palmini, A.1
Andermann, F.2
Aicardi, J.3
-
9
-
-
0026567180
-
Gray matter heterotopias: MR characteristics and correlation with developmental and neurological manifestations
-
Barkovich AJ, Kjos BO. Gray matter heterotopias: MR characteristics and correlation with developmental and neurological manifestations. Radiology 1992;182:493-499
-
(1992)
Radiology
, vol.182
, pp. 493-499
-
-
Barkovich, A.J.1
Kjos, B.O.2
-
10
-
-
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;341:608-612
-
(1993)
Lancet
, vol.341
, pp. 608-612
-
-
Kuzniecky, R.1
Andermann, F.2
Guerrini, R.3
-
11
-
-
0026721692
-
Neurological findings and seizure outcome in children with bilateral opercular macrogyriclike changes detected by MR1
-
Guerrini R, Dravet C, Raybaud C, et al. Neurological findings and seizure outcome in children with bilateral opercular macrogyriclike changes detected by MR1. Dev Med Child Neurol 1992;34:694
-
(1992)
Dev Med Child Neurol
, vol.34
, pp. 694
-
-
Guerrini, R.1
Dravet, C.2
Raybaud, C.3
-
12
-
-
0028902001
-
Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results
-
Palmini A, Gambardella A, Andermann F, et al. Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical results. Ann Neurol 1995;37:476-487
-
(1995)
Ann Neurol
, vol.37
, pp. 476-487
-
-
Palmini, A.1
Gambardella, A.2
Andermann, F.3
-
14
-
-
0028021189
-
Subcortical laminar heterotopia and lissencephaly in 2 families: A single X-linked dominant gene
-
Pinard JM, Motte J, Chiron C, Brian R, Andermann E, Dulac O. Subcortical laminar heterotopia and lissencephaly in 2 families: a single X-linked dominant gene. J Neurol Neurosurg Psychiatry 1994;57:914-920
-
(1994)
J Neurol Neurosurg Psychiatry
, vol.57
, pp. 914-920
-
-
Pinard, J.M.1
Motte, J.2
Chiron, C.3
Brian, R.4
Andermann, E.5
Dulac, O.6
-
15
-
-
0004042407
-
-
Oxford, England: Oxford University Press
-
Norman MG, McGillivray BC, Kalousek DK, Hill A, Poskitt KJ. Congenital Malformations of the Brain: Pathologic, Embryologic, Clinical, Radiologic and Genetic Aspects. Oxford, England: Oxford University Press; 1995:223-307
-
(1995)
Congenital Malformations of the Brain: Pathologic, Embryologic, Clinical, Radiologic and Genetic Aspects
, pp. 223-307
-
-
Norman, M.G.1
McGillivray, B.C.2
Kalousek, D.K.3
Hill, A.4
Poskitt, K.J.5
-
16
-
-
0003092862
-
Chromosome abnormalities: Origin and etiology in abortions and live births
-
Vogel F, Sperling K, eds. Berlin, Germany: Springer-Verlag
-
Jacobs PA, Hassold TJ. Chromosome abnormalities: origin and etiology in abortions and live births. In: Vogel F, Sperling K, eds. Human Genetics: Proceedings of the 7th International Congress., Berlin, Germany: Springer-Verlag; 1986:233-244
-
(1986)
Human Genetics: Proceedings of the 7th International Congress.
, pp. 233-244
-
-
Jacobs, P.A.1
Hassold, T.J.2
-
17
-
-
0002461619
-
Development of the human central nervous system
-
Haymaker W, Adams RD, eds. Springfield, III: Charles C Thomas
-
Sidman RL, Rakic P. Development of the human central nervous system. In: Haymaker W, Adams RD, eds. Histology and Histopathology of the Nervous System. Springfield, III: Charles C Thomas; 1982:73
-
(1982)
Histology and Histopathology of the Nervous System
, pp. 73
-
-
Sidman, R.L.1
Rakic, P.2
-
18
-
-
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
-
19
-
-
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. AJNR Am J Neuroradiol 1995;16:822-827
-
(1995)
AJNR Am J Neuroradiol
, vol.16
, pp. 822-827
-
-
Barkovich, A.J.1
Rowley, H.A.2
Bollen, A.3
-
20
-
-
0023624531
-
Walker-Warburg syndrome with skeletal muscle involvement: A report of three patients
-
Takada K, Becker LE, Takashima S. Walker-Warburg syndrome with skeletal muscle involvement: a report of three patients. Pediatr Neurosci 1987;13:202-209
-
(1987)
Pediatr Neurosci
, vol.13
, pp. 202-209
-
-
Takada, K.1
Becker, L.E.2
Takashima, S.3
-
21
-
-
0023891589
-
Cortical dysplasia in Fukuyama congenital muscular dystrophy: A Golgi and angioarchitectonic analysis
-
Takada K, Nakamura H, Takashima S. Cortical dysplasia in Fukuyama congenital muscular dystrophy: a Golgi and angioarchitectonic analysis. Acta Neuropathol 1988;76:170-178
-
(1988)
Acta Neuropathol
, vol.76
, pp. 170-178
-
-
Takada, K.1
Nakamura, H.2
Takashima, S.3
-
22
-
-
0027215439
-
Familial periventricular nodular heterotopia
-
Kamuro K, Tenokuchi Y. Familial periventricular nodular heterotopia. Brain Dev 1993;15:237-241
-
(1993)
Brain Dev
, vol.15
, pp. 237-241
-
-
Kamuro, K.1
Tenokuchi, Y.2
-
23
-
-
0027257653
-
Hereditary nodular heterotopia accompanied by mega cisterna magna
-
Oda T, Nagai Y, Fujimoto S, et al. Hereditary nodular heterotopia accompanied by mega cisterna magna. Am J Med Genet 1993; 47:268-271
-
(1993)
Am J Med Genet
, vol.47
, pp. 268-271
-
-
Oda, T.1
Nagai, Y.2
Fujimoto, S.3
-
24
-
-
0011259745
-
Familial band heterotopia: An X-linked dominant disorder with variable severity
-
Scheffer IE, Mitchell LA, Howell RA, et al. Familial band heterotopia: an X-linked dominant disorder with variable severity. Ann Neurol 1994;36:511
-
(1994)
Ann Neurol
, vol.36
, pp. 511
-
-
Scheffer, I.E.1
Mitchell, L.A.2
Howell, R.A.3
-
25
-
-
0027967042
-
X-linked pachygyria and agenesis of the corpus callosum: Evidence for an x chromosome lissencephaly locus
-
Berry-Kravis E, Israel J. X-linked pachygyria and agenesis of the corpus callosum: evidence for an x chromosome lissencephaly locus. Ann Neurol 1994;36:229-233
-
(1994)
Ann Neurol
, vol.36
, pp. 229-233
-
-
Berry-Kravis, E.1
Israel, J.2
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