ASDs

Related by string. ASDS * * autism spectrum disorders ASDs . Autism Spectrum Disorders ASDs . Dermatologic Surgery ASDS *

Related by context. All words. (Click for frequent words.) 74 autism spectrum disorders 74 autism spectrum disorder 69 ASD 67 autism spectrum disorders ASDs 67 autism 65 autism spectrum disorders ASD 65 Autism Spectrum Disorder ASD 64 ADHD 63 disorder ASD 63 autism spectrum 63 Autism Spectrum Disorder 62 attention-deficit/hyperactivity disorder ADHD 62 autistic spectrum 61 developmental disorders 61 mitochondrial disorders 61 PDD NOS 61 Autism Spectrum Disorders ASDs 61 developmental disorder 60 Autism Spectrum Disorders 60 neurodevelopmental 60 neuro developmental 60 neurodevelopmental disorders 59 dyscalculia 59 autistic traits 59 neurodevelopmental disorder 59 neurobehavioral disorder 59 Autistic Spectrum Disorder 59 developmental delays 59 congenital deafness 59 CHDs 59 sleep disordered breathing 59 tic disorders 59 neuropsychiatric disorder 59 mitochondrial dysfunction 59 neurological disorder affecting 58 neurobiological disorder 58 VCFS 58 NAFLD 58 syndromic 58 Autism Spectrum Disorders ASD 58 NF1 58 Pervasive Developmental Disorder 58 LQTS 58 juvenile idiopathic arthritis 57 cognitive impairments 57 Fragile X syndrome 57 epilepsy 57 disorders ASD 57 internalizing disorders 57 autism neurological disorder 57 neuroblastomas 57 Angelman syndrome 57 attention-deficit/hyperactivity disorder 57 subclinical hypothyroidism 57 neurobiological disorders 57 GBA mutations 57 autistics 57 habitual snoring 57 Autistic Disorder 57 neuro developmental disorder 57 generalized epilepsy 56 epilepsies 56 genetic abnormalities 56 neurologic disorders 56 autism Asperger 56 AAT deficiency 56 Rett syndrome 56 sensorineural hearing loss 56 SRBD 56 EoE 56 Major depressive disorder 56 inherited mutations 56 chromosomal disorder 56 verbal apraxia 56 comorbid disorders 56 FTLD 56 Joubert syndrome 56 apraxia 56 PANDAS 55 ciliopathies 55 disorder ADHD 55 High Functioning Autism 55 congenital anomalies 55 compulsive hoarding 55 HGPS 55 developmental disability 55 mitochondrial diseases 55 febrile convulsions 55 CNTNAP2 55 childhood disintegrative disorder 55 T1DM 55 mood disorders 55 sporadic ALS 55 VUR 55 RSV infections 55 neurobehavioral disorders 55 OSAHS 55 Autistic Spectrum Disorders 55 autism Asperger syndrome 55 Dravet syndrome 55 neurological impairments 55 NOMID 55 Down syndrome 55 maturational 55 CFS ME 55 psychiatric disorders 55 somatic symptoms 55 hereditary predisposition 55 febrile seizures 55 autistic 55 atopic 55 cochlear implantation 55 cognitive deficits 55 rhinosinusitis 55 auditory processing 55 Mitochondrial diseases 55 genetic syndromes 55 de novo mutations 55 ADHD Attention Deficit 54 #q# deletion 54 amblyopia 54 Attention Deficit Hyperactive Disorder 54 disfluencies 54 prenatally diagnosed 54 acute otitis media 54 inherited neurological disorder 54 autistic regression 54 Obstructive sleep apnea 54 maladaptive behaviors 54 trisomy 54 cognitive impairment 54 chromosomal abnormalities 54 neuropsychological impairments 54 ADD ADHD 54 chromosomal anomaly 54 CNVs 54 neuropsychiatric disorders 54 familial pancreatic cancer 54 perinatal depression 54 FASD 54 psychiatric illnesses 54 atopic eczema 54 WAGR syndrome 54 untreated celiac disease 54 nonautistic 54 Depressive disorders 54 Pervasive Developmental Disorders 54 mood dysregulation 54 Tourette syndrome TS 54 convergence insufficiency 54 learning disabilities 54 Chronic insomnia 54 pediatric bipolar disorder 54 intermittent exotropia 54 neonatal encephalopathy 54 JAK mutations 54 euthymic patients 54 diagnosing ADHD 54 myelomeningocele 54 intractable epilepsy 54 chromosomal disorders 54 Dental caries 54 alexithymia 54 intellectual disability 53 gene mutations 53 Math LD 53 Iron deficiency anemia 53 Genetic variants 53 Childhood Disorder 53 POAG 53 esotropia 53 Asperger syndrome Rett syndrome 53 diagnosing autism 53 autism dyslexia 53 GH deficiency 53 proliferative diabetic retinopathy 53 Anxiety disorders 53 enlarged tonsils 53 Mental retardation 53 Hyperactivity 53 ADPKD 53 gene variants 53 Primary IGFD 53 bronchopulmonary dysplasia 53 ASD prevalence 53 neurological abnormalities 53 reflux symptoms 53 seizure disorders 53 pyloric stenosis 53 chromosome abnormalities 53 familial hypercholesterolemia 53 narcolepsy cataplexy 53 Severe Primary IGFD 53 medulloblastoma 53 epigenetic changes 53 clefting 53 mental retardation epilepsy 53 repetitive behaviors 53 astrocytomas 53 cardiac hypertrophy 53 hyperactivity 53 cardiac abnormalities 53 unprovoked seizures 53 prediabetes 53 autosomal dominant inheritance 53 spastic diplegia 53 otitis media 53 NF2 53 atopic disorders 53 Hurler syndrome 53 Atopic dermatitis 53 sensory impairments 53 bronchiolitis 53 respiratory viral infections 53 exotropia 53 middle ear effusion 53 mild cognitive 53 brain lesions 53 white matter hyperintensities 53 inattention hyperactivity 53 #q#.# deletion syndrome 53 HbF 53 neurodevelopmental outcomes 53 recurrent wheezing 53 Peanut allergy 53 neurocognitive deficits 53 HNPCC 53 irreversible blindness 53 SNHL 53 bipolar disorders 53 Obsessive compulsive disorder 53 gastroesophageal reflux GERD 53 orofacial clefts 53 metabolic abnormalities 53 profound deafness 53 utero exposure 53 abnormalities 52 Irlen Syndrome 52 IUGR 52 premorbid 52 dyslexia dyspraxia 52 varicella infection 52 developmental abnormalities 52 LRRK2 mutations 52 DiGeorge syndrome 52 preterm deliveries 52 autism cerebral palsy 52 obstructive sleep apnea 52 Peutz Jeghers syndrome 52 CA MRSA infections 52 CdLS 52 Rh incompatibility 52 born preterm 52 Oppositional Defiant Disorder 52 Leber congenital amaurosis LCA 52 Autism 52 Acute lymphoblastic leukemia 52 prodrome 52 germline mutations 52 Attention-Deficit/Hyperactivity Disorder 52 primary biliary cirrhosis 52 myopia nearsightedness 52 disorders 52 molecular abnormalities 52 familial ALS 52 recurrent abdominal pain 52 congenital CMV 52 Postnatal depression 52 epigenetic alterations 52 dyslexics 52 schizotypal traits 52 antenatal depression 52 Hyperactivity Disorder 52 juvenile idiopathic arthritis JIA 52 comorbid anxiety 52 affective psychoses 52 Genetic predisposition 52 neurofibromatosis type 52 behavioral disorders 52 genetic variations 52 neurologic disorder 52 Prader Willi syndrome 52 untreated sleep apnea 52 congenital abnormalities 52 auditory neuropathy 52 pilocytic astrocytomas 52 allergic sensitization 52 neurocognitive impairment 52 Brugada syndrome 52 recurrent seizures 52 autism diagnoses 52 Fragile X Syndrome 52 HLHS 52 paternal discrepancy 52 chronic periodontitis 52 deafblindness 52 neurodegenerative disorder 52 IgA deficiency 52 highly heritable 52 eosinophilic esophagitis 52 obsessive compulsive disorder OCD 52 ependymoma 52 involuntary tics 52 FXTAS 52 presbycusis 52 medulloblastomas 52 Asperger Disorder 52 primary immunodeficiency 52 persistent pulmonary hypertension 52 Asperger disorder 52 familial adenomatous polyposis 52 pharmacologic treatments 52 neurodevelopmental impairment 52 recurrent miscarriage 52 neuromotor 52 familial clustering 52 Down syndrome cerebral palsy 52 myeloproliferative neoplasms 51 malformations 51 causative gene 51 autistic tendencies 51 genetic abnormality 51 autism Asperger Syndrome 51 amblyopic 51 synaesthesia 51 subclinical hyperthyroidism 51 chromosomal abnormality 51 Excessive daytime sleepiness 51 Asperger 51 unmeasured factors 51 tic disorder 51 subclinical atherosclerosis 51 Usher Syndrome 51 complex neurobiological disorder 51 hyperactive impulsive 51 renal scarring 51 rheumatic diseases 51 Sjögren syndrome 51 dystrophies 51 enuresis 51 neurological disorder 51 syndrome FAS 51 probands 51 FASPS 51 somatoform disorders 51 adolescents 51 Gliomas 51 neurodevelopmental disability 51 generalized tonic clonic seizures 51 neurobiological 51 ARVD 51 ADHD symptoms 51 gastrointestinal dysfunction 51 microdeletions 51 psychiatric disorder 51 uncontrolled epilepsy 51 RLS sufferers 51 progressive neurodegenerative disorder 51 precocious puberty 51 cerebral palsy Down syndrome 51 dyspraxia 51 CNTNAP2 gene 51 enterovirus infection 51 Mild cognitive impairment 51 Li Fraumeni syndrome 51 genetic disorder 51 trichotillomania 51 neurodevelopment 51 psychiatric comorbidities 51 Aortic stenosis 51 aspergers 51 ectodermal dysplasia 51 APOE ε4 51 impulsive behaviors 51 nonmelanoma skin cancers 51 externalizing disorders 51 neuroimaging studies 51 Parkinson sufferers 51 habitual snorers 51 chromosomal defect 51 phonological 51 recurrent tonsillitis 51 unexplained mental retardation 51 meningiomas 51 depressive disorders 51 Autism Asperger Syndrome 51 neuroendocrine 51 FeNO 51 neural tube defect 51 overactivity 51 thyroid hormone deficiency 51 Klinefelter syndrome 51 susceptibility genes 51 sensorimotor 51 Febrile seizures 51 MMSE scores 51 Hoarseness 51 sickle cell disease 51 Tourette syndrome 51 CALHM1 51 genetic susceptibility 51 disorder FASD 51 AUDs 51 airway hyperresponsiveness 51 recurrent miscarriages 51 #q# deletion syndrome 51 pseudotumor cerebri 51 thrombophilia 51 bronchopulmonary dysplasia BPD 51 undiagnosed celiac disease 51 schizophrenia 51 frontotemporal dementia 51 refractive error 51 structural abnormalities 51 developmental dyslexia 51 affective disorders 51 Bruxism 51 enterocolitis 51 REM sleep behavior 51 spinocerebellar ataxia 51 FMRP protein 51 untreated tooth decay 51 neurotypical 51 medulloblastoma tumors 51 rhinoconjunctivitis 51 heritable diseases 50 pathogenic mutations 50 cryptogenic stroke 50 extrapyramidal symptoms 50 neurosensory 50 dyslexia 50 anaphylaxis 50 modifiable risk 50 atopic dermatitis 50 vestibular dysfunction 50 fatal neuromuscular disorder 50 bacteraemia 50 mental retardation 50 Foetal Alcohol Spectrum Disorder 50 chromosome abnormality 50 infantile spasms 50 Angelman Syndrome 50 PCNSL 50 phenylketonuria 50 MCAD deficiency 50 Marfan 50 impaired cognition 50 MYH9 gene 50 sCJD 50 pervasive developmental 50 galactosemia 50 Myotonic dystrophy 50 LHON 50 basal cell nevus syndrome 50 bicuspid aortic valves 50 MYCN amplification 50 atopy 50 gluten sensitive enteropathy 50 adenotonsillectomy 50 spontaneous mutations 50 MGUS 50 amnestic MCI 50 allergic asthma 50 non syndromic 50 inattention impulsivity 50 etiologic 50 nonmelanoma skin cancer 50 syndromal 50 anxiety disorders 50 asthma exacerbations 50 severe dehydrating diarrhea 50 pneumococcal meningitis 50 generalized seizures 50 Rotavirus infection 50 degenerative neurological diseases 50 febrile seizure 50 disorders FASD 50 Gestational diabetes 50 dentin hypersensitivity 50 hypovitaminosis D 50 Lafora disease 50 eczema asthma 50 osteosarcomas 50 rhinovirus infection 50 penetrance 50 functioning autistics 50 polycystic ovary syndrome PCOS 50 cognitive dysfunction 50 proliferative retinopathy 50 asthma rhinitis 50 silent myocardial ischemia 50 craniofacial anomalies 50 Longitudinal studies 50 Irritable bowel syndrome IBS 50 hypochondriasis 50 microalbuminuria 50 dietary interventions 50 nondemented 50 mitochondrial disease 50 deafness blindness 50 perfusion abnormalities 50 BRCA1 mutations 50 syndromes 50 neurological impairment 50 pulmonary hypertension PH 50 juvenile myoclonic epilepsy 50 Parkinson disease PD 50 intraventricular hemorrhage 50 hyperactivity impulsivity 50 postnatally 50 KIBRA 50 monogenic 50 fetal malformations 50 enamel defects 50 dementias 50 emotional lability 50 familial hypercholesterolaemia FH 50 APOE e4 50 #q#.# [001] 50 myeloproliferative disorders 50 Generalized anxiety disorder 50 CIDP 50 neuropathologic 50 Chronic sinusitis 50 diagnosable mental disorders 50 olfactory dysfunction 50 dyskeratosis congenita 50 clinically heterogeneous 50 causal pathways 50 de ath 50 depressive episodes 50 chromosomal rearrangement 50 congenital hypothyroidism 50 Reactive Attachment Disorder 50 nondepressed 50 bipolar diagnoses 50 pathogenic mechanisms 50 neurodegenerative disease 50 neuropsychiatric symptoms 50 Rubinstein Taybi syndrome 50 RSV infection 50 neuropsychological deficits 50 MYH9 50 ichthyosis vulgaris 50 neuroblastoma 50 Systemic lupus 50 motor tics 50 Coeliac disease 50 developmentally delayed 50 savant syndrome 50 mutated genes 50 dissociative disorders 50 anatomical abnormalities 50 tinnitus sufferers 50 Chronic Myeloid Leukaemia 50 hypophosphatasia 50 eosinophilic disorders 50 diabetes mellitus DM 50 underdiagnosis 50 cognitive 50 nerve degeneration 50 INF2 50 ASD autism spectrum 50 behavioral abnormalities 50 ataxia telangiectasia 50 cerebral palsy blindness 50 leukemia ALL 50 autoimmune thyroiditis 50 Peanut allergies 50 uncontrolled asthma 50 colorectal carcinogenesis 50 comorbid ADHD 50 postoperative delirium 50 FMR1 50 asymptomatic PAD 50 OAB symptoms 50 nonsense mutation 50 ADEs 50 Down syndrome autism 50 Periodontitis 50 Chronic fatigue 50 dystonias 50 aneuploidies 50 dementing 49 fatty liver disease 49 mental retardation cerebral palsy 49 dysbindin 49 pathophysiologic mechanism 49 anticholinergic effects 49 allergic rhinitis 49 affective psychosis 49 hyperbilirubinemia 49 Premature infants 49 gestational diabetes mellitus 49 asymptomatic carotid stenosis 49 childhood leukemias 49 achromatopsia 49 DVT PE 49 ADHD ADD 49 myoclonus 49 sarcomas 49 Progeria 49 predisposing factors 49 congenital CMV infection 49 psychotic symptoms 49 infantile hemangioma 49 Essential tremor 49 Tourette Syndrome TS 49 osteogenesis imperfecta 49 underlying pathophysiology 49 BMPR2 49 cardioembolic stroke 49 sleep disorders 49 SADS 49 chromosomal anomalies 49 migraineurs 49 severe hyperbilirubinemia 49 acute leukemias 49 neuronal dysfunction 49 elevated serum ALT 49 sensory gating 49 AIOD 49 craniofacial abnormalities 49 IKZF1 49 hypothalamic pituitary adrenal axis 49 genetic determinants 49 autosomal dominant disorder 49 T2DM 49 adenoidectomy 49 ataxias 49 tic severity 49 genetic heterogeneity 49 hyperplastic 49 G6PD deficiency 49 non affective psychosis 49 electrophysiologic 49 prosopagnosia 49 Periodontal disease 49 DNA methylation patterns 49 acute lymphoid leukemia 49 periodontal gum disease 49 muscular dystrophies 49 DQB1 * 49 lichen planus 49 CMV infection 49 congenital disorders 49 PIK3CA 49 Alzheimers disease 49 GERD symptoms 49 neurodevelopment disorders 49 ependymomas 49 ALK mutations 49 autosomal dominant 49 Alzheimer disease AD 49 genetic susceptibilities 49 LTBI 49 Postpartum depression 49 SORL1 49 postpartum mood 49 attentional 49 Duchenne Muscular Dystrophy DMD 49 fatal neurodegenerative disorder 49 OCD 49 Aspergers syndrome 49 Thyroid nodules 49 TCF#L# gene 49 ADHD dyslexia 49 tonic clonic seizures 49 atopic asthma 49 hyperkinetic disorder 49 S. aureus infection 49 ORMDL3 49 inherited predisposition 49 TGFBR1 * 6A 49 leptin deficiency 49 nasal allergies 49 dental decay 49 EBV infection 49 thyroid dysfunction 49 chronic rhinosinusitis 49 primary ciliary dyskinesia 49 mental retardation syndromes 49 progranulin mutations 49 parkinsonism 49 pediatric GERD 49 #q#.# [002] 49 puerperal psychosis 49 Myelodysplastic syndromes MDS 49 airway remodeling 49 subclinical 49 Becker muscular dystrophy 49 schizophrenia schizoaffective disorder 49 Irritable bowel syndrome 49 geriatric syndromes 49 contagious yawning 49 Secondhand smoke exposure 49 colorectal cancer CRC 49 allergic eczema 49 TACI mutations 49 immunodeficiencies 49 Attention Deficit Disorder ADD 49 Iron deficiency 49 Molnar Szakacs 49 reflux disease 49 myelination 49 motor neuron diseases 49 EEGs 49 Leber Hereditary Optic Neuropathy 49 nighttime awakenings 49 ELBW infants 49 otitis 49 Vitamin B# deficiency 49 Bipolar disorder 49 chronicity 49 unknown etiology 49 Reefhuis 49 neurobehavioural 49 dominantly inherited 49 microvascular disease 49 synaptic function 49 mental disorders 49 Asperger syndrome milder 49 disabling neurological 49 androgen depletion 49 hiatal hernias 49 Attention-Deficit/Hyperactivity Disorder ADHD 49 breast cancer susceptibility genes 49 Retinoblastoma 49 deafness 49 vesicoureteral reflux 49 internalizing behaviors 49 TEAEs 49 obstructive lung 49 achondroplasia 49 primitive neuroectodermal tumors 49 hyperparathyroidism 49 XMRV infection 49 craniofacial deformities 49 phonic tics 49 Wilms tumor 49 Fragile X 49 NPHP 49 dental caries 49 Fecal incontinence 49 congenital toxoplasmosis 49 aetiology 49 cerebral palsy mental retardation 49 bulimia nervosa 49 APOE e4 gene 49 genetic mutations 49 PIDD 49 Marfan syndrome 49 MECP2 gene 49 subconjunctival hemorrhage 49 Rett Syndrome 49 congenital malformations 49 somatic mutations 49 lymphangioleiomyomatosis LAM 49 primary generalized tonic 49 GIST tumors 49 kinesthetic learners 49 endophenotypes 49 asthma 49 Menkes disease 49 medulloblastoma malignant brain tumor 49 LRRK2 49 atherothrombotic disease 49 bruxism 49 neurological sequelae 49 skeletal fluorosis 49 pathophysiologic 49 atopic disease 49 stimulant medications 49 Autistic 49 Retinopathy 49 herpes simplex encephalitis 49 ApoE4 gene 49 vitamin B# deficiency 49 motor neuron degeneration 49 undergone bariatric surgery 49 SHANK3 49 nongenetic 49 pharmacological interventions 49 airflow obstruction 49 Fatty Liver Disease 49 Fanconi anemia 49 APOE genotype 49 neurodermatitis 49 autism susceptibility genes 49 brain tumors 49 psychosocial distress 49 mtDNA mutations 49 hypotonia 49 chromosomal deletions 49 psychopathology 49 holoprosencephaly 49 autoinflammatory diseases 48 Hirschsprung disease 48 neurologic sequelae 48 atherothrombosis 48 CHARGE syndrome 48 gene mutation 48 GH deficient 48 autism spectrum diagnoses 48 Picky eating 48 tics involuntary 48 Allergic rhinitis 48 mitochondrial mutations 48 dysfunctional mirror neuron 48 physiological mechanisms 48 disorder ADD 48 myotonic dystrophy 48 neurocognitive functioning 48 Down syndrome chromosomal disorder 48 slow metabolizers 48 UGT#A# * 48 status epilepticus 48 endometrial cancers 48 microdeletion 48 depressive symptoms 48 rheumatologic 48 #p#.# [002] 48 PTEN mutations 48 FSGS 48 torticollis 48 progressive neurodegenerative disease 48 shorter telomere length 48 mitochondrial disorder 48 inflammatory bowel disease 48 distractibility 48 developmental pediatrician 48 leukoencephalopathy 48 Seasonal allergies 48 celiac disease 48 prematurity ROP 48 preterm babies 48 Schizophrenia affects 48 SHANK3 gene 48 dysbindin gene 48 disease NAFLD 48 Developmentally 48 diffuse gastric 48 TMJD 48 androgen deficiency 48 Antisocial Personality Disorder 48 primary immunodeficiencies 48 subsyndromal 48 tourette syndrome 48 genetically inherited 48 persistent wheezing 48 disorder PTSD 48 folate deficiency 48 neurodevelopment disorder 48 socioeconomic status SES 48 TYMS 48 activating mutation 48 peanut allergies 48 visual impairment 48 malignant brain 48 immunodeficiency 48 Juvenile Idiopathic Arthritis JIA 48 T1D 48 phonological awareness 48 lacunar 48 Wernicke Korsakoff syndrome 48 mutations 48 Cochlear implants 48 coprolalia 48 anencephaly 48 Uterine fibroids 48 Fragile X gene 48 urolithiasis 48 Bronchiolitis 48 pneumococcal infections 48 heterotaxy 48 disordered breathing 48 systemic lupus erythematosus SLE 48 chromosomal translocations 48 vasomotor rhinitis 48 metastatic brain tumor 48 genetic defect 48 Medulloblastoma 48 untreated OSA 48 comorbid depression 48 MPS VI 48 fatal neurodegenerative 48 neuroendocrine tumors 48 Autism PDD 48 prenatal exposures 48 IPAH 48 inconsolable crying 48 intracranial hemorrhage ICH 48 infantile hemangiomas 48 Heavy menstrual bleeding 48 retinal dysfunction 48 RSV bronchiolitis 48 basal cell carcinomas 48 neuropathies 48 metabolic abnormality 48 rheumatic disease 48 pyelonephritis 48 breastfed exclusively 48 pneumococci 48 optic atrophy 48 prefrontal regions 48 demyelinating diseases 48 hypersomnia 48 airway responsiveness 48 etiology 48 congenital adrenal hyperplasia CAH 48 idiopathic scoliosis 48 Pathological gambling 48 non metastatic osteosarcoma 48 epididymitis 48 cotinine levels 48 perceptual reasoning 48 primary aldosteronism 48 spontaneous preterm birth 48 gluten sensitivity 48 Aspergers 48 FMR1 gene 48 GISTs 48 hamartomas 48 delusions hallucinations 48 etiologies 48 comorbid 48 autism mental retardation 48 Amblyopia 48 chlamydial infection 48 nocturnal enuresis 48 MLL2 48 milder Asperger syndrome 48 Lennox Gastaut Syndrome 48 BCL#A 48 umbilical hernias 48 atypical nevi 48 proband 48 neuro developmental disorders 48 psychiatric morbidity 48 Fetal alcohol 48 invasive meningococcal disease 48 Severe acute malnutrition 48 hypospadias 48 enteroviruses 48 PTPN# 48 N myc 48 behavioral disinhibition 48 plagiocephaly 48 degenerative disorder 48 BRCA carriers 48 dysphagia 48 brainwave patterns 48 epigenetic markers 48 MetS 48 neurological 48 Li Fraumeni 48 CHD7 48 gastrointestinal symptoms 48 Binge eating 48 cystic fibrosis CF 48 squamous cell lung cancer 48 neurobiological underpinnings 48 GABAergic interneurons 48 Premature birth 48 dopaminergic therapy 48 monolinguals 48 eczema hay fever 48 apnea OSA 48 thimerosal exposure 48 genetic variants 48 diagnosable disorder 48 prediabetic 48 cystic fibrosis muscular dystrophy 48 vitamin D deficiency 48 Polycystic ovary syndrome PCOS 48 suicidality 48 Lactose intolerance 48 Aspergers Syndrome 48 dopamine receptor gene 48 Sleep disordered breathing 48 susceptibility loci 48 phenotypes 48 HER2 overexpression 48 PDGFRA 48 comorbid psychiatric disorders 48 neurocognitive disorder 48 Chronic ITP 48 lumbar disc disease 48 neurological disorders 48 multisystemic 48 celiac sprue 48 cerebral infarction 48 neuropsychiatric diseases 48 chronic eosinophilic leukemia 48 Parkinsonian Syndromes 48 onset seizures 48 atherothrombotic 48 Sensorineural hearing loss 48 Lennox Gastaut syndrome

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