Neurodevelopmental disorders and disruptive. Medical search. Frequent questions

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Anatomy26

Brain Chromosomes, Human, Pair 15 Neurons Cerebral Cortex Chromosomes, Human, X Nervous System Chromosomes, Human, Pair 16 Amygdala Nerve Net Neural Pathways Synapses Hippocampus Chromosomes, Human, Pair 7 Cerebellum Frontal Lobe Dendritic Spines Dendrites Chromosomes, Human, Pair 2 Embryo, Mammalian Cerebral Ventricles Cells, Cultured Central Nervous System Septum Pellucidum Corpus Callosum Prefrontal Cortex Chromosomes, Human, Pair 22

Organisms6

Animals, Newborn Mice, Knockout Mice, Inbred C57BL Mice, Mutant Strains Mice, Transgenic Rats, Sprague-Dawley

Diseases65

Rett Syndrome Williams Syndrome Angelman Syndrome Nervous System Diseases Intellectual Disability Prader-Willi Syndrome Prenatal Exposure Delayed Effects Disease Models, Animal Learning Disorders Neuronal Migration Disorders Psychomotor Disorders Communication Disorders Fetal Alcohol Spectrum Disorders Fragile X Syndrome Microcephaly Brain Diseases Central Nervous System Diseases Genetic Predisposition to Disease Cerebral Palsy Neurofibromatoses Tourette Syndrome Infant, Premature, Diseases Leukomalacia, Periventricular Abnormalities, Multiple Seizures Epilepsy Chromosome Deletion Syndrome Asphyxia Neonatorum Brain Damage, Chronic Hypoxia-Ischemia, Brain Tic Disorders Agenesis of Corpus Callosum Bronchopulmonary Dysplasia Substance-Related Disorders Nervous System Malformations Mercury Poisoning, Nervous System Heredodegenerative Disorders, Nervous System Language Development Disorders Movement Disorders Infant, Newborn, Diseases Respiratory Distress Syndrome, Newborn Macrocephaly Hydrocephalus Sleep Disorders Neurotoxicity Syndromes Blindness Intracranial Hemorrhages Encephalomalacia Hypoplastic Left Heart Syndrome Hearing Loss, Bilateral Language Disorders Spasms, Infantile Lymphoproliferative Disorders Neuromuscular Diseases Heart Defects, Congenital Alcohol-Related Disorders Diseases in Twins Premature Birth Speech Disorders Chromosome Duplication Dandy-Walker Syndrome Enterocolitis, Necrotizing Neurodegenerative Diseases Cerebral Hemorrhage

Chemicals and Drugs18

Methyl-CpG-Binding Protein 2 Nerve Tissue Proteins Thimerosal Cell Adhesion Molecules, Neuronal Chromosomal Proteins, Non-Histone Fragile X Mental Retardation Protein gamma-Aminobutyric Acid Repressor Proteins Brain-Derived Neurotrophic Factor Ubiquitin-Protein Ligases DNA-Binding Proteins Membrane Proteins Methylmercury Compounds Genetic Markers Environmental Pollutants Transcription Factors Chlorpyrifos Antipsychotic Agents

Analytical, Diagnostic and Therapeutic Techniques and Equipment37

Disease Models, Animal Magnetic Resonance Imaging Rotarod Performance Test Neurologic Examination Case-Control Studies Analysis of Variance Risk Factors Genetic Association Studies Cohort Studies Pedigree Electroencephalography Echoencephalography Severity of Illness Index Follow-Up Studies Brain Mapping Genetic Testing Genome-Wide Association Study Organ Culture Techniques DNA Mutational Analysis Reproducibility of Results Prospective Studies Norwood Procedures Oligonucleotide Array Sequence Analysis Organ Size Neuroimaging Treatment Outcome Models, Genetic Chromosome Mapping Longitudinal Studies Models, Biological Gene Expression Profiling Intensive Care, Neonatal Prevalence Retrospective Studies Hypothermia, Induced Diagnostic Techniques, Neurological Startle Reaction

Psychiatry and Psychology58

Developmental Disabilities Autistic Disorder Child Development Disorders, Pervasive Child Development Intellectual Disability Mental Disorders Schizophrenia Attention Deficit Disorder with Hyperactivity Bipolar Disorder Learning Disorders Psychomotor Disorders Communication Disorders Cognition Disorders Stereotyped Behavior Social Behavior Behavior, Animal Anxiety Disorders Tourette Syndrome Mood Disorders Neuropsychological Tests Cognition Exploratory Behavior Self-Injurious Behavior Motor Skills Disorders Psychotic Disorders Depressive Disorder, Major Motor Activity Anxiety Maze Learning Depressive Disorder Intelligence Intelligence Tests Obsessive-Compulsive Disorder Vocalization, Animal Stress Disorders, Post-Traumatic Tic Disorders Phobic Disorders Substance-Related Disorders Psychiatric Status Rating Scales Child Behavior Disorders Schizophrenic Psychology Conduct Disorder Motor Skills Psychomotor Performance Borderline Personality Disorder Schizotypal Personality Disorder Somatoform Disorders Sleep Disorders Affective Disorders, Psychotic Alcohol-Related Disorders Adolescent Development Psychometrics Combat Disorders Attention Deficit and Disruptive Behavior Disorders Impulse Control Disorders Startle Reaction Delirium, Dementia, Amnestic, Cognitive Disorders Wechsler Scales

Phenomena and Processes49

Child Development Chromosomes, Human, Pair 15 Pregnancy DNA Copy Number Variations Phenotype Genetic Predisposition to Disease Paternal Age Mutation Genomic Imprinting Haploinsufficiency Neurogenesis Chromosomes, Human, X Chromosomes, Human, Pair 16 Chromosome Deletion Neuronal Plasticity Gene Dosage Genotype Chromosomes, Human, Pair 7 Motor Activity Gene Expression Regulation, Developmental Time Factors Gestational Age Chromosomes, Human, Pair 2 Polymorphism, Single Nucleotide Epigenesis, Genetic Genetic Linkage Gene Expression Regulation Sex Characteristics Heterozygote Signal Transduction Synaptic Transmission Exons Gene Deletion Genetic Variation DNA Methylation Sequence Deletion Alleles Aging Genetic Markers Organ Size Base Sequence Psychomotor Performance Cell Differentiation Endophenotypes Adolescent Development Sensory Gating Chromosome Duplication Chromosomes, Human, Pair 22 Startle Reaction

Anthropology, Education, Sociology and Social Phenomena2

Social Behavior Disorders Adoption

Information Science5

Diagnostic and Statistical Manual of Mental Disorders Image Processing, Computer-Assisted Base Sequence Molecular Sequence Data Prevalence

Named Groups5

Infant, Newborn Infant, Extremely Low Birth Weight Infant, Premature Infant, Extremely Premature Infant, Very Low Birth Weight

Health Care22

Case-Control Studies Analysis of Variance Age Factors Risk Factors Family Health Cohort Studies Severity of Illness Index Follow-Up Studies Genetic Testing Sex Factors Genome-Wide Association Study Reproducibility of Results Prospective Studies Comorbidity Treatment Outcome Longitudinal Studies Age of Onset Maternal Exposure Intensive Care, Neonatal Prevalence Retrospective Studies Intensive Care Units, Neonatal

Geographicals2

Seychelles United States

Anatomy Organisms Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Anthropology, Education, Sociology and Social Phenomena Information Science Named Groups Health Care Geographicals

Rett Syndrome Developmental Disabilities Methyl-CpG-Binding Protein 2 Autistic Disorder Child Development Disorders, Pervasive Williams Syndrome Angelman Syndrome Nervous System Diseases Brain Child Development Intellectual Disability Mental Disorders Schizophrenia Prader-Willi Syndrome Infant, Newborn Attention Deficit Disorder with Hyperactivity Prenatal Exposure Delayed Effects Bipolar Disorder Chromosomes, Human, Pair 15 Disease Models, Animal Pregnancy Learning Disorders Neuronal Migration Disorders Psychomotor Disorders Communication Disorders Neurons DNA Copy Number Variations Fetal Alcohol Spectrum Disorders Phenotype Social Behavior Disorders Cognition Disorders Fragile X Syndrome Infant, Extremely Low Birth Weight Stereotyped Behavior Microcephaly Brain Diseases Social Behavior Infant, Premature Nerve Tissue Proteins Central Nervous System Diseases Genetic Predisposition to Disease Cerebral Palsy Magnetic Resonance Imaging Thimerosal Behavior, Animal Anxiety Disorders Neurofibromatoses Tourette Syndrome Mood Disorders Cerebral Cortex Neuropsychological Tests Paternal Age Infant, Premature, Diseases Mutation Leukomalacia, Periventricular Cell Adhesion Molecules, Neuronal Cognition Genomic Imprinting Haploinsufficiency Rotarod Performance Test Animals, Newborn Exploratory Behavior Neurogenesis Abnormalities, Multiple Chromosomes, Human, X Nervous System Seizures Chromosomes, Human, Pair 16 Mice, Knockout Mice, Inbred C57BL Diagnostic and Statistical Manual of Mental Disorders Neurologic Examination Self-Injurious Behavior Amygdala Epilepsy Case-Control Studies Chromosome Deletion Chromosomal Proteins, Non-Histone Neuronal Plasticity Gene Dosage Nerve Net Syndrome Neural Pathways Synapses Fragile X Mental Retardation Protein Genotype Infant, Extremely Premature Analysis of Variance Hippocampus Age Factors Risk Factors Chromosomes, Human, Pair 7 Motor Skills Disorders gamma-Aminobutyric Acid Psychotic Disorders Asphyxia Neonatorum Family Health Depressive Disorder, Major Genetic Association Studies Cerebellum

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