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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1994 1
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2000 5
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2003 3
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2005 4
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2008 6
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2010 4
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57 results

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Page 1
Lissencephaly: Update on diagnostics and clinical management.
Koenig M, Dobyns WB, Di Donato N. Koenig M, et al. Eur J Paediatr Neurol. 2021 Nov;35:147-152. doi: 10.1016/j.ejpn.2021.09.013. Epub 2021 Oct 7. Eur J Paediatr Neurol. 2021. PMID: 34731701 Review.
Lissencephaly represents a spectrum of rare malformations of cortical development including agyria, pachygyria and subcortical band heterotopia. The progress in molecular genetics has led to identification of 31 lissencephaly-associated genes with the overall …
Lissencephaly represents a spectrum of rare malformations of cortical development including agyria, pachygyria and subcortical ban …
Neuronal migration disorders.
Guerrini R, Parrini E. Guerrini R, et al. Neurobiol Dis. 2010 May;38(2):154-66. doi: 10.1016/j.nbd.2009.02.008. Epub 2009 Feb 23. Neurobiol Dis. 2010. PMID: 19245832 Review.
Lissencephaly-pachygyria-severe band heterotopia are diffuse neuronal migration disorders (NMDs) causing severe, global neurological impairment. Abnormalities of the LIS1, DCX, ARX, TUBA1A and RELN genes have been associated with these malformations. NMDs only affec …
Lissencephaly-pachygyria-severe band heterotopia are diffuse neuronal migration disorders (NMDs) causing severe, global neurol …
The genetics of lissencephaly.
Fry AE, Cushion TD, Pilz DT. Fry AE, et al. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):198-210. doi: 10.1002/ajmg.c.31402. Epub 2014 May 23. Am J Med Genet C Semin Med Genet. 2014. PMID: 24862549 Review.
Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
Leventer RJ, Pilz DT, Matsumoto N, Ledbetter DH, Dobyns WB. Leventer RJ, et al. Mol Med Today. 2000 Jul;6(7):277-84. doi: 10.1016/s1357-4310(00)01730-5. Mol Med Today. 2000. PMID: 10859564 Review.
Consequently, it is evident that cortical malformations are more common than previously thought. Among the most severe is classical lissencephaly, in which the cortex lacks the complex folding that characterizes the normal human brain. Lissencephaly includes agyria and pac …
Consequently, it is evident that cortical malformations are more common than previously thought. Among the most severe is classical l …
Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.
Leventer RJ. Leventer RJ. J Child Neurol. 2005 Apr;20(4):307-12. doi: 10.1177/08830738050200040701. J Child Neurol. 2005. PMID: 15921231 Review.
Lissencephaly and subcortical band heterotopia are closely related cortical malformations and are true disorders of neuronal migration. ...This review answers some of the key questions regarding the genotype-phenotype correlation for lissencephaly and subc …
Lissencephaly and subcortical band heterotopia are closely related cortical malformations and are true disorders of neu …
Cerebral developmental disorders.
Lian G, Sheen V. Lian G, et al. Curr Opin Pediatr. 2006 Dec;18(6):614-20. doi: 10.1097/MOP.0b013e328010542d. Curr Opin Pediatr. 2006. PMID: 17099359 Review.
Mutations in genes that direct the onset of neuroblast migration give rise to periventricular heterotopia (clusters of neurons along the ventricles of the brain). Mutations in genes that are required for neuroblast migration cause type I lissencephaly (smooth brain) and …
Mutations in genes that direct the onset of neuroblast migration give rise to periventricular heterotopia (clusters of neurons along …
Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin.
Gleeson JG. Gleeson JG. Curr Opin Neurol. 2000 Apr;13(2):121-5. doi: 10.1097/00019052-200004000-00002. Curr Opin Neurol. 2000. PMID: 10987567 Review.
Classical lissencephaly and double cortex are genetic neuronal migration disorders associated with mental retardation and epilepsy. In classical lissencephaly, the six-layered cortex is replaced by a four layered structure lacking normal gyri or sulci. ...
Classical lissencephaly and double cortex are genetic neuronal migration disorders associated with mental retardation and epilepsy. I …
The doublecortin gene family and disorders of neuronal structure.
Dijkmans TF, van Hooijdonk LW, Fitzsimons CP, Vreugdenhil E. Dijkmans TF, et al. Cent Nerv Syst Agents Med Chem. 2010 Mar;10(1):32-46. doi: 10.2174/187152410790780118. Cent Nerv Syst Agents Med Chem. 2010. PMID: 20236041 Review.
The doublecortin gene family is associated with subcortical band heterotopia, lissencephaly, epilepsy, developmental dyslexia and retinitis pigmentosa. ...
The doublecortin gene family is associated with subcortical band heterotopia, lissencephaly, epilepsy, developmental dy …
Malformations of cortical development.
Pang T, Atefy R, Sheen V. Pang T, et al. Neurologist. 2008 May;14(3):181-91. doi: 10.1097/NRL.0b013e31816606b9. Neurologist. 2008. PMID: 18469675 Free PMC article. Review.
Disorders of early neuroblast migration give rise to periventricular heterotopia (neurons located along the ventricles), whereas abnormalities later in migration lead to lissencephaly (smooth brain) or subcortical band heterotopia (smooth brain with a …
Disorders of early neuroblast migration give rise to periventricular heterotopia (neurons located along the ventricles), whereas abno …
Diffuse malformations of cortical development.
Bahi-Buisson N, Guerrini R. Bahi-Buisson N, et al. Handb Clin Neurol. 2013;111:653-65. doi: 10.1016/B978-0-444-52891-9.00068-3. Handb Clin Neurol. 2013. PMID: 23622213 Review.
Up to now, eight genes have been involved in different types of MCD. Lissencephaly-pachygyria and subcortical band heterotopia (SBH) represent a malformative spectrum resulting from mutations of either LIS1 or DCX genes. ...Bilateral perisylvian polymicrogyri …
Up to now, eight genes have been involved in different types of MCD. Lissencephaly-pachygyria and subcortical band heteroto …
57 results