X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
pachygyria (165) 165
index medicus (155) 155
humans (152) 152
female (104) 104
male (104) 104
clinical neurology (88) 88
magnetic resonance imaging (77) 77
child (66) 66
infant (65) 65
child, preschool (63) 63
lissencephaly (57) 57
cerebral cortex - abnormalities (56) 56
epilepsy (49) 49
neuronal migration (49) 49
genetics & heredity (48) 48
adolescent (40) 40
brain (40) 40
pediatrics (40) 40
infant, newborn (38) 38
polymicrogyria (38) 38
brain - pathology (37) 37
brain - abnormalities (36) 36
syndrome (34) 34
adult (33) 33
agyria-pachygyria (31) 31
malformations (30) 30
neurosciences (28) 28
mutation (27) 27
cerebral cortex - pathology (25) 25
electroencephalography (24) 24
mutations (23) 23
cortical dysplasia (22) 22
abnormalities, multiple - genetics (21) 21
cortical development (18) 18
pedigree (18) 18
phenotype (18) 18
spectrum (18) 18
cerebral-cortex (17) 17
cerebellar hypoplasia (16) 16
consanguinity (16) 16
neurons - pathology (16) 16
intellectual disability - genetics (15) 15
lissencephaly - genetics (15) 15
miller-dieker syndrome (15) 15
mri (15) 15
tomography, x-ray computed (15) 15
gene (14) 14
heterotopia (14) 14
mental retardation (14) 14
mental-retardation (14) 14
schizencephaly (14) 14
dysplasia (13) 13
epilepsy - genetics (13) 13
microcephaly (13) 13
abnormalities, multiple - pathology (12) 12
agyria (12) 12
children (12) 12
cortex (12) 12
disorders (12) 12
eeg (12) 12
neuroimaging (12) 12
abridged index medicus (11) 11
cell movement (11) 11
epilepsy - pathology (11) 11
genes, recessive (11) 11
miller-dieker (11) 11
neuronal migration disorders (11) 11
radiology, nuclear medicine & medical imaging (11) 11
abnormalities (10) 10
cerebral cortex - physiopathology (10) 10
epilepsy - etiology (10) 10
lis1 (10) 10
neurology (10) 10
pregnancy (10) 10
seizures (10) 10
subcortical band heterotopia (10) 10
animals (9) 9
genes (9) 9
genetic aspects (9) 9
hemimegalencephaly (9) 9
intellectual disability - pathology (9) 9
lissencephaly - pathology (9) 9
microcephaly - genetics (9) 9
microtubule-associated proteins - genetics (9) 9
neuropeptides - genetics (9) 9
pathology (9) 9
tubulin - genetics (9) 9
young adult (9) 9
abnormalities, multiple - diagnosis (8) 8
anomalies (8) 8
cerebral cortex - embryology (8) 8
congenital muscular-dystrophy (8) 8
developmental disabilities - genetics (8) 8
epilepsy - diagnosis (8) 8
genetic disorders (8) 8
genetic linkage (8) 8
genetics (8) 8
middle aged (8) 8
neuronal migration disorder (8) 8
neurons (8) 8
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Dusunen Adam, ISSN 1018-8681, 2015, Volume 28, Issue 2, pp. 175 - 178
Journal Article
Turk Noroloji Dergisi, ISSN 1301-062X, 2017, Volume 23, Issue 1, pp. 26 - 28
Journal Article
03/2007
Pachygyria is a disorder of neuronal migration. We report an Indian family with four siblings with developmental delay, infrequent seizures, normal head size... 
microcephaly | mental retardation | magnetic resonance imaging | Developmental delay | pachygyria
Web Resource
The American Journal of Human Genetics, ISSN 0002-9297, 11/2016, Volume 99, Issue 5, pp. 1117 - 1129
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2011, Volume 43, Issue 6, pp. 590 - 594
Journal Article
Humana Mente, 2018, Volume 4, Issue 3, pp. 45 - 50
Journal Article
Brain, ISSN 0006-8950, 2014, Volume 137, Issue 6, pp. 1676 - 1700
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 12/2018, Volume 176, Issue 12, pp. 2808 - 2812
We describe a mother and son with focal epilepsy, mild cognitive impairment, and pachygyria, which was parieto‐occipital in the mother and with remarkable... 
epilepsy | LIS1 | malformations of cortical development | pachygyria | PAFAH1B1 | DOUBLECORTIN | ACETYLHYDROLASE | GENETICS & HEREDITY | LISSENCEPHALY GENE | CHILD | MISSENSE MUTATIONS | Phenotypes | Epilepsy | Cortex | Cognitive ability | LIS1 protein | Mutation | Gene expression
Journal Article
by Chang, JZ and Zhao, LJ and Chen, C and Peng, Y and Xia, Y and Tang, GZ and Bai, T and Zhang, YH and Ma, RY and Guo, RL and Mei, LB and Liang, DS and Cao, QY and Wu, LQ
GENE, ISSN 0378-1119, 09/2015, Volume 569, Issue 1, pp. 46 - 50
22q11.2 microduplication syndrome was recently described as a new disorder with variable clinical features that ranged from normal to mental retardation and... 
VARIABLE PHENOTYPES | DISTAL | LOW COPY REPEATS | CLINICAL VARIABILITY | Pachygyria | MECHANISMS | SNP array | DELETION | 22q11.2 duplication | GENOMIC DISORDERS | GENETICS & HEREDITY | DUPLICATION | Copy number variation analysis
Journal Article
BRAIN, ISSN 0006-8950, 09/2008, Volume 131, pp. 2304 - 2320
Journal Article
Clinical Nuclear Medicine, ISSN 0363-9762, 01/2012, Volume 37, Issue 1, pp. e4 - e6
Journal Article
Child's Nervous System, ISSN 0256-7040, 4/2019, Volume 35, Issue 4, pp. 607 - 612
Arachnoid cysts are commonly considered congenital lesions, but this has not been proven. With the development of neuroimaging and DNA testing technology, more... 
Neuroimaging | FOXC2 | Neurosciences | Medicine & Public Health | Central nervous system disease | Arachnoid cyst | Neurosurgery | Genetic diseases | LOCATION | SURGERY | PACHYGYRIA | MENTAL-RETARDATION | FOSSA | SIDEDNESS | PREVALENCE | NATURAL-HISTORY | SEX DISTRIBUTION | CLINICAL NEUROLOGY | MONOZYGOTIC TWINS | PEDIATRICS | DISTICHIASIS | Family | Nervous system diseases | Genetic aspects | Genetic disorders | Cysts | Gene mutations
Journal Article
Brain, ISSN 0006-8950, 11/2010, Volume 133, Issue 11, pp. 3194 - 3209
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 1/2017, Volume 32, Issue 1, pp. 127 - 131
Journal Article
No results were found for your search.

Cannot display more than 1000 results, please narrow the terms of your search.