Keywords: سندرم DiGeorge; pediatric cardiac transplantation; chromosomal anomalies; Down syndrome; Turner syndrome; DiGeorge syndrome;
مقالات ISI سندرم DiGeorge (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 DiGeorge; thyroid; parathyroid; hypoparathyroidism; pseudohypoparathyroidism; DiGeorge syndrome;
Keywords: سندرم DiGeorge; 22q11.2 deletion syndrome (22q11DS); Velocardiofacial syndrome; DiGeorge syndrome; Psychiatric diagnosis; Treatment; Psychosocial; Functioning;
Keywords: سندرم DiGeorge; Severe combined immunodeficiency; severe combined immunodeficiency newborn screening; next-generation sequencing; molecular diagnostics; AT; Ataxia telangiectasia; CGH; Comparative genomic hybridization; CHARGE; Coloboma, heart defects, choanal atresia, g
Keywords: سندرم DiGeorge; milk-alkali syndrome; pancreatitis; hypercalcemia; hypocalcemia; acute renal failure; calcium carbonate; DiGeorge syndrome
Keywords: سندرم DiGeorge; MRKH syndrome; Uterovaginal aplasia; Associated malformations; Associated syndromes; Abnormal karyotype; Klippel-Feil syndrome; VACTERL association; DiGeorge syndrome
Keywords: سندرم DiGeorge; DiGeorge syndrome; hematopoietic cell transplantation; primary immunodeficiency; severe combined immunodeficiency; T-cell lymphopenia; T-cell receptor excision circle (TREC);
Keywords: سندرم DiGeorge; Obstructive sleep apnea; DiGeorge Syndrome; Sleep disordered breathing; Anterior cricoid suspension; Anterior tracheal wall suspension;
Keywords: سندرم DiGeorge; 22q11.2 Deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Obstructive sleep apnea; Velopharyngeal insufficiency
Keywords: سندرم DiGeorge; anesthesia; cardiovascular surgical procedures; DiGeorge syndrome; hypocalcemia; immunosuppression; infection
Keywords: سندرم DiGeorge; 22q11.2 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Velopharyngeal dysfunction;
Keywords: سندرم DiGeorge; 22q11.2 microdeletion syndrome; DiGeorge syndrome; Velocardiofacial syndrome; Hearing loss; Cleft palate; Speech articulation disorder
Keywords: سندرم DiGeorge; 22q11.2 microdeletion syndrome; DiGeorge syndrome; Velocardiofacial syndrome; Velopharyngeal insufficiency; Cleft palate; Speech articulation disorder
Congenital respiratory tract disorders in 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; 22q11 deletion; Velocardiofacial syndrome; DiGeorge syndrome; Airway malacia; Subglottic stenosis; Laryngeal web;
Deletion of the T-box transcription factor gene, Tbx1, in mice induces differential expression of genes associated with cleft palate in humans
Keywords: سندرم DiGeorge; Tbx1; DiGeorge syndrome; Velocardiofacial syndrome; Soft palate; Bifid uvula; Cleft palate;
The interaction between neurocognitive functioning, subthreshold psychotic symptoms and pharmacotherapy in 22q11.2 deletion syndrome: A longitudinal comparative study
Keywords: سندرم DiGeorge; DiGeorge Syndrome; Velocardiofacial Syndrome; SIPS; Williams Syndrome; Neurocognitive functioning;
Wrodzone zaroÅniÄcie krtani i przeÅyku u dziewczynki z delecjÄ
22q11.2 - opis przypadku
Keywords: سندرم DiGeorge; ZespóÅ DiGeorge'a; wrodzone zaroÅniÄciu przeÅyku; wady dróg oddechowych; niedobór odpornoÅci; niedodma; DiGeorge syndrome; Esophagus atresia; Structural airway anomalies; Immune deficiency; Atelectasis;
Social cognitive impairment in 22q11 deletion syndrome: A review
Keywords: سندرم DiGeorge; Cognition; Social perception; Theory of mind; DiGeorge Syndrome; Psychotic disorders;
Archival ReportThe Psychosis Spectrum in 22q11.2 Deletion Syndrome Is Comparable to That of Nondeleted Youths
Keywords: سندرم DiGeorge; Clinical high risk; DiGeorge syndrome; Prodromal; Psychosis; 22q11.2 Deletion syndrome; Schizophrenia;
Thymus transplantation for complete DiGeorge syndrome: European experience
Keywords: سندرم DiGeorge; DiGeorge syndrome; athymia; thymus transplantation; AIRE; Autoimmune regulator; ATG; Antithymocyte globulin; cDGS; Complete DiGeorge syndrome; CHARGE; Coloboma, heart defects, atresia choanae, retardation of growth and development, genital abnormalities,
B cell development in chromosome 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; DiGeorge syndrome; Follicular helper T cells; Somatic hypermutation; TBX1; Immunoglobulin; 22q11.2 deletion syndrome; Switched memory B cells;
Reduction of CRKL expression in patients with partial DiGeorge syndrome is associated with impairment of T-cell functions
Keywords: سندرم DiGeorge; CRKL; DiGeorge syndrome; c-Fos; proliferation; T-cell receptor activation; IL-2; signal transducer and activator of transcription 5; AP-1; Activator protein 1; APC; Allophycocyanin; CFSE; Carboxyfluorescein succinimidyl ester; CRKL; Crk-like; del22q11; De
Early onset intellectual disability in chromosome 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; DiGeorge syndrome; Velocardiofacial syndrome; Microdeletion syndrome; 22q11 deletion syndrome; Tetralogy of Fallot; Cognitive impairment; Intellectual disability disordersSíndrome de DiGeorge; Síndrome velocardiofacial; Síndrome de microdeleción; Síndrome
Noncardiac DiGeorge syndrome diagnosed with multiplex ligation-dependent probe amplification: A case report
Keywords: سندرم DiGeorge; deletion 22q11; DiGeorge syndrome; multiplex ligation-dependent probe amplification
Short CommunicationChromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review
Keywords: سندرم DiGeorge; aCGH; array comparative genomic hybridization; OMIM; Online Mendelian Inheritance in Man; DGS; DiGeorge syndrome; VCFS; velocardiofacial syndrome; del; deletion; MLPA; multiplex ligation-dependent probe amplification; VSD; ventricular septal defect; FISH;
Short CommunicationPrenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome
Keywords: سندرم DiGeorge; sSMC; small supernumerary marker chromosome; CES; cat eye syndrome; inv dup; inverted duplication; mar; marker chromosome; LCR; low-copy repeats; DGS; DiGeorge syndrome; aCGH; array comparative genomic hybridization; IUGR; intrauterine growth restriction;
Association of IL-12p70 and IL-6:IL-10 ratio with autism-related behaviors in 22q11.2 deletion syndrome: A preliminary report
Keywords: سندرم DiGeorge; DiGeorge syndrome; Velo-cardio-facial syndrome; Autism; Repetitive behaviors; Cytokines; Immunity; Inflammation; T cell; Schizophrenia;
Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; Chromosome 22q11.2 deletion syndrome; 22q11DS; Velocardiofacial syndrome; DiGeorge syndrome; Cognitive remediation; Schizophrenia;
Subtypes in 22q11.2 deletion syndrome associated with behaviour and neurofacial morphology
Keywords: سندرم DiGeorge; Velo-cardio-facial syndrome (VCFS); 22q11.2 deletion syndrome (22q11DS); DiGeorge syndrome; Cluster analysis; k-Means; Subtype; Behavioural phenotype;
RNA binding proteins in the regulation of heart development
Keywords: سندرم DiGeorge; 3â² UTR; 3â² untranslated region; AVC; atrioventricular canal; CELF; CUG-BP, Elav-like family; CHAMP; cardiac helicase activated by MEF2 protein; Csm; cardiac-specific isoform of Mov10l1; DGCR8; DiGeorge Syndrome critical region gene 8; DM; dystrophia m
Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: Results of the first 2 years
Keywords: سندرم DiGeorge; Severe combined immunodeficiency; newborn screening; T-cell receptor excision circle; T-cell lymphopenia; DiGeorge syndrome; CHARGE; Coloboma (ocular), heart anomaly, atresia (choanal), retardation, genital and ear anomalies; CHH; Cartilage-hair hypoplasi
A longitudinal examination of the psychoeducational, neurocognitive, and psychiatric functioning in children with 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; 22q11.2 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Psychoeducational functioning in 22q11DS; Neurocognitive functioning in 22q11DS; Psychiatric functioning in 22q11DS; Schizophrenia genetics
Sindrome di DiGeorge: il caso di Laura
Keywords: سندرم DiGeorge; Sindrome di DiGeorge; Del22; Linfociti T; Ipocalcemia; DiGeorge syndrome; Del22; T lymphocytes; Hypocalcemia;
Altered Development of the Dorsolateral Prefrontal Cortex in Chromosome 22q11.2 Deletion Syndrome: An In Vivo Proton Spectroscopy Study
Keywords: سندرم DiGeorge; ADHD; chromosome 22q11.2 deletion syndrome; DiGeorge syndrome; 1H MRS; NAA; N-acetylaspartate; neuropsychology; spectroscopy; velocardiofacial syndrome
Chromosome 22 microdeletion in children with syndromic congenital heart disease by fluorescent in situ hybridization (FISH)
Keywords: سندرم DiGeorge; Chromosome 22 microdeletion; Syndromic congenital heart disease; DiGeorge syndrome; Hypocalcemia; Velocardiofacial syndrome
The neural crest in cardiac congenital anomalies
Keywords: سندرم DiGeorge; Cardiac neural crest; Aortic arch arteries; Persistent truncus arteriosus; Congentital heart defects; DiGeorge syndrome; Second heart field
Otolaryngologic Manifestations of Craniofacial Syndromes
Keywords: سندرم DiGeorge; Craniofacial; Apert syndrome; Crouzon syndrome; Treacher Collins syndrome; DiGeorge syndrome; Velocardiofacial syndrome; Opitz G/BBB syndrome; Moebius syndrome;
How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease
Keywords: سندرم DiGeorge; Neural crest; Right ventricle; DiGeorge syndrome; Heterotaxy syndrome; Cilium; Congenital heart disease;
Reactive lymphoid hyperplasia in association with 22q11.2 deletion syndrome and a BRCA2 mutation
Keywords: سندرم DiGeorge; DiGeorge syndrome; Immunodeficiency; Lymphoma; Malignancy
Adolescente con sÃndrome de deleción 22q11.2 y endocrinopatÃa múltiple
Keywords: سندرم DiGeorge; Deleción 22q11.2; SÃndrome de DiGeorge; Diabetes mellitus tipo 1; Facies asimétrica con el llanto; Manifestaciones endocrinológicas; 22q11.2 deletion; DiGeorge Syndrome; Type 1 diabetes mellitus; Facial asymmetry with crying; Endocrine manifestations;
Epstein-Barr virus–positive T-cell lymphoma cells having chromosome 22q11.2 deletion: an autopsy report of DiGeorge syndrome
Keywords: سندرم DiGeorge; EBV-associated T-cell lymphoma; DiGeorge syndrome; CAEBV; FISH
Céphalométrie du syndrome vélocardiofacial : les conséquences phonatoires de la dysmorphose
Keywords: سندرم DiGeorge; DiGeorge syndrome; Velopharyngeal insufficiency; Cephalometry; Phonation; Syndrome de DiGeorge; Insuffisance vélopharyngée; Céphalométrie; Phonation;
Discordance in diagnoses and treatment of psychiatric disorders in children and adolescents with 22q11.2 deletion syndrome
Keywords: سندرم DiGeorge; 22q11.2DS; Velocardiofacial syndrome; DiGeorge syndrome; Children/adolescents; Psychopathology; Service utilization
Partial rescue of the Tbx1 mutant heart phenotype by Fgf8: Genetic evidence of impaired tissue response to Fgf8
Keywords: سندرم DiGeorge; T-box; Cardiac outflow tract septation; DiGeorge syndrome; FGF signaling pathway; Cardiac progenitors;
22q11 chromosome abnormalities and the cleft service
Keywords: سندرم DiGeorge; 22q11 deletion syndrome; Velocardiofacial syndrome; DiGeorge syndrome; Cleft palate; Submucous cleft; Velophayngeal insuffiency
Genetic factors are important determinants of neurodevelopmental outcomes after neonatal cardiac surgery
Keywords: سندرم DiGeorge; Apolipoprotein E; Cardiac surgery; Cardiopulmonary bypass; Central nervous system; Congenital heart disease; DiGeorge syndrome; Genetics; Hypoplastic left heart syndrome; Neurodevelopment; Neurodevelopmental testing; Tetralogy of Fallot; Velo-cardio-facia
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)
Keywords: سندرم DiGeorge; DiGeorge syndrome; Th1; Th2; Allergy; Th17; B cells; Autoimmunity; Antibody
Tbx1 regulates progenitor cell proliferation in the dental epithelium by modulating Pitx2 activation of p21
Keywords: سندرم DiGeorge; Tbx1; PITX2; p21; DiGeorge syndrome; Tooth development
Juvenile myoclonic epilepsy with photosensitivity in a female with Velocardiofacial syndrome (del(22)(q11.2))—Causal relationship or coincidence?
Keywords: سندرم DiGeorge; JME; Microdeletion; 22q11.2; DiGeorge syndrome
Seizures and EEG findings in an adult patient with DiGeorge syndrome: A case report and review of the literature
Keywords: سندرم DiGeorge; 22q11.2 deletion syndrome; DiGeorge syndrome; EEG; Epilepsy; Hypocalcemia; Seizures