-
1
-
-
0023122493
-
Disorders of neuronal migration
-
Barth PG. (1987) Disorders of neuronal migration. Can J Neurol Sci 14: 1-16.
-
(1987)
Can J Neurol Sci
, vol.14
, pp. 1-16
-
-
Barth, P.G.1
-
3
-
-
0033770467
-
Worster-Drought syndrome, a mild tetraplegic perisylvian cerebral palsy. Review of 47 cases
-
Clark M, Carr L, Reilly S, Neville BGR. (2000) Worster-Drought syndrome, a mild tetraplegic perisylvian cerebral palsy. Review of 47 cases. Brain 123: 2160-2170.
-
(2000)
Brain
, vol.123
, pp. 2160-2170
-
-
Clark, M.1
Carr, L.2
Reilly, S.3
Neville, B.G.R.4
-
4
-
-
0036211908
-
MECP2 mutation in a boy with severe neonatal encephalopathy
-
Geerdink N, Rotteveel JJ, Lammens M, Sistermans EA, Heikens GT, Gabreels FJ, Mullaart RA, Hamel BC. (2002) MECP2 mutation in a boy with severe neonatal encephalopathy. Neuropediatrics 33: 33-36.
-
(2002)
Neuropediatrics
, vol.33
, pp. 33-36
-
-
Geerdink, N.1
Rotteveel, J.J.2
Lammens, M.3
Sistermans, E.A.4
Heikens, G.T.5
Gabreels, F.J.6
Mullaart, R.A.7
Hamel, B.C.8
-
5
-
-
0036224299
-
Polymicrogyria in chromosome 22q11 deletion syndrome
-
Ghariani S, Dahan K, Saint-Martin C, Kadhim H, Morsomme F, Moniotte S, Verellen-Dumoulin C, Sebire G. (2002) Polymicrogyria in chromosome 22q11 deletion syndrome. Eur J Paediatr Neurol 6: 73-77.
-
(2002)
Eur J Paediatr Neurol
, vol.6
, pp. 73-77
-
-
Ghariani, S.1
Dahan, K.2
Saint-Martin, C.3
Kadhim, H.4
Morsomme, F.5
Moniotte, S.6
Verellen-Dumoulin, C.7
Sebire, G.8
-
6
-
-
0033930097
-
Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment
-
Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G et al. (2000) Familial perisylvian polymicrogyria: A new familial syndrome of cortical maldevelopment. Ann Neurol 48: 39-48.
-
(2000)
Ann Neurol
, vol.48
, pp. 39-48
-
-
Guerreiro, M.M.1
Andermann, E.2
Guerrini, R.3
Dobyns, W.B.4
Kuzniecky, R.5
Silver, K.6
Van Bogaert, P.7
Gillain, C.8
David, P.9
Ambrosetto, G.10
-
7
-
-
0036265092
-
Epileptgenic brain malformations: Clinical presentation, malformative patterns and indications for genetic testing
-
quiz 544-547
-
Guerrini R, Carrozzo R. (2001) Epileptgenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing. Seizure 10: 532-543; quiz 544-547.
-
(2001)
Seizure
, vol.10
, pp. 532-543
-
-
Guerrini, R.1
Carrozzo, R.2
-
8
-
-
0028604469
-
The association of cortical dysplasia and anterior horn arthrogryposis: A case report
-
Hageman G, Hoogenraad TU, Prevo RL. (1994) The association of cortical dysplasia and anterior horn arthrogryposis: A case report. Brain Dev 16: 463-466.
-
(1994)
Brain Dev
, vol.16
, pp. 463-466
-
-
Hageman, G.1
Hoogenraad, T.U.2
Prevo, R.L.3
-
9
-
-
0014775056
-
Arthrogryposis following treatment of maternal tetanus with muscle relaxants
-
Jago RH. (1970) Arthrogryposis following treatment of maternal tetanus with muscle relaxants. Arch Dis Child 45: 277-279.
-
(1970)
Arch Dis Child
, vol.45
, pp. 277-279
-
-
Jago, R.H.1
-
10
-
-
1842533446
-
Club feet with congenital perisylvian polymicrogyria possibly due to bifocal ischaemic damage of the neuroaxis in utero
-
Kammoun F, Tanguy A, Boesplug-Tanguy O, Bensahel H, Khouri N, Landrieu P. (2004) Club feet with congenital perisylvian polymicrogyria possibly due to bifocal ischaemic damage of the neuroaxis in utero. Am J Med Genetics 126A: 191-196.
-
(2004)
Am J Med Genetics
, vol.126 A
, pp. 191-196
-
-
Kammoun, F.1
Tanguy, A.2
Boesplug-Tanguy, O.3
Bensahel, H.4
Khouri, N.5
Landrieu, P.6
-
11
-
-
0027473939
-
Congenital bilateral perisylvian syndrome: Study of 31 patients
-
The CBPS Multicenter collaborative Study
-
Kuzniecky R, Andemann F, Guerrini R. (1993) Congenital bilateral perisylvian syndrome: Study of 31 patients. The CBPS Multicenter collaborative Study. Lancet 341: 608-612.
-
(1993)
Lancet
, vol.341
, pp. 608-612
-
-
Kuzniecky, R.1
Andemann, F.2
Guerrini, R.3
-
12
-
-
0030789806
-
Is there a zone of vascular vulnerability in the fetal brainstem?
-
Leong S, Ashwell KW. (1997) Is there a zone of vascular vulnerability in the fetal brainstem? Neurotoxicol Teratol 19: 265-275.
-
(1997)
Neurotoxicol Teratol
, vol.19
, pp. 265-275
-
-
Leong, S.1
Ashwell, K.W.2
-
13
-
-
0002785599
-
Perisylvian malforation - Vascular aetiology?
-
In: Tuxhorn I, Holthausen H, and Boenigk H, editors. London: John Libbey Press
-
Meencke HJ, Veith G. (1997) Perisylvian malforation - vascular aetiology? In: Tuxhorn I, Holthausen H, and Boenigk H, editors. Paediatric Epilepsy Syndromes and their Surgical Treatment. London: John Libbey Press. p 190-198.
-
(1997)
Paediatric Epilepsy Syndromes and Their Surgical Treatment
, pp. 190-198
-
-
Meencke, H.J.1
Veith, G.2
-
14
-
-
0021090597
-
Fetal akinesia sequence: An animal model
-
Moessinger AC. (1983) Fetal akinesia sequence: An animal model. Pediatrics 72: 857-863.
-
(1983)
Pediatrics
, vol.72
, pp. 857-863
-
-
Moessinger, A.C.1
-
15
-
-
0030659671
-
The Worster-Drought syndrome: A severe test of paediatric neurodisability services?
-
Neville BGR. (1997) The Worster-Drought syndrome: A severe test of paediatric neurodisability services? Dev Med Child Neurol 39: 782-784.
-
(1997)
Dev Med Child Neurol
, vol.39
, pp. 782-784
-
-
Neville, B.G.R.1
-
18
-
-
0038150802
-
Brainstem dysgenesis: Report of five patients with congenital hypotonia, multiple cranial nerve involvement, and ocular motor apraxia
-
Roig M, Gratacos M, Vazquez E, Del-Toro M, Foguet A, Ferrer I, Macaya A. (2003) Brainstem dysgenesis: Report of five patients with congenital hypotonia, multiple cranial nerve involvement, and ocular motor apraxia. Dev Med Child Neurol 45: 489-493.
-
(2003)
Dev Med Child Neurol
, vol.45
, pp. 489-493
-
-
Roig, M.1
Gratacos, M.2
Vazquez, E.3
Del-Toro, M.4
Foguet, A.5
Ferrer, I.6
Macaya, A.7
-
19
-
-
0344841407
-
Pediatric electromyography
-
(Chapter 3) In: Jones HR, De Vivo DC, Darras BT, editors. Philadelphia: Butterworth Heinemann
-
Swoboda KJ, Edebol-Eeg-Olofsson K, Harmon RL, Bolton CE, Harper MC, Pitt M, Darras BT, Jones HT Jr. (2003) Pediatric electromyography (Chapter 3). In: Jones HR, De Vivo DC, Darras BT, editors. Neuromuscular Disorders of Infancy, Childhood and Adolescence. A clinician's approach. Philadelphia: Butterworth Heinemann.
-
(2003)
Neuromuscular Disorders of Infancy, Childhood and Adolescence. A Clinician's Approach
-
-
Swoboda, K.J.1
Edebol-Eeg-Olofsson, K.2
Harmon, R.L.3
Bolton, C.E.4
Harper, M.C.5
Pitt, M.6
Darras, B.T.7
Jones Jr., H.T.8
-
20
-
-
0036201466
-
A locus for bilateral perisylvian polymicrogyria maps to Xq28
-
Villard L, Nguyen K, Cardoso C, Martin CL, Weiss AM, Sifry-Platt M, Grix AW, Graham JM Jr, Winter RM, Leventer RJ, Dobyns WB. (2002) A locus for bilateral perisylvian polymicrogyria maps to Xq28. Am J Hum Genet 70: 1003-1008.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1003-1008
-
-
Villard, L.1
Nguyen, K.2
Cardoso, C.3
Martin, C.L.4
Weiss, A.M.5
Sifry-Platt, M.6
Grix, A.W.7
Graham Jr., J.M.8
Winter, R.M.9
Leventer, R.J.10
Dobyns, W.B.11
|