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classical lissencephalies and subcortical band heterotopias - physiopathology (32) 32
humans (30) 30
index medicus (28) 28
clinical neurology (20) 20
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classical lissencephalies and subcortical band heterotopias - genetics (16) 16
classical lissencephalies and subcortical band heterotopias - pathology (14) 14
magnetic resonance imaging (14) 14
microtubule-associated proteins - genetics (13) 13
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electroencephalography (9) 9
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neurology (9) 9
1-alkyl-2-acetylglycerophosphocholine esterase - genetics (8) 8
brain - pathology (8) 8
classical lissencephalies and subcortical band heterotopias - complications (8) 8
classical lissencephalies and subcortical band heterotopias - diagnosis (8) 8
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lissencephaly (7) 7
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subcortical band heterotopia (7) 7
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cerebral cortex - pathology (4) 4
classical lissencephalies and subcortical band heterotopias - diagnostic imaging (4) 4
encephalopathy (4) 4
epilepsy - etiology (4) 4
gene (4) 4
lissencephaly - physiopathology (4) 4
malformations (4) 4
miller-dieker syndrome (4) 4
neurons (4) 4
retrospective studies (4) 4
band heterotopia (3) 3
cerebellar hypoplasia (3) 3
cerebral cortex - physiopathology (3) 3
children (3) 3
chromosome deletion (3) 3
chromosomes, human, pair 17 - genetics (3) 3
classical lissencephalies and subcortical band heterotopias - epidemiology (3) 3
cortical dysplasia (3) 3
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double cortex (3) 3
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guillain-barre syndrome - physiopathology (3) 3
homeodomain proteins - genetics (3) 3
infant, newborn (3) 3
lissencephaly - genetics (3) 3
medicine & public health (3) 3
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research (3) 3
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surgery (3) 3
temporal-lobe epilepsy (3) 3
transcription factors - genetics (3) 3
treatment outcome (3) 3
1-alkyl-2-acetylglycerophosphocholine esterase - deficiency (2) 2
1-alkyl-2-acetylglycerophosphocholine esterase - metabolism (2) 2
14-3-3 proteins - genetics (2) 2
absent corpus-callosum (2) 2
agyria (2) 2
analysis (2) 2
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articles (2) 2
arx (2) 2
autopsy (2) 2
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choristoma - pathology (2) 2
classical lissencephalies and subcortical band heterotopias - classification (2) 2
classical lissencephalies and subcortical band heterotopias - psychology (2) 2
classification (2) 2
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American Journal of Medical Genetics Part A, ISSN 1552-4825, 06/2017, Volume 173, Issue 6, pp. 1473 - 1488
Lissencephaly (“smooth brain,” LIS) is a malformation of cortical development associated with deficient neuronal migration and abnormal formation of cerebral... 
lissencephaly | tubulinopathy | classification | agyria | subcortical band heterotopia | pachygyria | OSTEODYSPLASTIC PRIMORDIAL DWARFISM | MILLER-DIEKER SYNDROME | CORTICAL DEVELOPMENT | INTELLECTUAL DISABILITY | MUTATIONS CAUSE | CORPUS-CALLOSUM | GENETICS & HEREDITY | MOLECULAR-BASIS | NEURONAL MIGRATION DEFECTS | CEREBELLAR HYPOPLASIA | Microtubule-Associated Proteins - genetics | Humans | Child, Preschool | Infant | Male | Lissencephaly - classification | Lissencephaly - diagnostic imaging | Cerebral Cortex - physiopathology | Classical Lissencephalies and Subcortical Band Heterotopias - diagnostic imaging | Young Adult | 1-Alkyl-2-acetylglycerophosphocholine Esterase - genetics | Lissencephaly - physiopathology | Adult | Female | Neuropeptides - genetics | Child | Infant, Newborn | Classical Lissencephalies and Subcortical Band Heterotopias - genetics | Cerebral Cortex - diagnostic imaging | Classical Lissencephalies and Subcortical Band Heterotopias - physiopathology | Magnetic Resonance Imaging | Phenotype | Adolescent | Lissencephaly - genetics | Mutation | Classical Lissencephalies and Subcortical Band Heterotopias - classification | Medical genetics | Neuroimaging | Leukocyte migration | Lissencephaly | Subcortical band heterotopia | Cortex | Classification | Doublecortin protein | Genetic counselling | Cell migration | Genetic screening | Agyria
Journal Article
Annals of Neurology, ISSN 0364-5134, 09/2014, Volume 76, Issue 3, pp. 428 - 442
Journal Article
Journal of Neuroendocrinology, ISSN 0953-8194, 08/2014, Volume 26, Issue 8, pp. 528 - 541
Thyroid hormones (TH) play crucial roles in brain maturation and are important for neuronal migration and neocortical lamination. Subcortical band heterotopia... 
hypothyroxinaemia | thyroid hormone propylthiouracil | foetal brain | neuronal migration | Foetal brain | Thyroid hormone propylthiouracil | Neuronal migration | Hypothyroxinaemia | NEUROPSYCHOLOGICAL DEVELOPMENT | IODINE DEFICIENCY | BRAIN-DEVELOPMENT | ADULT-RATS | NEUROSCIENCES | PROPYLTHIOURACIL-INDUCED HYPOTHYROIDISM | CEREBRAL-CORTEX | THYROID-HORMONE INSUFFICIENCY | IMPAIRS SYNAPTIC-TRANSMISSION | ENDOCRINOLOGY & METABOLISM | DENTATE GYRUS | DEVELOPMENTAL EXPOSURE | Hypothyroidism - chemically induced | Neurons - pathology | Neuroglia - pathology | Hypothyroidism - complications | Neuroanatomical Tract-Tracing Techniques | Thyroxine - blood | Seizures - complications | Seizures - chemically induced | Dose-Response Relationship, Drug | Maternal Exposure - adverse effects | Female | Classical Lissencephalies and Subcortical Band Heterotopias - pathology | Pentylenetetrazole - pharmacology | Thyrotropin - blood | Brain - physiopathology | Rats | Prenatal Exposure Delayed Effects - physiopathology | Pregnancy | Propylthiouracil - pharmacology | Triiodothyronine - blood | Classical Lissencephalies and Subcortical Band Heterotopias - physiopathology | Animals | Classical Lissencephalies and Subcortical Band Heterotopias - complications | Membrane Potentials | Brain - pathology | Hypothyroidism - blood | Prenatal Exposure Delayed Effects - chemically induced | Prenatal Exposure Delayed Effects - pathology | Dextran | Propylthiouracil | Hypothyroidism | Epilepsy | Thyroxine | Index Medicus
Journal Article
Journal Article
Human Genetics, ISSN 0340-6717, 2009, Volume 126, Issue 1, pp. 173 - 193
Epilepsy is the most common neurological disorder affecting young people. The etiologies are multiple and most cases are sporadic. However, some rare families... 
CHILDHOOD ABSENCE EPILEPSY | DOUBLE CORTEX SYNDROME | TEMPORAL-LOBE EPILEPSY | FEBRILE SEIZURES PLUS | IDIOPATHIC GENERALIZED EPILEPSY | PERIVENTRICULAR NODULAR HETEROTOPIA | GENETICS & HEREDITY | SEVERE MYOCLONIC EPILEPSY | SUBCORTICAL BAND HETEROTOPIA | INTERLEUKIN-1-BETA IL-1-BETA GENE | FAMILIAL PARTIAL EPILEPSY | Paired Box Transcription Factors - genetics | Periventricular Nodular Heterotopia - diagnostic imaging | Brain - anatomy & histology | Cathepsin B - genetics | Humans | Child, Preschool | Male | Periventricular Nodular Heterotopia - physiopathology | Epilepsy - physiopathology | Epilepsy - etiology | Lissencephaly - diagnostic imaging | Classical Lissencephalies and Subcortical Band Heterotopias - diagnostic imaging | Chromosomes, Human, Pair 3 | Lissencephaly - physiopathology | Malformations of Cortical Development - physiopathology | Epilepsy - genetics | Chromosomes, Human, Pair 22 | Eye Proteins - genetics | Cerebral Cortex - abnormalities | Lissencephaly - complications | Collagen Type XVIII | Procollagen N-Endopeptidase - genetics | Repressor Proteins - genetics | PAX6 Transcription Factor | Transcription Factors - genetics | Malformations of Cortical Development - complications | Nerve Tissue Proteins - genetics | T-Box Domain Proteins - genetics | Cerebral Cortex - diagnostic imaging | Homeodomain Proteins - genetics | ADAMTS4 Protein | Radiography | Classical Lissencephalies and Subcortical Band Heterotopias - physiopathology | Classical Lissencephalies and Subcortical Band Heterotopias - complications | Chromosomes, Human, Pair 16 | Cerebral Cortex - growth & development | Malformations of Cortical Development - diagnostic imaging | Receptors, G-Protein-Coupled - genetics | Mutation | ADAM Proteins - genetics | Periventricular Nodular Heterotopia - complications
Journal Article
Child's Nervous System, ISSN 0256-7040, 2/2016, Volume 32, Issue 2, pp. 377 - 380
Journal Article
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 10/2010, Volume 120, Issue 4, pp. 503 - 515
Journal Article