Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 218,279,234 papers from all fields of science
Search
Sign In
Create Free Account
Kuzniecky syndrome
Known as:
PACHYGYRIA WITH MENTAL RETARDATION, SEIZURES, AND ARACHNOID CYSTS
, Pachygyria with mental retardation and seizures
, Pachygyria, mental retardation and epilepsy
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
9 relations
Arachnoid Cysts
Autosomal recessive inheritance
Global developmental delay
Mental Retardation
Expand
Broader (3)
Epilepsy
Intellectual Disability
Lissencephaly
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Sincipital Encephaloceles: A Study of Associated Brain Malformations
Shashidhar Achar
,
H. K. Dutta
Journal of Clinical Imaging Science
2016
Corpus ID: 25438799
Objective: The aim of this study was to evaluate the associated intracranial malformations in patients with sincipital…
Expand
2011
2011
Evaluation of White Matter Changes in Agyria–Pachygyria Complex Using Diffusion Tensor Imaging
Yu-Chia Kao
,
S. Peng
,
W. Weng
,
Ming-I Lin
,
Wang-Tso Lee
Journal of Child Neurology
2011
Corpus ID: 2877492
Associated abnormalities of the white matter in patients with agyria–pachygyria complex have rarely been investigated using new…
Expand
Highly Cited
2003
Highly Cited
2003
Nonsyndromic mental retardation and cryptogenic epilepsy in women with Doublecortin gene mutations
R. Guerrini
,
F. Moro
,
+17 authors
Soma Das
Annals of Neurology
2003
Corpus ID: 44962324
DCX mutations cause mental retardation in male subjects with lissencephalypachygyria and in female subjects with subcortical band…
Expand
2002
2002
Agyria-pachygyria: clinical, neuroimaging, and neurophysiologic correlations.
Jao-Shwann Liang
,
Wang-Tso Lee
,
C. Young
,
S. Peng
,
Yu‐Zen Shen
Pediatric Neurology
2002
Corpus ID: 22901537
Highly Cited
1999
Highly Cited
1999
Assignment of the muscle-eye-brain disease gene to 1p32-p34 by linkage analysis and homozygosity mapping.
B. Cormand
,
K. Avela
,
+5 authors
A. Lehesjoki
American Journal of Human Genetics
1999
Corpus ID: 13461478
Muscle-eye-brain disease (MEB) is an autosomal recessive disease of unknown etiology characterized by severe mental retardation…
Expand
1995
1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up study
H. Pihko
,
M. Lappi
,
+4 authors
P. Santavuori
Brain & development (Tokyo. )
1995
Corpus ID: 33926340
1994
1994
Serial EEG and sleep polygraphic studies on lissencephaly (agyria-pachygyria)
K. Mori
,
T. Hashimoto
,
+4 authors
Y. Kuroda
Brain & development (Tokyo. )
1994
Corpus ID: 4767317
1993
1993
Ependymal Abnormalities in Lissencephaly/Pachygyria
H. Darwish
,
P. Barth
,
+5 authors
R. Korobkin
Journal of Neuropathology and Experimental…
1993
Corpus ID: 22538519
The ependyma was examined in eight children with neuroblast migratory disorders of diverse origin: three cases of lissencephaly…
Expand
Review
1991
Review
1991
The agyria-pachygyria complex: A spectrum of cortical malformations
J. Aicardi
Brain & development (Tokyo. )
1991
Corpus ID: 4702437
Highly Cited
1976
Highly Cited
1976
Agyria-Pachygyria (Lissencephaly Syndrome)
K. Jellinger
,
A. Rett
Neuropadiatrie
1976
Corpus ID: 34360086
Rakic Sidman Rakic Sidman
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE