Keywords: سندرم حذف 22q11.2; Schizophrenia; 22q11.2 deletion syndrome; Modeling; Psychoeducation; Social skills training; Cognitive-behavioral therapy;
مقالات ISI سندرم حذف 22q11.2 (ترجمه نشده)
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Keywords: سندرم حذف 22q11.2; Cleft palate; 22q11.2 deletion syndrome; Velopharyngeal insufficiency; Velopharyngoplasty; Speech
Keywords: سندرم حذف 22q11.2; 22q11.2 Deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Obstructive sleep apnea; Velopharyngeal insufficiency
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Velopharyngeal dysfunction;
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; 22q11DS; Behavioural phenotype; Cognitive phenotype; Psychiatric disorder; Psychosis; Review
Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; Primary lymphedema; Primary lymphatic dysplasia; 22q11.2 deletion syndrome; TBX1; VEGFR3; Lymphatic anomalies;
Psychiatric manifestations of 22q11.2 deletion syndrome: A literature review
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Psychiatric comorbidity; Genetics; SÃndrome de deleción 22q11.2; Comorbilidades psiquiátricas; Genética;
Manifestaciones psiquiátricas del sÃndrome de deleción 22q11.2: una revisión de la literatura
Keywords: سندرم حذف 22q11.2; SÃndrome de deleción 22q11.2; Comorbilidades psiquiátricas; Genética; 22q11.2 deletion syndrome; Psychiatric comorbidity; Genetics;
Psychotic symptoms influence the development of anterior cingulate BOLD variability in 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; BOLD signal variability; Psychotic symptoms; 22q11.2 deletion syndrome; Salience network;
Exploratory study on cognitive abilities and social responsiveness in children with 22q11.2 deletion syndrome (22q11DS) and children with idiopathic intellectual disability (IID)
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Idiopathic intellectual disability; Cognitive abilities; Social responsiveness; Developmental trajectories;
A pilot study on immuno-psychiatry in the 22q11.2 deletion syndrome: A role for Th17 cells in psychosis?
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Schizophrenia spectrum disorder; Th17 cells; T-cell immune deficiency; Psychosis; Neuro-inflammation;
Adults with 22q11.2 deletion syndrome have a different velopharyngeal anatomy with predisposition to velopharyngeal insufficiency
Keywords: سندرم حذف 22q11.2; Cleft palate; Levator veli palatini; 22q11.2 deletion syndrome; Velocardiofacial syndrome; VPI;
Atypical language characteristics and trajectories in children with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Idiopathic intellectual disability; Autism spectrum disorders; Language development;
Association of airway abnormalities with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Airway anomalies; Trachea; Larynx; Polyhydramnios;
Original articleParkinson's disease associated with 22q11.2 deletion: Clinical characteristics and response to treatment
Keywords: سندرم حذف 22q11.2; Genetics; 22q11.2 deletion syndrome; Early-onset Parkinson's disease; Phenotype; Deep brain stimulation;
Archival ReportThe Psychosis Spectrum in 22q11.2 Deletion Syndrome Is Comparable to That of Nondeleted Youths
Keywords: سندرم حذف 22q11.2; Clinical high risk; DiGeorge syndrome; Prodromal; Psychosis; 22q11.2 Deletion syndrome; Schizophrenia;
White matter microstructural deficits in 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Diffusion tensor imaging; Psychosis; Fractional anisotropy; Cingulum bundle;
Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study
Keywords: سندرم حذف 22q11.2; (22q11.2DS); 22q11.2 deletion syndrome; (AD); axial diffusivity; (DTI); diffusion tensor imaging; (DWI); diffusion weighted image; (dTP); dorsal temporal pole; (EmC); extreme capsule; (FOV); field of view; (FA); fractional anisotropy; (-fp); fronto-pariet
Cerebral microbleeds: A new presenting feature of chromosome 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 2q11.2DS; 22q11.2 deletion syndrome; CNS; central nervous system; CMB; cerebral microbleeds; Array CGH; array - comparative genomic hybridization; EEG; electroencephalography; CT; computed tomography; MRI; magnetic resonance imaging; FFE; fast-field-echo;
Cardiac sympathetic activity in 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; AMPT; Monoamine depletion; Cardiac sympathetic activity; Planar MIBG myocardial scintigraphy;
Abnormal gait, reduced locomotor activity and impaired motor coordination in Dgcr2-deficient mice
Keywords: سندرم حذف 22q11.2; EGFP, enhanced green fluorescent proteinDgcr2 gene; knock-out mice; 22q11.2 deletion syndrome; Motor coordination; Abnormal gait; Purkinje cell
B cell development in chromosome 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; DiGeorge syndrome; Follicular helper T cells; Somatic hypermutation; TBX1; Immunoglobulin; 22q11.2 deletion syndrome; Switched memory B cells;
Neurocognitive profile in psychotic versus nonpsychotic individuals with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Neurocognition; Schizophrenia; Psychosis; Penn computerized neurocognitive battery;
The Immune Phenotype of Patients with CHARGE Syndrome
Keywords: سندرم حذف 22q11.2; CHARGE syndrome; 22q11.2 deletion syndrome; Lymphopenia; Specific antibody deficiency; CHARGE; Coloboma, Heart disease, choanal Atresia, growth/mental Retardation, Genitourinary malformations, Ear abnormalities; CHD7; Chromodomain Helicase DNA-binding pro
Congenital Heart Defects and Measures of Fetal Growth in Newborns with Down Syndrome or 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; birth weight; congenital heart defects; Down syndrome; epidemiology; fetal growth; head circumference; CHD; Congenital heart defects; EUROCAT; European Surveillance of Congenital Anomalies;
Abordaje inmunológico del síndrome por deleción 22q11.2
Keywords: سندرم حذف 22q11.2; Síndrome de DiGeorge; Síndrome por deleción 22q11.2; Cardiopatía troncoconal; Inmunodeficiencia; Linfopenia congénita; Hipoplasia tímica; Aplasia tímicaDiGeorge syndrome; 22q11.2 deletion syndrome; Congenital heart disease; Immunodeficiency; Congenital ly
Schizophrenia patients and 22q11.2 deletion syndrome adolescents at risk express the same deviant patterns of resting state EEG microstates: A candidate endophenotype of schizophrenia
Keywords: سندرم حذف 22q11.2; Schizophrenia; 22q11.2 deletion syndrome; Endophenotype; Microstates; Resting-state
Perspectives actuelles dans la microdélétion 22q11.2Â : prise en charge du phénotype neurocomportemental
Keywords: سندرم حذف 22q11.2; 22q11.2; Syndrome de DiGeorge; Remédiation cognitive; ADHD; Psychose; Anomalies cytogénétiques; Neurocognition; Cognition sociale; Schizophrénie; 22q11.2 deletion syndrome; DiGeorge's syndrome; Chromosomal abnormalities; Psychosis; Cognitive remediati
El sÃndrome 22q11.2DÂ S como un subtipo genético de esquizofrenia
Keywords: سندرم حذف 22q11.2; Esquizofrenia; Microdeleción 22q11.2; SÃndrome de deleción 22q11.2; 22q11.2DS; Schizophrenia; 22q11.2 microdeletion; 22q11.2 deletion syndrome; 22q11.2DS;
Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; congenital heart defects; prenatal diagnosis
Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcome
Keywords: سندرم حذف 22q11.2; 22q11.2 Deletion syndrome; Negative symptoms; Psychotic symptoms; Cluster
Clinical Features and Follow-Up in Patients with 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11.2; 22q11DS; 22q11.2 deletion syndrome; AIEOP; Italian Association of Pediatric Haematology and Oncology; MIM; Mendelian Inheritance in Man;
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 حذف 22q11.2; 22q11.2 deletion syndrome; Williams syndrome; Executive functions; Visuospatial functions; Psychiatric manifestation
Subthreshold Psychotic Symptoms in 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; psychosis; schizophrenia; prodromal; Structured Interview for Prodromal Syndromes;
Congenital heart disease is associated with reduced cortical and hippocampal volume in patients with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; Cardiac defects; Velo-cardio-facial syndrome; Brain morphometry; Volumetric MRI; Neurodevelopmental disorders; CHD; congenital heart disease; 22q11DS; 22q11.2 deletion syndrome;
Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion
Keywords: سندرم حذف 22q11.2; Pleiotropy; Copy number variant (CNV); Autism; Schizophrenia; 22q11.2 deletion syndrome;
A candidate gene approach to identify modifiers of the palatal phenotype in 22q11.2 deletion syndrome patients
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Cleft palate; Candidate gene;
Exploring a neurogenic basis of velopharyngeal dysfunction in Tbx1 mutant mice: No difference in volumes of the nucleus ambiguus
Keywords: سندرم حذف 22q11.2; Tbx1; Nucleus ambiguus; Velopharyngeal dysfunction; 22q11.2 Deletion syndrome;
Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Schizophrenia; Premorbid adjustment
A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Psychoeducational functioning in 22q11DS; Neurocognitive functioning in 22q11DS; Psychiatric functioning in 22q11DS; Schizophrenia genetics
Converging levels of analysis on a genomic hotspot for psychosis: Insights from 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 Deletion Syndrome; Velocardiofacial syndrome; Dopamine; Schizophrenia; Psychosis; Copy number variant; Animal models
Adolescents at ultra-high risk for psychosis with and without 22q11 deletion syndrome: A comparison of prodromal psychotic symptoms and general functioning
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Ultra-high risk; Schizophrenia; Early intervention; Prodrome;
Occurrence of affective disorders compared to other psychiatric disorders in children and adolescents with 22q11.2 deletion syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; Major depression; Bipolar disorder; Anxiety disorders; Psychosis;
Association of MB-COMT polymorphisms with schizophrenia-susceptibility and symptom severity in an African cohort
Keywords: سندرم حذف 22q11.2; 22qDS; 22q11.2 deletion syndrome; A; adenine; bp; base pairs; C; cytosine; CI; confidence interval; COMT; catechol-O-methyltransferase; DNA; deoxyribonucleic acid; DSM-IV; diagnostic and statistical manual of mental disorders; G; guanine; gDNA; genomic DN
Underlying Genetic Diagnosis of Pierre Robin Sequence: Retrospective Chart Review at Two Children's Hospitals and a Systematic Literature Review
Keywords: سندرم حذف 22q11.2; 22qDS; 22q11.2 deletion syndrome; CGH; Comparative genomic hybridization; FAS; Fetal alcohol syndrome; FISH; Fluorescence in situ hybridization; PRS; Pierre Robin sequence; RBCH; Rainbow Babies and Children's Hospital; SS; Stickler syndrome; VCFS; Veloc
Relationship between reaction time, fine motor control, and visual–spatial perception on vigilance and visual-motor tasks in 22q11.2 Deletion Syndrome
Keywords: سندرم حذف 22q11.2; 22q11.2 Deletion Syndrome; Intellectual disability; Visual-motor function; Reaction time; Vigilance
The chromosome 22q11.2 deletion: From the unification of biomedical fields to a new kind of genetic condition
Keywords: سندرم حذف 22q11.2; 22q11.2 Deletion Syndrome; Genomic designation; Genetics; Nosology; Citation analysis; Boundary object; Actant; Diagnostic categories
Cognitive phenotype of velocardiofacial syndrome: A review
Keywords: سندرم حذف 22q11.2; Cognitive phenotype; Velocardiofacial syndrome; Intellectual developmental disability; Psychiatric disorder; 22q11.2 deletion syndrome
Neuroanatomic Predictors to Prodromal Psychosis in Velocardiofacial Syndrome (22q11.2 Deletion Syndrome): A Longitudinal Study
Keywords: سندرم حذف 22q11.2; 22q11.2 deletion syndrome; brain development; longitudinal; MRI; prodromal; psychosis; schizophrenia; temporal lobe
Prodromal symptoms in adolescents with 22q11.2 deletion syndrome and schizotypal personality disorder
Keywords: سندرم حذف 22q11.2; Prodrome; Psychosis; Ultra high risk; Genetic deletion syndrome; Schizotypal personality disorder; 22q11.2 Deletion Syndrome