Classical Lissencephaly

Known as: Classic Lissencephaly, Lissencephaly Sequence, Isolated, Lissencephaly, type I 
A genetic disorder caused by mutations in the LIS1, XLIS, or TUBA1A genes. It results in brain malformation characterized by the underdevelopment or… (More)
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Ionic liquids (ILs) have been widely investigated as novel solvents, electrolytes, and soft functional materials. Nevertheless… (More)
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Review
2007
Review
2007
Classical lissencephaly is a human developmental brain disorder characterized by a paucity of cortical gyration and thickening of… (More)
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Highly Cited
2006
Highly Cited
2006
OBJECTIVE Diabetes Prevention Program (DPP) participants randomized to the intensive lifestyle intervention (ILS) had… (More)
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Highly Cited
2004
Highly Cited
2004
RICHARD M. FELDER and JONI SPURLIN North Carolina State University, Raleigh, North Carolina 27695±7905, USA. E-mail: rmfelder… (More)
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Highly Cited
2004
Highly Cited
2004
Correct neuronal migration and positioning during cortical development are essential for proper brain function. Mutations of the… (More)
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Highly Cited
2003
Highly Cited
2003
Deletions of 17p13.3, including the LIS1 gene, result in the brain malformation lissencephaly, which is characterized by reduced… (More)
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Highly Cited
2000
Highly Cited
2000
Normal development of the cerebral cortex requires long-range migration of cortical neurons from proliferative regions deep in… (More)
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Highly Cited
2000
Highly Cited
2000
Mutations in mammalian Lis1 (Pafah1b1) result in neuronal migration defects. Several lines of evidence suggest that LIS1… (More)
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Highly Cited
1998
Highly Cited
1998
Classical lissencephaly (LIS) is a neuronal migration disorder resulting in brain malformation, epilepsy and mental retardation… (More)
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Highly Cited
1997
Highly Cited
1997
Classical lissencephaly (smooth brain) or generalized agyria-pachygyria is a severe brain malformation which results from an… (More)
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