-
1
-
-
0035956478
-
Classification system for malformations of cortical development: Update 2001
-
Barkovich AJ, Kuzniecky RI, Jackson GD, Guerrini R, Dobyns WB. Classification system for malformations of cortical development: update 2001. Neurology 2001;57:2168-2178
-
(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
-
-
0035110971
-
Malformations of cortical development and epilepsy
-
Kuzniecky RI, Barkovich AJ. Malformations of cortical development and epilepsy. Brain Dev 2001;23:2-11
-
(2001)
Brain Dev
, vol.23
, pp. 2-11
-
-
Kuzniecky, R.I.1
Barkovich, A.J.2
-
3
-
-
0034794713
-
Epilepsy and genetic malformations of the cerebral cortex
-
Guerrini R, Carrozzo R. Epilepsy and genetic malformations of the cerebral cortex. Am J Med Genet 2001;106:160-173
-
(2001)
Am J Med Genet
, vol.106
, pp. 160-173
-
-
Guerrini, R.1
Carrozzo, R.2
-
5
-
-
0035067350
-
Cell migration and cerebral cortical development
-
Golden JA. Cell migration and cerebral cortical development. Neuropathol Appl Neurobiol 2001;27:22-28
-
(2001)
Neuropathol Appl Neurobiol
, vol.27
, pp. 22-28
-
-
Golden, J.A.1
-
7
-
-
0034700961
-
Bilateral frontal polymicrogyria: A newly recognized brain malformation syndrome
-
Guerrini R, Barkovich AJ, Sztriha L, Dobyns WB. Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome. Neurology 2000;54:909-913
-
(2000)
Neurology
, vol.54
, pp. 909-913
-
-
Guerrini, R.1
Barkovich, A.J.2
Sztriha, L.3
Dobyns, W.B.4
-
8
-
-
0030822047
-
Pediatric congenital bilateral perisylvian syndrome: Clinical and MRI features in 12 patients
-
Gropman AL, Barkovich AJ, Vezina LG, Conry JA, Dubovsky EC, Packer RJ. Pediatric congenital bilateral perisylvian syndrome: clinical and MRI features in 12 patients. Neuropediatrics 1997;28:198-203
-
(1997)
Neuropediatrics
, vol.28
, pp. 198-203
-
-
Gropman, A.L.1
Barkovich, A.J.2
Vezina, L.G.3
Conry, J.A.4
Dubovsky, E.C.5
Packer, R.J.6
-
9
-
-
18244413664
-
Bilateral parasagittal parietooccipital polymicrogyria and epilepsy
-
Guerrini R, Dubeau F, Dulac O, et al. Bilateral parasagittal parietooccipital polymicrogyria and epilepsy. Ann Neurol 1997;41:65-73
-
(1997)
Ann Neurol
, vol.41
, pp. 65-73
-
-
Guerrini, R.1
Dubeau, F.2
Dulac, O.3
-
10
-
-
18344389160
-
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21
-
Piao X, Basel-Vanagaite L, Straussberg R, et al. An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21. Am J Hum Genet 2001;70:1028-1033
-
(2001)
Am J Hum Genet
, vol.70
, pp. 1028-1033
-
-
Piao, X.1
Basel-Vanagaite, L.2
Straussberg, R.3
-
11
-
-
0036201466
-
A locus for bilateral perisylvian polymicrogyria maps to Xq28
-
Villard L, Nguyen K, Cardoso C, et al. A locus for bilateral perisylvian polymicrogyria maps to Xq28. Am J Hum Genet 2001;70:1003-1008
-
(2001)
Am J Hum Genet
, vol.70
, pp. 1003-1008
-
-
Villard, L.1
Nguyen, K.2
Cardoso, C.3
-
12
-
-
0000757793
-
High-definition magnetic resonance imaging identification of cortical dysplasias: Micropolygyria versus lissencephaly
-
Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin B, Pfanner P, eds. Philadelphia: Lippincott-Raven
-
Raybaud C, Girard N, Canto-Moreira N, Poncet M. High-definition magnetic resonance imaging identification of cortical dysplasias: micropolygyria versus lissencephaly. In: Guerrini R, Andermann F, Canapicchi R, Roger J, Zifkin B, Pfanner P, eds. Dysplasias of Cerebral Cortex and Epilepsy. Philadelphia: Lippincott-Raven; 1996:131-143
-
(1996)
Dysplasias of Cerebral Cortex and Epilepsy
, pp. 131-143
-
-
Raybaud, C.1
Girard, N.2
Canto-Moreira, N.3
Poncet, M.4
-
13
-
-
0025734430
-
The spectrum of lissencephaly: Report of ten patients analyzed by magnetic resonance imaging
-
Barkovich AJ, Koch TK, Carol CL. The spectrum of lissencephaly: report of ten patients analyzed by magnetic resonance imaging. Ann Neurol 1991;30:139-146
-
(1991)
Ann Neurol
, vol.30
, pp. 139-146
-
-
Barkovich, A.J.1
Koch, T.K.2
Carol, C.L.3
-
14
-
-
0037919879
-
Pathological aspects: General
-
Crone J, Stern J, eds. Edinburgh: Churchill Livingstone
-
Crone J, Stern J. Pathological aspects: general. In: Crone J, Stern J, eds. Pathology of Mental Retardation. 2nd ed. Edinburgh: Churchill Livingstone; 1972:121-191
-
(1972)
Pathology of Mental Retardation. 2nd Ed.
, pp. 121-191
-
-
Crone, J.1
Stern, J.2
-
15
-
-
0003026864
-
Dysplasias of cerebral cortex
-
Freide RL, ed. Berlin: Springer
-
Friede RL. Dysplasias of cerebral cortex. In: Freide RL, ed. Developmental Neuropathology. 2nd ed. Berlin: Springer; 1989:330-346
-
(1989)
Developmental Neuropathology. 2nd Ed.
, pp. 330-346
-
-
Friede, R.L.1
-
16
-
-
0002390720
-
Neuronal proliferation, migration, organization, and myelination
-
Volpe JJ, ed. Philadelphia: Saunders
-
Volpe JJ. Neuronal proliferation, migration, organization, and myelination. In: Volpe JJ, ed. Neurology of the Newborn. 4th ed. Philadelphia: Saunders; 2001:45-102
-
(2001)
Neurology of the Newborn. 4th Ed.
, pp. 45-102
-
-
Volpe, J.J.1
-
17
-
-
0001792841
-
Normal development of the neonatal and infant brain, skull, and spine
-
Barkovich AJ, ed. New York: Lippincott Williams & Wilkins
-
Barkovich AJ. Normal development of the neonatal and infant brain, skull, and spine. In: Barkovich AJ, ed. Pediatric Neuroimaging. 3rd ed. New York: Lippincott Williams & Wilkins; 2000:9-54
-
(2000)
Pediatric Neuroimaging. 3rd Ed.
, pp. 9-54
-
-
Barkovich, A.J.1
-
18
-
-
0001790128
-
Myelination and retarded myelination
-
van der Knaap MS, Valk J, eds. Berlin: Springer
-
van der Knaap MS, Valk J Myelination and retarded myelination. In: van der Knaap MS, Valk J, eds. Magnetic Resonance of Myelin, Myelination, and Myelin Disorders. 2nd ed. Berlin: Springer; 1995:31-52
-
(1995)
Magnetic Resonance of Myelin, Myelination, and Myelin Disorders. 2nd Ed.
, pp. 31-52
-
-
Van der Knaap, M.S.1
Valk, J.2
-
19
-
-
0031948919
-
Fukuyama congenital muscular dystrophy
-
Aida N. Fukuyama congenital muscular dystrophy. J Mag Reson Imaging 1998;8:317-326
-
(1998)
J Mag Reson Imaging
, vol.8
, pp. 317-326
-
-
Aida, N.1
-
20
-
-
0021136592
-
Cortical dysplasia in congenital muscular dystrophy with central nervous involvement (Fukuyama type)
-
Takada K, Nakamura H, Tanaka J. Cortical dysplasia in congenital muscular dystrophy with central nervous involvement (Fukuyama type). J Neuropathol Exp Neurol 1984;43:395-407
-
(1984)
J Neuropathol Exp Neurol
, vol.43
, pp. 395-407
-
-
Takada, K.1
Nakamura, H.2
Tanaka, J.3
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