-
1
-
-
0029877369
-
Arthrogryposis multiplex congenital and bilateral parietal polymicrogyria in association with the intrauterine death of a twin
-
Baker, E. M., M. G. Khorasgani, D. Gardner-Medwin, A. Gholkar, P. D. Griffiths: Arthrogryposis multiplex congenital and bilateral parietal polymicrogyria in association with the intrauterine death of a twin. Neuropediatrics 27 (1996) 54-56
-
(1996)
Neuropediatrics
, vol.27
, pp. 54-56
-
-
Baker, E.M.1
Khorasgani, M.G.2
Gardner-Medwin, D.3
Gholkar, A.4
Griffiths, P.D.5
-
2
-
-
0023553576
-
MR of neuronal migration anomalies
-
Barkovich, A. J., S. H. Chuang, D. Norman: MR of neuronal migration anomalies. AJR 150 (1988) 179-187
-
(1988)
AJR
, vol.150
, pp. 179-187
-
-
Barkovich, A.J.1
Chuang, S.H.2
Norman, D.3
-
3
-
-
0026563229
-
Schizencephaly: Correlation of clinical findings with MR characteristics
-
Barkovich, A. J., B. O. Kjos: Schizencephaly: correlation of clinical findings with MR characteristics. AJNR 13 (1992) 85-94
-
(1992)
AJNR
, vol.13
, pp. 85-94
-
-
Barkovich, A.J.1
Kjos, B.O.2
-
4
-
-
0028968605
-
Correlation of prenatal events with the development of polymicrogyria
-
Barkovich, A. J., H. A. Rowley, A. Bollen: Correlation of prenatal events with the development of polymicrogyria. AJNR 16 (1995) 822-827
-
(1995)
AJNR
, vol.16
, pp. 822-827
-
-
Barkovich, A.J.1
Rowley, H.A.2
Bollen, A.3
-
5
-
-
0018942032
-
Unilateral delayed opercularization in a case of Sotos' syndrome (cerebral gigantism)
-
Barth, P. G., L. Vlasveld, J. Valk: Unilateral delayed opercularization in a case of Sotos' syndrome (cerebral gigantism). Neuroradiology 20 (1980) 49-52
-
(1980)
Neuroradiology
, vol.20
, pp. 49-52
-
-
Barth, P.G.1
Vlasveld, L.2
Valk, J.3
-
6
-
-
0023122493
-
Disorders of neuronal migration
-
Barth, P. G.: Disorders of neuronal migration. Can. J. Neurol. Sci. 14 (1987) 1-16
-
(1987)
Can. J. Neurol. Sci.
, vol.14
, pp. 1-16
-
-
Barth, P.G.1
-
8
-
-
0025438203
-
Developmental Foix-Chavany-Marie syndrome. Polymicrogyria or macrogyria
-
Becker, P. S.: Developmental Foix-Chavany-Marie syndrome. Polymicrogyria or macrogyria (letter). Ann. Neurol. 27 (1990) 693
-
(1990)
Ann. Neurol.
, vol.27
, pp. 693
-
-
Becker, P.S.1
-
9
-
-
0026697329
-
Epilepsy and anomalies of neuronal migration: MRI and clinical aspects
-
Brodtkorb, E., G. Nilsen, O. Smevik, P. A. Rinck: Epilepsy and anomalies of neuronal migration: MRI and clinical aspects. Acta Neurol. Scand. 86 (1992) 24-32
-
(1992)
Acta Neurol. Scand.
, vol.86
, pp. 24-32
-
-
Brodtkorb, E.1
Nilsen, G.2
Smevik, O.3
Rinck, P.A.4
-
10
-
-
0028077058
-
Epileptic seizures, arthrogryposis and migrational brain disorders: A syndrome?
-
Brodtkorb, E., T. Torbergsen, K. O. Nakken, K. Anderson, R. Gimse, O. Sjaastad: Epileptic seizures, arthrogryposis and migrational brain disorders: a syndrome? Acta Neurol. Scand. 90 (1994) 232-240
-
(1994)
Acta Neurol. Scand.
, vol.90
, pp. 232-240
-
-
Brodtkorb, E.1
Torbergsen, T.2
Nakken, K.O.3
Anderson, K.4
Gimse, R.5
Sjaastad, O.6
-
11
-
-
0030065606
-
Germline mutations in the homeobox gene Emx2 in patients with severe schizencephaly
-
Brunelli, S., A. Faiella, V. Capra, V. Nigro, A. Simeone, A. Cama et al: Germline mutations in the homeobox gene Emx2 in patients with severe schizencephaly. Nature Genetics 12 (1996) 94-96
-
(1996)
Nature Genetics
, vol.12
, pp. 94-96
-
-
Brunelli, S.1
Faiella, A.2
Capra, V.3
Nigro, V.4
Simeone, A.5
Cama, A.6
-
12
-
-
0029000061
-
Lissencephaly and other malformations of cortical development: 1995 Update
-
Dobyns, W. B., C. L. Truwit: Lissencephaly and other malformations of cortical development: 1995 Update. Neuropediatrics 26 (1995) 132-147
-
(1995)
Neuropediatrics
, vol.26
, pp. 132-147
-
-
Dobyns, W.B.1
Truwit, C.L.2
-
13
-
-
0027362039
-
Neurogenic arthrogryposis multiplex congenita: Clinical and MRI findings
-
Fedrizzi, E., G. Botteon, M. Inverno, E. Ciceri, L. D'Incerti, F. Dworzak: Neurogenic arthrogryposis multiplex congenita: Clinical and MRI findings. Pediatr. Neurol. 9 (1993) 343-348
-
(1993)
Pediatr. Neurol.
, vol.9
, pp. 343-348
-
-
Fedrizzi, E.1
Botteon, G.2
Inverno, M.3
Ciceri, E.4
D'Incerti, L.5
Dworzak, F.6
-
14
-
-
0000456560
-
Diplegie facio-linguo-masticatrice d'origine cortico-sous-corticale sans paralysie des membres
-
Foix, C., J. A. Chavany, J. Marie: Diplegie facio-linguo-masticatrice d'origine cortico-sous-corticale sans paralysie des membres. Rev. Neurol. 33 (1926) 214-219
-
(1926)
Rev. Neurol.
, vol.33
, pp. 214-219
-
-
Foix, C.1
Chavany, J.A.2
Marie, J.3
-
15
-
-
0028125573
-
Regulation of the POU domain gene SCIP during cerebral cortical development
-
Frantz, G. D., A. P. Bohner, R. M. Akers, S. K. McConnell: Regulation of the POU domain gene SCIP during cerebral cortical development. J. Neurosci. 14 (1994) 472-485
-
(1994)
J. Neurosci.
, vol.14
, pp. 472-485
-
-
Frantz, G.D.1
Bohner, A.P.2
Akers, R.M.3
McConnell, S.K.4
-
16
-
-
0027994280
-
Otx1 and Otx2 define the layers and regions in the developing cerebral cortex and cerebellum
-
Frantz, G.D., J. M. Weimann, M. E. Levine, S. K. McConnell: Otx1 and Otx2 define the layers and regions in the developing cerebral cortex and cerebellum. J. Neurosci. 14 (1994) 5725-5740
-
(1994)
J. Neurosci.
, vol.14
, pp. 5725-5740
-
-
Frantz, G.D.1
Weimann, J.M.2
Levine, M.E.3
McConnell, S.K.4
-
17
-
-
0018149535
-
Postencephalitic porencephaly, hydranencephaly or polymicrogyria. A review
-
Berl
-
Friede, R. L., J. Mikolasek: Postencephalitic porencephaly, hydranencephaly or polymicrogyria. A review. Acta Neuropathol. (Berl) 43 (1978) 161-168
-
(1978)
Acta Neuropathol.
, vol.43
, pp. 161-168
-
-
Friede, R.L.1
Mikolasek, J.2
-
18
-
-
0023022648
-
Developmental Foix-Chavany-Marie syndrome in identical twins
-
Graff-Radford, N. R., E. P. Bosch, J. C. Stears, D. Tranel: Developmental Foix-Chavany-Marie syndrome in identical twins. Ann. Neurol. 20 (1986) 632-635
-
(1986)
Ann. Neurol.
, vol.20
, pp. 632-635
-
-
Graff-Radford, N.R.1
Bosch, E.P.2
Stears, J.C.3
Tranel, D.4
-
19
-
-
0024503103
-
Acute pseudobulbar palsy due to bilateral focal cortical damage: The opercular syndrome of Foix-Chavany-Marie
-
Grattan Smith, P. J., I. J. Hopkins, L. K. Shield, D. W. Boldt: Acute pseudobulbar palsy due to bilateral focal cortical damage: The opercular syndrome of Foix-Chavany-Marie. J. Child Neurol. 4 (1989) 131-136
-
(1989)
J. Child Neurol.
, vol.4
, pp. 131-136
-
-
Grattan Smith, P.J.1
Hopkins, I.J.2
Shield, L.K.3
Boldt, D.W.4
-
20
-
-
0026721692
-
Neurologic findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI
-
Guerrini, R., C. Dravet, C. Raybaud, J. Roger, M. Bureau, A. Battaglia et al: Neurologic findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI. Dev. Med. Child. Neurol. 34 (1992) 694-705
-
(1992)
Dev. Med. Child. Neurol.
, vol.34
, pp. 694-705
-
-
Guerrini, R.1
Dravet, C.2
Raybaud, C.3
Roger, J.4
Bureau, M.5
Battaglia, A.6
-
21
-
-
0029871937
-
Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse
-
Gulisano, M., V. Broccoli, C. Pardini, E. Boncinelli: Emx1 and Emx2 show different patterns of expression during proliferation and differentiation of the developing cerebral cortex in the mouse. Eur. J. Neurosci. 8 (1996) 1037-1050
-
(1996)
Eur. J. Neurosci.
, vol.8
, pp. 1037-1050
-
-
Gulisano, M.1
Broccoli, V.2
Pardini, C.3
Boncinelli, E.4
-
22
-
-
0007558926
-
Über eine Kohlenoxydvergiftung im Fetalleben mit Entwicklungsstörung der Hirnrinde
-
Hallervorden, J.: Über eine Kohlenoxydvergiftung im Fetalleben mit Entwicklungsstörung der Hirnrinde. Allg. Z. Psychiatr. 124 (1949) 289-298
-
(1949)
Allg. Z. Psychiatr.
, vol.124
, pp. 289-298
-
-
Hallervorden, J.1
-
23
-
-
0024376029
-
Expression of a large family of POU-domain regulatory genes in mammalian brain development
-
He, X., M. N. Treacy, D. M. Simmons, H. A. Ingraham, L. W. Swanson, M. G. Rosenfeld: Expression of a large family of POU-domain regulatory genes in mammalian brain development. Nature 340 (1989) 35-41
-
(1989)
Nature
, vol.340
, pp. 35-41
-
-
He, X.1
Treacy, M.N.2
Simmons, D.M.3
Ingraham, H.A.4
Swanson, L.W.5
Rosenfeld, M.G.6
-
24
-
-
0023893655
-
Focal cortical myoclonus and rolandic cortical dysplasia: Clarification by MRI
-
Kuzniecky, R., S. Berkovic, F. Andermann, D. Melanson, A. Olivier, Y. Robitaille: Focal cortical myoclonus and rolandic cortical dysplasia: clarification by MRI. Ann. Neurol. 23 (1988) 317-325
-
(1988)
Ann. Neurol.
, vol.23
, pp. 317-325
-
-
Kuzniecky, R.1
Berkovic, S.2
Andermann, F.3
Melanson, D.4
Olivier, A.5
Robitaille, Y.6
-
25
-
-
0024323989
-
Bilateral central macrogyria: Epilepsy, pseudobulbar palsy, and mental retardation - A recognizable neuronal migration disorder
-
Kuzniecky, R., F. Andermann, D. Tampieri, D. Melanson, A. Olivier, I. Leppik: Bilateral central macrogyria: epilepsy, pseudobulbar palsy, and mental retardation - a recognizable neuronal migration disorder. Ann. Neurol. 25 (1989) 547-554
-
(1989)
Ann. Neurol.
, vol.25
, pp. 547-554
-
-
Kuzniecky, R.1
Andermann, F.2
Tampieri, D.3
Melanson, D.4
Olivier, A.5
Leppik, I.6
-
26
-
-
0027473939
-
Congenital bilateral perisylvian syndrome: Study of 31 patients
-
Kuzniecky, R., F. Andermann, R. Guerrini, CBPS Multicenter Collaborative Study: Congenital bilateral perisylvian syndrome: study of 31 patients. Lancet 341 (1993) 608-612
-
(1993)
Lancet
, vol.341
, pp. 608-612
-
-
Kuzniecky, R.1
Andermann, F.2
Guerrini, R.3
-
27
-
-
0028294602
-
The epileptic spectrum in the congenital bilateral perisylvian syndrome
-
Kuzniecky, R., F. Andermann, R. Guerrini, CBPS Multicenter Collaborative Study: The epileptic spectrum in the congenital bilateral perisylvian syndrome. Neurology 44 (1994) 379-385
-
(1994)
Neurology
, vol.44
, pp. 379-385
-
-
Kuzniecky, R.1
Andermann, F.2
Guerrini, R.3
-
28
-
-
0002976338
-
Malformations of the Nervous System
-
Adams, J. H., J. A. N. Corsellas, L. W. Duchen (Eds.): New York, John Wiley and Sons
-
Larroche, J.-C.: Malformations of the Nervous System. In: Adams, J. H., J. A. N. Corsellas, L. W. Duchen (Eds.): Greenfield's Neuropathology, 4th ed., New York, John Wiley and Sons, (1984) 385-450
-
(1984)
Greenfield's Neuropathology, 4th Ed.
, pp. 385-450
-
-
Larroche, J.-C.1
-
29
-
-
0018958918
-
Bilateral perisylvian softening: Bilateral anterior opercular syndrome (Foix-Chavany-Marie Syndrome)
-
Mariani, C., H. Spinnler, R. Sterzi, G. Vallar: Bilateral perisylvian softening: bilateral anterior opercular syndrome (Foix-Chavany-Marie Syndrome). J. Neurol. 223 (1980) 269-284
-
(1980)
J. Neurol.
, vol.223
, pp. 269-284
-
-
Mariani, C.1
Spinnler, H.2
Sterzi, R.3
Vallar, G.4
-
30
-
-
0019997554
-
Pathogenesis of four-layered microgyric cortex in man
-
Berl
-
McBride, M. C., T. L. Kemper: Pathogenesis of four-layered microgyric cortex in man. Acta Neoropathol. (Berl) 57 (1982) 93-98
-
(1982)
Acta Neoropathol.
, vol.57
, pp. 93-98
-
-
McBride, M.C.1
Kemper, T.L.2
-
31
-
-
0028340659
-
The developing cerebral surface: Preliminary report on the patterns of sulcal and gyral maturation - Anatomy, ultrasound, and magnetic resonance imaging
-
Naidich, T. P., J. L. Grant, N. Altman, R. Zimmerman, S. B. Birchansky, B. Braffman et al.: The developing cerebral surface: preliminary report on the patterns of sulcal and gyral maturation - anatomy, ultrasound, and magnetic resonance imaging. Neuro Imaging Clinic North America 4 (1994) 201-240
-
(1994)
Neuro Imaging Clinic North America
, vol.4
, pp. 201-240
-
-
Naidich, T.P.1
Grant, J.L.2
Altman, N.3
Zimmerman, R.4
Birchansky, S.B.5
Braffman, B.6
-
32
-
-
0004042407
-
-
Oxford, Oxford University Press
-
Norman, M. G., B. C. McGillivray, D. K. Kalousek, A. Hill, K. J. Poskitt: Congenital Malformations of the Brain: Pathologic, Embryologic, Clinical, Radiologic, and Genetic Aspects. Oxford, 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
-
34
-
-
0026759308
-
Nested expression domains of four homeobox genes in the developing rostral brain
-
Simeons, A., D. Acampora, M. Gulisano, A. Stornaiuolo, E. Boncinelli: Nested expression domains of four homeobox genes in the developing rostral brain. Nature 358 (1992) 687-690
-
(1992)
Nature
, vol.358
, pp. 687-690
-
-
Simeons, A.1
Acampora, D.2
Gulisano, M.3
Stornaiuolo, A.4
Boncinelli, E.5
-
35
-
-
0026663463
-
Telencephalon-restricted expression of BF-1, a new member of the HNF-3/fork head gene family, in the developing rat brain
-
Tao, W., E. Lai: Telencephalon-restricted expression of BF-1, a new member of the HNF-3/fork head gene family, in the developing rat brain. Neuron 8 (1992) 957-966
-
(1992)
Neuron
, vol.8
, pp. 957-966
-
-
Tao, W.1
Lai, E.2
|