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Lissencephaly

Known as: Lissencephaly [Disease/Finding], Lissencephalies, Lissencephalia 
A smooth brain malformation of the CEREBRAL CORTEX resulting from the abnormal location of developing neurons during corticogenesis. It is… Expand
National Institutes of Health

Papers overview

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Review
2018
Review
2018
A large number of genes encoding for tubulin proteins are expressed in the developing brain. Each is subject to specific spatial… Expand
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Review
2017
Review
2017
Lissencephaly (“smooth brain,” LIS) is a malformation of cortical development associated with deficient neuronal migration and… Expand
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Highly Cited
2007
Highly Cited
2007
Summary The development of the mammalian brain is dependent on extensive neuronal migration. Mutations in mice and humans that… Expand
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Highly Cited
2002
Highly Cited
2002
Male embryonic mice with mutations in the X-linked aristaless-related homeobox gene (Arx) developed with small brains due to… Expand
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Highly Cited
2000
Highly Cited
2000
Mutations in the LIS1 gene cause gross histological disorganization of the developing human brain, resulting in a brain surface… Expand
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Highly Cited
1998
Highly Cited
1998
X-linked lissencephaly and "double cortex" are allelic human disorders mapping to Xq22.3-Xq23 associated with arrest of migrating… Expand
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Highly Cited
1998
Highly Cited
1998
X-SCLH/LIS syndrome is a neuronal migration disorder with disruption of the six-layered neocortex. It consists of subcortical… Expand
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Highly Cited
1994
Highly Cited
1994
PLATELET-ACTIVATING factor (PAF) is involved in a variety of biological and pathological processes1 and PAF acetylhydrolase… Expand
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Highly Cited
1993
Highly Cited
1993
LISSENCEPHALY (agyria-pachygyria) is a human brain malformation manifested by a smooth cerebral surface and abnormal neuronal… Expand
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Highly Cited
1993
Highly Cited
1993
Lissencephaly (agyria-pachygyria) is a human brain malformation manifested by a smooth cerebral surface and abnormal neuronal… Expand
Is this relevant?