Keywords: سندرم ویلیامس; Williams syndrome; Low-gamma oscillations; 3D integration; Visual coherence; EEG/ERP;
مقالات ISI سندرم ویلیامس (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: سندرم ویلیامس; Williams syndrome; Colour discrimination; Colour categorisation; Visual perception;
Keywords: سندرم ویلیامس; Williams syndrome; Down syndrome; Executive function;
Keywords: سندرم ویلیامس; Causal inference; Contextual integration; Central coherence; Williams syndrome;
Keywords: سندرم ویلیامس; Williams syndrome; Mental states; Emotion; Eye gaze; Eye tracking;
Keywords: سندرم ویلیامس; Drawing; Williams syndrome; Attention; Developmental disability; Strategy use;
Keywords: سندرم ویلیامس; Metaphor; Metonymy; Williams syndrome; Semantic knowledge;
Keywords: سندرم ویلیامس; Williams syndrome; Down syndrome; Short-term memory; Developmental trajectories;
Keywords: سندرم ویلیامس; Development; Brain connectivity; DTI; HARDI; rs-fMRI; Autism; ADHD; Fragile X; 22q11.2 DS; Turner syndrome; Williams syndrome;
Keywords: سندرم ویلیامس; Williams syndrome; Spanish; Syntax; Phrase rules; Recursion; Binding; Control; Computation; Chomsky hierarchy
Keywords: سندرم ویلیامس; Williams syndrome; Hearing loss; Otoacoustic emissions;
Parada cardÃaca relacionada con la anestesia en el sÃndrome Williams-Beuren
Keywords: سندرم ویلیامس; SÃndrome Williams; Parada cardiaca; Anestesia; CardiopatÃa; Muerte súbita; Isquemia miocárdica; Williams syndrome; Cardiac arrest; Anaesthesia; Cardiopathy; Death sudden; Myocardial ischaemia;
The interaction between neurocognitive functioning, subthreshold psychotic symptoms and pharmacotherapy in 22q11.2 deletion syndrome: A longitudinal comparative study
Keywords: سندرم ویلیامس; DiGeorge Syndrome; Velocardiofacial Syndrome; SIPS; Williams Syndrome; Neurocognitive functioning;
The contribution of GTF2I haploinsufficiency to Williams syndrome
Keywords: سندرم ویلیامس; GTF2I; Williams syndrome; Hypersociability; TRPC3;
Hyperacusis in children: A clinical profile
Keywords: سندرم ویلیامس; Hyperacusis; Otitis media with effusion; Sensory gating; Conductive hearing loss; Sensorineural hearing loss; Williams syndrome; Sensory processing disorder;
Negative subthreshold psychotic symptoms distinguish 22q11.2 deletion syndrome from other neurodevelopmental disorders: A two-site study
Keywords: سندرم ویلیامس; Velocardiofacial syndrome; Williams syndrome; Negative symptoms; Structured Interview for Prodromal Symptoms (SIPS); Computerized Neurocognitive Battery (CNB);
Original articleDisparities in visuo-spatial constructive abilities in Williams syndrome patients with typical deletion on chromosome 7q11.23
Keywords: سندرم ویلیامس; Williams syndrome; Visuo-spatial construction; Inter-individual differences;
CYP24A1 loss of function: Clinical phenotype of monoallelic and biallelic mutations
Keywords: سندرم ویلیامس; FGF23; fibroblastic growth factor 23; PTH; parathyroid hormone; WS; Williams syndrome; 1,25-(OH)2D; 1,25-dihydroxyvitamin D; 24,25-(OH)2D; 24,25-dihydroxyvitamin D; 25-OHD; 25-hydroxyvitamin D; 24-hydroxylase; hypercalcemia; hypercalciuria; vitamin D; Wil
CongenitalSurgical Correction of Congenital Supravalvular Aortic Stenosis
Keywords: سندرم ویلیامس; supravalvular aortic stenosis; Williams syndrome; congenital heart disease; surgery;
Audio-visual speech perception in infants and toddlers with Down syndrome, fragile X syndrome, and Williams syndrome
Keywords: سندرم ویلیامس; Down syndrome; fragile X syndrome; Williams syndrome; Audio-visual speech integration; Language acquisition; the McGurk effect;
Williams syndrome and mature B-Leukemia: A random association?
Keywords: سندرم ویلیامس; Williams syndrome; Mature B-Leukemia; Cancer predisposition;
Cerebral and cerebellar MRI volumes in Williams syndrome
Keywords: سندرم ویلیامس; Cerebellum; Williams syndrome; MRI;
A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: Velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes
Keywords: سندرم ویلیامس; 22q11.2 deletion syndrome; Williams syndrome; Executive functions; Visuospatial functions; Psychiatric manifestation
Accelerometer-determined physical activity and walking capacity in persons with Down syndrome, Williams syndrome and Prader-Willi syndrome
Keywords: سندرم ویلیامس; Accelerometer; Physical activity; Six-minute walk test; Down syndrome; Williams syndrome; Prader-Willi syndrome;
Sleep is atypical across neurodevelopmental disorders in infants and toddlers: A cross-syndrome study
Keywords: سندرم ویلیامس; Sleep; Language development; Neurodevelopmental disorders; Down syndrome; Fragile X syndrome; Williams syndrome;
Cardiovascular manifestations of Williams syndrome: Imaging findings
Keywords: سندرم ویلیامس; Williams syndrome; Cardiovascular CT angiography; Supravalvular aortic stenosis; Pulmonary artery stenosis; Pediatric cardiothoracic surgery
Cross syndrome comparison of sleep problems in children with Down syndrome and Williams syndrome
Keywords: سندرم ویلیامس; Sleep problems; Williams syndrome; Down syndrome; Actigraphy; Developmental disorders
Global dot integration in typically developing children and in Williams Syndrome
Keywords: سندرم ویلیامس; Glass patterns; Global integration; Development; Williams Syndrome; Illusory motion; Form processing; Motion processing
Facilitating complex shape drawing in Williams syndrome and typical development
Keywords: سندرم ویلیامس; Drawing; Developmental disorders; Williams syndrome; Typical development; Perception; Graphic planning; Remediation
Caregiver survey of pharmacotherapy to treat attention deficit/hyperactivity disorder in individuals with Williams syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Stimulant medication; ADHD medication; Methylphenidate; Amphetamine
Familiarity and recollection in Williams syndrome
Keywords: سندرم ویلیامس; Familiarity; Recollection; Williams syndrome; Declarative memory; Recognition memory
Psycholinguistic abilities of children with Williams syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Psycholinguistic abilities; Visual and auditory processing
The production of figurative language in typically developing children and Williams Syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Figurative language; Language production; Development;
How executive functions are related to intelligence in Williams syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Executive functions; Intelligence
The neuroanatomy of the autistic phenotype
Keywords: سندرم ویلیامس; Autism; Fragile X syndrome; Williams syndrome; Gray matter; White matter; Neuroimaging
Colour as an environmental cue when learning a route in a virtual environment: Typical and atypical development
Keywords: سندرم ویلیامس; Williams syndrome; Route learning; Wayfinding; Colour perception; Visuo-spatial cognition
Examining reports of mental health in adults with Williams syndrome
Keywords: سندرم ویلیامس; Informant and respondent; Mental health; Stroop; Williams syndrome
Mutation of Gtf2ird1 from the Williams-Beuren syndrome critical region results in facial dysplasia, motor dysfunction, and altered vocalisations
Keywords: سندرم ویلیامس; KO; homozygous Gtf2ird1 knockout; PND; postnatal day; USV; ultrasound vocalisation; WBS; Williams-Beuren syndrome; WSCP; Williams syndrome cognitive profile; WT; wild-type; BEN; GTF3; Knockout; Mouse model; MusTRD1; Neurodevelopmental disorder; Ultrasou
Understanding motor acts and motor intentions in Williams syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Social cognition; Understanding motor acts; Understanding motor intention; Motor skills;
Sleep EEG fingerprints reveal accelerated thalamocortical oscillatory dynamics in Williams syndrome
Keywords: سندرم ویلیامس; Williams syndrome; Sleep EEG; Sleep spindles; Cortical synchronization; NREM
Effect of nonrigid registration algorithms on deformation-based morphometry: a comparative study with control and Williams syndrome subjects
Keywords: سندرم ویلیامس; Nonrigid registration; Deformation-based morphometry; Williams syndrome; Brain atlas
Williams Syndrome Transcription Factor is critical for neural crest cell function in Xenopus laevis
Keywords: سندرم ویلیامس; WSTF; Neural crest; Xenopus; Williams Syndrome; BAZ1b; Chromatin remodeler
How useful are landmarks when learning a route in a virtual environment? Evidence from typical development and Williams syndrome
Keywords: سندرم ویلیامس; Spatial cognition; Route learning; Navigation; Virtual reality; Williams syndrome; Landmarks
Parent report of antidepressant, anxiolytic, and antipsychotic medication use in individuals with Williams syndrome: Effectiveness and adverse effects
Keywords: سندرم ویلیامس; Williams syndrome; Anxiety; SSRI; Antidepressant; Anxiolytic; Antipsychotic;
Anxious, hypoactive phenotype combined with motor deficits in Gtf2ird1 null mouse model relevant to Williams syndrome
Keywords: سندرم ویلیامس; Gtf2ird1; Williams syndrome; Anxiety; Motor coordination; Mouse model
Behavioral phenotypes of genetic syndromes with intellectual disability: Comparison of adaptive profiles
Keywords: سندرم ویلیامس; Mental retardation; Down Syndrome; Williams Syndrome; Angelman Syndrome; Prader-Willi Syndrome; Fragile-X Syndrome; Adaptation
MRI amygdala volume in Williams Syndrome
Keywords: سندرم ویلیامس; Williams Syndrome; Hypersociability; Amygdala; Neurodevelopment
Characterisation of sleep problems in children with Williams syndrome
Keywords: سندرم ویلیامس; CSHQ, Child Sleep Habits Questionnaire; SRE, sleep-related enuresis; TD, typically developing children; WS, Williams syndromeSleep; Genetic disorders; Williams syndrome
A Comparative Study of Hearing Loss in Two Microdeletion Syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) Syndromes
Keywords: سندرم ویلیامس; AR; Acoustic reflex; COMT; Catechol-O-methyltransferase; DD; Developmental disability; ENT; Ear, nose, and throat; SRT; Speech reception threshold; TD; Typically developing; VCFS; Velocardiofacial syndrome; WS; Williams syndrome;
ADHD and genetic syndromes
Keywords: سندرم ویلیامس; Attention Deficit/Hyperactivity Disorder; Genetic syndromes; Fragile X Syndrome; Neurofibromatosis type 1; Tuberous Sclerosis Complex; Williams Syndrome; Sexual aneuploidies; Mental retardation