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Turkish Journal Of Neurology, ISSN 1301-062X, 03/2018, Volume 24, Issue 1, pp. 1 - 2
Cerebral palsy (CP), is a permanent, but not progressive, postural and movement disorder caused by brain injury or dysgenesis during rapid brain development... 
T?p | Cerebral palsy | ataxic | genetics | dyskinetic | spastic
Journal Article
Developmental Medicine & Child Neurology, ISSN 0012-1622, 05/2017, Volume 59, Issue 5, pp. 462 - 469
Although prematurity and hypoxic–ischaemic injury are well‐recognized contributors to the pathogenesis of cerebral palsy (CP), as many as one‐third of children... 
POLYMORPHISMS | BRAIN-INJURY | COPY NUMBER VARIATIONS | MUTATION | PEDIATRICS | ACTIN CYTOSKELETON | MODEL | PREVALENCE | APOLIPOPROTEIN-E GENOTYPE | ASSOCIATION | CLINICAL NEUROLOGY | DEFICIENCY CAUSES | DNA Copy Number Variations - genetics | Mutation - genetics | Humans | Risk Factors | Cerebral Palsy - genetics
Journal Article
Journal Article
BMJ : British Medical Journal, ISSN 0959-8138, 7/2014, Volume 349, Issue jul15 2, pp. g4294 - g4294
Objective To investigate risks of recurrence of cerebral palsy in family members with various degrees of relatedness to elucidate patterns of... 
RESEARCH | MEDICINE, GENERAL & INTERNAL | ASSOCIATIONS | GESTATIONAL-AGE | NORWAY | DISEASE | SURVEILLANCE | RECURRENCE | PREVALENCE | AGGREGATION | BIRTHS | Diseases in Twins - genetics | Prevalence | Pedigree | Cerebral Palsy - epidemiology | Humans | Norway - epidemiology | Risk Factors | Diseases in Twins - epidemiology | Cerebral Palsy - genetics | Cohort Studies
Journal Article
NeuroMolecular Medicine, ISSN 1535-1084, 12/2014, Volume 16, Issue 4, pp. 821 - 844
An ongoing challenge in children presenting with motor delay/impairment early in life is to identify neurogenetic disorders with a clinical phenotype, which... 
Neurology | Cerebral palsy | Neurosciences | Biomedicine | Masqueraders | Internal Medicine | Spastic, dyskinetic, and ataxic phenotypes | Neurogenetic | RISK-FACTORS | PRETERM INFANTS | NEUROSCIENCES | COENZYME-Q10 DEFICIENCY | CEREBELLAR-ATAXIA | INTRAVENTRICULAR HEMORRHAGE | ACIDURIA TYPE-I | GLUTARIC ACIDURIA | GLOBUS-PALLIDUS INTERNUS | PELIZAEUS-MERZBACHER DISEASE | DEEP BRAIN-STIMULATION | Brain - embryology | Leukoencephalopathies - genetics | Genomics | Humans | Movement Disorders - diagnosis | Child, Preschool | Male | Nervous System Diseases - diagnosis | Stroke - congenital | Exome | Asphyxia Neonatorum - genetics | Brain Diseases, Metabolic - diagnosis | Cerebral Palsy - diagnosis | Leukoencephalopathies - diagnosis | Chromosome Disorders - diagnosis | Child | Hypoxia, Brain - diagnosis | Infant, Newborn | Brain Diseases, Metabolic - genetics | Neurotransmitter Agents - metabolism | Lysosomal Storage Diseases, Nervous System - genetics | Movement Disorders - genetics | Muscle Spasticity - genetics | Cerebral Palsy - genetics | Hypoxia, Brain - genetics | Cell Movement | Tissue Array Analysis | Stroke - diagnosis | Genetic Diseases, Inborn - genetics | Developmental Disabilities - genetics | Nervous System Diseases - genetics | Molecular Diagnostic Techniques | Diagnostic Errors | Asphyxia Neonatorum - diagnosis | Adult | Female | Birth Injuries - genetics | Developmental Disabilities - diagnosis | Genetic Diseases, Inborn - diagnosis | Globus Pallidus - pathology | Lysosomal Storage Diseases, Nervous System - diagnosis | Mitochondrial Diseases - genetics | Diagnosis, Differential | Genome-Wide Association Study | Leukoencephalopathies - metabolism | Birth Injuries - diagnosis | Muscle Spasticity - diagnosis | Chromosome Disorders - genetics | Mitochondrial Diseases - diagnosis | Medical colleges | Molecular genetics | Children's hospitals | Development and progression | Diagnostic imaging | Diagnosis | masqueraders | dyskinetic and ataxic phenotypes | neurogenetic | spastic
Journal Article
Neurology, ISSN 0028-3878, 04/2015, Volume 84, Issue 16, pp. 1660 - 1668
OBJECTIVE:To determine the prevalence and characteristics of copy number variations (CNVs) in children with cerebral palsy (CP) of unknown etiology, comprising... 
INDIVIDUALS | CHROMOSOMAL MICROARRAY | GENE | FUNCTION CLASSIFICATION-SYSTEM | DISABILITY | EPILEPSY | AUTISM SPECTRUM DISORDERS | CLINICAL NEUROLOGY | CHILDREN | DELETION | Prevalence | Israel - epidemiology | Cerebral Palsy - epidemiology | Humans | Adolescent | Cerebral Palsy - physiopathology | Child, Preschool | Female | Male | DNA Copy Number Variations - genetics | Child | Cerebral Palsy - genetics
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 2014, Volume 22, Issue 1, pp. 40 - 45
Journal Article