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1 cy of LIS1 results in lissencephaly, a human neuronal migration disorder.
2 (encoding LIS1) cause lissencephaly, a human neuronal migration disorder.
3 s cause a clinically recognizable, syndromic neuronal migration disorder.
4 ogressive cognitive decline in patients with neuronal migration disorders.
5 otential to reveal common cellular causes of neuronal migration disorders.
6 correlation between pediatric epilepsies and neuronal migration disorders.
7 haracterised forms of muscular dystrophy and neuronal migration disorders.
8 r using nonrodent model systems for studying neuronal migration disorders.
9 y linking DYX1C1 with many genes involved in neuronal migration disorders.
10 ging from mild cognitive impairment (MCI) to neuronal migration disorders.
11 ive neurodevelopmental trait consisting of a neuronal migration disorder, and our data implicate GCP2
12                                              Neuronal migration disorders are often associated with i
13                                              Neuronal migration disorders are often identified in pat
14 mutated in X-linked lissencephaly (X-LIS), a neuronal migration disorder associated with epilepsy and
15  lissencephaly and double cortex are genetic neuronal migration disorders associated with mental reta
16 ales but manifests in females as a localized neuronal migration disorder, called periventricular nodu
17                    Type I lissencephaly is a neuronal migration disorder caused by haploinsuffiency o
18 so known as subcortical band heterotopia), a neuronal migration disorder causing epilepsy and mental
19                      Type I lissencephaly, a neuronal migration disorder characterized by cognitive d
20    Cobblestone brain malformation (COB) is a neuronal migration disorder characterized by protrusions
21                       Genes mutated in human neuronal migration disorders encode tubulin proteins and
22 ht into how cortactin and DCX, a known human neuronal migration disorder gene, participate in this pr
23  Periventricular heterotopia (PH) is a human neuronal migration disorder in which many neurons destin
24 ding these proteins in humans cause distinct neuronal migration disorders, including periventricular
25 ous deletions of 17p13.3 result in the human neuronal migration disorders isolated lissencephaly sequ
26  a gene whose hemi-deletion causes the human neuronal migration disorder Miller-Dieker lissencephaly.
27                        Recent data show that neuronal migration disorders (NMD) lower the seizure thr
28 sense variants in heterozygous patients with neuronal migration disorders (NMDs) as diverse as pachyg
29         The investigators also showed that a neuronal migration disorder occurs in both the myd mouse
30 ing a forebrain anomaly resembling the human neuronal migration disorder of double cortex.
31  (SBH) and lissencephaly (LIS), two distinct neuronal migration disorders producing epilepsy and vari
32               Human cortical heterotopia and neuronal migration disorders result in epilepsy; however
33           Classical lissencephaly (LIS) is a neuronal migration disorder resulting in brain malformat
34  patients with occipitotemporal syndrome had neuronal migration disorder, suggesting a developmental
35 rtin is a cytoplasmic protein mutated in the neuronal migration disorder X-linked lissencephaly.
36 rated periventricular nodular heterotopia, a neuronal migration disorder, yet overexpression of stabi