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Pediatric Neurology, ISSN 0887-8994, 10/2008, Volume 39, Issue 4, p. 298
Journal Article
Pediatric Neurology, ISSN 0887-8994, 10/2008, Volume 39, Issue 4, p. 298
Journal Article
Annals of Neurology, ISSN 0364-5134, 06/2014, Volume 75, Issue 6, pp. 943 - 958
Journal Article
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2008, Volume 39, Issue 4, pp. 298 - 298
Journal Article
BRAIN SCIENCES, ISSN 2076-3425, 08/2019, Volume 9, Issue 8, p. 190
Pediatric epilepsy presents with various diagnostic challenges. Recent advances in neuroimaging play an important role in the diagnosis, management and in... 
WADA TEST | AMERICAN ACADEMY | temporal lobe epilepsy | ICTAL SPECT | PRESURGICAL EVALUATION | extra-temporal lobe epilepsy | refractory epilepsy | ILAE COMMISSION | MRI | SEIZURE FOCI | NEUROSCIENCES | neuroimaging | CHILDREN | TASK-FORCE | pediatric epilepsy | FMRI
Journal Article
Langmuir, ISSN 0743-7463, 04/2018, Volume 34, Issue 14, pp. 4282 - 4288
In this study, we introduce the possibility of applying a colloidal amorphous array composed of fine silica particles as a structural-color material to... 
COLORS | RAPID FABRICATION | FILMS | MATERIALS SCIENCE, MULTIDISCIPLINARY | CHEMISTRY, PHYSICAL | NANOSTRUCTURES | DOTS | PIGMENTS | CHEMISTRY, MULTIDISCIPLINARY | SATURATION | INVISIBLE SECURITY INK
Journal Article
Organic Electronics, ISSN 1566-1199, 04/2017, Volume 43, pp. 156 - 161
We demonstrate efficiency enhancement in perovskite solar cells (PSCs) utilizing a free-dopant hole transporting material (HTM), non-peripherally substituted... 
Phthalocyanine | Small molecule | Thermal annealing | Hole transport material | Perovskite solar cells | PHYSICS, APPLIED | MATERIALS SCIENCE, MULTIDISCIPLINARY | LENGTHS | ORGANIC SEMICONDUCTORS | Perovskite | Annealing | Phthalocyanins
Journal Article
Epilepsia, ISSN 0013-9580, 05/2011, Volume 52, Issue 5, pp. 984 - 992
Summary Purpose:  ARX, the aristaless‐related homeobox gene, is implicated in cerebral, testicular, and pancreatic development. ARX mutations are associated... 
Ohtahara syndrome | Interneurons | Neuropsychiatric disorders | Early infantile epileptic encephalopathy | ARX | POLYALANINE EXPANSION | ABNORMAL GENITALIA | SUPPRESSION | CLINICAL NEUROLOGY | INFANTILE EPILEPTIC ENCEPHALOPATHY | LINKED MENTAL-RETARDATION | WEST-SYNDROME | FAMILIES | NEURONS | DYSFUNCTION | HOMEOBOX GENE | Frameshift Mutation | Humans | Infant | Male | Developmental Disabilities - genetics | Genes, Homeobox - genetics | Spasms, Infantile - genetics | Mental Disorders - genetics | Adult | Epilepsy - genetics | Female | Mental Disorders - diagnosis | Child | Developmental Disabilities - diagnosis | Disorders of Sex Development - diagnosis | Transcription Factors - genetics | Disorders of Sex Development - genetics | Mutation - genetics | Homeodomain Proteins - genetics | Syndrome | Epilepsy - diagnosis | Phenotype | Pedigree | Sex Distribution | Heterozygote | Medical colleges | Nervous system diseases | Analysis | Depression, Mental | Epilepsy | Genetic research | Schizophrenia | Genetic aspects | Medical research | Mutation | Animal models | Mental disorders | Exons | Central nervous system | X chromosome | Cognition | Mental retardation | Homeobox | Learning | Lissencephaly | Encephalopathy | Development | Anxiety | Children | Pancreas | Genitalia | Depression | ARX protein | Hospitals | Motor skill learning | Testes | Pleomorphism
Journal Article
Journal of Child Neurology, ISSN 0883-0738, 1/2019, Volume 34, Issue 1, pp. 17 - 21
Background/Aims: Seizures, strokelike episodes, and headaches are common complications in patients with Sturge-Weber syndrome. Based on our experience, we... 
seizures | strokelike episode | Sturge-Weber syndrome | hemorrhage | ischemia | neuroimaging | ANGIOMATOSIS | DISEASE | PEDIATRICS | CLINICAL NEUROLOGY | CHILDREN
Journal Article
Epilepsia, ISSN 0013-9580, 08/2014, Volume 55, Issue 8, pp. 1235 - 1244
Journal Article
Epilepsy & Behavior Case Reports, ISSN 2213-3232, 2017, Volume 11, pp. 125 - 128
Abstract PRRT2 pathogenic variants have been described in benign familial infantile epilepsy, episodic ataxia, paroxysmal kinesigenic dyskinesia, and... 
Neurology | Ataxia | Kinesigenic dyskinesia | PRRT2 | Genetic epilepsies | Epilepsy
Journal Article