Literature DB >> 8000973

The place of neuronal migration abnormalities in child neurology.

J Aicardi1.   

Abstract

With the development of modern imaging techniques, disturbances of neuronal migration appear to be a major cause of epilepsy, mental retardation and chronic neurological disability in childhood. Sixty-nine cases are presented, including 46 of diffuse migration abnormalities and 23 of localized dysplasia. Patients with diffuse migration disorders presented with mental retardation, gross motor impairment and severe seizure disorders whereas in those with focal anomalies, epilepsy was the chief complaint. Magnetic resonance imaging, although usually diagnostic of migration disorders often does not allow definition of the pathologic type. Some EEG patterns, such as high amplitude fast rhythms or the theta-delta pattern are highly suggestive. Most cases of abnormal migration are sporadic and probably acquired. Some are due to chromosomal anomalies, especially of chromosome 17p where a gene for lissencephaly has been mapped. Familial cases occur with both recessive and possibly dominant inheritance. Epilepsy due to migration abnormalities is often intractable. Resection of dysplastic cortex may be effective for localized disease and callosotomy has been proposed for diffuse anomalies.

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Year:  1994        PMID: 8000973     DOI: 10.1017/s0317167100041159

Source DB:  PubMed          Journal:  Can J Neurol Sci        ISSN: 0317-1671            Impact factor:   2.104


  8 in total

1.  Extracellular signals that regulate the tangential migration of olfactory bulb neuronal precursors: inducers, inhibitors, and repellents.

Authors:  H A Mason; S Ito; G Corfas
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

2.  Developmental disruptions and behavioral impairments in rats following in utero RNAi of Dyx1c1.

Authors:  Steven W Threlkeld; Melissa M McClure; Jilin Bai; Yu Wang; Joe J LoTurco; Glenn D Rosen; R Holly Fitch
Journal:  Brain Res Bull       Date:  2006-12-05       Impact factor: 4.077

Review 3.  Classification and pathological characteristics of the cortical dysplasias.

Authors:  Richard A Prayson
Journal:  Childs Nerv Syst       Date:  2014-10-09       Impact factor: 1.475

4.  Hippocampal heterotopia lack functional Kv4.2 potassium channels in the methylazoxymethanol model of cortical malformations and epilepsy.

Authors:  P A Castro; E C Cooper; D H Lowenstein; S C Baraban
Journal:  J Neurosci       Date:  2001-09-01       Impact factor: 6.167

5.  Neuroprotective changes of striatal degeneration-related gene expression by acupuncture in an MPTP mouse model of Parkinsonism: microarray analysis.

Authors:  Yeong-Gon Choi; Sujung Yeo; Yeon-Mi Hong; Sabina Lim
Journal:  Cell Mol Neurobiol       Date:  2010-11-25       Impact factor: 5.046

Review 6.  Cell migration in the normal and pathological postnatal mammalian brain.

Authors:  Myriam Cayre; Peter Canoll; James E Goldman
Journal:  Prog Neurobiol       Date:  2009-02-11       Impact factor: 11.685

7.  Brainstem respiratory oscillators develop independently of neuronal migration defects in the Wnt/PCP mouse mutant looptail.

Authors:  Muriel Thoby-Brisson; Julien Bouvier; Derrick M Glasco; Michelle E Stewart; Charlotte Dean; Jennifer N Murdoch; Jean Champagnat; Gilles Fortin; Anand Chandrasekhar
Journal:  PLoS One       Date:  2012-02-17       Impact factor: 3.240

Review 8.  LIS1 and DCX: Implications for Brain Development and Human Disease in Relation to Microtubules.

Authors:  Orly Reiner
Journal:  Scientifica (Cairo)       Date:  2013-03-17
  8 in total

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