Works matching IS 08830738 AND DT 2005 AND VI 20 AND IP 4
Results: 20
X-Linked Lissencephaly With Abnormal Genitalia as a Tangential Migration Disorder Causing Intractable Epilepsy: Proposal for a New Term, "Interneuronopathy"
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 392, doi. 10.1177/08830738050200042001
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Long-Term Prognosis of Epilepsies and Related Seizure Disorders in Fukuyama-iype Congenital Muscular Dystrophy.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 385, doi. 10.1177/08830738050200041901
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Recurrent Intractable Seizures in Children With Cortical Dysplasia Adjacent to Dysembryoplastic Neuroepithelial Tumor.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 377, doi. 10.1177/08830738050200041801
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Electroencephalographic Recordings of Focal Seizures in Patients Affected by Periventricular Nodular Heterotopia: Role of the Heterotopic Nodules in the Genesis of Epileptic Discharges.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 369, doi. 10.1177/08830738050200041701
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Dynamic Statistical Parametric Mapping for Analyzing the Magnetoencephalographic Epileptiform Activity in Patients With Epilepsy.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 363, doi. 10.1177/08830738050200041601
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Neurophysiologic Findings of Neuronal Migration Disorders: Intrinsic Epileptogenicity of Focal Cortical Dysplasia on Electroencephalography, Electrocorticography, and Magnetoencephalography.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 357, doi. 10.1177/08830738050200041501
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Clinical Application of Experimental Cortical Dysplasia in Rats.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 351, doi. 10.1177/08830738050200041401
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Pathologic Features of Dysplasia and Accompanying Alterations Observed in Surgical Specimens From Patients With Intractable Epilepsy.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 341, doi. 10.1177/08830738050200041301
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Clinical Aspects of Hemimegalencephaly by Means of a Nationwide Survey.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 337, doi. 10.1177/08830738050200041201
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Molecular Pathogenesis of Focal Cortical Dysplasia and Hemimegalencephaly.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 330, doi. 10.1177/08830738050200041101
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Molecular and Neurologic Findings of Peroxisome Biogenesis Disorders.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 326, doi. 10.1177/08830738050200041001
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Intractable Seizures in Tuberous Sclerosis Complex: From Molecular Pathogenesis to the Rationale for Treatment.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 318, doi. 10.1177/08830738050200040901
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Schizencephaly: Clinical Spectrum, Epilepsy, and Pathogenesis.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 313, doi. 10.1177/08830738050200040801
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Genotype-Phenotype Correlation in Lissencephaly and Subcortical Band Heterotopia: The Key Questions Answered.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 307, doi. 10.1177/08830738050200040701
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Activated Remodeling and N-Methyl-D-Aspartate (NMDA) Receptors in Cortical Dysplasia.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 303, doi. 10.1177/08830738050200040601
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Cortical Malformation and Pediatric Epilepsy: A Molecular Genetic Approach.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 300, doi. 10.1177/08830738050200040501
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Neuronal Migration Disorders, Genetics, and Epileptogenesis.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 287, doi. 10.1177/08830738050200040401
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Neuronal Migration in Developmental Disorders.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 280, doi. 10.1177/08830738050200040301
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Neuronal Migration in Cortical Development.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 274, doi. 10.1177/08830738050200040201
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Neuronal Migration Disorders and Their Impact on Pediatric Epileptology.
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- Journal of Child Neurology, 2005, v. 20, n. 4, p. 273, doi. 10.1177/08830738050200040101
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