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Lissencephaly
Known as:
Lissencephaly [Disease/Finding]
, Lissencephalies
, Lissencephalia
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A smooth brain malformation of the CEREBRAL CORTEX resulting from the abnormal location of developing neurons during corticogenesis. It is…
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National Institutes of Health
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Related topics
Related topics
24 relations
Agyria
Congenital neurologic anomalies
In Blood
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
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Narrower (6)
Kuzniecky syndrome
LISSENCEPHALY SYNDROME, NORMAN-ROBERTS TYPE
Massa Casaer Ceulemans syndrome
Pachygyria, frontotemporal
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2009
Highly Cited
2009
Inhibition of calpain increases LIS1(PAFAH1B1) and partially rescues in vivo phenotypes in a mouse model of lissencephaly
Masami Yamada
,
Yuko Yoshida
,
+9 authors
S. Hirotsune
Nature Network Boston
2009
Corpus ID: 839297
Lissencephaly is a devastating neurological disorder caused by defective neuronal migration. LIS1 (official symbol PAFAH1B1, for…
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2003
2003
Quantitative MRI detects abnormalities in relatives of patients with epilepsy and malformations of cortical development
M. Merschhemke
,
T. Mitchell
,
+7 authors
J. Duncan
NeuroImage
2003
Corpus ID: 6953630
2003
2003
Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia
H. Miyata
,
D. Chute
,
J. Fink
,
P. Villablanca
,
H. Vinters
Acta Neuropathologica
2003
Corpus ID: 22161983
Lissencephaly with agenesis of the corpus callosum and rudimentary dysplastic cerebellum may represent a subset of lissencephaly…
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Highly Cited
2002
Highly Cited
2002
Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance
S. V. Gestel
,
Thomas Forsgren
,
+6 authors
C. Broeckhoven
Molecular Psychiatry
2002
Corpus ID: 37713286
Epistatic effect of genes from the dopamine and serotonin systems on the temperament traits of Novelty Seeking and Harm Avoidance
Review
2001
Review
2001
LIS1: from cortical malformation to essential protein of cellular dynamics
R. Leventer
,
C. Cardoso
,
D. Ledbetter
,
W. Dobyns
Trends in Neurosciences
2001
Corpus ID: 29132401
1999
1999
Analysis of lissencephaly-causing LIS1 mutations.
T. Sapir
,
M. Eisenstein
,
+7 authors
O. Reiner
European Journal of Biochemistry
1999
Corpus ID: 31593035
Mutations in the LIS1 gene may result in severe abnormalities of brain cortical layering known as lissencephaly. Most…
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Highly Cited
1996
Highly Cited
1996
Scrambler, a new neurological mutation of the mouse with abnormalities of neuronal migration
H. Sweet
,
R. Bronson
,
K. Johnson
,
Susan A. Cook
,
M. Davisson
Mammalian Genome
1996
Corpus ID: 10057791
A novel spontaneous neurological mutation, scrambler (scm), appeared in the inbred mouse strain DC/Le (dancer) in 1991. Mice…
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1993
1993
Fukuyama-type congenital muscular dystrophy and the Walker-Warburg syndrome
S. Kimura
,
Y. Sasaki
,
+7 authors
N. Misugi
Brain & development (Tokyo. )
1993
Corpus ID: 4779381
1990
1990
Visual and auditory evoked potential correlates of cerebral malformations
S. Coupland
,
H. Sarnat
Brain & development (Tokyo. )
1990
Corpus ID: 4704794
1979
1979
Lissencephaly (Agyria) on Computed Tomography
K. Ohno
,
T. Enomoto
,
J. Imamoto
,
K. Takeshita
,
M. Arima
Journal of computer assisted tomography
1979
Corpus ID: 23126167
Unusual computed tomographic findings were observed in two infants with similar clinical pictures including delay in…
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