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1 ological evidence of developmental tumors or cortical dysplasia.
2 arachnoid space results in the formation of cortical dysplasia.
3 y, centrally predominant polymicrogyria-like cortical dysplasia.
4 l organization consistent with type Ia focal cortical dysplasia.
5 terotopia and diffuse megalencephaly without cortical dysplasia.
6 to differentiate between type I and type II cortical dysplasia.
7 factors are involved in the pathogenesis of cortical dysplasia.
8 ly had schizencephaly, heterotopia, or focal cortical dysplasia.
9 athological aging, and the presence of focal cortical dysplasia.
10 meningeal differentiation can lead to severe cortical dysplasia.
11 aches for childhood epilepsy associated with cortical dysplasia.
12 daptor proteins, FE65 and FE65L1, results in cortical dysplasia.
13 t in epilepsy and mental retardation without cortical dysplasia.
14 bitory synaptic transmission in experimental cortical dysplasia.
15 y a causal role in the pathogenesis of focal cortical dysplasias.
16 well as in the pathogenesis of certain human cortical dysplasias.
18 velopmental abnormalities consisted of focal cortical dysplasia (5), heterotopia (2), hamartoma (3),
19 aly and intractable epilepsy, one with focal cortical dysplasia and intractable epilepsy, and one dys
20 is linked to the first description of focal cortical dysplasia and limbic encephalitis, the patholog
22 n utero irradiation of rats produces diffuse cortical dysplasia and neuronal heterotopia in the neoco
23 a, two focal cortical dysplasia, one diffuse cortical dysplasia and one microdysgenesis), acquired in
25 f central pachygyria and polymicrogyria-like cortical dysplasia and simplified gyral malformation syn
26 cytomegalic neurons in focal or hemispheric cortical dysplasia and to determine whether the activity
27 ficial, particularly for patients with focal cortical dysplasia and unilateral hemispheric malformati
28 out the prevalence of HPV infection in focal cortical dysplasias and about its potential importance a
30 ents, including hemimegalencephaly and focal cortical dysplasia, are common causes of intractable pae
31 egalencephaly, hemimegalencephaly, and focal cortical dysplasia as part of a single pathogenic spectr
32 Long-term overexpression of Wnt3a led to cortical dysplasia associated with the formation of larg
37 two groups: patients with highly asymmetric cortical dysplasia caused by the common p.E17K mutation,
39 in brain samples resected from patients with cortical dysplasia (CD), which was correlated with durat
42 ons of cortical development, including focal cortical dysplasia (FCD) and hemimegalencephaly (HME), a
44 nd ultrastructural patterns in type II focal cortical dysplasia (FCD) have been studied to explain th
48 f tuberous sclerosis complex (TSC) and focal cortical dysplasia (FCD) is early life refractory epilep
52 x (TSC)-associated cortical tubers and focal cortical dysplasia (FCD), we performed qualitative and s
56 pithelial tumours (DNTs; eight cases), focal cortical dysplasia (FCD; 14 cases) and hippocampal scler
57 ohistochemistry in the core of type II focal cortical dysplasias (FCD-II), at the FCD boundary (peril
60 of CNTNAP2 in Old Order Amish children with cortical dysplasia, focal epilepsy, relative macrocephal
61 In the developmental group, low-grade focal cortical dysplasias had better outcome than heterotopia
63 he complex structural abnormalities of focal cortical dysplasia have been proposed - from Taylor et a
64 splay type I lissencephaly, a severe form of cortical dysplasia hypothesized to result from abnormal
67 lioneuronal heterotopias are a focal type of cortical dysplasia in which neural cells migrate aberran
70 h drug-resistant epilepsy.However, in type I cortical dysplasia, MR imaging is often normal, and also
71 ) central pachygyria and polymicrogyria-like cortical dysplasia (n = 24); (iv) generalized polymicrog
72 = 24); (iv) generalized polymicrogyria-like cortical dysplasia (n = 6); and (v) a 'simplified' gyral
73 eveal the presence and the border of type II cortical dysplasia on MRI, a quantitative ROI-based anal
74 egalencephaly, two polymicrogyria, two focal cortical dysplasia, one diffuse cortical dysplasia and o
75 diagnosed with multiple sclerosis, one with cortical dysplasia, one with pineal hemorrhage and one w
76 suggests that new cells may arrive in focal cortical dysplasia, perhaps deriving in part from the su
77 f the most common or enlightening MCD: focal cortical dysplasia, periventricular heterotopia, polymic
79 tardation and seizures associated with focal cortical dysplasias, subependymal nodules, and subependy
80 growth (megalencephaly) as well as segmental cortical dysplasia (such as hemimegalencephaly, focal co
81 ranges from lissencephalic to polymicrogyric cortical dysplasias, suggesting shared pathogenic mechan
82 n large dysplastic cells microdissected from cortical dysplasia surgical specimens was used to identi
83 for surgical outcome in patients with focal cortical dysplasia than the presence of a lesion on magn
84 megalencephaly, hemimegalencephaly and focal cortical dysplasia, the most common cause of intractable
85 ype II dysplasias and in only some of type I cortical dysplasias.THE MOST COMMON FINDINGS ON MRI IMAG
86 trocytes of all hemimegalencephaly and focal cortical dysplasia type II specimens, regardless of the
92 association between HPV infection and focal cortical dysplasia type IIb, and its reproducibility acr
93 roportion of pathological specimens of focal cortical dysplasia type IIb, but not in control specimen
95 thological diagnosis among adults, and focal cortical dysplasia was the most common diagnosis among c
96 ions of cortical development in 19.8% (focal cortical dysplasia was the most common type, 52.7% of ca
97 or the cognitive impairment in the rats with cortical dysplasia was the underlying brain substrate, n
98 with focal or multifocal polymicrogyria-like cortical dysplasia with abnormal and simplified gyral pa
99 rtical dysplasia are recognized.Type I focal cortical dysplasia with mild symptomatic expression and
101 esected TSC tubers, FCDs with balloon cells, cortical dysplasia without balloon cells, and histologic
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