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Nature Medicine, ISSN 1078-8956, 01/2009, Volume 15, Issue 1, pp. 84 - 90
Disorders of neuronal migration can lead to malformations of the cerebral neocortex that greatly increase the risk of seizures. It remains untested whether... 
MEDICINE, RESEARCH & EXPERIMENTAL | DOUBLECORTIN | BIOCHEMISTRY & MOLECULAR BIOLOGY | SUSCEPTIBILITY | RAT NEOCORTEX | LAMINAR HETEROTOPIA | CORTICAL DEVELOPMENT | CEREBRAL-CORTEX | CELL BIOLOGY | METHYLAZOXYMETHANOL | DOUBLE CORTEX SYNDROME | GENETIC MALFORMATIONS | EPILEPSY | Genetic Therapy | Neurons - pathology | Malformations of Cortical Development, Group II - pathology | Seizures - genetics | Microtubule-Associated Proteins - genetics | Neuropeptides - physiology | Cell Movement - genetics | Gene Knockdown Techniques | Seizures - pathology | Classical Lissencephalies and Subcortical Band Heterotopias - veterinary | Neurons - physiology | Female | Neuropeptides - genetics | Classical Lissencephalies and Subcortical Band Heterotopias - pathology | RNA Interference - physiology | Disease Models, Animal | Malformations of Cortical Development, Group II - embryology | Severity of Illness Index | Classical Lissencephalies and Subcortical Band Heterotopias - genetics | Genetic Predisposition to Disease | Animals, Genetically Modified | Rats | Microtubule-Associated Proteins - antagonists & inhibitors | Malformations of Cortical Development, Group II - genetics | Seizures - therapy | Microtubule-Associated Proteins - physiology | Pregnancy | Animals | Malformations of Cortical Development, Group II - veterinary | Models, Biological | Classical Lissencephalies and Subcortical Band Heterotopias - therapy | Neuropeptides - antagonists & inhibitors | Gene mutations | Neurons | Epilepsy | Physiological aspects | Genetic aspects | Research | Gene expression | Health aspects | Risk factors | Brain | Convulsions & seizures | Rodents | Cell adhesion & migration
Journal Article
No to hattatsu = Brain and development, ISSN 0029-0831, 09/2016, Volume 48, Issue 5, p. 347
X-linked lissencephaly with ambiguous genitalia (XLAG) syndrome is a disorder associated with severe intellectual disability and intractable epilepsy.... 
Ethanol | Central Venous Catheters | Humans | Infant | Male | Classical Lissencephalies and Subcortical Band Heterotopias - therapy
Journal Article
Journal of Pediatric Hematology/Oncology, ISSN 1077-4114, 11/2008, Volume 30, Issue 11, pp. 865 - 868
Journal Article
Journal Article
Brain & Development, ISSN 0387-7604, 2015, Volume 38, Issue 4, pp. 399 - 406
Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2013, Volume 161, Issue 6, pp. 1453 - 1458
We describe a female patient with mild lissencephaly (pachygyria), severe intellectual disability, and facial dysmorphisms with an inverted 1.4 Mb... 
YWHAE | lissencephaly | 17p13.3 duplication | PAFAH1B1 | Lissencephaly | NEURONAL MIGRATION | DUPLICATIONS | TIBIA | MILLER-DIEKER-SYNDROME | GENE | MOLECULAR DIAGNOSIS | MICRODELETIONS | GENETICS & HEREDITY | MALFORMATION-SEVERITY | MUTATIONS | DELETIONS | Lissencephaly - diagnosis | Sequence Inversion - genetics | Microtubule-Associated Proteins - genetics | Humans | DNA, Complementary - genetics | Infant | Developmental Disabilities - genetics | Chromosome Duplication - genetics | Nervous System Malformations - diagnostic imaging | Lissencephaly - diagnostic imaging | Classical Lissencephalies and Subcortical Band Heterotopias - diagnostic imaging | Intellectual Disability - genetics | RNA - genetics | Developmental Disabilities - diagnostic imaging | 1-Alkyl-2-acetylglycerophosphocholine Esterase - genetics | Chromosome Disorders - diagnosis | Chromosome Disorders - diagnostic imaging | Female | Muscle Hypotonia | Nervous System Malformations - genetics | Developmental Disabilities - diagnosis | 14-3-3 Proteins - genetics | Classical Lissencephalies and Subcortical Band Heterotopias - genetics | Introns - genetics | Classical Lissencephalies and Subcortical Band Heterotopias - diagnosis | In Situ Hybridization, Fluorescence | Sequence Analysis, DNA | Haploinsufficiency | DNA - genetics | Radiography | DNA - chemistry | Phenotype | Comparative Genomic Hybridization | Intellectual Disability - diagnosis | Nervous System Malformations - diagnosis | Lissencephaly - genetics | DNA, Complementary - chemistry | Chromosome Disorders - genetics | Encephalopathy | Autism
Journal Article
Epilepsia, ISSN 0013-9580, 09/2012, Volume 53, Issue 4, pp. 81 - 91
Journal Article