-
1
-
-
0024319579
-
The lissencephaly syndromes
-
Aicardi J. The lissencephaly syndromes. Int Pediatr 1989: 4: 118-126.
-
(1989)
Int Pediatr
, vol.4
, pp. 118-126
-
-
Aicardi, J.1
-
2
-
-
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
-
-
0025734430
-
The spectrum of lissencephaly: Report often patients analyzed by magnetic resonance imaging
-
Barkovich AJ, Koch TK, Carrol CL. The spectrum of lissencephaly: report often 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
Carrol, C.L.3
-
5
-
-
0344433739
-
Apparent X-linked pachygyria/lissencephaly with agenesis of the corpus callosum
-
Bhatt S. Dobyns WB, Pressman BD, Graham JM. Apparent X-linked pachygyria/lissencephaly with agenesis of the corpus callosum. Am J Hum Genet 1994: 55(Suppl): A78.
-
(1994)
Am J Hum Genet
, vol.55
, Issue.SUPPL.
-
-
Bhatt, S.1
Dobyns, W.B.2
Pressman, B.D.3
Graham, J.M.4
-
6
-
-
0021174658
-
Syndromes with lissencephaly I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly
-
Dobyns WB. Stratton RF, Greenberg F. Syndromes with lissencephaly I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly. Am J Med Genet 1984: 18: 509-526.
-
(1984)
Am J Med Genet
, vol.18
, pp. 509-526
-
-
Dobyns, W.B.1
Stratton, R.F.2
Greenberg, F.3
-
7
-
-
0025968152
-
Clinical and molecular diagnosis of Miller-Dieker syndrome
-
Dobyns WB, Curry CJR, Hoyme HE, Turlington LT. Ledbetter DH. Clinical and molecular diagnosis of Miller-Dieker syndrome. Am J Hum Genet 1991: 48: 584-594.
-
(1991)
Am J Hum Genet
, vol.48
, pp. 584-594
-
-
Dobyns, W.B.1
Curry, C.J.R.2
Hoyme, H.E.3
Turlington, L.T.4
Ledbetter, D.H.5
-
8
-
-
0026780723
-
Causal heterogeneity in isolated lissencephaly
-
Dobyns WB, Elias ER, Newlin AC, Pagon RA, Ledbetter DH. Causal heterogeneity in isolated lissencephaly. Neurology 1992: 42: 1375-1388.
-
(1992)
Neurology
, vol.42
, pp. 1375-1388
-
-
Dobyns, W.B.1
Elias, E.R.2
Newlin, A.C.3
Pagon, R.A.4
Ledbetter, D.H.5
-
9
-
-
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
-
10
-
-
0027200304
-
A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema
-
Hourihane JOB, Bennett CP, Chaudhuri R, Robb SA. Martin NDT. A sibship with a neuronal migration defect, cerebellar hypoplasia and congenital lymphedema. Neuropediatrics 1993: 24: 43-46.
-
(1993)
Neuropediatrics
, vol.24
, pp. 43-46
-
-
Hourihane, J.O.B.1
Bennett, C.P.2
Chaudhuri, R.3
Robb, S.A.4
Martin, N.D.T.5
-
11
-
-
0028353910
-
Familial diffuse cortical dysplasia
-
Kuzniecky R. Familial diffuse cortical dysplasia. Arch Neurol 1994: 51: 307-310.
-
(1994)
Arch Neurol
, vol.51
, pp. 307-310
-
-
Kuzniecky, R.1
-
14
-
-
0020554785
-
Pachygyria and congenital nephrosis. Disorder of migration and neuronal orientation
-
Robain O, Deonna T. Pachygyria and congenital nephrosis. Disorder of migration and neuronal orientation. Acta Neuropathol 1983: 60: 137-141.
-
(1983)
Acta Neuropathol
, vol.60
, pp. 137-141
-
-
Robain, O.1
Deonna, T.2
-
15
-
-
0024375162
-
Muscle-eye-brain disease (MEB)
-
Santavuori P, Somer H, Sainio K, Rapola J, Kruus S, Nikitin T, Ketonen L, Leisti J. Muscle-eye-brain disease (MEB). Brain Dev 1989: 11: 147-153.
-
(1989)
Brain Dev
, vol.11
, pp. 147-153
-
-
Santavuori, P.1
Somer, H.2
Sainio, K.3
Rapola, J.4
Kruus, S.5
Nikitin, T.6
Ketonen, L.7
Leisti, J.8
-
16
-
-
0015267348
-
Cerebrohepatorenal syndrome of Zellweger: An inherited disorder of neuronal migration
-
Volpe JJ, Adams RD. Cerebrohepatorenal syndrome of Zellweger: an inherited disorder of neuronal migration. Acta Neuropathol 1972: 20: 175-198.
-
(1972)
Acta Neuropathol
, vol.20
, pp. 175-198
-
-
Volpe, J.J.1
Adams, R.D.2
|