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

Year Number of Results
2000 3
2001 2
2002 1
2003 1
2004 1
2005 2
2006 1
2008 2
2009 2
2010 1
2011 2
2012 1
2013 1
2014 1
2016 1
2017 2
2018 2
2019 1
2020 1
2021 1
2024 1

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Page 1
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.
LCHa is related to mutation in LIS1 or DCX, LCHb with mutation of the RELN gene, and LCHd could be related to the TUBA1A gene. Polymicrogyria encompasses a wide range of clinical, etiological, and histological findings. Among several syndromes, recessive bilateral fronto-p …
LCHa is related to mutation in LIS1 or DCX, LCHb with mutation of the RELN gene, and LCHd could be related to the TUBA1A gene. Polymicrog
Polymicrogyria: a common and heterogeneous malformation of cortical development.
Stutterd CA, Leventer RJ. Stutterd CA, et al. Am J Med Genet C Semin Med Genet. 2014 Jun;166C(2):227-39. doi: 10.1002/ajmg.c.31399. Epub 2014 May 28. Am J Med Genet C Semin Med Genet. 2014. PMID: 24888723 Review.
Polymicrogyria (PMG) is one of the most common malformations of cortical development. ...It may occur as an isolated cortical malformation, or in association with other malformations within the brain or body as part of a multiple congenital anomaly syndrome. Polymicrogy
Polymicrogyria (PMG) is one of the most common malformations of cortical development. ...It may occur as an isolated cortical malform
Neuroimaging findings in Pallister-Killian syndrome.
Barkovich EJ, Lateef TM, Whitehead MT. Barkovich EJ, et al. Neuroradiol J. 2018 Aug;31(4):403-411. doi: 10.1177/1971400917744798. Epub 2017 Dec 20. Neuroradiol J. 2018. PMID: 29260614 Free PMC article. Review.
MRI abnormalities common to PKS include cerebral volume loss, malformations of cortical development, corpus callosum dysgenesis, white matter disease, and craniofacial malformations. In our patient, new findings of perisylvian with occipital polymicrogyria, vermian …
MRI abnormalities common to PKS include cerebral volume loss, malformations of cortical development, corpus callosum dysgenesis, white matte …
Polymicrogyria associated with 17p13.3p13.2 duplication: Case report and review of the literature.
Stutterd CA, Francis D, McGillivray G, Lockhart PJ, Leventer RJ. Stutterd CA, et al. Eur J Med Genet. 2020 Apr;63(4):103774. doi: 10.1016/j.ejmg.2019.103774. Epub 2019 Oct 1. Eur J Med Genet. 2020. PMID: 31585183 Review.
We present the case of a male infant with bilateral perisylvian polymicrogyria associated with a de novo duplication of chromosome region 17p13.3p13.2. To our knowledge, this is the first report of polymicrogyria associated with the 17p13.3 contiguous gene du …
We present the case of a male infant with bilateral perisylvian polymicrogyria associated with a de novo duplication of chromo …
New trends in neuronal migration disorders.
Verrotti A, Spalice A, Ursitti F, Papetti L, Mariani R, Castronovo A, Mastrangelo M, Iannetti P. Verrotti A, et al. Eur J Paediatr Neurol. 2010 Jan;14(1):1-12. doi: 10.1016/j.ejpn.2009.01.005. Epub 2009 Mar 4. Eur J Paediatr Neurol. 2010. PMID: 19264520 Review.
It is characterized by a cluster of disorganized neurons in abnormal locations and it is divided into three main groups: periventricular nodular heterotopia, subcortical heterotopia and marginal glioneural heterotopia. Polymicrogyria develops at the final stages of neurona …
It is characterized by a cluster of disorganized neurons in abnormal locations and it is divided into three main groups: periventricular nod …
Genetic malformations of cortical development.
Guerrini R, Marini C. Guerrini R, et al. Exp Brain Res. 2006 Aug;173(2):322-33. doi: 10.1007/s00221-006-0501-z. Epub 2006 May 25. Exp Brain Res. 2006. PMID: 16724181 Review.
Carrier female patients can have isolated corpus callosum agenesis. Among several syndromes featuring polymicrogyria, bilateral perisylvian polymicrogyria shows genetic heterogeneity, including linkage to chromosome Xq28 in some pedigrees, autosomal dominant …
Carrier female patients can have isolated corpus callosum agenesis. Among several syndromes featuring polymicrogyria, bilateral pe
X-linked malformations of cortical development.
Leventer RJ, Mills PL, Dobyns WB. Leventer RJ, et al. Am J Med Genet. 2000 Fall;97(3):213-20. doi: 10.1002/1096-8628(200023)97:3<213::AID-AJMG1039>3.0.CO;2-W. Am J Med Genet. 2000. PMID: 11449490 Review.
This review will discuss four cortical malformation syndromes, which are known or likely to have an X-linked inheritance pattern: bilateral periventricular nodular heterotopia, X-linked lissencephaly/subcortical band heterotopia, X-linked lissencephaly with abnormal genitalia, an …
This review will discuss four cortical malformation syndromes, which are known or likely to have an X-linked inheritance pattern: bilateral …
Cortical dysplasias and epilepsy: a review of the architectonic, clinical, and seizure patterns.
Andermann F. Andermann F. Adv Neurol. 2000;84:479-96. Adv Neurol. 2000. PMID: 11091890 Review.
Cortical malformations due to disorganization, occurring later in intrauterine life, are represented by micropolygyria. These lesions are often bilateral and perisylvian, but at times they are unilateral and in some patients may be occipital or frontal. ...Interesting and …
Cortical malformations due to disorganization, occurring later in intrauterine life, are represented by micropolygyria. These lesions are of …
Epilepsy and genetic malformations of the cerebral cortex.
Guerrini R, Carrozzo R. Guerrini R, et al. Am J Med Genet. 2001 Summer;106(2):160-73. doi: 10.1002/ajmg.1569. Am J Med Genet. 2001. PMID: 11579436 Review.
Fukuyama congenital muscular dystrophy is due to mutations of the fukutin gene and is accompanied by polymicrogyria. Febrile seizures and epilepsy with generalized tonic-convulsions appear in about 50% of children but are usually not severe. ...TSC1 mutations seem to cause …
Fukuyama congenital muscular dystrophy is due to mutations of the fukutin gene and is accompanied by polymicrogyria. Febrile seizures …
25 results