-
1
-
-
0025767294
-
The predictive value of microcephaly during the first year of life for mental retardation at seven years
-
Dolk H. The predictive value of microcephaly during the first year of life for mental retardation at seven years. Dev Med Child Neurol 1991;33:974-983.
-
(1991)
Dev Med Child Neurol
, vol.33
, pp. 974-983
-
-
Dolk, H.1
-
2
-
-
11144350990
-
Microcephaly associated with abnormal gyral pattern
-
Sztriha L, Dawodu A, Gururaj A, et al. Microcephaly associated with abnormal gyral pattern. Neuropediatrics 2004; 35:346-352.
-
(2004)
Neuropediatrics
, vol.35
, pp. 346-352
-
-
Sztriha, L.1
Dawodu, A.2
Gururaj, A.3
-
4
-
-
0031869221
-
Microlissen-cephaly: A heterogeneous malformation of cortical development
-
Barkovich AJ, Ferriero DM, Barr RM, et al. Microlissen-cephaly: a heterogeneous malformation of cortical development. Neuropediatrics 1998;29:113-119.
-
(1998)
Neuropediatrics
, vol.29
, pp. 113-119
-
-
Barkovich, A.J.1
Ferriero, D.M.2
Barr, R.M.3
-
5
-
-
32144433872
-
A developmental and genetic classification for malformations of cortical development
-
Barkovich AJ, Kuzniecky RI, Jackson GD, et al. A developmental and genetic classification for malformations of cortical development. Neurology 2005;65:1873-1887.
-
(2005)
Neurology
, vol.65
, pp. 1873-1887
-
-
Barkovich, A.J.1
Kuzniecky, R.I.2
Jackson, G.D.3
-
6
-
-
56149096865
-
Diffusion-weighted and conventional MR imaging in neonatal hy-poxic ischemia: Two-year follow-up study
-
Vermeulen RJ, van Schie PE, Hendrikx L, et al. Diffusion-weighted and conventional MR imaging in neonatal hy-poxic ischemia: two-year follow-up study. Radiology 2008; 249:631-639.
-
(2008)
Radiology
, vol.249
, pp. 631-639
-
-
Vermeulen, R.J.1
Van Schie, P.E.2
Hendrikx, L.3
-
7
-
-
0029992752
-
Normal gyration and sulcation in preterm and term neo-nates: Appearance on MR images
-
van der Knaap MS, van Wezel-Meijler G, Barth PG, et al. Normal gyration and sulcation in preterm and term neo-nates: appearance on MR images. Radiology 1996;200: 389-396.
-
(1996)
Radiology
, vol.200
, pp. 389-396
-
-
Van Der Knaap, M.S.1
Van Wezel-Meijler, G.2
Barth, P.G.3
-
8
-
-
0024274659
-
The human pattern of gyrification in the cerebral cortex
-
Zilles K, Armstrong E, Schleicher A, et al. The human pattern of gyrification in the cerebral cortex. Anat Embryol (Berl) 1988;179:173-179.
-
(1988)
Anat Embryol (Berl)
, vol.179
, pp. 173-179
-
-
Zilles, K.1
Armstrong, E.2
Schleicher, A.3
-
9
-
-
0025295738
-
Quantitative morphometric analysis of brain growth using magnetic resonance imaging
-
Schaefer GB, Thompson JN, Bodensteiner JB, et al. Quantitative morphometric analysis of brain growth using magnetic resonance imaging. J Child Neurol 1990;5:127-130.
-
(1990)
J Child Neurol
, vol.5
, pp. 127-130
-
-
Schaefer, G.B.1
Thompson, J.N.2
Bodensteiner, J.B.3
-
10
-
-
11144282429
-
Neonatal seizure monitoring using non-linear EEG analysis
-
Smit LS, Vermeulen RJ, Fetter WP, et al. Neonatal seizure monitoring using non-linear EEG analysis. Neuropediat-rics 2004;35:329-335.
-
(2004)
Neuropediat-rics
, vol.35
, pp. 329-335
-
-
Smit, L.S.1
Vermeulen, R.J.2
Fetter, W.P.3
-
11
-
-
17644399484
-
Autosomal recessive primary microcephaly (MCPH): A review of clinical, molecular, and evolutionary findings
-
Woods CG, Bond J, Enard W. Autosomal recessive primary microcephaly (MCPH): a review of clinical, molecular, and evolutionary findings. Am J Hum Genet 2005;76: 717-728.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 717-728
-
-
Woods, C.G.1
Bond, J.2
Enard, W.3
-
12
-
-
33750086043
-
Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus
-
de Wit MC, de Coo IF, Julier C, et al. Microcephaly and simplified gyral pattern of the brain associated with early onset insulin-dependent diabetes mellitus. Neurogenetics 2006;7:259-263.
-
(2006)
Neurogenetics
, vol.7
, pp. 259-263
-
-
De Wit, M.C.1
De Coo, I.F.2
Julier, C.3
-
13
-
-
24944465271
-
ASPM mutations identified in patients with primary microcephaly and seizures
-
Shen J, Eyaid W, Mochida GH, et al. ASPM mutations identified in patients with primary microcephaly and seizures. J Med Genet 2005;42:725-729.
-
(2005)
J Med Genet
, vol.42
, pp. 725-729
-
-
Shen, J.1
Eyaid, W.2
Mochida, G.H.3
-
14
-
-
50449089620
-
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum
-
Najm J, Horn D, Wimplinger I, et al. Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum. Nat Genet 2008;40:1065-1067.
-
(2008)
Nat Genet
, vol.40
, pp. 1065-1067
-
-
Najm, J.1
Horn, D.2
Wimplinger, I.3
-
15
-
-
0032955891
-
Microcephaly with simplified gyral pattern in six related children
-
Peiffer A, Singh N, Leppert M, et al. Microcephaly with simplified gyral pattern in six related children. Am J Med Genet 1999;84:137-144.
-
(1999)
Am J Med Genet
, vol.84
, pp. 137-144
-
-
Peiffer, A.1
Singh, N.2
Leppert, M.3
-
16
-
-
16844364796
-
Extreme microcephaly with agyria-pachygyria, partial agenesis of the corpus callosum, and pontocerebellar dysplasia
-
Sztriha L, Johansen JG, Al-Gazali LI. Extreme microcephaly with agyria-pachygyria, partial agenesis of the corpus callosum, and pontocerebellar dysplasia. J Child Neurol 2005;20:170-172.
-
(2005)
J Child Neurol
, vol.20
, pp. 170-172
-
-
Sztriha, L.1
Johansen, J.G.2
Al-Gazali, L.I.3
-
17
-
-
0020075263
-
Familial lissenceph-aly with extreme neopallial hypoplasia
-
Barth PG, Mullaart R, Stam FC, et al. Familial lissenceph-aly with extreme neopallial hypoplasia. Brain Dev 1982;4: 145-151.
-
(1982)
Brain Dev
, vol.4
, pp. 145-151
-
-
Barth, P.G.1
Mullaart, R.2
Stam, F.C.3
-
18
-
-
0029804898
-
Lissencephaly with extreme cerebral and cerebellar hypoplasia: A magnetic resonance imaging study
-
Kroon AA, Smit BJ, Barth PG, et al. Lissencephaly with extreme cerebral and cerebellar hypoplasia: a magnetic resonance imaging study. Neuropediatrics 1996;27:273-276.
-
(1996)
Neuropediatrics
, vol.27
, pp. 273-276
-
-
Kroon, A.A.1
Smit, B.J.2
Barth, P.G.3
-
19
-
-
0033060614
-
Microcephaly with simplified gyral pattern (oligogyric microcephaly) and microlissen-cephaly: Reply
-
Dobyns WB, Barkovich AJ. Microcephaly with simplified gyral pattern (oligogyric microcephaly) and microlissen-cephaly: reply. Neuropediatrics 1999;30:104-106.
-
(1999)
Neuropediatrics
, vol.30
, pp. 104-106
-
-
Dobyns, W.B.1
Barkovich, A.J.2
-
20
-
-
0036113638
-
MR imaging appearance of fetal cerebral ventricular morphology
-
Levine D, Trop I, Mehta TS, et al. MR imaging appearance of fetal cerebral ventricular morphology. Radiology 2002;223:652-660.
-
(2002)
Radiology
, vol.223
, pp. 652-660
-
-
Levine, D.1
Trop, I.2
Mehta, T.S.3
-
21
-
-
33748436802
-
In utero magnetic resonance of non-isolated ventriculomegaly: Does ventricular size or morphology reflect pathology?
-
Rickard S, Morris J, Paley M, et al. In utero magnetic resonance of non-isolated ventriculomegaly: Does ventricular size or morphology reflect pathology? Clin Radiol 2006;61:844-853.
-
(2006)
Clin Radiol
, vol.61
, pp. 844-853
-
-
Rickard, S.1
Morris, J.2
Paley, M.3
-
22
-
-
0038416095
-
Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16
-
Chang BS, Piao X, Bodell A, et al. Bilateral frontoparietal polymicrogyria: clinical and radiological features in 10 families with linkage to chromosome 16. Ann Neurol 2003;53:596-606.
-
(2003)
Ann Neurol
, vol.53
, pp. 596-606
-
-
Chang, B.S.1
Piao, X.2
Bodell, A.3
-
23
-
-
33751326164
-
Links between abnormal brain structure and cognition in holoprosencephaly
-
Roesler CP, Paterson SJ, Flax J, et al. Links between abnormal brain structure and cognition in holoprosencephaly. Pediatr Neurol 2006;35:387-394.
-
(2006)
Pediatr Neurol
, vol.35
, pp. 387-394
-
-
Roesler, C.P.1
Paterson, S.J.2
Flax, J.3
-
24
-
-
0037044287
-
Neuroanatomy of holoprosencephaly as predictor of function: Beyond the face predicting the brain
-
Plawner LL, Delgado MR, Miller VS, et al. Neuroanatomy of holoprosencephaly as predictor of function: beyond the face predicting the brain. Neurology 2002;59:1058-1066.
-
(2002)
Neurology
, vol.59
, pp. 1058-1066
-
-
Plawner, L.L.1
Delgado, M.R.2
Miller, V.S.3
-
25
-
-
0033933649
-
Voxel-based morphometry: The methods
-
Ashburner J, Friston KJ. Voxel-based morphometry: the methods. Neuroimage 2000;11:805-821.
-
(2000)
Neuroimage
, vol.11
, pp. 805-821
-
-
Ashburner, J.1
Friston, K.J.2
-
26
-
-
50049103785
-
Structural MR-imaging studies of the brain in children: Issues and opportunities
-
Wilke M, Holland SK. Structural MR-imaging studies of the brain in children: issues and opportunities. Neuroem-bryol Aging 2008;5:6-13.
-
(2008)
Neuroem-bryol Aging
, vol.5
, pp. 6-13
-
-
Wilke, M.1
Holland, S.K.2
-
27
-
-
0042916498
-
New syndrome of simplified gyral pattern, micromelia, dysmorphic features and early death
-
Basel-Vanagaite L, Marcus N, Klinger G, et al. New syndrome of simplified gyral pattern, micromelia, dysmorphic features and early death. Am J Med Genet A 2003;119: 200-206.
-
(2003)
Am J Med Genet A
, vol.119
, pp. 200-206
-
-
Basel-Vanagaite, L.1
Marcus, N.2
Klinger, G.3
-
28
-
-
0036990776
-
Microlissen-cephaly in microcephalic osteodysplastic primordial dwarf-ism: A case report and review of the literature
-
Klinge L, Schaper J, Wieczorek D, et al. Microlissen-cephaly in microcephalic osteodysplastic primordial dwarf-ism: a case report and review of the literature. Neuropediatrics 2002;33:309-313.
-
(2002)
Neuropediatrics
, vol.33
, pp. 309-313
-
-
Klinge, L.1
Schaper, J.2
Wieczorek, D.3
-
29
-
-
0032783118
-
Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis
-
Sztriha L, Al-Gazali LI, Varady E, et al. Autosomal recessive micrencephaly with simplified gyral pattern, abnormal myelination and arthrogryposis. Neuropediatrics 1999;30: 141-145.
-
(1999)
Neuropediatrics
, vol.30
, pp. 141-145
-
-
Sztriha, L.1
Al-Gazali, L.I.2
Varady, E.3
-
30
-
-
0034961955
-
Microlissen-cephaly with cardiac, spinal and urogenital defects
-
Gardner RJ, Savarirayan R, Dunne KB, et al. Microlissen-cephaly with cardiac, spinal and urogenital defects. Clin Dysmorphol 2001;10:203-208.
-
(2001)
Clin Dysmorphol
, vol.10
, pp. 203-208
-
-
Gardner, R.J.1
Savarirayan, R.2
Dunne, K.B.3
-
31
-
-
33748549916
-
Unusual association of simplified gyral pattern and sparse hair in an Egyptian patient with microcephaly-lymphoedema
-
Mazen I, Zaki MS. Unusual association of simplified gyral pattern and sparse hair in an Egyptian patient with microcephaly-lymphoedema. Clin Dysmorphol 2006;15: 245-247.
-
(2006)
Clin Dysmorphol
, vol.15
, pp. 245-247
-
-
Mazen, I.1
Zaki, M.S.2
|