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2005, 2d ed., Advances in neurology, ISBN 9780781751698, Volume 96, 400
Thoroughly revised to reflect the latest advances in treatment and research, this volume is the most comprehensive, current clinical reference on psychiatric... 
Basal Ganglia Diseases | physiopathology | complications | Movement Disorders | etiology | Movement disorders
eBook
Nature, ISSN 0028-0836, 11/2010, Volume 468, Issue 7321, pp. 263 - 269
Mutations in the X-linked MECP2 gene, which encodes the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), cause Rett syndrome and several... 
GLUTAMIC-ACID DECARBOXYLASE | GENE | 67 KDA | MULTIDISCIPLINARY SCIENCES | MOUSE MODEL | MUTATION | NEURONAL MECP2 | SCHIZOPHRENIA | MICE | CPG-BINDING PROTEIN-2 | YOUNG GIRLS | Autistic Disorder - physiopathology | gamma-Aminobutyric Acid - metabolism | Methyl-CpG-Binding Protein 2 - metabolism | Male | Psychomotor Disorders - complications | Methyl-CpG-Binding Protein 2 - deficiency | Compulsive Behavior - physiopathology | Neurons - metabolism | Disease Models, Animal | Autistic Disorder - genetics | Signal Transduction | Compulsive Behavior - genetics | Genotype | Mice, Transgenic | Survival Rate | Hippocampus - pathology | Rett Syndrome - physiopathology | Self-Injurious Behavior - genetics | Phenotype | Neuronal Plasticity | Long-Term Potentiation | Stereotypic Movement Disorder - genetics | Compulsive Behavior - complications | Glutamate Decarboxylase - metabolism | Mice | Hippocampus - physiopathology | Autistic Disorder - pathology | Rett Syndrome - complications | Neural Inhibition | Stereotypic Movement Disorder - pathology | Reflex, Startle - genetics | Electroencephalography | Methyl-CpG-Binding Protein 2 - genetics | Synaptic Transmission | Psychomotor Disorders - genetics | Self-Injurious Behavior - complications | Psychomotor Disorders - physiopathology | Inhibitory Postsynaptic Potentials | Stereotypic Movement Disorder - physiopathology | Brain - cytology | Homeodomain Proteins - genetics | Stereotypic Movement Disorder - complications | Self-Injurious Behavior - physiopathology | Animals | Rett Syndrome - pathology | Vesicular Inhibitory Amino Acid Transport Proteins - genetics | Presynaptic Terminals - metabolism | Autistic Disorder - complications | Respiration | Rett Syndrome - genetics | Autism | Care and treatment | Rett syndrome | Schizophrenia | GABA | Genetic aspects | Diagnosis | Cognition disorders | Seizures (Medicine) | Health aspects | Studies | Anxieties | Social interaction | Neurons | Rodents | Bipolar disorder | Behavior | Gene expression | Index Medicus
Journal Article
Journal Article
American Journal of Psychiatry, ISSN 0002-953X, 01/2009, Volume 166, Issue 1, pp. 83 - 94
Objective: Among children, attention deficit hyperactivity disorder (ADHD) and conduct disorder are often comorbid and overlap clinically. Neuropsychological... 
DISRUPTIVE BEHAVIOR DISORDERS | METABOLISM | PSYCHIATRY | DEFICIT HYPERACTIVITY DISORDER | FRONTAL-CORTEX | INHIBITORY CONTROL | VALIDATION | HOSPITALIZED ADOLESCENTS | DEFICIT/HYPERACTIVITY DISORDER | BRAIN ABNORMALITIES | CHILDREN | Attention Deficit Disorder with Hyperactivity - physiopathology | Conduct Disorder - diagnosis | Humans | Prefrontal Cortex - physiopathology | Pattern Recognition, Visual - physiology | Parietal Lobe - physiopathology | Psychomotor Performance - physiology | Cerebral Cortex - physiopathology | Attention - physiology | Conduct Disorder - psychology | Motivation | Limbic System - physiopathology | Attention Deficit Disorder with Hyperactivity - diagnosis | Nerve Net - physiopathology | Comorbidity | Brain - physiopathology | Cerebellum - physiopathology | Conduct Disorder - physiopathology | Neuropsychological Tests | Magnetic Resonance Imaging | Arousal - physiology | Temporal Lobe - physiopathology | Image Processing, Computer-Assisted | Thalamus - physiopathology | Attention Deficit Disorder with Hyperactivity - psychology | Brain Mapping | Gyrus Cinguli - physiopathology | Reward | Complications and side effects | Magnetic resonance imaging | Conduct disorder | Prefrontal cortex | Diagnosis | Health aspects | Methods | Attention deficit disorder | Brain | Medical imaging | Hyperactivity | Children & youth | Index Medicus | Abridged Index Medicus
Journal Article
American Journal of Psychiatry, ISSN 0002-953X, 2/2011, Volume 168, Issue 2, pp. 152 - 162
Objective:Dysfunction in the amygdala and orbitofrontal cortex has been reported in youths and adults with psychopathic traits. The specific nature of the... 
PROBABILISTIC RESPONSE REVERSAL | CALLOUS-UNEMOTIONAL TRAITS | VENTROMEDIAL PREFRONTAL CORTEX | HUMAN BRAIN | PSYCHIATRY | COMMON STEREOTACTIC SPACE | BASOLATERAL AMYGDALA | DISSOCIABLE ROLES | PASSIVE-AVOIDANCE | DORSAL ANTERIOR CINGULATE | CHILDREN | Amygdala - physiopathology | Conduct Disorder - diagnosis | Humans | Male | Reference Values | Pattern Recognition, Visual - physiology | Caudate Nucleus - physiopathology | Feedback, Psychological | Oxygen Consumption - physiology | Psychomotor Performance - physiology | Attention Deficit and Disruptive Behavior Disorders - diagnosis | Attention Deficit and Disruptive Behavior Disorders - physiopathology | Conduct Disorder - psychology | Antisocial Personality Disorder - physiopathology | Motivation | Female | Attention Deficit and Disruptive Behavior Disorders - psychology | Nerve Net - physiopathology | Antisocial Personality Disorder - psychology | Frontal Lobe - physiopathology | Reinforcement (Psychology) | Avoidance Learning - physiology | Conduct Disorder - physiopathology | Association Learning - physiology | Magnetic Resonance Imaging | Image Processing, Computer-Assisted | Adolescent | Brain Mapping | Signal Transduction - physiology | Decision Making - physiology | Antisocial Personality Disorder - diagnosis | Psychological aspects | Brain | Oppositional defiant disorder in children | Physiological aspects | Conduct disorder | Youth | Teenagers | Research | Antisocial personality disorder | Sociopathic personality | Decision making | Mental health | Pharmacology | Behavior disorders | Psychopathology | Child & adolescent psychiatry | Index Medicus | Abridged Index Medicus
Journal Article
1995, ISBN 9780781701747, Volume 65., xix, 341
Book
American Journal of Medical Genetics Part A, ISSN 1552-4825, 02/2018, Volume 176, Issue 2, pp. 455 - 459
KAT6B sequence variants have been identified in both patients with the Say-Barber-Biesecker-Young-Simpson syndrome (SBBYSS) and in the genitopatellar syndrome... 
skeletal anomalies | related disorders | KAT6B | focused exome sequencing | KAT6B-related disorders | RETARDATION | GENETICS & HEREDITY | HISTONE ACETYLTRANSFERASE | MUTATIONS | PHENOTYPIC SPECTRUM | Patella - physiopathology | Scrotum - abnormalities | Scrotum - physiopathology | Exons | Humans | Joint Instability - genetics | Histone Acetyltransferases - genetics | Craniofacial Abnormalities - physiopathology | Intellectual Disability - genetics | Blepharophimosis - genetics | Heart Defects, Congenital - genetics | Psychomotor Disorders - genetics | Congenital Hypothyroidism - genetics | Facies | Patella - abnormalities | Female | Psychomotor Disorders - physiopathology | Urogenital Abnormalities - physiopathology | Child | Abnormalities, Multiple - genetics | Craniofacial Abnormalities - genetics | Kidney - physiopathology | Haploinsufficiency - genetics | Genetic Association Studies | Congenital Hypothyroidism - physiopathology | Abnormalities, Multiple - physiopathology | Intellectual Disability - physiopathology | Phenotype | Kidney - abnormalities | Alleles | Heart Defects, Congenital - physiopathology | Mutation | Joint Instability - physiopathology | Blepharophimosis - physiopathology | Urogenital Abnormalities - genetics | Medical genetics | Intellectual disabilities | Genotypes | Haploinsufficiency | Index Medicus
Journal Article