Keywords: agenesis corpus callosum; Corpus callosum agenesis; Corpus callosum hypoplasia; Prevalence; Prenatal diagnosis; Termination of pregnancy;
مقالات ISI agenesis corpus callosum (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: agenesis corpus callosum; Cognitive outcome; Corpus callosum agenesis; Population-based prospective study; ACC; Agenesis of the Corpus Callosum; MRI; Magnetic Resonance Imaging; WPPSI-III/WPPSI-IV; the Wechsler Pre-school and Primary Scale of Intelligence 3rd/4th edition; WISC-IV;
Keywords: agenesis corpus callosum; Motor cortex; Interhemispheric inhibition; Corpus callosum agenesis; DTI; fMRI;
Keywords: agenesis corpus callosum; Corpus callosum dysgenesis; agenesis; Hypoplasia; MRI; Diffusion tensor imaging DTI; Tractography; Child; White matter bundles; Probst bundle; Atlas; AF; arcuate fasciculus (postAF, posterior segment); CC; corpus callosum; CCD; corpus callosum dysgenesis;
Disrupted developmental organization of the structural connectome in fetuses with corpus callosum agenesis
Keywords: agenesis corpus callosum; CCA; corpus callosum agenesis; DTI; diffusion tensor imaging; FA; fractional anisotropy; FDR; false discovery rate; FWER; familywise error rate; GLM; general linear model; GW; gestational week; ROI; region of interest; SSE; sum of squares for errors; Corp
An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects
Keywords: agenesis corpus callosum; Chromosome 1p31.3; Microdeletion; NFIA gene; Corpus callosum agenesis; Craniofacial defects
160Â kb deletion in ISPD unmasking a recessive mutation in a patient with Walker-Warburg syndrome
Keywords: agenesis corpus callosum; ISPD; Walker-Warburg syndrome; Dystroglycanopathy; Hydrocephalus; Seizures; Cerebellar hypoplasia; Corpus callosum agenesis;
Interhemispheric and Quadrigeminal Cysts
Keywords: agenesis corpus callosum; Arachnoid cyst; Corpus callosum agenesis; Hydrocephalus; Intracranial cyst; Neuroendoscopy; CSF; Cerebrospinal fluid; ETV; Endoscopic third ventriculostomy; MRI; Magnetic resonance imaging;
Coffin–Siris syndrome with multiple congenital malformations and intrauterine death: Towards a better delineation of the severe end of the spectrum
Keywords: agenesis corpus callosum; Array-CGH; Brain malformation; Coffin–Siris syndrome; Corpus callosum agenesis; Dandy Walker; Intrauterine death
A 6.9 Mb 1qter deletion/4.4 Mb 18pter duplication in a boy with extreme microcephaly with simplified gyral pattern, vermis hypoplasia and corpus callosum agenesis
Keywords: agenesis corpus callosum; Array-CGH; 1qter Deletion; 18pter Duplication; Microcephaly; Simplified gyral pattern; Vermis hypoplasia; Corpus callosum agenesis; AKT3
Inherited 18q23 duplication in a fetus with multiple congenital anomalies
Keywords: agenesis corpus callosum; 18q duplication; Telomeres; Corpus callosum agenesis; Congenital heart defect; Pierre–Robin sequence; Toriello–Carey syndrome
Clinical and genetic aspects of craniofrontonasal syndrome: Towards resolving a genetic paradox
Keywords: agenesis corpus callosum; Craniofrontonasal syndrome; CFND; Hypertelorism; Corpus callosum agenesis; Midline defect; X chromosome; Ephrin-B1; EFNB1; Cellular interference; Neurocristopathology;
Aicardi syndrome
Keywords: agenesis corpus callosum; Corpus callosum agenesis; Infantile spasms; Chorioretinal abnormalities; Intracranial cysts; X-linked inheritance; Papilloma of the choroid plexus;
Prenatal diagnosis of ring chromosome 6 in a fetus with cerebellar hypoplasia and partial agenesis of corpus callosum: case report and review of the literature
Keywords: agenesis corpus callosum; Ring chromosome 6; Prenatal diagnosis; Corpus callosum agenesis; Cerebellar hypoplasia;