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(Click for frequent words.) 71 neurodevelopment 70 neuro developmental 67 neurodevelopmental disorders 65 neuromotor 65 utero exposure 63 developmental abnormalities 63 chromosomal anomaly 62 IUGR 62 cognitive deficits 62 cognitive 61 neurobehavioral 61 neurobiological 61 developmental delays 61 Angelman syndrome 61 neurodevelopmental disorder 61 neonatal encephalopathy 61 mitochondrial dysfunction 61 prenatal exposure 60 neurocognitive deficits 60 ASDs 60 neurological 60 mild cognitive 60 CNTNAP2 60 Genetic predisposition 60 metabolic abnormalities 60 gastrointestinal dysfunction 60 neuronal dysfunction 60 psychomotor 59 inattention hyperactivity 59 hyperactivity inattention 59 reproductive abnormalities 59 premorbid 59 bronchopulmonary dysplasia 59 antenatal depression 59 obesity insulin resistance 59 neuropsychiatric disorder 59 neurodevelopmental outcomes 59 synaptic function 59 hematological abnormalities 58 alexithymia 58 neurocognitive 58 cognitive impairment 58 neurological abnormalities 58 cognitive dysfunction 58 autism spectrum disorders ASD 58 SRBD 58 airway responsiveness 58 thyroid dysfunction 58 neuroendocrine 58 persistent pulmonary hypertension 58 etiologic 58 developmental disorders 58 behavioral disinhibition 58 Rubinstein Taybi syndrome 58 neuropsychiatric diseases 58 pathophysiologic 58 NF1 58 disorder ASD 57 epilepsy cerebral palsy 57 attention-deficit/hyperactivity disorder ADHD 57 Klinefelter syndrome 57 hyperbilirubinemia 57 neurological impairments 57 chronicity 57 prenatal exposures 57 cognitive functioning 57 neuropsychiatric disorders 57 behavioral abnormalities 57 Rh incompatibility 57 nongenetic 57 malformations 57 auditory processing 57 diagnosing autism 57 inherited mutations 57 maturational 57 hippocampal function 57 neurobehavioural 57 autonomic dysfunction 57 chromosomal disorder 57 attention-deficit/hyperactivity disorder 57 neurosensory 56 pathophysiological 56 Folic acid deficiency 56 neuro developmental disorders 56 dyscalculia 56 comorbid disorders 56 autistic spectrum 56 genetic susceptibility 56 allergic sensitization 56 autistic traits 56 neuropsychological deficits 56 orofacial clefts 56 fetal malformations 56 parkinsonism 56 psychiatric disorders 56 mood disorders 56 hypotonia 56 mental retardation epilepsy 56 highly heritable 56 attentional 56 cerebral palsy blindness 56 MECP2 gene 56 adult neurogenesis 56 cerebellar 56 dysregulation 56 cognition 56 enterocolitis 56 Hyperactivity 56 airway hyperresponsiveness 56 Pervasive Developmental Disorder 56 #q#.# deletion syndrome 56 preterm deliveries 55 recurrent abdominal pain 55 postnatally 55 comorbid anxiety 55 callous unemotional traits 55 neurotoxic effects 55 aetiological 55 neurodevelopmental outcome 55 low birthweight 55 mtDNA mutations 55 prefrontal cortical 55 congenital anomalies 55 sensorimotor 55 predisposing factor 55 hypothalamic pituitary adrenal axis 55 thyroid hormone levels 55 Comorbid 55 chromosomal anomalies 55 Asperger Disorder 55 intraventricular hemorrhage 55 brain neurochemistry 55 autism spectrum disorders ASDs 55 GH deficiency 55 phthalate exposure 55 skeletal abnormalities 55 impaired cognition 55 dopamine receptor gene 55 verbal apraxia 55 autism spectrum disorders 55 autism dyslexia 55 dietary interventions 55 recurrent miscarriage 55 Maternal obesity 55 dyslexia dyspraxia 55 metabolic acidosis 55 subclinical hypothyroidism 55 synaptic proteins 55 neurodevelopmental impairment 55 holoprosencephaly 55 neuropathology 55 Hurler syndrome 55 endocrine disruption 55 neurodevelopmental disability 55 de novo mutations 55 ADHD 55 CNTNAP2 gene 55 malignant transformation 55 Dysregulation 55 thyroid hormone deficiency 55 chromosomal abnormalities 55 T1DM 55 #q# deletion syndrome 55 chromosomal disorders 55 airway remodeling 55 neuropathological 55 AUDs 54 APOE ε4 54 proliferative diabetic retinopathy 54 neuro developmental disorder 54 impulsivity 54 menstrual irregularity 54 bronchopulmonary dysplasia BPD 54 neurocognitive functioning 54 cryptorchidism 54 neurological impairment 54 atopic 54 thyroid function 54 neurologic disorders 54 aneuploidy 54 microdeletion 54 idiopathic Parkinson disease 54 clefting 54 prostate carcinogenesis 54 HGPS 54 neuroinflammation 54 psychosocial functioning 54 mitochondrial disorders 54 autism spectrum disorder 54 hyperinsulinemia 54 VCFS 54 neuroimaging studies 54 Sociodemographic 54 ASD autism spectrum 54 androgen depletion 54 metabolic dysfunction 54 Asperger disorder 54 tic disorders 54 chromosome abnormalities 54 Wernicke Korsakoff syndrome 54 term potentiation LTP 54 epigenetic changes 54 phthalate syndrome 54 CHD7 54 structural abnormalities 54 diagnosing ADHD 54 emotional dysregulation 54 mental retardation cerebral palsy 54 neurophysiological 54 mood dysregulation 54 adenotonsillectomy 54 biochemical abnormalities 54 cognitive affective 54 monoclonal gammopathy 54 precocious puberty 54 genetic abnormalities 54 metabolic abnormality 54 congenital hypothyroidism 54 juvenile idiopathic arthritis 54 motor neuron degeneration 54 fetal chromosomal 54 cerebral palsy mental retardation 54 chorioamnionitis 54 behavioral 54 syndrome FAS 54 LRRK2 mutations 54 Longitudinal studies 54 generalized epilepsy 54 FMRP protein 54 prepubertal 54 penetrance 54 cerebellar hypoplasia 54 Iron deficiency 54 subclinical atherosclerosis 54 mitochondrial mutations 54 Secondhand smoke exposure 54 neurologic 54 gastric carcinoma 54 Genetic variants 53 circadian genes 53 pubertal maturation 53 congenital abnormalities 53 prenatally diagnosed 53 neural tube defect 53 colorectal carcinogenesis 53 insulin resistance 53 birthweight 53 apraxia 53 immunodeficiencies 53 lactase deficiency 53 neuropsychological impairments 53 onset puberty 53 sensory gating 53 PON1 53 neuropsychiatric 53 cataract formation 53 neuropsychological functioning 53 environmental toxicants 53 atopic disease 53 Oppositional Defiant Disorder 53 postpartum mood 53 Noonan Syndrome 53 breastfed infants 53 sonographic diagnosis 53 Cushing syndrome 53 chromosomal defects 53 affective disorders 53 neuroligins 53 behavioral disorders 53 Mental retardation 53 ectodermal dysplasia 53 Autistic Spectrum Disorder 53 neuroanatomical 53 Prenatal exposure 53 folate deficiency 53 carotid atherosclerosis 53 underlying pathophysiology 53 causal pathway 53 monogenic 53 dominantly inherited 53 internalizing disorders 53 generalized seizures 53 pubertal 53 galactosemia 53 pulmonary hypoplasia 53 atopic eczema 53 G6PD deficiency 53 genomic imprinting 53 hormonal abnormalities 53 polyhydramnios 53 facial clefts 53 untreated sleep apnea 53 psychotic symptoms 53 pathogenic mechanisms 53 synaptic plasticity 53 subsyndromal 53 behavioral disturbances 53 ERK signaling 53 channelopathies 53 neurogenesis 53 neurocognitive impairment 53 neonatal morbidity 53 IgA deficiency 53 cardio metabolic 53 STAT4 53 mcg dl 53 Neuropsychological 53 chromosomal instability 53 neurologic dysfunction 53 somatoform disorders 53 reproductive toxicity 53 calcium homeostasis 53 Mood disorders 53 epigenetic alterations 53 psychobiological 53 causal pathways 53 endothelial dysfunction 53 neuronal plasticity 53 oculomotor 53 paraneoplastic 52 endophenotypes 52 neurological disorder affecting 52 serum BDNF 52 unmeasured confounders 52 autism 52 cortical plasticity 52 autism cerebral palsy 52 Chronic ITP 52 neuritic 52 mitochondrial diseases 52 maladaptive behaviors 52 learning disabilities 52 recurrent wheezing 52 autism Asperger 52 epilepsies 52 congenital adrenal hyperplasia 52 activate AMPK 52 autistic tendencies 52 NAFLD 52 visuospatial 52 nerve degeneration 52 biopsychosocial 52 dysgraphia 52 thrombophilia 52 multisystemic 52 Depressive symptoms 52 heritable 52 perinatal 52 BLLs 52 autism spectrum 52 genetic syndromes 52 residual confounding 52 spina bifida cerebral palsy 52 utero 52 comorbid psychiatric 52 cognitive function 52 neurotransmission 52 autosomal recessive genetic 52 genital defects 52 intrauterine 52 Autistic Disorder 52 HPA axis 52 GBA mutations 52 hyperactivity 52 atopy 52 neuronal differentiation 52 neural plasticity 52 systemic inflammation 52 cognitive abilities 52 Childhood Disorder 52 medium chain acyl 52 synaptogenesis 52 PTPN# 52 ADHD symptoms 52 intelligence quotient IQ 52 somatic symptoms 52 muscular dystrophy cystic fibrosis 52 juvenile idiopathic arthritis JIA 52 craniosynostosis 52 Prader Willi syndrome 52 parkinsonian 52 adrenal function 52 pseudotumor cerebri 52 vascular dysfunction 52 progressive neurodegenerative disorder 52 Neurocognitive 52 polycystic ovary syndrome 52 depressive symptoms 52 pervasive developmental 52 leptin deficiency 52 heritable diseases 52 psychosocial variables 52 schizophreniform disorder 52 neuroinflammatory 52 hippocampal volume 52 cognitive impairments 52 p# activation 52 congenital adrenal hyperplasia CAH 52 hydrops 52 hypopituitarism 52 rhinovirus infection 52 RSV infection 52 thiopurine 52 neuromotor delays 52 phonological 52 disorders FASD 52 hypophosphatasia 52 OSAHS 52 disorders ASD 52 gastrointestinal disturbances 52 pharmacologic treatments 52 Neurodevelopmental 52 emotional lability 52 #q#.# [001] 52 REM sleep behavior 52 bone metabolism 52 hormone imbalances 52 etiological 52 cerebral palsy Down syndrome 52 dysregulated 52 psychiatric comorbidity 52 Primary IGFD 52 hormone secretion 52 Mitochondrial dysfunction 52 HbF 52 eyeblink conditioning 52 autosomal recessive 52 vitamin B# deficiency 52 myelination 52 infertility miscarriage 52 dopamine signaling 52 neurotoxicity 52 fibrotic disease 52 hyperprolactinemia 52 syndrome OSAS 52 serotonin deficiency 52 neurocognitive function 52 ataxias 52 extrapyramidal symptoms 52 menarche 52 Rett syndrome 52 developmental neurotoxicity 52 esotropia 52 allergic eczema 52 Vitamin D insufficiency 52 chromosomal abnormality 52 excitotoxicity 52 torsade de pointes 52 IGF1 52 cognitive dysfunctions 52 prenatally 52 genetic imprinting 52 craniofacial anomalies 52 Iron deficiency anemia 52 undescended testicles 52 airway reactivity 51 Fragile X syndrome 51 childhood disintegrative disorder 51 genetic polymorphisms 51 Sjögren syndrome 51 necrotizing enterocolitis 51 Six3 51 inherited neurological disorder 51 neurobiological disorders 51 familial clustering 51 aetiology 51 perceptual reasoning 51 FASPS 51 myelomeningocele 51 Socioeconomic status 51 pathophysiological mechanisms 51 immunotoxicity 51 heritable disorders 51 cognitive stimulation 51 mania hypomania 51 congenital toxoplasmosis 51 Apgar scores 51 primary ciliary dyskinesia 51 Dravet syndrome 51 SGPT 51 hypercalciuria 51 retinal dysfunction 51 organophosphate exposure 51 immunological 51 neuro cognitive 51 dysbindin gene 51 myeloproliferative neoplasms 51 aneuploidies 51 sleep disturbances 51 tic severity 51 severe hyperbilirubinemia 51 Navas Acien 51 pituitary hormone 51 Peutz Jeghers syndrome 51 ovarian hormones 51 neurodevelopment disorder 51 asthma rhinitis 51 heterotaxy 51 amygdala reactivity 51 hypogonadotropic hypogonadism 51 Beckwith Wiedemann syndrome 51 microcephaly 51 neuronal signaling 51 hypocalcaemia 51 daytime alertness 51 probiotic supplementation 51 molecular mechanisms underlying 51 NMDA receptors 51 Decety 51 preterm delivery 51 salivary cortisol 51 myopathies 51 unmeasured confounding 51 FeNO 51 cAMP signaling 51 prodrome 51 middle ear effusion 51 neurodevelopment disorders 51 externalizing disorders 51 spontaneous mutations 51 anovulation 51 phthalate metabolites 51 neurological sequelae 51 neuronal degeneration 51 neurological dysfunction 51 thyrotropin levels 51 untreated celiac disease 51 sensory disturbances 51 #q# deletion 51 cholinergic tone 51 BCL#A 51 methodologic 51 growth hormone secretion 51 Chronic insomnia 51 phenotypes 51 mito 51 cortical thinning 51 missense mutations 51 Sleep disordered breathing 51 abdominal adiposity 51 deformational plagiocephaly 51 deafness blindness 51 asthma exacerbations 51 ataxia 51 sensory impairments 51 polycystic ovary syndrome PCOS 51 impair cognitive 51 involuntary tics 51 sleep disordered breathing 51 blindness deafness 51 depressive symptomatology 51 Fragile X gene 51 undiagnosed celiac disease 51 Fetal alcohol 51 overt nephropathy 51 glucose tolerance 51 congenital malformations 51 onset diabetes mellitus 51 eczema asthma 51 ADHD dyslexia 51 abnormalities 51 MetS 51 hyperparathyroidism 51 affective psychoses 51 fetuses infants 51 prothrombotic 51 Apert syndrome 51 mental retardation blindness 51 hypovitaminosis D 51 neurobehavioral disorder 51 inbred strains 51 recurrent miscarriages 51 coronary calcification 51 exposed prenatally 51 Retinopathy 51 remyelination 51 affective psychosis 51 inhibitory neurotransmitters 51 pathophysiological processes 51 neurophysiologic 51 elevated cortisol 51 Hashimoto thyroiditis 51 neurofibrillary 51 euthymic patients 51 hematopoietic cancers 51 dysmorphic features 51 GABAergic interneurons 51 endocrine dysfunction 51 Neurogenesis 51 Clinical manifestations 51 predisposing factors 51 pediatric bipolar disorder 51 ependymoma 51 Hutchinson Gilford progeria 51 serum vitamin D 51 Alzheimer Disease AD 51 preterm infants 51 myotonic dystrophy 51 untreated obstructive sleep 51 psychopathology 51 cognitive functions 51 Irva Hertz Picciotto 51 reproductive endocrine 51 daytime sleepiness 51 perinatal asphyxia 51 brain plasticity 51 hyperactivity impulsivity 51 Fragile X Syndrome 51 mental retardation 51 neurologic complications 51 preeclampsia 51 CHDs 51 dysbindin 51 transgenic mouse models 51 hypothyroidism 51 febrile seizure 51 fat malabsorption 51 intrapartum 51 chromosome abnormality 51 CAG repeats 50 incurable neurological disorder 50 lethargy irritability 50 Autistic Spectrum Disorders 50 neuropathologic 50 familial adenomatous polyposis 50 autosomal dominant 50 temper dysregulation disorder 50 bipolar disorder schizophrenia 50 cardiac conduction 50 congential 50 physiologic 50 myoclonus 50 locomotor 50 dissociative disorders 50 neurobiological basis 50 chromosome #q#.# [001] 50 beta1 integrin 50 elevated serum ALT 50 metabolic 50 atopic asthma 50 thimerosal exposure 50 untreated hypothyroidism 50 subclinical hyperthyroidism 50 born preterm 50 coagulopathy 50 cortisol secretion 50 cognitive domains 50 folate metabolism 50 neuropsychological 50 disorder ADHD 50 Severe Primary IGFD 50 disc degeneration 50 prenatal testosterone 50 MYCN amplification 50 serotonin transporter 50 infantile colic 50 comorbid psychiatric disorders 50 developmental trajectories 50 neurodegeneration 50 puerperal psychosis 50 PON1 activity 50 causative gene 50 spastic diplegia 50 carotid IMT 50 gene MECP2 50 neurologic sequelae 50 pathogenetic mechanisms 50 cerebral palsy epilepsy 50 telomere length 50 coma convulsions 50 genetic defects 50 Menkes disease 50 Disorder ADHD 50 Thyroid hormone 50 CYP#D# 50 congenital disorders 50 nocturnal enuresis 50 Reye syndrome rare 50 neurobiological underpinnings 50 Dr. Gozal 50 Child Behavior Checklist 50 unmeasured factors 50 Leydig cell 50 #q#.# [002] 50 proliferative retinopathy 50 hereditary nonpolyposis colorectal cancer 50 intestinal inflammation 50 STAT3 signaling 50 SHANK3 50 Developmental Disorders 50 embryo biopsy 50 Attention-Deficit/Hyperactivity Disorder 50 Autism Spectrum Disorder 50 APOE e4 50 pulmonary hypertension PH 50 LIS1 50 Cognitive impairment 50 leaky gut 50 headaches irritability 50 neural degeneration 50 ADD ADHD 50 Down syndrome cerebral palsy 50 autosomal dominant disorder 50 neonatal respiratory distress 50 Electrophysiological 50 genetically inherited 50 prenatal 50 autosomal dominant inheritance 50 gene mutations 50 parasomnias 50 Alzheimer pathology 50 myeloproliferative diseases 50 SNHL 50 Gestational diabetes 50 habitual snoring 50 potentially modifiable 50 tremors numbness 50 autoimmune thyroid 50 Functional neuroimaging 50 reproductive hormones 50 chromosomal alterations 50 hyperphenylalaninemia HPA due 50 poststroke 50 neurodegenerative 50 depressive disorders 50 hemoglobinopathies 50 intracranial hypertension 50 daytime drowsiness 50 nondemented 50 gonococcal 50 protein tau 50 coinfection 50 placental function 50 elevated homocysteine 50 hepatotoxicity 50 diagnosing bipolar disorder 50 schizophrenia 50 microvascular disease 50 progressive neurologic 50 hydrocephaly 50 congenital cytomegalovirus 50 hirsutism 50 transaminase elevations 50 respiratory distress syndrome 50 renal scarring 50 hypoxic ischemic brain 50 oncogenesis 50 prenatal phthalate exposure 50 comorbidity 50 neurological degeneration 50 lymphocyte activation 50 hypersomnia 50 antiphospholipid syndrome 50 subclinical 50 cerebral vasospasm 50 lipid metabolism 50 neurologic symptoms 50 hereditary predisposition 50 shorter telomere length 50 nongenetic factors 50 chromosomal aberrations 50 cochlear implantation 50 CP CPPS 50 dysautonomia 50 cortical excitability 50 insulin resistance syndrome 50 hyperammonemia 50 de ath 50 TCF#L# gene 50 urinary excretion 50 intra uterine 50 genes predisposing 50 VUR 50 postoperative delirium 50 PGD PGS 50 proband 50 tardive dyskinesia TD 50 physiologic mechanisms 50 rheumatic disease 50 chronic periodontitis 50 dopamine neurotransmission 50 torticollis 50 endocrine abnormalities 50 meningitis encephalitis pulmonary edema 50 histone methylation 50 obstetric complications 50 metacognitive 50 periventricular leukomalacia 50 PB1 F2 50 singleton pregnancy 50 glial tumors 50 bronchiolitis 50 mitochondrial function 50 hemolytic 50 liver fibrosis 50 AAT deficiency 50 autistics 50 FTLD 50 clinically heterogeneous 50 synapse formation 50 neuronal 50 BH4 deficiency 50 astrocytomas 50 Raynaud syndrome 50 congenital CMV infection 50 disorder ADD 50 #q# [001] 50 KIBRA 50 androgen excess 50 Becker muscular dystrophy 50 p# mutations 50 visuospatial processing 50 multigenic 50 disfluencies 50 white matter hyperintensities 50 mGluR2 NAM 50 plasma lipid 50 cortical activation 50 disorder FASD 50 hypokalemia hypomagnesemia 50 thyrotropin 50 exotropia 50 modifiable risk 50 cytomegalovirus infection 50 Glucocorticoids 50 amenorrhea 50 Circadian rhythm 50 intestinal microflora 50 inherited neurodegenerative 50 cholesterol metabolism 50 untreated psychosis 50 familial pancreatic cancer 50 Autism Spectrum Disorders ASD 50 ELBW infants 50 endocrine diseases 50 neurogenic 50 uncharacterized genes 50 Cognitive behavioral 50 DiGeorge syndrome 50 causative genes 49 cholestasis 49 carcinogenesis 49 spinocerebellar ataxia 49 brain lesions 49 cardiovascular disease hypertension 49 HNPCC 49 orofacial 49 amblyopic 49 Elevated serum 49 neurobehavioral disorders 49 axonal degeneration 49 Hippocampal 49 M. vaccae 49 SHANK3 gene 49 postnatal 49 Repeated concussions 49 levodopa induced 49 Brugada syndrome 49 monoamine 49 attention-deficit/hyperactivity 49 Postpartum depression 49 amyloid deposition 49 impulsive behaviors 49 ovarian dysfunction 49 developmental disorder 49 apoE 49 esophageal reflux 49 Down syndrome chromosomal disorder 49 severe dehydrating diarrhea 49 degenerative neurological diseases 49 Cockayne Syndrome 49 hyperglycaemia 49 physiological abnormalities 49 dysarthria 49 Chronic fatigue 49 neurologic impairment 49 repetitive stereotyped 49 familial aggregation 49 PTEN mutations 49 Marc Weisskopf 49 irregular menstrual periods 49 axonal damage 49 genetic alterations 49 genetic polymorphism 49 mIU L 49 PLMs 49 male hormone androgen 49 atypical neuroleptics 49 idiopathic intracranial hypertension 49 organogenesis 49 organophosphate pesticides 49 neurodegenerative disorder 49 Antisocial personality 49 premenopause 49 TMEM#B 49 neurogenetic 49 adiponectin levels 49 neurodegenerative disease 49 trisomy 49 biochemical imbalance 49 thyroid hormones 49 preterm 49 endocrine 49 serum estradiol 49 VLBW 49 congenital blindness 49 FGF2 49 adrenal suppression 49 mitochondrial oxidative 49 dysgenesis 49 postoperative pulmonary 49 susceptibility gene 49 psychotic illnesses 49 infantile amnesia 49 Impulsivity 49 Postnatal depression 49 psychiatric illnesses 49 excitotoxic 49 comorbid depression 49 comorbid 49 Neural tube defects 49 adiposity 49 PANDAS 49 immunodeficiency 49 gastric carcinogenesis 49 skeletal fluorosis 49 GABRA2 gene 49 retinol binding protein 49 teratogenic 49 multifactorial 49 spinocerebellar ataxia type 49 glutamatergic 49 hyperexcitability 49 cardiac malformations 49 autistic regression 49 endotoxemia 49 intracellular signal transduction 49 synaptic dysfunction 49 gene locus 49 muscle degeneration 49 mitochondrial defects 49 psychosocial 49 diabetic microvascular complications 49 signaling cascades 49 Mild cognitive impairment 49 neurofibromatosis type 49 Spinal muscular atrophy 49 MTHFR 49 Magnesium deficiency 49 torsades de pointes 49 hyperreflexia 49 vascular cognitive impairment 49 longitudinal studies 49 bicuspid aortic valves 49 teratogens 49 coronary artery atherosclerosis 49 genetic neuromuscular disorder 49 neuropsychiatric symptoms 49 sleep deprivation impairs 49 bacteriuria 49 myelogenous leukemia 49 obsessive compulsive behaviors 49 Bardet Biedl Syndrome 49 MMRV vaccine 49 Periodontitis 49 Disrupted sleep 49 psychopathological disorders 49 intravascular hemolysis 49 hippocampal atrophy 49 fluoxetine Prozac 49 syndromic 49 HRQL 49 tumor progression 49 disorders 49 serum phosphate 49 ELBW 49 pharmacological interventions 49 neurocognition 49 primary biliary cirrhosis 49 kernicterus 49 non affective psychosis 49 gait disturbance 49 Major depressive disorder 49 upregulates 49 Meckel Gruber 49 mRNA expression 49 extrapyramidal 49 prolactin levels 49 overactivity 49 neurologic disorder 49 chromosomal imbalance 49 fatty liver disease 49 cerebral palsy muscular dystrophy 49 dopaminergic therapy 49 ORMDL3 49 nonalcoholic steatohepatitis 49 metabolite concentrations 49 neurobiological mechanisms 49 Foetal Alcohol Spectrum Disorder